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FL118-C3-O-C-amide-C-NH2-d<sub>5</sub> formate

" in MedChemExpress (MCE) Product Catalog:

By Targets:	ADC Cytotoxin (5) ADC Linker (11) Amino Acid Derivatives (1) Amyloid-β (1) Apoptosis (4) Autophagy (2) Bacterial (2) Biochemical Assay Reagents (4) Calcium Channel (2) Cathepsin (1) Cholecystokinin Receptor (1) DNA/RNA Synthesis (4) Drug Derivative (3) Drug Intermediate (2) Drug Isomer (1) Drug Metabolite (1) Drug-Linker Conjugates for ADC (3) E3 Ligase Ligand-Linker Conjugates (4) Endogenous Metabolite (1) Fluorescent Dye (6) GHSR (1) GnRH Receptor (1) HIV (1) IAP (1) Integrin (1) Isotope-Labeled Compounds (4) Ligands for Target Protein for PROTAC (2) MMP (1) Opioid Receptor (1) Parasite (1) PKC (2) PKG (1) PROTAC Linkers (6) Protease Activated Receptor (PAR) (13) PTHR (1) Radionuclide-Drug Conjugates (RDCs) (1) STAT (3) STING (2) Survivin (1) Topoisomerase (3)
By Research Areas:	Cancer (50) Cardiovascular Disease (2) Endocrinology (1) Infection (4) Inflammation/Immunology (8) Metabolic Disease (7) Neurological Disease (7)

By Targets:

ADC Cytotoxin (5)

ADC Linker (11)

Amino Acid Derivatives (1)

Amyloid-β (1)

Apoptosis (4)

Autophagy (2)

Bacterial (2)

Biochemical Assay Reagents (4)

Calcium Channel (2)

Cathepsin (1)

Cholecystokinin Receptor (1)

DNA/RNA Synthesis (4)

Drug Derivative (3)

Drug Intermediate (2)

Drug Isomer (1)

Drug Metabolite (1)

Drug-Linker Conjugates for ADC (3)

E3 Ligase Ligand-Linker Conjugates (4)

Endogenous Metabolite (1)

Fluorescent Dye (6)

GHSR (1)

GnRH Receptor (1)

HIV (1)

IAP (1)

Integrin (1)

Isotope-Labeled Compounds (4)

Ligands for Target Protein for PROTAC (2)

MMP (1)

Opioid Receptor (1)

Parasite (1)

PKC (2)

PKG (1)

PROTAC Linkers (6)

Protease Activated Receptor (PAR) (13)

PTHR (1)

Radionuclide-Drug Conjugates (RDCs) (1)

STAT (3)

STING (2)

Survivin (1)

Topoisomerase (3)

By Research Areas:

Cancer (50)

Cardiovascular Disease (2)

Endocrinology (1)

Infection (4)

Inflammation/Immunology (8)

Metabolic Disease (7)

Neurological Disease (7)

Inhibitors & Agonists

Screening Libraries

Fluorescent Dye

Peptides

MCE Kits

Natural
Products

Recombinant Proteins

Isotope-Labeled Compounds

Antibodies

Targets Recommended: FAAH P-glycoprotein

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-161022S1

**FL118-C3-O-C-amide-C-NH2-d5 formate**	Isotope-Labeled Compounds ADC Linker	Cancer
FL118-C3-O-C-amide-C-NH2-d5 formate is a deuterium labeled FL118-C3-O-C-amide-C-NH2 formate. FL118-C3-O-C-amide-C-NH2 formate is an ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .

HY-161022A

**FL118-C3-O-C-amide-C-NH2 formate**	ADC Linker	Cancer
FL118-C3-O-C-amide-C-NH2 format is an ADC linker for the synthesis of synthetic antibody conjugate active molecules (ADCs)..

HY-12486

*FL118* 10,11-(Methylenedioxy)-20(S)-camptothecin	Survivin Apoptosis IAP	Cancer
FL118 (10,11-(Methylenedioxy)-20(S)-camptothecin), a Camptothecin (HY-16560) analogue, is a potent and orally active survivin inhibitor. FL118 binds to oncoprotein DDX5 (p68) to dephosphorylates and degrades DDX5. FL118 can be used for the research of cancer ^[2].

HY-156856

FL118-14-Propanol	ADC Cytotoxin	Cancer
FL118-14-Propanol is a FL118 derivative. FL118-14-Propanol synthesized ADC molecule has good anti-tumor effect in mice .

HY-15792

(R)-FL118 10,11-(Methylenedioxy)-20(R)-camptothecin	Drug Derivative	Cancer
(R)-FL118 (10,11-(Methylenedioxy)-20(R)-camptothecin) is the R-enantiomer of FL118 (HY-12486). (R)-FL118 shows anticancer activity .

