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<i>Lagotis yunnanensis<_i> W. W. Smith

" in MedChemExpress (MCE) Product Catalog:

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Transcriptase (4) RIP kinase (5) ROCK (9) ROR (2) ROS Kinase (3) RSV (2) SARS-CoV (13) Ser/Thr Protease (2) Serotonin Transporter (3) SF3B1 (1) SHMT (1) SHP2 (2) Sigma Receptor (1) Sirtuin (2) Small Interfering RNA (siRNA) (19) Sodium Channel (23) Somatostatin Receptor (2) SphK (4) Src (2) STAT (18) Stearoyl-CoA Desaturase (SCD) (1) Steroid Sulfatase (1) STING (16) Survivin (4) TAM Receptor (3) Tau Protein (1) TGF-beta/Smad (8) TGF-β Receptor (30) Thymidylate Synthase (1) Thyroid Hormone Receptor (3) TMV (3) TNF Receptor (19) Toll-like Receptor (TLR) (12) Topoisomerase (186) Transketolase (1) Transthyretin (TTR) (5) Trk Receptor (5) TROP2 (1) TRP Channel (7) TrxR (3) Tyrosinase (6) URAT1 (1) VD/VDR (3) VEGFR (12) Wnt (5) Xanthine Oxidase (2) YAP (4) α-synuclein (3) β-catenin (4) γ-secretase (1)
By Research Areas:	Cancer (1221) Cardiovascular Disease (206) Endocrinology (89) Infection (298) Inflammation/Immunology (376) Metabolic Disease (237) Neurological Disease (294)
Click Chemistry:	TCO (1) DBCO (2) Azide (22) Tetrazine (2) Alkynes (15)
Oligonucleotides:	miRNA mimics (10) Solvents (1) miRNA antagomirs (10) Nucleosides and their Analogs (33) Thickeners (1) Nucleoside Phosphoramidites (5) Flavoring Agents (1) miRNA inhibitors (10) Phospholipids (2) Solubilizing Agents (1) mRNA (3) Antisense Oligonucleotides (2) Bases (1) siRNAs (18) miRNA agomirs (10) MicroRNAs (40) Aptamers (5) Pre-designed siRNA Sets (18) Emulsifiers (1) Polymers (1)

2941

Inhibitors & Agonists

Screening Libraries

145

Fluorescent Dye

Biochemical Assay Reagents

252

Peptides

MCE Kits

Inhibitory Antibodies

461

Natural
Products

373

Recombinant Proteins

332

Isotope-Labeled Compounds

140

Antibodies

Click Chemistry

113

Oligonucleotides

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-16992A

W-54011 5 Publications Verification	Complement System Reactive Oxygen Species	Inflammation/Immunology
W-54011 is a potent and orally active non-peptide C5a receptor antagonist. W-54011 inhibits the binding of ¹²⁵I-labeled C5a to human neutrophils with a K_i value of 2.2 nM. W-54011 also inhibits C5a-induced intracellular Ca ²⁺ mobilization, chemotaxis, and generation of ROS in human neutrophils with IC₅₀s of 3.1 nM, 2.7 nM, and 1.6 nM, respectively .

HY-100911

W-5 hydrochloride	Calmodulin	Neurological Disease
W-5 hydrochloride is a calmodulin antagonist. W-5 hydrochloride inhibits phosphodiesterase activation with an IC₅₀ value of 240 µM. W-5 hydrochloride can be used as a negative control for W-7 (HY-100912) .

HY-100913

W-7 isomer hydrochloride	Calmodulin	Cancer
W-7 isomer hydrochloride is an isomer of W-7 hydrochloride (HY-100912). W-7 hydrochloride is a selective calmodulin antagonist .

HY-100912

W-7 hydrochloride 5 Publications Verification	Phosphodiesterase (PDE) Myosin Apoptosis Calmodulin	Cancer
W-7 hydrochloride is a selective calmodulin antagonist. W-7 hydrochloride inhibits the Ca ²⁺-calmodulin-dependent phosphodiesterase and myosin light chain kinase with IC₅₀ values of 28 μM and 51 μM, respectively . W-7 hydrochloride induces apoptosis and has antitumor activity .

HY-100910

W-13 hydrochloride	CaMK	Cancer
W-13 hydrochloride is a calmodulin antagonist. W-13 hydrochloride can inhibit Tamoxifen (HY-13757A)-resistant human breast cancer cell growth .

HY-145482

W36017	Drug Metabolite	Neurological Disease
W3601 is the impurity of Lidocaine. W3601 exhibits nerve blocking activity with the pK_a of 7.4 .

HY-163106

W000113414_I13	Ceramidase	Cancer
W000113414_I13 is an acid ceramidase (AC) inhibitor. W000113414_I13 exhibits dose-dependent inhibition of AC with an IC₅₀ value of 6.6?μM. W000113414_I13 can be used for the research of cancer .

HY-Y0407A

Tetrapropylammonium hydroxide (40% w/w in water) TPAOH (40% w/w in water)	Biochemical Assay Reagents	Others
Tetrapropylammonium hydroxide (40% w/w in water)It is a compound belonging to the class of quaternary ammonium compounds and is a strong base with cationic properties. Tetrapropylammonium hydroxide (40% w/w in water)It is usually used as a phase transfer catalyst to promote the transfer of reactants between immiscible phases in various organic synthesis reactions. It is also used in the production of semiconductors, especially the manufacture of thin-film transistors and other electronic devices.

HY-145012S

W-19-d4 hydrochloride	Isotope-Labeled Compounds	Others
W-19-d₄ (hydrochloride) is the deuterium labeled W-19 hydrochloride[1].

HY-145415

W13	Bacterial	Infection
W13 is a potent MsbA inhibitor. W13 is an ATPase stimulator with an EC₅₀ of 5.5 µM .

HY-107928B

Iron–Dextran(Fe 35-40% w/w)	Biochemical Assay Reagents	Others
Iron–Dextran(Fe 35-40% w/w) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-100979

W-84 dibromide HDMPPA	mAChR	Others
W-84 (dibromide) is a potent allosteric modulator of M2-cholinoceptors, which retards [ ³H]N-methylscopolamine dissociation. W-84 dibromide can stabilize cholinergic antagonist-receptor complexes. W-84 (dibromide) is a non-competitive muscarinic acetylcholine receptors antagonist with allosteric effects. W-84 (dibromide) protects over additively against an organophosphate-intoxication when applied in combination with atropine .

