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stereoisomer

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51

Inhibitors & Agonists

1

Biochemical Assay Reagents

2

Peptides

16

Natural
Products

4

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-15954A
    NVP-CGM097 (stereoisomer)

    CGM097 stereoisomer

    		 Others Others
    NVP-CGM097 (stereoisomer) is a stereoisomer of NVP-CGM097, with no special bioactivity. NVP-CGM097 is a potent and selective MDM2 inhibitor.
    NVP-CGM097 (stereoisomer)
  • HY-15536A
    Cebranopadol ((1α,4α)stereoisomer)

    GRT6005 (1α,4α)stereoisomer

    		 Opioid Receptor Neurological Disease
    Cebranopadol ((1α,4α)stereoisomer) is a stereoisomer of cebranopadol. Cebranopadol is a potent agonist activity on ORL-1.
    Cebranopadol ((1α,4α)stereoisomer)
  • HY-10013B
    Taranabant ((1R,2R)stereoisomer)

    MK0364 (1R,2R)stereoisomer

    		 Cannabinoid Receptor Others
    Taranabant (1R,2R)stereoisomer is the R-enantiomer of Taranabant. Taranabant is a highly potent and selective cannabinoid 1 (CB1) receptor inverse agonist.
    Taranabant ((1R,2R)stereoisomer)
  • HY-W001959
    D-Allothreonine

    		Endogenous Metabolite Metabolic Disease
    D-Allothreonine is the D type stereoisomer of Allothreonine. D-Allothreonine is a peptido-lipid derived from bacteria. D-Allothreonine, amide-linked to the D-galacturonic acid, is also a constituent in the polysaccharide .
    D-Allothreonine
  • HY-B1871
    Metolachlor

    		Others Others
    Metolachlor is a pre-emergent selective, chloroacetanilide herbicide for the control of a variety of annual grass and broad leaf weeds in corn and other crops. Metolachlor is a chiral herbicide consisting of four stereoisomers .
    Metolachlor
  • HY-112382
    Iso-Olomoucine

    		Others Others
    Iso-olomoucine is an inactive stereoisomer of the CDK5 inhibitor olomoucine with IC50 >1 mM .
    Iso-Olomoucine
  • HY-118670A
    16(R)-Iloprost

    		Others Cardiovascular Disease
    16(R)-Iloprost is a stereoisomer of Iloprost. 16(R)-Iloprost inhibited platelet aggregation with IC50 value of 65 nM .
    16(R)-Iloprost
  • HY-113887A
    11β-Prostaglandin F1β

    11β-PGF1β

    		 Others Endocrinology
    11β-Prostaglandin F1β (11β-PGF1β) is a stereoisomer of PGF1α with inverted C-9 and C-11 hydroxyl groups .
    11β-Prostaglandin F1β
  • HY-118670
    16(S)-Iloprost

    		Others Cardiovascular Disease
    16(S)-Iloprost is a stereoisomer of Iloprost. 16(S)-Iloprost inhibited platelet aggregation with IC50 value of 3.5 nM, and balanced binding with platelet membrane receptors Kd value of 13.4 nM .
    16(S)-Iloprost
  • HY-114029
    Ep vinyl quinidine

    3-Epiquinine; Epivinylquinidine

    		 Parasite Infection Cardiovascular Disease
    Ep vinyl quinidine (3-Epiquinine) is an epi-vinyl stereoisomer of Quinidine. Quinidine is an antiarrhythmic agent. Quinidine is a potent, orally active, selective cytochrome P450db inhibitor. Quinidine is also a K+ channel blocker with an IC50 of 19.9 μM. Quinidine can be used for malaria research .
    Ep vinyl quinidine
  • HY-B1871R
    Metolachlor (Standard)

    		Others Others
    Metolachlor (Standard) is the analytical standard of Metolachlor. This product is intended for research and analytical applications. Metolachlor is a pre-emergent selective, chloroacetanilide herbicide for the control of a variety of annual grass and broad leaf weeds in corn and other crops. Metolachlor is a chiral herbicide consisting of four stereoisomers .
    Metolachlor (Standard)
  • HY-N0181A
    Lumisterol