HY-164569

NH2 DOTA-GA	Radionuclide-Drug Conjugates (RDCs)	Cancer
NH2 DOTA-GA is a DOTA-based metal chelator that can be used to prepare radionuclide drug conjugates (RDCs) whose carboxylic acid groups can complex metal ions. For example, NH2 DOTA-GA complexes Gd(III) ions.

HY-161022S

FL118-C3-O-C-amide-C-NH2-d5	Isotope-Labeled Compounds ADC Linker	Cancer
FL118-C3-O-C-amide-C-NH2-d₅ is a deuterium labeled FL118-C3-O-C-amide-C-NH2 .

HY-161022

**FL118-C3-O-C-amide-C-NH2**	ADC Linker	Cancer
FL118-C3-O-C-amide-C-NH2 (compound 6a) is an ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .

HY-170868

CL2A-FL118	Drug-Linker Conjugates for ADC	Cancer
CL2A-FL118 is a drug-linker for synthesis of ADC molecule Sac-CL2A-FL118 .

HY-164181

*Fmoc-protected DMT-Dt PEG2 NH2* amidite**	DNA/RNA Synthesis	Cancer
Fmoc-protected DMT-Dt PEG2 NH2 amidite is a phosphoramidite monomer.

HY-156315A

SCO-PEG2-NH2 formate	ADC Linker	Cancer
SCO-PEG2-NH2 formate is a cleavable ADC Linker containing 2 PEG units. SCO-PEG2-NH2 formate can be used as a copper-free click chemical reagent for catalyst-free click reactions.

HY-156316A

SCO-PEG3-NH2 formate	ADC Linker	Cancer
SCO-PEG3-NH2 formate is a cleavable ADC Linker containing 3 PEG units. SCO-PEG3-NH2 formate can be used as a copper-free click chemical reagent for catalyst-free click reactions .

HY-157419

FL77-24 7-(4-Ethylphenyl)-FL118	Apoptosis	Cancer
FL77-24, a FL118 analog and apoptosis inducer, possesses antitumor activity, with IC₅₀ values of 99.4 nM, 118 nM, <6.4 nM, 28.5 nM and <6.4 nM in HCT116, HepG2, MCF-7, A549 and HeLa cells, respectively. FL77-24 mainly causes cell cycle arrest in S and G2/M phases .

HY-148470A

C4-Amide-C4-NH2	Drug Derivative	Others
C4-Amide-C4-NH2 is an active compound. C4-Amide-C4-NH2 can be used in a variety of biochemical studies.

HY-P2638

Cholecystokinin (27-32)-amide CCK-27-32-NH2	Cholecystokinin Receptor	Neurological Disease
Cholecystokinin (27-32)-amide (CCK-27-32-NH2) is a potent cholecystokinin receptor CCK receptor antagonist .

HY-148471A

C3-Amide-C4-NH2	ADC Linker	Others
C3-Amide-C4-NH2 is a potent linker .

HY-148472A

C2-Amide-C4-NH2	ADC Linker	Others
C2-Amide-C4-NH2 is a potent linker .

HY-148080

Indole-C2-amide-C2-NH2	ADC Linker	Others
Indole-C2-amide-C2-NH2 is a potent linker .

HY-138530

Thiol-PEG4-amide-NH2	PROTAC Linkers	Cancer
Thiol-PEG4-amide-NH2 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .

HY-148346

STING agonist-20-Ala-amide-PEG2-C2-NH2	Drug-Linker Conjugates for ADC STING	Cancer
STING agonist-20-Ala-amide-PEG2-C2-NH2 is an active scaffold comprising a stimulator of interferon genes (STING). STING agonist-20-Ala-amide-PEG2-C2-NH2 can be used to synthesize immune-stimulating antibody conjugate (ISAC). STING agonist-20-Ala-amide-PEG2-C2-NH2 can be used for the research of cancer .

HY-W096148

Biotin-C4-amide-C5-NH2	ADC Linker	Cancer
Biotin-C4-amide-C5-NH2 is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .

HY-161933

1-Adamantane-amide-C7-NH2	PROTAC Linkers	Cancer
1-Adamantane-amide-C7-NH2 is the linker, which can be used for syntheisis of PROTAC GPX4 degrader-3 (HY-161930) .

HY-141423

Thalidomide-O-amide-C5-NH2	E3 Ligase Ligand-Linker Conjugates Autophagy Apoptosis	Cancer
Thalidomide-O-amide-C5-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology .

HY-148346A

*STING agonist-20-Ala-amide-PEG2-C2-NH2* TFA**	Drug-Linker Conjugates for ADC STING	Cancer
STING agonist-20-Ala-amide-PEG2-C2-NH2 (Compound 30b) TFA is an active scaffold comprising a stimulator of interferon genes (STING). STING agonist-20-Ala-amide-PEG2-C2-NH2 TFA can be used to synthesize immune-stimulating antibody conjugate (ISAC). STING agonist-20-Ala-amide-PEG2-C2-NH2 TFA can be used for the research of cancer .

HY-141423A

*Thalidomide-O-amide-C5-NH2* TFA**	E3 Ligase Ligand-Linker Conjugates Autophagy Apoptosis	Cancer
Thalidomide-O-amide-C5-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology .

HY-139085A

*XL388-C2-amide-PEG9-NH2* hydrochloride**	Drug Intermediate	Cancer
XL388-C2-amide-PEG9-NH2 hydrochloride is an intermediate used in the synthesis of C26-linked Rapamycin analog .

HY-139085B

*XL388-C2-amide-PEG9-NH2* TFA**	Drug Intermediate	Cancer
XL388-C2-amide-PEG9-NH2 TFA is an intermediate used in the synthesis of C26-linked Rapamycin analog .

HY-P4701

*pTH-Related Protein (1-34) amide* (human, mouse, rat)** Human PTHrP-(1-34)NH2	PTHR	Metabolic Disease
pTH-Related Protein (1-34) amide (human, mouse, rat) (Human PTHrP-(1-34)NH2) is a N-terminal fragments of PTHrP. pTH-Related Protein (1-34) amide (human, mouse, rat) induces hypercalcemia, and can be used for research of humoral hypercalcaemia of malignancy .

HY-P4832

Acetyl-Tau Peptide (273-284) amide	Amyloid-β	Neurological Disease
Acetyl-Tau Peptide (273-284) amide is an acetylated Tau peptide fragment. Acetyl-Tau Peptide (273-284) amide limits the substantial aggregation of Ac-Aβ(25–35)-NH2 and can be used as an inhibitor of Ac-Aβ(25–35)-NH2. Acetyl-Tau Peptide (273-284) amide can be used as an experimental model to investigate the Aβ/Tau cross-interaction ^[2].

HY-W007497S

*H-β-Ala-NH2.-d4HCl* H-β-Ala-NH2·HCl-d<sub>4sub>	Isotope-Labeled Compounds	Others
H-β-Ala-NH2.-d₄ HCl is the deuterium labeled H-β-Ala-NH2.HCl[1].

HY-P1311

RLLFT-NH2	Drug Isomer	Others
RLLFT-NH2 is a reversed amino acid sequence negative control peptide for TFLLR-NH2 .

HY-P10215

Ac-{Cpg}-Thr-Ala-{Ala(CO)}-Asp-{Cpg}-NH2	Parasite	Infection
Ac-{Cpg}-Thr-Ala-{Ala(CO)}-Asp-{Cpg}-NH2 (compound 40) is a potent **Plasmodium subtilisin-like protease 1 (SUB1)** inhibitor. SUB1-IN-1 shows IC₅₀ values of 12 nM and 10 nM against P. vivax and P. falciparum SUB1 (Pv- and PfSUB1), respectively .

HY-P1310

VKGILS-NH2 1 Publications Verification	Protease Activated Receptor (PAR)	Inflammation/Immunology
VKGILS-NH2 is a reversed amino acid sequence control peptide for SLIGKV-NH2 (protease-activated receptor 2 (PAR2) agonist). VKGILS-NH2 has no effect on DNA synthesis in cells ^[2].

HY-138523

**NH2-PEG3500-NH2**	PROTAC Linkers	Cancer
NH2-PEG3500-NH2 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .

HY-P10930

*wrwyar-NH2* TFA**	DNA/RNA Synthesis	Cancer
wrwyar-NH2 (TFA) is a control peptide for wrwycr-NH2 (HY-P10930A) .

HY-130988

Ipatasertib-NH2 GDC-0068-NH2; RG7440-NH2	Ligands for Target Protein for PROTAC	Cancer
Ipatasertib-NH2 (GDC-0068-NH2;RG7440-NH2) is a ligand for target protein AKT for PROTAC (INY-03-041). INY-03-041 is composed of Ipatasertib-NH2, a ten-hydrocarbon linker, and a CRBN ligand Lenalidomide for E3 ubiquitin ligase .

HY-P0283

Protease-Activated Receptor-2, amide 2 Publications Verification	Protease Activated Receptor (PAR)	Cancer
Protease-Activated Receptor-2, amide (SLIGKV-NH₂) is a highly potent protease-activated receptor-2 (PAR2) activating peptide.