HY-163192

W6134	ROR	Cancer
W6134 is highly potent and selective RORγ covalent inhibitor with IC₅₀ of 0.21 μM. W6134 exhibits superior activity ini nhibiting the proliferation and colony formation and inducing apoptosis. W6134 can be used for the research of cancer .

HY-18731

1400W Dihydrochloride 10+ Cited Publications	NO Synthase Apoptosis	Cardiovascular Disease Inflammation/Immunology Cancer
1400W dihydrochloride is the dihydrochloride form of 1400W (HY-18730). 1400W is a slow, tight binding, and highly selective inducible nitric-oxide synthase (iNOS) inhibitor, with a K_d value ≤ 7 nM. 1400W inhibits iNOS induction in microglial cells, and reduces generation of NO, thereby mitigating oxidative stress and neuronal cell apoptosis in the rat cerebral cortex, and improving the spatial memory dysfunction caused by acute hypobaric hypoxia-reoxygenation .

HY-168035

W4275	Histone Methyltransferase	Cancer
W4275 (Compound 42) is a selective NSD2 inhibitor with oral activity, showing an IC₅₀ value of 17 nM. W4275 exhibits antiproliferative activity with an IC₅₀ of 230 nM against RS411 cells and significantly inhibits tumor growth in the RS411 tumor xenograft model. Pharmacokinetic analysis in mice demonstrates that W4275 has good oral bioavailability (F of 27.34%). W4275 holds promise for use in cancer research .

HY-N8097

Kushenol W	Bacterial	Infection
Kushenol W is a prenylated flavonoid that can be isolated from the root of Sophora flavescens. Kushenol W has antimicrobial effect, with a MIC of 10 μg/mL for Staphylococcus aureus .

HY-18730

1400W W1400	NO Synthase Apoptosis	Cardiovascular Disease Inflammation/Immunology Cancer
1400W is a slow, tight binding, and highly selective inducible nitric-oxide synthase (iNOS) inhibitor, with a K_d value ≤ 7 nM. 1400W inhibits iNOS induction in microglial cells, and reduces generation of NO, thereby mitigating oxidative stress and neuronal cell apoptosis in the rat cerebral cortex, and improving the spatial memory dysfunction caused by acute hypobaric hypoxia-reoxygenation .

HY-153190

W1131	Oxidative Phosphorylation STAT Ferroptosis	Cancer
W1131 is a potent STAT3 inhibitor, triggering ferroptosis. W1131 suppresses cancer progression in gastric cancer cell subcutaneous xenograft model, organoids model, and PDX model. W1131 effectively alleviates chemical resistance of cancer cells to 5-FU (HY-90006). W1131 regulates cell cycle, DNA damage response, and oxidative phosphorylation, including IL6-JAK-STAT3 pathway and ferroptosis pathway .

HY-19282A

(5R)-BW-4030W92	Sodium Channel	Neurological Disease
(5R)-BW-4030W92 is the R enantiomer of BW-4030W92. BW-4030W92 is a non-selective, voltage-, and use-dependent sodium channel antagonist.

HY-153190A

W1131 TFA	Ferroptosis STAT	Cancer
W1131 TFA is a potent STAT3 inhibitor that induces ferroptosis. W1131 inhibits cancer progression in subcutaneous xenograft, organoid, and PDX models of gastric cancer. W1131 effectively alleviates cancer cell chemoresistance to 5-FU (HY-90006). W1131 regulates the cell cycle, DNA damage response, and oxidative phosphorylation, including the IL6-JAK-STAT3 pathway and the ferroptosis pathway .

HY-U00204

Nisobamate W1015	Others	Neurological Disease
Nisobamate (W1015) is a tranquilizer.

HY-118311

(Z)-W 3699 (Z)-Probilin; (Z)-Secrebil; (Z)-Piprozolin	Others	Metabolic Disease
(Z)-W 3699 is a potential choleretic. (Z)-W 3699 can increase the solubility of cholesterol in the gallbladder by altering the secretion of micellar bile acids. (Z)-W 3699 can prevent the formation of cholesterol-containing gallstones in dogs.

HY-116088

W123	LPL Receptor	Inflammation/Immunology
W123, a FTY720 analog, is a competitive sphingosine 1-phosphate type 1 (S1P1) receptor antagonist. W123 is measured by GTPγS activation, MAPK recruitment, cell migration, and ligand-induced receptor internalization .

HY-P1175

L-R4W2	TRP Channel	Neurological Disease
L-R4W2 is a potent antagonist of vanilloid receptor 1 (VR1, TRPV1), with an IC₅₀ of 0.1 μM. L-R4W2 may act as a potent analgesic .

HY-19264

264W94	Apical Sodium-Dependent Bile Acid Transporter	Metabolic Disease
264W94 is a potent ileal bile acid transporter (IBAT) inhibitor and a new cholesterol lowering agent. 264W94 has CYP7A1 induction, and antilipemic action .

HY-N5154

Sanggenon W	Others	Others
Sanggenon W is an isoprenyl flavonoid extracted from mulberry root bark .

HY-106537

W 3699 Probilin; Secrebil; Piprozolin	Others	Metabolic Disease
W 3699 (Probilin; Secrebil; Piprozolin) is a choleretic agent that 参 be used in the study of biliary diseases .

HY-N1262

Scutebarbatine W Scutehenanine B	Others	Inflammation/Immunology
Scutebarbatine W is a 13-spiro subtype neo-clerodane diterpenoid. Scutebarbatine W inhibits NO production with an IC₅₀ value of 34.7 μM .

HY-N7294

Taxuspine W	Others	Others
Taxuspine W is a natural product, that can be isolated from the Japanese Yew Taxus cuspidata .

HY-N11531

Kuwanon W	Others	Others
Kuwanon W is a natural product that can be isolated from the root bark of Morus lhou .

HY-100174

W-2429 NSC294836	Others	Neurological Disease
W-2429 (NSC294836) is considerably more effective than acetylsalicylic acid in inhibiting carrageenan-induced edema and in reducing brewer's yeast-induced fever in rats .

HY-P3087

Tyr-W-MIF-1	Opioid Receptor	Neurological Disease
Tyr-W-MIF-1 is an opioid tetrapeptide with opiate and antiopiate activity. Tyr-W-MIF-1 can induce analgesia .

HY-143665S

Nor-W-18-d4	Isotope-Labeled Compounds	Others
Nor-W-18-d₄ is the deuterium labeled Nor-W-18[1].