    9β,10α-Ergosterol

    		 Endogenous Metabolite Metabolic Disease
    Lumisterol (9β,10α-Ergosterol), a steroid compound, is the (9β,10α)-stereoisomer of Ergosterol (HY-N0181). Lumisterol is a photoprotective agent against UVB-induced DNA damage and anti-proliferative activities .
    Lumisterol
  • HY-17626C
    (R)-Alalevonadifloxacin mesylate

    (R)-WCK-2349

    		 Others Others
    (R)-Alalevonadifloxacin mesylate is an isomer of Alalevonadifloxacin mesylate (HY-17626B). Alalevonadifloxacin mesylate is a oraly active anti-methicillin-resistant Staphylococcus aureus (MRSA) antibiotic .
    (R)-Alalevonadifloxacin mesylate
  • HY-100587
    D-Glutamine
    2 Publications Verification

    		 Autophagy Mitophagy Endogenous Metabolite Ferroptosis Metabolic Disease
    D-Glutamine is a cell-permeable D type stereoisomer of Glutamine.
    D-Glutamine
  • HY-18500
    (βS)-β-Hydroxy-L-histidine hydrochloride

    		Others Others
    (βS)-β-Hydroxy-L-histidine hydrochloride is a stereoisomer of β-hydroxyhistidine .
    (βS)-β-Hydroxy-L-histidine hydrochloride
  • HY-B1871S
    Metolachlor-d6

    		Isotope-Labeled Compounds Others
    Metolachlor-d6 is the deuterium labeled Metolachlor[1]. Metolachlor is a pre-emergent selective, chloroacetanilide herbicide for the control of a variety of annual grass and broad leaf weeds in corn and other crops. Metolachlor is a chiral herbicide consisting of four stereoisomers[2][3].
    Metolachlor-d6
  • HY-121962
    neo-Inositol

    		Endogenous Metabolite Metabolic Disease
    neo-Inositol, a stereoisomer of inositol, has been isolated from calf brain .
    neo-Inositol
  • HY-Y1804
    D-Lysine monohydrochloride

    		Endogenous Metabolite Others
    D-Lysine monohydrochloride is an Lysine stereoisomer which can be used as a component of surfactants .
    D-Lysine monohydrochloride
  • HY-117881
    CJ-15208

    		Others Neurological Disease
    CJ-15208 is a potent and selective κ-opioid receptor antagonist with significant opioid activity. CJ-15208 exhibited strong analgesic effects in the warm water tail withdrawal test in mice and was mediated through multiple opioid receptors. The stereoisomers of CJ-15208 exhibited different opioid activity characteristics, for example, one stereoisomer exhibited κ-opioid receptor antagonism, while the other exhibited δ-opioid receptor antagonism. All stereoisomers of CJ-15208 had no significant effects on respiration. The stereoisomers of CJ-15208 did not lead to the development of drug tolerance, which makes it potential in the further development of safe opioid analgesics .
    CJ-15208
  • HY-W012479
    H-D-Trp-OH

    D-Tryptophan

    		 Endogenous Metabolite Metabolic Disease
    H-D-Trp-OH is a D-stereoisomer of tryptophan and occasionally found in naturally produced peptides such as the marine venom peptide.
    H-D-Trp-OH
  • HY-N12868
    25-Epi-28-epi-cyasterone

    		Others Endocrinology
    25-Epi-28-epi-cyasterone (3) is a stereoisomer of cyasterone that can be isolated from Cyathula officinalis .
    25-Epi-28-epi-cyasterone
  • HY-I1060
    L-Alloisoleucine
    1 Publications Verification

    (3R)-LS-Isoleucine; L-Allo-isoleucine

    		 Endogenous Metabolite Others
    L-Alloisoleucine is a branched chain amino acid and is a stereo-isomer of L-isoleucine. L-Alloisoleucine is a common constituent of human plasma (albeit at low levels).
    L-Alloisoleucine
  • HY-N10924
    Strychnistenolide

    		Others Others
    Strychnistenolide is a sesquiterpene lactone that can be isolated from the roots of Lindera strychnifolia. Strychnistenolide exists as a single stereoisomer in CHCl3, but exomeric in pyridine .
    Strychnistenolide
  • HY-158554
    2-Ethylethcathinone hydrochloride