HY-P1310A

*VKGILS-NH2* TFA**	Protease Activated Receptor (PAR)	Inflammation/Immunology
VKGILS-NH2 TFA is a reversed amino acid sequence control peptide for SLIGKV-NH2 (protease-activated receptor 2 (PAR2) agonist). VKGILS-NH2 TFA has no effect on DNA synthesis in cells ^[2].

HY-D2442

Cy3-PEG-NH2	Fluorescent Dye	Cancer
Cy3-PEG-NH2 is a polyethylene glycol derivative containing Cy3 (HY-D0822) fluorescent dye and polyethylene glycol (PEG) and an amino group. The Cy3 fluorophore is commonly used in applications such as immunolabeling, nucleic acid labeling, fluorescence microscopy, and flow cytometry. Cy3 has an emission maximum around 562-570 nm. Cy3-PEG-NH2 can be used for fluorescence imaging, fluorescence tracing and fluorescence labeling .

HY-P1311A

*RLLFT-NH2* TFA**	Protease Activated Receptor (PAR)	Others
RLLFT-NH2 TFA is a reversed amino acid sequence negative control peptide for TFLLR-NH2 (HY-P0226) .

HY-P1263

tcY-NH2 (trans-Cinnamoyl)-YPGKF-NH2	Protease Activated Receptor (PAR)	Metabolic Disease Inflammation/Immunology
tcY-NH2 ((trans-Cinnamoyl)-YPGKF-NH2) is a potent selective PAR4 antagonist peptide. tcY-NH2 inhibits thrombin- and AY-NH₂-induced platelet aggregation and endostatin release, and can be used in the research of inflammation, immunology ^[2] .

HY-P5638

FLGFVGQALNALLGKL-NH2	Bacterial	Infection
FLGFVGQALNALLGKL-NH2 is an antimicrobial peptide of frog origin. FLGFVGQALNALLGKL-NH2 has activity against Staphylococcus aureus ATCC 29213 (MIC=32 μM) .

HY-148872

*Thalidomide-5-NH2-C8-NH2* TFA**	Biochemical Assay Reagents	Others
Thalidomide-5-NH2-C8-NH2 TFA can be used for compound synthesis .

HY-P10201A

*Ac-GpYLPQTV-NH2* acetate**	STAT	Cancer
Ac-GpYLPQTV-NH2 acetate is a STAT3 inhibitor with an IC₅₀ value of 0.33 μM. Ac-GpYLPQTV-NH2 acetate has antitumor activity .

HY-P10201

Ac-GpYLPQTV-NH2	STAT	Cancer
Ac-GpYLPQTV-NH2 is a STAT3 inhibitor with an IC₅₀ value of 0.33 μM. Ac-GpYLPQTV-NH2 has antitumor activity .

HY-P10667

Ac-MRGDH-NH2	Integrin	Cancer
Ac-MRGDH-NH2 is a pentapeptide containing the RGD sequence. Ac-MRGDH-NH2 can be used to synthesize the diastereoisomeric prodrugs Λ- and Δ-[Ru(Ph2phen)2(κS,κN-(Ac-MRGDH-NH2))]Cl2. In these prodrugs, Ac-MRGDH-NH2 serves as a photolabile protecting group for the cytotoxic bis-aqua ruthenium warhead [Ru(Ph2phen)2(OH2)2]2+, and Ac-MRGDH-NH2 possesses integrin targeting ability and photosubstitution properties. Therefore, Ac-MRGDH-NH2 can be utilized in research on tumor-targeted photodynamic activation chemotherapy (PACT) .

HY-40171S

NH2-C2-NH-Boc-d4 PROTAC Linker 22-d<sub>4sub>	PROTAC Linkers	Cancer
NH2-C2-NH-Boc-d₄ is the deuterium labeled NH2-C2-NH-Boc[1]. NH2-C2-NH-Boc (PROTAC Linker 22) is a alkyl chain-based PROTAC linker can be used in the synthesis of PROTACs[2].

HY-P10673

KwFwLL-NH2	GHSR	Metabolic Disease
KwFwLL-NH2, a hexapeptide, is a ghrelin receptor ligand. KwFwLL-NH2 can act as a specific inverse agonist at the ghrelin receptor but with moderate potency (EC₅₀=45.6 nM) .

HY-P10065

RKLLW-NH2	Cathepsin	Inflammation/Immunology
RKLLW-NH2 is a Cathepsin L inhibitor .