HY-107094

MT-7716 hydrochloride W-212393 hydrochloride	Opioid Receptor	Neurological Disease
MT-7716 hydrochloride (W-212393 hydrochloride) is a selective non-peptide nociceptin receptor (NOP) agonist and promising potential treatment drug for alcohol abuse and relapse prevention .

HY-122491

Dimethyl-W84 dibromide	mAChR	Neurological Disease
Dimethyl-W84 (dibromide) modulates M2 muscarinic acetylcholine receptors. Dimethyl-W84 (dibromide) can be used in nervous system related research .

HY-B2056

Triforine CELA W 524	Fungal	Infection Inflammation/Immunology
Triforine (CELA W 524), a systemic fungicide, was shown to display a moderate to distinct fungitoxic activity in vitro towards several pathogenic and non-pathogenic fungi .

HY-P1175A

L-R4W2 TFA	TRP Channel	Neurological Disease
L-R4W2 TFA is a potent antagonist of vanilloid receptor 1 (VR1, TRPV1), with an IC₅₀ of 0.1 μM. L-R4W2 TFA may act as a potent analgesic .

HY-B2081

Etozolin W-2900A	Others	Cardiovascular Disease Metabolic Disease
Etozolin (W-2900A) is a diuretic agent. Etozolin inhibits fluid and electrolyte reabsorption in the loop of Henle. Etozolin can be used in research of congestive heart failure, hypertension and edema .

HY-B0184A

Felbamate hydrate W-554 hydrate; ADD-03055 hydrate	iGluR	Neurological Disease
Felbamate hydrate (W-554 hydrate) is a potent nonsedative anticonvulsant whose clinical effect may be related to the inhibition of N-methyl-D-aspartate (NMDA) .

HY-B0184

Felbamate 1 Publications Verification W-554; ADD-03055	iGluR	Neurological Disease
Felbamate (W-554) is a potent nonsedative anticonvulsant whose clinical effect may be related to the inhibition of N-methyl-D-aspartate (NMDA).

HY-P10287

Neuropeptide W-30 (human) NPW30, human	Neuropeptide B/W Receptor	Neurological Disease
Neuropeptide W-30 (human) is an important stress mediator in the central nervous system that modulates the hypothalamus-pituitary-adrenal (HPA) axis and sympathetic outflow. Neuropeptide W-30 (human) is an endogenous ligand for the two structurally related orphan G-protein-coupled receptors (GPCRs) GPR7 and GPR8. Neuropeptide W-30 (human) activates and binds to both GPR7 and GPR8 at similar effective doses .

HY-101395

W146 1 Publications Verification	LPL Receptor Apoptosis	Metabolic Disease Cancer
W146 is a selective antagonist of sphingosine-1-phosphate receptor 1 (S1PR1) with an EC₅₀ value of 398 nM.

HY-U00157

Meseclazone W2395; NSC297623	Others	Inflammation/Immunology
Meseclazone (W2395;NSC297623) exhibits inhibitory potency of secondary phase ADP aggregation. Meseclazone possesses anti-inflammatory, analgesic and antipyretic activity.

HY-P5082

α-Synuclein 4554W	α-synuclein	Neurological Disease
α-Synuclein 4554W is an inhibitor of α-Synuclein (aSyn) aggregation with associated toxicity. α-Synuclein 4554W consists of GIVNGVKA sequences, previously identified through intracellular library screening. α-Synuclein 4554W reduces fibril formation of aSyn mutants assocaited with Parkinson’s disease .

HY-R01701

hsa-miR-548w mimic	MicroRNA	Cancer
hsa-miR-548w mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.

hsa-miR-548w mimic hsa-miR-548w mimic

HY-150755

Topo I/COX-2-IN-2	Topoisomerase COX Apoptosis Reactive Oxygen Species	Cancer
Topo I/COX-2-IN-2 (Compound W10) is a potent dual-target inhibitor of Topo I and COX-2 with IC₅₀ values of 0.90 μM and 2.31 μM, respectively. Topo I/COX-2-IN-2 induces cancer cell apoptosis through the mitochondrial pathway .

HY-136908

W140 TFA	Biochemical Assay Reagents	Others
W140 (TFA) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-101578

2614W94	Monoamine Oxidase	Neurological Disease
2614W94 is a selective, reversible inhibitor of monoamine oxidase-A with a competitive mechanism of inhibition and IC₅₀ of 5 nM and K_i of 1.6 nM with serotonin as substrate.

HY-107094A

MT-7716 free base W-212393	Opioid Receptor	Neurological Disease
MT-7716 free base (W-212393) is a selective non-peptide nociceptin receptor (NOP) agonist and promising potential treatment drug for alcohol abuse and relapse prevention .

HY-101395A

W146 TFA 1 Publications Verification	LPL Receptor Apoptosis	Metabolic Disease Cancer
W146 TFA is a selective antagonist of sphingosine-1-phosphate receptor 1 (S1PR1) with an EC₅₀ value of 398 nM.

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-N11531

Kuwanon W	Structural Classification Flavonoids Flavones Source classification Plants Moraceae Morus alba Linn.	Others
Kuwanon W is a natural product that can be isolated from the root bark of Morus lhou .

HY-N8097

Kushenol W	Infection Flavonoids Classification of Application Fields Leguminosae Flavonones Source classification Phenols Polyphenols Plants Sophora flavescens Aiton Disease Research Fields	Bacterial
Kushenol W is a prenylated flavonoid that can be isolated from the root of Sophora flavescens. Kushenol W has antimicrobial effect, with a MIC of 10 μg/mL for Staphylococcus aureus .

HY-N5154

Sanggenon W	Structural Classification Flavonoids Flavones Source classification Plants Moraceae Morus alba Linn.	Others
Sanggenon W is an isoprenyl flavonoid extracted from mulberry root bark .

HY-N1262

Scutebarbatine W Scutehenanine B	Structural Classification Terpenoids Labiatae Source classification Derris robusta Diterpenoids Plants	Others
Scutebarbatine W is a 13-spiro subtype neo-clerodane diterpenoid. Scutebarbatine W inhibits NO production with an IC₅₀ value of 34.7 μM .

HY-N7294

Taxuspine W	Structural Classification Taxus cuspidata Siebold & Zucc. Ketones, Aldehydes, Acids Source classification Taxaceae Plants	Others
Taxuspine W is a natural product, that can be isolated from the Japanese Yew Taxus cuspidata .