    2-Eec hydrochloride

    		 Biochemical Assay Reagents Others
    2-Ethylethcathinone hydrochloride (2-Eec hydrochloride) is a substituted cathinone (compounds with potential for abuse). 2-Ethylethcathinone hydrochloride is a stereoisomer of 2-fluoroethcathinone .
    2-Ethylethcathinone hydrochloride
  • HY-14856A
    iso-Atagabalin hydrochloride

    iso-PD 0200390 hydrochloride

    		 Others Others
    iso-Atagabalin (iso-PD 0200390) hydrochloride is a stereoisomer of Atagabalin (HY-14856). Atagabalin is a selective GABA (gamma-aminobutyric acid) receptor agonist with antianxiety effect .
    iso-Atagabalin hydrochloride
  • HY-122294
    Rociverine

    		Others Neurological Disease
    Rociverine is an anticholinergic compound with smooth muscle relaxant activity. Rociverine showed different binding modes in five cloned muscarinic receptors. The cis stereoisomer of Rociverine showed a higher affinity change compared to the trans stereoisomer. The (1R,2R) configuration of Rociverine showed significantly higher affinity, even up to 240 times. The (1S,2S) configuration of Rociverine is very important for binding selectivity .
    Rociverine
  • HY-Y1804S
    D-Lysine-d4 monohydrochloride

    		Isotope-Labeled Compounds Endogenous Metabolite Others
    D-Lysine-d4 (monohydrochloride) is the deuterium labeled D-Lysine. D-Lysine monohydrochloride is an Lysine stereoisomer which can be used as a component of surfactants[1].
    D-Lysine-d4 monohydrochloride
  • HY-115429
    Calcium dextrofolinate

    6R-Leucovorin calcium; (6R)-Folinic acid calcium

    		 Others Metabolic Disease
    Calcium dextrofolinate is a stereoisomer of Calcium folinate. Calcium folinate (Folinic acid calcium) is a biological folic acid and is generally administered along with methotrexate (MTX) as a rescue agent to decrease MTX-induced toxicity .
    Calcium dextrofolinate
  • HY-13030A
    (R)-(-)-JQ1 Enantiomer
    Maximum Cited Publications
    10 Publications Verification

    		 Epigenetic Reader Domain Cancer
    (R)-(-)-JQ1 Enantiomer is the stereoisomer of (+)-JQ1. (+)-JQ1 potently decreases expression of both BRD4 target genes, whereas (R)-(-)-JQ1 Enantiomer has no effect.
    (R)-(-)-JQ1 Enantiomer
  • HY-I1060S
    L-Alloisoleucine-d10

    		Isotope-Labeled Compounds Endogenous Metabolite Others
    L-Alloisoleucine-d10 is the deuterium labeled L-Alloisoleucine. L-Alloisoleucine is a branched chain amino acid and is a stereo-isomer of L-isoleucine. L-Alloisoleucine is a common constituent of human plasma (albeit at low levels).
    L-Alloisoleucine-d10
  • HY-N9487
    (R)-(-)-α-Phellandrene

    (-)-α-Phellandrene

    		 Bacterial Infection Inflammation/Immunology
    (R)-(-)-α-Phellandrene ((-)-α-Phellandrene) is an the (R)-(-)-stereoisomer of α-phellandrene. α-phellandrene is an orally active cyclic monoterpene that attenuates inflammatory response, and induces DNA damage .
    (R)-(-)-α-Phellandrene
  • HY-137428
    (S,S)-EDDS

    		Biochemical Assay Reagents Others
    (S,S)-EDDS is a stereoisomer of EDTA (HY-Y0682), and exhibits ability to chelate metal ions. (S,S)-EDDS exhibits good biodegradability in the environment, and can be used in environmental management and biotechnology .
    (S,S)-EDDS
  • HY-137261
    UDP-β-D-glucose disodium

    		Others Metabolic Disease
    UDP-β-D-glucose disodium is a the stereoisomer of UDP-α-D-glucose. UDP-β-D-glucose disodium is an oligosaccharide that can be used to synthesize glycoproteins and glycolipids. UDP-β-D-glucose disodium can be used as a substrate .
    UDP-β-D-glucose disodium
  • HY-117682
    L-(+)-threo-Chloramphenicol