HY-P1263A

*tcY-NH2* TFA** 1 Publications Verification (trans-Cinnamoyl)-YPGKF-NH2 TFA	Protease Activated Receptor (PAR)	Metabolic Disease Inflammation/Immunology
tcY-NH2 ((trans-Cinnamoyl)-YPGKF-NH2) TFA is a potent selective PAR4 antagonist peptide. tcY-NH2 TFA inhibits thrombin- and AY-NH₂-induced platelet aggregation and endostatin release, and can be used in the research of inflammation, immunology ^[2] .

Cat. No.	Product Name

HY-L907

MCE Kinase Hinge Binder Fragment Library

10,000 compounds

The most prominent mechanism of action of kinase inhibitors is their competition with ATP by binding to the hinge region of the kinase protein. Once the kinase is blocked by an inhibitor, it loses the ability to transfer phosphate groups from ATP to other molecules, resulting in the loss of kinase activity.

The hinge-binding region of kinase inhibitors mimics the interaction pattern between the ATP nucleobase and the kinase. MCE extracted thousands of kinase inhibitors from the ChEMBL database and isolated their molecular fragments. In certain cases, the amino and amide groups on the molecular fragments are crucial for binding in the hinge region. Therefore, we enhanced the diversity of the collected results by adding these two groups to unoccupied positions on the ring system. Subsequently, the fragments were assessed for their hinge region binding ability via docking at distinct kinases, we also applied pharmacophore constraints to ensure interactions with key amino acids in the kinase hinge region, ultimately obtaining kinase-related molecular fragments.

MCE provides over 10,000 kinase fragment molecules that meet the above requirements and are available off the shelf, serving as an effective tool for screening and developing drugs targeting kinases.

Cat. No.	Product Name	Type

HY-103684

RT-NH2 Real Thiol-NH2	Fluorescent Dyes/Probes
RT-NH2 is a RealThiol prototype without the carboxylic acid groups. RT-NH2 is fairly hydrophobic and cannot distribute in the nucleus, which is a hallmark of protein binding for fluorescent probe.

HY-D2442

Cy3-PEG-NH2

Fluorescent Dyes/Probes

Cy3-PEG-NH2 is a polyethylene glycol derivative containing Cy3 (HY-D0822) fluorescent dye and polyethylene glycol (PEG) and an amino group. The Cy3 fluorophore is commonly used in applications such as immunolabeling, nucleic acid labeling, fluorescence microscopy, and flow cytometry. Cy3 has an emission maximum around 562-570 nm. Cy3-PEG-NH2 can be used for fluorescence imaging, fluorescence tracing and fluorescence labeling .

HY-D2098

TAMRA-PEG2-NH2	Fluorescent Dyes/Probes
TAMRA-PEG2-NH2 is a dye derivative of TAMRA (HY-135640) containing 4 PEG units. TAMRA-PEG2-NH2 contains NH2 groups, which can undergo condensation reactions with carboxyl groups to form covalent bonds.

HY-D2101

TAMRA-PEG3-NH2	Fluorescent Dyes/Probes
TAMRA-PEG3-NH2 is a dye derivative of TAMRA (HY-135640) containing 3 PEG units. TAMRA-PEG3-NH2 contains NH2 groups, which can undergo condensation reactions with carboxyl groups to form covalent bonds.

HY-D2102

TAMRA-PEG7-NH2	Fluorescent Dyes/Probes
TAMRA-PEG7-NH2 is a dye derivative of TAMRA (HY-135640) containing 7 PEG units. TAMRA-PEG7-NH2 contains NH2 groups, which can undergo condensation reactions with carboxyl groups to form covalent bonds.

Cat. No.	Product Name	Target	Research Area

HY-P1310

VKGILS-NH2 1 Publications Verification	Protease Activated Receptor (PAR)	Inflammation/Immunology
VKGILS-NH2 is a reversed amino acid sequence control peptide for SLIGKV-NH2 (protease-activated receptor 2 (PAR2) agonist). VKGILS-NH2 has no effect on DNA synthesis in cells ^[2].

HY-P10930

*wrwyar-NH2* TFA**	DNA/RNA Synthesis	Cancer
wrwyar-NH2 (TFA) is a control peptide for wrwycr-NH2 (HY-P10930A) .

HY-P5755

SWELYYPLRANL-NH2	Peptides	Cancer
SWELYYPLRANL-NH2 is an E-cadherin and N-cadherin antagonist. SWELYYPLRANL-NH2 inhibits phage clone binding to E- or N-cad/Fc chimeric protein (IC₅₀: 0.7 and 0.09 μM respectively). SWELYYPLRANL-NH2 inhibits cell aggregation. SWELYYPLRANL-NH2 can be used to promote drug delivery through epithelial and endothelial permeability barriers .

HY-P0283

Protease-Activated Receptor-2, amide 2 Publications Verification	Protease Activated Receptor (PAR)	Cancer
Protease-Activated Receptor-2, amide (SLIGKV-NH₂) is a highly potent protease-activated receptor-2 (PAR2) activating peptide.