HY-122949

Momordicine I	Triterpenes Structural Classification Terpenoids Source classification Cucurbitaceae Plants Momordica charantia Linn.	DGK
Momordicine I, a triterpenoid compound extracted from momordica charantia L. Momordicine I alleviates isoproterenol-induced cardiomyocyte hypertrophy through suppression of PLA2G6 and DGK-ζ .

HY-121050

Ambruticin W7783	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Fungal
Ambruticin (W7783) is an orally active and potent antifungal antibiotic. Ambruticin represents a class of antibiotics, that can be isolated from a strain of Polyangium cellulosum var. fulvum, a bacterium belonging to the class Myxobacteriales. Ambruticin is a cyclopropyl-polyene-pyran acid and is active against fungi .

HY-N12370

Tenaxin I	Structural Classification Flavonoids Flavones Labiatae Source classification Plants Medicago truncatula Gaertn.	Others
Tenaxin I is a component extracted from Radix Scutellariae with neuraminidase inhibitory activity .

HY-N12073

Monofucosyllacto-N-hexaose I MFLNH I	Structural Classification Polysaccharides Animals Source classification Saccharides	Others
Monofucosyllacto-N-hexaose I (MFLNH I) is a composition of human milk oligosaccharide .

HY-N2013R

Aristolactam I (Standard)	Structural Classification Natural Products other families Source classification Plants	Caspase Apoptosis
Aristolactam I (Standard) is the analytical standard of Aristolactam I. This product is intended for research and analytical applications. Aristololactam I (AL-I), is the main metabolite of aristolochic acid I (AA-I), participates in the processes that lead to renal damage. Aristololactam I (AL-I) directly injures renal proximal tubule cells, the cytotoxic potency of AL-I is higher than that of AA-I and that the cytotoxic effects of these molecules are mediated through the induction of apoptosis in a caspase-3-dependent pathway .

HY-P3055

Dendrotoxin-I DTX-I	Structural Classification Animals Cyclopeptides Source classification Animal Venoms	Potassium Channel
Dendrotoxin-I (DTX-I) is a potent K ⁺ channels blocker with IC₅₀s of 0.13-50 nM for voltage-gated potassium channel subunits K_V1.1, K_V1.2 and K_V1.6, respectively. Dendrotoxin-I, a neurotoxin, has the potential for cancer research .

HY-N11172

Schibitubin I	Structural Classification Source classification Lignans Schisandra bicolor Cheng Phenylpropanoids Plants Schisandraceae	Others
Schibitubin I is a lignin. Schibitubin I has neuroprotective activity. Schibitubin I can be isolated from the fruits of Schisandra bicolor var. tuberculata .

HY-N12727

Okaramine I	Structural Classification Alkaloids Microorganisms Source classification Indole Alkaloids	Bacterial
Okaramine I is an Escherichia coli glycosyltransferase (MurG) inhibitor. Okaramine I can be used as an antibacterial agent. Okaramine I can be found in Aspergillus aculeatus .

HY-N12316

Goshuyuamide I	Structural Classification Alkaloids Source classification Evodia rutaecarpa (Juss.) Benth. Rutaceae Plants Indole Alkaloids	Others
Goshuyuamide-I (compound 4) is a kind of alkaloid. Goshuyuamide-I can be isolated from the fruits of Euodia rutaecarpa. Goshuyuamide-I can be used in the research of analgesics .

HY-107301

Dehydrosoyasaponin I Soyasaponin Be; DHS-I	Structural Classification Polysaccharides Leguminosae Source classification Plants Saccharides Medicago sativa L.	Potassium Channel
Dehydrosoyasaponin I (Soyasaponin Be;DHS-I), a triterpene glycoside, is a potent and reversible calcium-activated potassium (maxi-K) channels activator .

HY-N0407R

Picroside I (Standard)	Structural Classification Iridoids Terpenoids Source classification Scrophulariaceae Plants Picrorhiza scrophulariiflora Pennell	STAT
Picroside I (Standard) is the analytical standard of Picroside I. This product is intended for research and analytical applications. Picroside I is the major ingredient of Picrorhiza scrophulariiflora. Picrorhiza scrophulariiflora is a high value medicinal herb due to rich source of hepatoprotective metabolites, Picroside-I and Picroside-II . Picroside I is a promising agent for the management of asthma. Picroside I reduces the inflammation significantly at its higher dose. Picroside I also downregulates pSTAT6 and GATA3 expressions. Picroside I dose-dependently increases the serum levels of IFN-γ .

HY-N2013

Aristolactam I 1 Publications Verification Aristololactam; Aristolactam	Structural Classification Natural Products other families Classification of Application Fields Source classification Plants Inflammation/Immunology Disease Research Fields	Caspase Apoptosis
Aristololactam I (AL-I), is the main metabolite of aristolochic acid I (AA-I), participates in the processes that lead to renal damage. Aristololactam I (AL-I) directly injures renal proximal tubule cells, the cytotoxic potency of AL-I is higher than that of AA-I and that the cytotoxic effects of these molecules are mediated through the induction of apoptosis in a caspase-3-dependent pathway .

HY-N1628

1β-Hydroxybaccatin I 1-Hydroxybaccatin I	Structural Classification Terpenoids Source classification Taxaceae Diterpenoids Plants Taxus wallichiana Zucc.	Others
1β-Hydroxybaccatin I (1-Hydroxybaccatin I) can be extracted from Taxus wallichiana .

HY-N8171

Lagotisoide D 10-O-[(E)-3,4-Dimethoxycinnamoyl]-catalpol	Iridoids Classification of Application Fields Simple Phenylpropanols Terpenoids Source classification Other Diseases Scrophulariaceae Lagotis yunnanensis W. W. Smith Phenylpropanoids Plants Disease Research Fields	Others
Lagotisoide D is a lridoid glycoside from Lagotis yunnanensis .

HY-N11430

F1839-I	Structural Classification Monophenols Microorganisms Source classification Phenols	HIV
F1839-I is a compound that can be isolated from Stachybotrys. F1839-I has weak cytotoxicity and anti-HIV activity with an IC₅₀ value of 15.6 μM .

HY-N10076

Ganomycin I	Structural Classification Microorganisms Source classification Phenols Polyphenols	HMG-CoA Reductase (HMGCR) Glucosidase HIV Protease
Ganomycin I is a dual inhibitor of α-Glucosidase and HMG-CoA reductase. Ganomycin I can also inhibits HIV protease. Ganomycin I exhibits anti-diabetic and anti-osteoclastogenesis effects .