    (+)-Chloramphenicol; Dextramycine; Dextromycetin

    		 Antibiotic Infection
    L-(+)-threo-Chloramphenicol ((+)-Chloramphenicol) is the S,S-stereoisomer of Chloramphenicol (HY-B0239). L-(+)-Threo-chloramphenicol inhibits protein synthesis in reticulocytes. L-(+)-threo-Chloramphenicol also inhibits the oxidative activity of isolated mitochondria .
    L-(+)-threo-Chloramphenicol
  • HY-142162A
    (S,R)-LSN3318839

    		Others Others
    (S,R)-LSN3318839 is the stereoisomer of LSN3318839 (HY-142162). LSN3318839 is an orally active positive allosteric modulator of the glucagon-like peptide-1 receptor (GLP-1R) .
    (S,R)-LSN3318839
  • HY-I1070
    D-Isoleucine

    (R)-Isoleucine

    		 Others Neurological Disease
    D-Isoleucine ((R)-Isoleucine), an isoleucine stereoisomer, is a selective activator of Asc-1 antiporter, which enhances long-term potentiation at the hippocampal CA1-CA3 via release of endogenous D-serine .
    D-Isoleucine
  • HY-W012479R
    H-D-Trp-OH (Standard)

    		Endogenous Metabolite Metabolic Disease
    H-D-Trp-OH (Standard) is the analytical standard of H-D-Trp-OH. This product is intended for research and analytical applications. H-D-Trp-OH is a D-stereoisomer of tryptophan and occasionally found in naturally produced peptides such as the marine venom peptide.
    H-D-Trp-OH (Standard)
  • HY-W048718
    Fmoc-D-Tle-OH

    Fmoc-D-α-t-butylglycine

    		 Amino Acid Derivatives Others
    Fmoc-D-Tle-OH (Fmoc-D-α-t-butylglycine) is an amino acid derivative with an Fmoc protecting group, which can be used to synthesize chelating agents that can form a single stereoisomer-enriched form after coordination with metal centers .
    Fmoc-D-Tle-OH
  • HY-108437
    exo-IWR-1

    		Wnt Infection Cancer
    exo-IWR-1, an inactive stereoisomer of Endo-IWR-1, is a negative control of IWR-1 (HY-12238). IWR-1 is a tankyrase inhibitor which inhibits Wnt/β-catenin signaling pathway .
    exo-IWR-1
  • HY-W012479S
    H-D-Trp-OH-d5

    D-Tryptophan-d5

    		 Isotope-Labeled Compounds Endogenous Metabolite Metabolic Disease
    H-D-Trp-OH-d5 (D-Tryptophan-d5) is the deuterium labeled H-D-Trp-OH. H-D-Trp-OH is a D-stereoisomer of tryptophan and occasionally found in naturally produced peptides such as the marine venom peptide.
    H-D-Trp-OH-d5
  • HY-W016733
    D-Citrulline

    H-D-Cit-OH

    		 Endogenous Metabolite Cardiovascular Disease
    D-Citrulline (H-D-Cit-OH) is a stereoisomer of L-citrulline (HY-N0391). D-Citrulline significantly attenuates polymorphonuclear leukocyte (PMN)-induced cardiac contractile dysfunction in the isolated perfused rat heart subjected to ischemia/reperfusion via a non-NO-mediated mechanism .
    D-Citrulline
  • HY-N6935
    Sennidin B

    		HCV Akt GLUT Infection Metabolic Disease
    Sennidin B, a stereoisomer isolated from the leaves of Cassia angustifolia, has lower activity than Sennidin A. Sennidin A inhibits HCV NS3 helicase, with an IC50 of 0.8 μM. Sennidin A induces phosphorylation of Akt and glucose transporter 4 (GLUT4) translocation. Sennidin A stimulates the glucose incorporation .
    Sennidin B
  • HY-111827
    S-1-Propenyl-L-cysteine
    4 Publications Verification