HY-P2638

Cholecystokinin (27-32)-amide CCK-27-32-NH2	Cholecystokinin Receptor	Neurological Disease
Cholecystokinin (27-32)-amide (CCK-27-32-NH2) is a potent cholecystokinin receptor CCK receptor antagonist .

HY-P4701

*pTH-Related Protein (1-34) amide* (human, mouse, rat)** Human PTHrP-(1-34)NH2	PTHR	Metabolic Disease
pTH-Related Protein (1-34) amide (human, mouse, rat) (Human PTHrP-(1-34)NH2) is a N-terminal fragments of PTHrP. pTH-Related Protein (1-34) amide (human, mouse, rat) induces hypercalcemia, and can be used for research of humoral hypercalcaemia of malignancy .

HY-P4832

Acetyl-Tau Peptide (273-284) amide	Amyloid-β	Neurological Disease
Acetyl-Tau Peptide (273-284) amide is an acetylated Tau peptide fragment. Acetyl-Tau Peptide (273-284) amide limits the substantial aggregation of Ac-Aβ(25–35)-NH2 and can be used as an inhibitor of Ac-Aβ(25–35)-NH2. Acetyl-Tau Peptide (273-284) amide can be used as an experimental model to investigate the Aβ/Tau cross-interaction ^[2].

HY-P1311

RLLFT-NH2	Drug Isomer	Others
RLLFT-NH2 is a reversed amino acid sequence negative control peptide for TFLLR-NH2 .

HY-P10215

Ac-{Cpg}-Thr-Ala-{Ala(CO)}-Asp-{Cpg}-NH2	Parasite	Infection
Ac-{Cpg}-Thr-Ala-{Ala(CO)}-Asp-{Cpg}-NH2 (compound 40) is a potent **Plasmodium subtilisin-like protease 1 (SUB1)** inhibitor. SUB1-IN-1 shows IC₅₀ values of 12 nM and 10 nM against P. vivax and P. falciparum SUB1 (Pv- and PfSUB1), respectively .

HY-P1310A

*VKGILS-NH2* TFA**	Protease Activated Receptor (PAR)	Inflammation/Immunology
VKGILS-NH2 TFA is a reversed amino acid sequence control peptide for SLIGKV-NH2 (protease-activated receptor 2 (PAR2) agonist). VKGILS-NH2 TFA has no effect on DNA synthesis in cells ^[2].

HY-P1311A

*RLLFT-NH2* TFA**	Protease Activated Receptor (PAR)	Others
RLLFT-NH2 TFA is a reversed amino acid sequence negative control peptide for TFLLR-NH2 (HY-P0226) .

HY-P5755A

*SWELYYPLRANL-NH2* TFA**	Peptides	Cancer
SWELYYPLRANL-NH2 TFA is an E-cadherin and N-cadherin antagonist. SWELYYPLRANL-NH2 TFA inhibits phage clone binding to E- or N-cad/Fc chimeric protein (IC₅₀: 0.7 and 0.09 μM respectively). SWELYYPLRANL-NH2 TFA inhibits cell aggregation. SWELYYPLRANL-NH2 can be used to promote drug delivery through epithelial and endothelial permeability barriers .

HY-P1263

tcY-NH2 (trans-Cinnamoyl)-YPGKF-NH2	Protease Activated Receptor (PAR)	Metabolic Disease Inflammation/Immunology
tcY-NH2 ((trans-Cinnamoyl)-YPGKF-NH2) is a potent selective PAR4 antagonist peptide. tcY-NH2 inhibits thrombin- and AY-NH₂-induced platelet aggregation and endostatin release, and can be used in the research of inflammation, immunology ^[2] .

HY-P5638

FLGFVGQALNALLGKL-NH2	Bacterial	Infection
FLGFVGQALNALLGKL-NH2 is an antimicrobial peptide of frog origin. FLGFVGQALNALLGKL-NH2 has activity against Staphylococcus aureus ATCC 29213 (MIC=32 μM) .

HY-P10201A

*Ac-GpYLPQTV-NH2* acetate**	STAT	Cancer
Ac-GpYLPQTV-NH2 acetate is a STAT3 inhibitor with an IC₅₀ value of 0.33 μM. Ac-GpYLPQTV-NH2 acetate has antitumor activity .

HY-P10201

Ac-GpYLPQTV-NH2	STAT	Cancer
Ac-GpYLPQTV-NH2 is a STAT3 inhibitor with an IC₅₀ value of 0.33 μM. Ac-GpYLPQTV-NH2 has antitumor activity .