HY-N11455

Lacto-N-difucohexaose I LDFH I	Structural Classification Polysaccharides Microorganisms Source classification Saccharides	Others
Lacto-N-difucohexaose I (LNDFH I), a linker, could be used to combine oligosaccharides containing Lewis b sugar chain to water insoluble polysaccharide .

HY-N3340

Macrocarpal I	Structural Classification Terpenoids Sesquiterpenes Source classification Phenols Polyphenols Myrtaceae Plants Eucalyptus globulus Labill.	Fungal
Macrocarpal I is a phloroglucinol coupled sesquiterpenoid with antifungal activity. Macrocarpal I against C. glabrata with an IC₅₀ value of 0.75 μg/mL. Macrocarpal I can be isolated from the juvenile leaves of E. maideni .

HY-N7141R

Spiramycin I (Standard)	Structural Classification Microorganisms Macrolide Antibiotics Antibiotics Source classification Anti-parasitic Disease Research	Parasite Antibiotic Bacterial
Spiramycin I (Standard) is the analytical standard of Spiramycin I. This product is intended for research and analytical applications. Spiramycin I is a macrolide antibiotic and antiparasitic .

HY-N8511

Acremine I	Structural Classification Natural Products Microorganisms Source classification	Fungal
Acremine I is a fungi inhibitor and also a metabolite of the endophytic fungus Acremonium byssoides. Acremine I can effectively inhibit Plasmopara viticola. Acremine I can be used for research on plant diseases, such as grape downy mildew .

HY-N8293

Eupalinolide I	Structural Classification Melilotus albus Desr. Terpenoids Sesquiterpenes Source classification Plants Compositae	Others
Eupalinolide I inhibits the viability of breast cancer cells. Eupalinolide I can be isolated from Eupatorium lindleyanum .

HY-B1411R

i-Inositol (Standard)	Structural Classification Natural Products Human Gut Microbiota Metabolites Immune System Disorder Microorganisms Source classification Disease markers Endocrine diseases Endogenous metabolite	Endogenous Metabolite
i-Inositol (Standard) is the analytical standard of i-Inositol. This product is intended for research and analytical applications. i-Inositol (myo-Inositol) is a compound of sugar alcohols. i-Inositol is involved in a series of biological processes such as insulin signal transduction and cytoskeletal transduction. i-Inositol mainly exists in glial cells and plays an osmotic role .

HY-N0612R

Siamenoside I (Standard)	Triterpenes Structural Classification Terpenoids Source classification Cucurbitaceae Siraitia grosvenorii (Swingle) C. Jeffrey ex Lu et Z. Y. Zhang Plants	Others
Siamenoside I (Standard) is the analytical standard of Siamenoside I. This product is intended for research and analytical applications. Siamenoside I is one of the mogrosides that has several kinds of bioactivities.

HY-N0331

Ziyuglycoside I	Triterpenes Structural Classification Classification of Application Fields Sanguisorba officinalis Linn. Terpenoids Source classification Rosaceae Plants Disease Research Fields Cancer	MDM-2/p53 Apoptosis
Ziyuglycoside I isolated from S. officinalis root, has anti-wrinkle activity, and increases the expression of type I collagen. Ziyuglycoside I could be used as an active ingredient for cosmetics . Ziyuglycoside I triggers cell cycle arrest and apoptosis mediated by p53, it can be a potential agent candidate for treating triple-negative breast cancer (TNBC) .

HY-N12127

Gymnoside I	Orchidaceae Gymnadenia conopsea (L.) R. Br. Source classification Plants	Others
Gymnoside I (compound 1) is a glycosidoxybenzyl 2-isobutylmalic acid. Gymnoside I shows antiallergic activity in passive cutaneous allergic reaction (PCA) in mice. Gymnoside I can be used in research to treat asthma, neurasthenia and chronic hepatitis .

HY-N8614

Peucedanocoumarin I	Structural Classification Natural Products Chrysanthemum × morifolium (Ramat.) Hemsl. Source classification Plants Umbelliferae	Others
Peucedanocoumarin I (compound 1) is a kind of dihydropyranocoumarin. Peucedanocoumarin I can be isolated from the root of f Peucedanum praeruptorum .

HY-N12718

Campneoside I	Structural Classification Source classification Phenols Polyphenols Bignoniaceae Plants Incarvillea compacta Maxim.	Others
Campneoside I is a bitter phenyl propanoid glycoside. Campneoside I can be isolated from the roots of Incarvillea compacta .

HY-N7218

Lysolipin I	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Bacterial
Lysolipin I is a lipophilic antibiotic from Streptomyces violaceoniger. Lysolipin I is active against Gram-positive and Gramnegative bacteria .

HY-N0331R

Ziyuglycoside I (Standard)	Triterpenes Structural Classification Sanguisorba officinalis Linn. Terpenoids Source classification Rosaceae Plants	MDM-2/p53 Apoptosis
Ziyuglycoside I (Standard) is the analytical standard of Ziyuglycoside I. This product is intended for research and analytical applications. Ziyuglycoside I isolated from S. officinalis root, has anti-wrinkle activity, and increases the expression of type I collagen. Ziyuglycoside I could be used as an active ingredient for cosmetics . Ziyuglycoside I triggers cell cycle arrest and apoptosis mediated by p53, it can be a potential agent candidate for treating triple-negative breast cancer (TNBC) .

HY-W019806

Lacto-N-fucopentaose I LNFP I	Infection Structural Classification Natural Products Polysaccharides Classification of Application Fields Animals Inflammation/Immunology Disease Research Fields Saccharides	Endogenous Metabolite CDK Reactive Oxygen Species Apoptosis Enterovirus Bacterial
Lacto-N-fucopentaose I (LNFPI) is a human milk oligosaccharide (HMO), possessing antiviral and antibacterial activity. Lacto-N-fucopentaose I can reduce capsid protein VP1 to block virus adsorption, promote CDK2 and reduce cyclin E to recover cell cycle S phase block. Lacto-N-fucopentaose I inhibits ROS production and apoptosis in virus-infected cells. Lacto-N-fucopentaose I can also regulate intestinal microbiota to affect immune system development .