    		 Histamine Receptor Cardiovascular Disease Others Metabolic Disease Inflammation/Immunology
    S-1-Propenyl-L-cysteine is a stereoisomer of S-allyl-l-cysteine, extracted from garlic, with immunomodulatory effects and reduces blood pressure in a hypertensive animal model . S-1-Propenyl-L-cysteine exhibits antioxidative efficacy through a NO-dependent BACH1 signaling pathway . S-1-Propenyl-L-cysteine is orally active.
    S-1-Propenyl-L-cysteine
  • HY-117239
    SB-206606

    		Adrenergic Receptor Cardiovascular Disease
    SB-206606, a stereoisomer of BRL 37344, is a potentially specific, beta 3-adrenergic receptor (β3-AR) ligand. The affinity of [3H]SB 206606 is 76 times higher for the β3-AR than for the beta 1/beta 2-adrenergic receptors .
    SB-206606
  • HY-W010042
    L-Glucose

    L-(-)-Glucose

    		 Others Metabolic Disease Cancer
    L-Glucose (L-(-)-Glucose) is a stereoisomer of D-Glucose (HY-B0389), which does not readily enter the brain. L-Glucose can promote food intake. L-glucose is combined with a fluorescence detector to produce a fluorescent probe that can be used to visualize and characterize cancer cells. L-Glucose also can be used in the research to enhance memory in mice .
    L-Glucose
  • HY-W012885
    (S)-Methyl 3-hydroxybutanoate

    		Biochemical Assay Reagents Others
    (S)-Methyl 3-hydroxybutanoate consists of a chiral center, resulting in two enantiomers, where (S)-Methyl 3-hydroxybutanoate means that the hydroxyl group is located on the third carbon atom of the S-configuration carboxylic acid group stereoisomers. This compound is often used as a building block for the synthesis of various pharmaceuticals and natural products. Due to its fruity taste, it is also used as a flavor and fragrance ingredient.
    (S)-Methyl 3-hydroxybutanoate
  • HY-116096
    15-epi-PGE1

    15(R)-Prostaglandin E1; 15-Epiprostaglandin E1

    		 15-PGDH Others
    15-epi-PGE1 (15R-Prostaglandin E1; 15-Epiprostaglandin E1) is a stereoisomer of PGE1 (HY-B0131) but with less biological activity . 15-epi-PGE1 is a non-competitive inhibitor for human placental 15-Hydroxyprostaglandin dehydrogenase (15-PGDH) with an IC50 of 170 μM .
    15-epi-PGE1
  • HY-N6935R
    Sennidin B (Standard)

    		HCV Akt GLUT Infection Metabolic Disease
    Sennidin B (Standard) is the analytical standard of Sennidin B. This product is intended for research and analytical applications. Sennidin B, a stereoisomer isolated from the leaves of Cassia angustifolia, has lower activity than Sennidin A. Sennidin A inhibits HCV NS3 helicase, with an IC50 of 0.8 μM. Sennidin A induces phosphorylation of Akt and glucose transporter 4 (GLUT4) translocation. Sennidin A stimulates the glucose incorporation .
    Sennidin B (Standard)
  • HY-117542
    D595

    		Others Neurological Disease
    D595 is a phenylethylamine calcium channel blocker with potent negative inotropic activity. D595 has shown significant efficacy in its corresponding pharmacological studies, especially in inhibiting the uptake of monoamine neurotransmitters. D595 has high affinity in binding to the dopamine transporter (DAT), serotonin transporter (SERT), and norepinephrine transporter (NET). Structural adjustments of D595, especially changes in the hydroxyl stereochemistry, significantly affect its interaction with the transporters, showing a specific preference for stereoisomers .
    D595
  • HY-147105A
    (+)-LRH-1 modulator-1

    		Interleukin Related Inflammation/Immunology
    (+)-LRH-1 modulator-1 is a stereoisomer of LRH-1 modulator-1. LRH-1 modulator-1 (compound 6N) is a potent LRH-1 (liver receptor homolog-1) modulator/agonist. LRH-1 modulator-1 has anti-inflammatory effects in intestinal organoids. LRH-1 modulator-1 induces the anti-inflammatory cytokine IL-10 and reduces the inflammatory cytokines IL-1b and TNFa .
    (+)-LRH-1 modulator-1

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