HY-P10667

Ac-MRGDH-NH2	Integrin	Cancer
Ac-MRGDH-NH2 is a pentapeptide containing the RGD sequence. Ac-MRGDH-NH2 can be used to synthesize the diastereoisomeric prodrugs Λ- and Δ-[Ru(Ph2phen)2(κS,κN-(Ac-MRGDH-NH2))]Cl2. In these prodrugs, Ac-MRGDH-NH2 serves as a photolabile protecting group for the cytotoxic bis-aqua ruthenium warhead [Ru(Ph2phen)2(OH2)2]2+, and Ac-MRGDH-NH2 possesses integrin targeting ability and photosubstitution properties. Therefore, Ac-MRGDH-NH2 can be utilized in research on tumor-targeted photodynamic activation chemotherapy (PACT) .

HY-P10673

KwFwLL-NH2	GHSR	Metabolic Disease
KwFwLL-NH2, a hexapeptide, is a ghrelin receptor ligand. KwFwLL-NH2 can act as a specific inverse agonist at the ghrelin receptor but with moderate potency (EC₅₀=45.6 nM) .

HY-P10065

RKLLW-NH2	Cathepsin	Inflammation/Immunology
RKLLW-NH2 is a Cathepsin L inhibitor .

HY-P1263A

*tcY-NH2* TFA** 1 Publications Verification (trans-Cinnamoyl)-YPGKF-NH2 TFA	Protease Activated Receptor (PAR)	Metabolic Disease Inflammation/Immunology
tcY-NH2 ((trans-Cinnamoyl)-YPGKF-NH2) TFA is a potent selective PAR4 antagonist peptide. tcY-NH2 TFA inhibits thrombin- and AY-NH₂-induced platelet aggregation and endostatin release, and can be used in the research of inflammation, immunology ^[2] .

HY-P1312

LRGILS-NH2	Protease Activated Receptor (PAR)	Others
LRGILS-NH2 is a reverse-sequence protease-activated receptor-2 (PAR-2)-inactive, negative control, and SLIGRL-NH2 is a PAR-2-activating peptide .

HY-P10139

Dnp-PLGLWAr-NH2	MMP	Others
Dnp-PLGLWAr-NH2 is a synthetic collagenase/gelatinase substrate. Dnp-PLGLWAR-NH2 can be used to quantify total MMP activity in APMA-activated conditioned medium samples .

HY-P10930A

*wrwycr-NH2* TFA**	DNA/RNA Synthesis	Cancer
wrwycr-NH2 (TFA) is a peptide. wrwycr-NH2 (TFA) is cytotoxic to multiple cancer cells, can induce DNA damage and cell cycle arrest, but does not induce endoplasmic reticulum stress. wrwycr-NH2 (TFA) has anti-tumor activity, and it shows better efficacy when used in combination with DNA-damaging agents .

HY-P3591

YMRF-NH2	Calcium Channel	Neurological Disease
YMRF-NH2 is a neuropeptide. YMRF-NH2 binds to FMRFa-R with an EC₅₀ value of 31 nM ^[2].

HY-P1309A

*PAR-4 Agonist Peptide, amide* TFA** 2 Publications Verification PAR-4-AP TFA; AY-NH2 TFA	Protease Activated Receptor (PAR)	Inflammation/Immunology
PAR-4 Agonist Peptide, amide TFA (PAR-4-AP TFA; AY-NH2 TFA) is a proteinase-activated receptor-4 (PAR-4) agonist, which has no effect on either PAR-1 or PAR-2 and whose effects are blocked by a PAR-4 antagonist .

HY-P1309

PAR-4 Agonist Peptide, amide 2 Publications Verification PAR-4-AP; AY-NH2	Protease Activated Receptor (PAR)	Inflammation/Immunology
PAR-4 Agonist Peptide, amide (PAR-4-AP; AY-NH2) is a proteinase-activated receptor-4 (PAR-4) agonist, which has no effect on either PAR-1 or PAR-2 and whose effects are blocked by a PAR-4 antagonist.

HY-P3784

FKKSFKL-NH2	PKC	Metabolic Disease Inflammation/Immunology Cancer
FKKSFKL-NH2 is a protein kinase C-selective peptide. FKKSFKL-NH2 can be used for the research of various biochemical .

HY-P1312A

*LRGILS-NH2* TFA**	Protease Activated Receptor (PAR)	Others
LRGILS-NH2 TFA is a reverse-sequence protease-activated receptor-2 (PAR-2)-inactive, negative control, and SLIGRL-NH2 is a PAR-2-activating peptide .