HY-N0432R

Astragaloside I (Standard)	Triterpenes Structural Classification other families Leguminosae Terpenoids Source classification Astragalus membranaceus var. mongholicus (Bunge)P.K.Hsiao Plants	Wnt β-catenin
Astragaloside I (Standard) is the analytical standard of Astragaloside I. This product is intended for research and analytical applications. Astragaloside I, one of the main active ingredients in Astragalus membranaceus, has osteogenic properties. Astragaloside I stimulates osteoblast differentiation through the Wnt/β-catenin signaling pathway .

HY-N7022R

Eclalbasaponin I (Standard)	Triterpenes Structural Classification other families Terpenoids Source classification Plants	Others
Eclalbasaponin I (Standard) is the analytical standard of Eclalbasaponin I. This product is intended for research and analytical applications. Eclalbasaponin I is isolated from Eclipta prostrata L with antitumor activity. Eclalbasaponin I inhibits the proliferation of hepatoma cell smmc-7721 with an IC₅₀ value of 111.1703 μg/ml .

HY-N2541

Gymnemic acid I	Triterpenes Classification of Application Fields Terpenoids Source classification Asclepiadaceae Metabolic Disease Plants Disease Research Fields Gymnema sylvestre (Retz.) Schult.	Apoptosis Autophagy
Gymnemic acid I is a bioactive triterpene saponin found in Gymnema sylvestre. Gymnemic acid I decreases the apoptosis under the high glucose stress .

HY-122530

Juvocimene I	Structural Classification Natural Products Ocimum basilicum L. Labiatae Source classification Plants	Others
Juvocimene I is a potent juvenile hormone mimic. Juvocimene I can be isolated from the essential oil of sweet basil,Ocimum basilicum L .

HY-N0360R

Dihydrotanshinone I (Standard)	Quinones Structural Classification Labiatae Samanea saman (Jacq.) Merr. Source classification Plants Phenanthrenequinones	SARS-CoV
Dihydrotanshinone I (Standard) is the analytical standard of Dihydrotanshinone I. This product is intended for research and analytical applications. Dihydrotanshinone I is a natural compound extracted from Salvia miltiorrhiza Bunge which has been widely used for treating cardiovascular diseases. Dihydrotanshinone I exhibits entry-blocking effect for MERS-CoV.

HY-N0890R

Tubeimoside I (Standard)	Triterpenes Structural Classification Terpenoids Source classification Cucurbitaceae Plants Bolbostemma paniculaum (Maxim)Franguet	Apoptosis
Tubeimoside I (Standard) is the analytical standard of Tubeimoside I. This product is intended for research and analytical applications.

HY-126476

Justicisaponin I	Justicia rotundifolia Nees Triterpenes Structural Classification Acanthaceae Terpenoids Source classification Plants	Others
Justicisaponin I can be used as an anti-fertility agent. Justicisaponin I stabilizes the acrosome membrane of sperm, and inhibits the release of acid hydrolase and sperm proteins .

HY-N1939R

Icariside I (Standard)	Flavonols Structural Classification Monophenols Flavonoids Source classification Phenols Epimedium brevicornu Maxim. Plants Berberidaceae	Others
Icariside I (Standard) is the analytical standard of Icariside I. This product is intended for research and analytical applications. Icariside I is a metabolite of Icarlin, which could regulate bone remodeling and is recognized as an effective agent for the treatment of osteoporosis.

HY-N8355

Beauveriolide I	Infection Alkaloids Structural Classification Microorganisms Classification of Application Fields Source classification Disease Research Fields	Endogenous Metabolite
Beauveriolide I is the metabolite of Entomopathogenic Fungi Beauveria sp.. Beauveriolide I (1) exhibits moderate insecticidal activities against Spodoptera litura and Callosobruchus chinensis .

HY-N0047R

Polyphyllin I (Standard)	Structural Classification Liliaceae Paris polyphylla Smith Plants Saccharides Steroids	JNK mTOR Akt PDK-1 Autophagy Apoptosis
Polyphyllin I (Standard) is the analytical standard of Polyphyllin I. This product is intended for research and analytical applications. Polyphyllin I is a bioactive constituent extracted from Paris polyphylla, has strong anti-tumor activity. Polyphyllin I is an activator of the JNK signaling pathway and is an inhibitor of PDK1/Akt/mTOR signaling. Polyphyllin I induces autophagy, G2/M phase arrest and apoptosis .

HY-N7052

Tubulysin I	Structural Classification Monophenols Microorganisms Classification of Application Fields Ketones, Aldehydes, Acids Source classification Phenols Disease Research Fields Cancer	ADC Cytotoxin Microtubule/Tubulin
Tubulysin I is a highly cytotoxic anti-microtubule toxin (anti-microtubule toxins) that is synthesized as an ADC cytotoxin (ADC Cytotoxin). Tubulysin I can be isolated from the myxobacteria Archangium geophyra and Angiococcus disciformis. Tubulysin I displays extremely potent cytotoxic activity in mammalian cells, including multidrug-resistant cell lines, with IC₅₀ values in the low nanomolar range. Tubulysin I inhibits microtubule/tubulin polymerization and leads to cell cycle arrest and apoptosis .

HY-N1985

Acetylastragaloside I	Structural Classification Natural Products Leguminosae Astragalus membranaceus var. mongholicus (Bunge)P.K.Hsiao Plants	Parasite
Acetylastragaloside I is a glycoside that can be isolated from the roots of Astragalus baibutensis. Acetylastragaloside I is the first cycloartane-type triterpene with remarkable trypanocidal activity with IC₅₀ values of 9.5 and 5.0 μg/mL for *T. brucei rhodesiense* and *T. cruzi*, respectively. Acetylastragaloside I can be used for the research of trypanosome infection .

HY-N0407

Picroside I 6'-Cinnamoylcatalpol	Structural Classification Iridoids Classification of Application Fields Terpenoids Source classification Scrophulariaceae Plants Picrorhiza scrophulariiflora Pennell Inflammation/Immunology Disease Research Fields	STAT
Picroside I is the major ingredient of Picrorhiza scrophulariiflora. Picrorhiza scrophulariiflora is a high value medicinal herb due to rich source of hepatoprotective metabolites, Picroside-I and Picroside-II . Picroside I is a promising agent for the management of asthma. Picroside I reduces the inflammation significantly at its higher dose. Picroside I also downregulates pSTAT6 and GATA3 expressions. Picroside I dose-dependently increases the serum levels of IFN-γ .

HY-N0887

Isoastragaloside I 1 Publications Verification Isoastragaloside-I	Triterpenes Structural Classification other families Classification of Application Fields Leguminosae Terpenoids Source classification Metabolic Disease Astragalus membranaceus var. mongholicus (Bunge)P.K.Hsiao Plants Disease Research Fields	Others
Isoastragaloside I is a natural compound from the medicinal herb Radix Astragali; possesses the activity of elevating adiponectin production.

HY-N1939

Icariside I Icarisid I	Flavonols Structural Classification Monophenols Flavonoids Classification of Application Fields Source classification Other Diseases Phenols Epimedium brevicornu Maxim. Plants Berberidaceae Disease Research Fields	Others
Icariside I is a metabolite of Icarlin, which could regulate bone remodeling and is recognized as an effective agent for the treatment of osteoporosis.

Cat. No.	Product Name	Chemical Structure

HY-16305S1

Maribavir-d6 TFA
Maribavir-d6 TFA (1263W94-d6 TFA; BW1263W94-d6 TFA; GW257406X-d6 TFA) is a deuterium labeled Maribavir (HY-16305). Maribavir is an orally active antiviral agent for cytomegalovirus (CMV) through inhibition of protein kinase UL97 and the following CMV DNA replication .

HY-16305S

Maribavir-d6
Maribavir-d₆ (1263W94-d₆) is a deuterium labeled Maribavir (HY-16305). Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC₅₀ of 3 nM .

HY-W010452S1

3-Hydroxybutyric acid-13C4 sodium
3-Hydroxybutyric acid- ¹³C₄ (sodium) is the ¹³C labeled 3-Hydroxybutyric acid sodium (HY-W010452). 3-Hydroxybutyric acid sodium is a metabolite that is elevated in type I diabetes, and can modulate the properties of membrane lipids[1].

HY-145012S

W-19-d4 hydrochloride
W-19-d₄ (hydrochloride) is the deuterium labeled W-19 hydrochloride[1].

HY-143665S

Nor-W-18-d4
Nor-W-18-d₄ is the deuterium labeled Nor-W-18[1].

HY-W010452S2

3-Hydroxybutyric acid-13C2 sodium
3-Hydroxybutyric acid- ¹³C₂ (sodium) is the ¹³C labeled 3-Hydroxybutyric acid sodium (HY-W010452). 3-Hydroxybutyric acid sodium is a metabolite that is elevated in type I diabetes, and can modulate the properties of membrane lipids[1].

HY-W890109S

Spiramycin I-d3-1
Spiramycin I-d₃-1 is deuterium-labeled Spiramycin I .

HY-143623S

Neo Spiramycin I-d3
Neo Spiramycin I-d₃is the deuterium labeledNeo Spiramycin I(HY-143623) . Neo Spiramycin I (NSPI) is the active metabolite of Spiramycin (SPI) with antimicrobial activity. Neo Spiramycin is widely used in veterinary medicine .

HY-124211S

Dibenzo(a,i)pyrene-d14
Dibenzo(a,i)pyrene-d₁₄ is the deuterium labeled Dibenzo(a,i)pyrene[1].

HY-W743804

Aclidinium-d5 bromide
Aclidinium-d₅ (LAS 34273-d₅; LAS-W 330-d₅) bromide is deuterium-labeled Aclidinium Bromide (HY-14144) .

HY-W008452S

H-Tyr(3-I)-OH-13C6
H-Tyr(3-I)-OH- ¹³C₆ is the ¹³C-labeled H-Tyr(3-I)-OH. H-Tyr(3-I)-OH is a potent and effective tyrosine hydroxylase inhibitor. H-Tyr(3-I)-OH is an intermediate in the production of thyroid hormones and has a role as a human or mouse metabolite[1][2].

HY-W019776

Sudan I-d5
Sudan I-d₅ is a the deuterated Sudan I. Sudan I is a diazo-conjugate red dye and can be used as an additive to products such as oils, solvents or polishes. Sudan I inhibits growth of bacterial strains Clostridium perfringens and L. rhamnosus[1].

HY-B0674S1

Ebastine-d6
Ebastine-d₆ is deuterated labeled Ebastine (HY-B0674). Ebastine (LAS-W 090) is an orally active, second-generation histamine H1 receptor antagonist. Ebastine can be used for the symptoms of allergic rhinitis and chronic idiopathic urticaria research .

HY-P1032S2

Angiotensin I-13C6,15N (human, mouse, rat) TFA
Angiotensin I-13C6,15N (human, mouse, rat) TFA is ¹³C and ¹⁵N labeled Angiotensin I (human, mouse, rat) TFA. Angiotensin I-13C6,15N (human, mouse, rat) TFA is a precursor of angiotensin II and is cleaved into angiotensin II by angiotensin converting enzyme (ACE) .

HY-W728545

Labetalol-d6 hydrochloride
Labetalol-d6 hydrochloride (AH5158-d6 hydrochloride; Sch-15719W-d6) is a deuterium labeled Labetalol (HY-121383). Labetalol is an orally active α1- and β-adrenergic receptors competitive antagonist, which exhibits anti-hypertensive property .

HY-B1411S1

i-Inositol-d1
i-Inositol-d is the deuterium labeled i-Inositol[1].

HY-B1411S

i-Inositol-d6
i-Inositol-d₆ is the deuterium labeled i-Inositol. i-Inositol is a chemical compound, associated lipids are found in many foods, in particular fruit, especially cantaloupe and oranges.

HY-B0175S

Toltrazuril-d3
Toltrazuril-d₃ is deuterated labeled Toltrazuril. Toltrazuril (BAY-i 9142) is an antiprotozoal agent that acts upon Coccidia parasites.

HY-B0184S

Felbamate-d4
Felbamate-d₄ (W-554-d4) is the deuterium labeled Felbamate. Felbamate (W-554) is a potent anticonvulsant whose clinical effect may be related to the inhibition of N-methyl-D-aspartate (NMDA).

HY-W015851S

3-Hydroxybutanoic acid-13C sodium
3-Hydroxybutanoic acid-13C- ¹³C (sodium) is the ¹³C labeled 3-Hydroxybutanoic acid sodium (HY-W010452). 3-Hydroxybutyric acid sodium (β-Hydroxybutyric acid sodium) is a metabolite that is elevated in type I diabetes. 3-Hydroxybutyric acid sodium can modulate the properties of membrane lipids .

HY-P1032S

Angiotensin I-13C19,15N3 (human, mouse, rat)

Angiotensin I- ¹³C₁₉, ¹⁵N₃ (human, mouse, rat) is the ¹³C and ¹⁵N labeled Angiotensin I (human, mouse, rat) (HY-P1032). Cellulose (Pectin glycosidase) is a natural high molecular weight polysaccharide found in many plants and organisms. It is widely used in manufacturing industries, such as in paper making, textiles, food and medicine, etc. As a renewable resource, Cellulose is biodegradable and sustainable, and can also be used to manufacture chemicals such as Cellulose Esters, Cellulose Acetate and Cellulose Nitrate. In addition, Cellulose is often used as a food additive to increase the stability and quality of food .

HY-13458S1

Droxidopa-13C2,15N hydrochloride
Droxidopa- ¹³C₂, ¹⁵N (hydrochloride) is deuterium labeled Droxidopa. Droxidopa(L-DOPS), the mixture of Droxidopa (w/w80%) and Pharmaceutical starch (w/w20%), acts as a proagent to the neurotransmitters norepinephrine (noradrenaline) and epinephrine (adrenaline); Droxidopa(L-DOPS) is capable of crossing the protective blood–brain barrier[1][2].

HY-W010248S

2-Phenylglycine-d5
2-Phenylglycine-d₅ is the deuterium labeled 2-Phenylglycine. 2-Phenylglycine (DL-α-Phenylglycine) is a metabolite in breast milk during the W2 to W4 lactation period[1].

HY-B0184S1

Felbamate-d5
Felbamate-d₅ is the deuterium labeled Felbamate[1]. Felbamate (W-554) is a potent nonsedative anticonvulsant whose clinical effect may be related to the inhibition of N-methyl-D-aspartate (NMDA)[2][3].

HY-W588193S

Cortol-d5
Cortol-d₅ is deuterium-labeled Cortol (HY-W588193) .

HY-W014375S3

Arginine-d7 hydrochloride
Arginine-d₇ hydrochloride is deuterium labeled Arginine (hydrochloride) (HY-W014375). Arginine hydrochloride is an arginine derivative.

HY-125678S

Jasmine lactone-d2
Jasmine lactone-d₂ is deuterated labeled (±)-Cotinine-N-β-Glucuronide (HY-W588194).

HY-W709575

Spermidine-d6 trihydrochloride
Spermidine-d6 trihydrochloride is the deuterium labeled Spermidine-d6 (trihydrochloride) (HY-W709575) .

HY-W750155

Tetramethrin-d6
Tetramethrin-d6 is the deuterium labeled Tetramethrin-d6 (HY-W750155) .

HY-W654119

CMPF-d3
CMPF-d3 is the deuterium labeled CMPF-d3 (HY-W654119) .

HY-W653875

Azithromycin-d5
Azithromycin-d5 is the deuterium labeled Azithromycin-d5 (HY-W653875) .

HY-W698871

(±) Anabasine-d4
(±) Anabasine-d4 is the deuterium labeled (±) Anabasine-d4 (HY-W698871) .

HY-W744599

Desoxymetasone-d5
Desoxymetasone-d5 is the deuterium labeled Desoxymetasone-d5 (HY-W744599) .

HY-W747795

Digitoxin-d3
Digitoxin-d3 is the deuterium labeled Digitoxin-d3 (HY-W747795) .

HY-W008440S

DL-Cycloserine-15N,d3
DL-Cycloserine- ¹⁵N,d₃is the deuterium labeledDL-Cycloserine(HY-W008440) .

HY-W014375S2

Arginine-13C6 hydrochloride
Arginine- ¹³C₆ hydrochloride is ¹³C-labeled Arginine (hydrochloride) (HY-W014375). Arginine hydrochloride is an arginine derivative.

HY-W701834S

4-Hydroxymethylambrisentan-d5
4-Hydroxymethylambrisentan-d₅ is deuterium-labeled 4-Hydroxymethylambrisentan (HY-W701834) .

HY-W741222S

N-Desmethyl Olopatadine-d6
N-Desmethyl Olopatadine-d₆ is deuterium-labeled N-Desmethyl Olopatadine (HY-W741222) .

HY-W088178S

N,N-Dimethylbenzenesulfonamide-d2
N,N-Dimethylbenzenesulfonamide-d2 is the deuterium labeled N,N-Dimethylbenzenesulfonamide (HY-W088178) .

HY-W700866S

4-Hydroxyclonidine-d4 acetate
4-Hydroxyclonidine-d4 acetate is the deuterium labeled 4-Hydroxyclonidine hydrochloride (HY-W700866) .

HY-W357090S

L-Idose-13C-3
L-Idose- ¹³C-3 is the ¹³C labeled L-Idose (HY-W357090)[1].

HY-W710495

N-Acetyl-L-aspartic acid-d3-1
N-Acetyl-L-aspartic acid-d₃-1is the deuterium labeledN-Acetyl-L-aspartic acid(HY-W710495) .

HY-124215S1

Fenchone-d3
Fenchone-d₃ is deuterated labeled Benzo[pqr]tetraphen-3-ol (HY-W585890).

HY-W001171S

3-Hydroxyanthranilic acid-d3
3-Hydroxyanthranilic acid-d₃ is deuterium-labeled 3-Hydroxyanthranilic acid (HY-W001171) .

HY-W725480

Carfentrazon-ethyl-d5
Carfentrazon-ethyl-d5 is the deuterium labeled Carfentrazon-ethyl-d5 (HY-W725480) .

HY-W012837S

Benzylmethylether-d2
Benzylmethylether-d2 (Methoxymethylbenzene-d2) is the deuterium labeled (Methoxymethyl)benzene (HY-W012837) .

HY-W143071S

1-(Methylthio)-pentane-d3
1-(Methylthio)-pentane-d3 is the deuterium labeled Amyl methyl sulfide (HY-W143071) .

HY-W750265

Dexamethasone Phosphate-d5
Dexamethasone Phosphate-d5 is the deuterium labeled Dexamethasone Phosphate-d5 (HY-W750265) .

HY-W050088S

Isoxepac-d6
Isoxepac-d₆ is the deuterium labeled Isoxepac (HY-W050088). Isoxepac is a nonsteroidal anti-inflammatory agent[1].

HY-W777535S

Naphthalene-13C6
Naphthalene- ¹³C₆ is ¹³C labeled Naphthalene-13C10 (HY-W777535).

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