HY-P4147

Ac-IHIHIQI-NH2	Peptides	Others
Ac-IHIHIQI-NH2 is a fibril-forming heptapeptide with high catalytic activity to laccase mimics. Ac-IHIHIQI-NH2 exhibits selectivity for hydrophobic p-nitrophenyl (ONp) ester substrates in the process of self-assembly ^[2].

HY-P10202

5-FAM-GpYLPQTV-NH2	STAT	Cancer
5-FAM-GpYLPQTV-NH2 is a fluorescently labeled peptide and has STAT3 inhibitory activity. 5-FAM-GpYLPQTV-NH2 can be used in cancer research .

HY-P4024

KKEDVV-Abu-CS-Abu-SYKK-NH2	Peptides	Others
KKEDVV-Abu-CS-Abu-SYKK-NH2 is a peptide. KKEDVV-Abu-CS-Abu-SYKK-NH2 can be used for various biochemical research.

HY-P5360

TFLLRN-NH2	Protease Activated Receptor (PAR)	Others
TFLLRN-NH2 is a biological active peptide. (PAR-1 Agonist)

HY-P5456

KRPpSQRHGSKY-NH2	PKC	Others
KRPpSQRHGSKY-NH2 is a biological active peptide. (This is a phosphorylated PKC substrate peptide)

HY-P4292

H-Gly-Pro-Gly-NH2	HIV Amino Acid Derivatives	Infection
H-Gly-Pro-Gly-NH2 is a tripeptide that inhibits HIV-1 replication. H-Gly-Pro-Gly-NH2 inhibits the activity of HIV-1 III_B and HIV-2 ROD with EC₅₀ values of 35 µM and 30 µM, respectively. H-Gly Pro Gly NH2 inhibits HIV-1 replication in vitro by interfering with capsid formation. H-Gly Pro Gly NH2 has antiviral activity and can be used for virus research ^[2] .

HY-P0226

TFLLR-NH2	Protease Activated Receptor (PAR)	Cardiovascular Disease
TFLLR-NH2 is a selective PAR1 agonist with an EC₅₀ of 1.9 μM.

HY-P1260

FSLLRY-NH2 5 Publications Verification	Protease Activated Receptor (PAR)	Neurological Disease
FSLLRY-NH2 is a protease-activated receptor 2 (PAR2) inhibitor .

HY-P10683

RAWVAWR-NH2	Bacterial	Infection
RAWVAWR-NH2 is a peptide derived from human lysozyme with antibacterial activity .

HY-P4487

H-Pro-Pro-Asp-NH2	Biochemical Assay Reagents	Others
H-Pro-Pro-Asp-NH2 is a potent and selective catalyst for asymmetric aldol reactions. H-Pro-Pro-Asp-NH2 catalyzes aldol reactions between acetone and several aldehydes ^[2].

HY-W015987

9-Fluorenylmethyl carbamate Fmoc-NH2	Biochemical Assay Reagents	Others
9-Fluorenylmethyl carbamate (Fmoc-NH2) is an amide compound with an Fmoc protecting group, which can be used as a photobase initiator to prepare organosilane-based proton exchange membranes .

HY-P5245

Ac-KLKKTETQ-NH2	Peptides	Metabolic Disease
Ac-KLKKTETQ-NH2, a peptide, has the potential for cosmetics research .

HY-P4233

H-Gly-Arg-Gly-Asp-Ser-NH2	Peptides	Cancer
Gly-Arg-Gly-Asp-Ser-NH2 is a pentapeptide with no N-terminal modification. Gly-Arg-Gly-Asp-Ser-NH2 can be coupled to carrriers ^[2].

HY-P3975

Glp-His-Pro-Gly-NH2 pGlu-His-Pro-Gly-NH2	GnRH Receptor	Endocrinology
Glp-His-Pro-Gly-NH2 (pGlu-His-Pro-Gly-NH2) is a peptide containing 4 amino acids. Glp-His-Pro-Gly-NH2 stimulates gonadotrophin, luteinizing hormone (LH) and follicle stimulating hormone (FSH) release ^[2].

HY-P5756

CSD-CH2(1,8)-NH2	Opioid Receptor	Neurological Disease
CSD-CH2(1,8)-NH2 is a selective and competitive KOR antagonist (K_i: 6.8 nM). CSD-CH2(1,8)-NH2 inhibits calcium mobilization in DRG neurons. CH2(1,8)-NH2 antagonizes the antinociceptive effect of U50,488. CSD-CH2(1,8)-NH2 can be used for research of neuropsychiatric disorders .

HY-P3593

LPLRF-NH2	Calcium Channel	Cardiovascular Disease Neurological Disease
LPLRF-NH2 is a member of RFamide peptide with anorexigenic effect. LPLRF-NH2 increases arterial blood pressure and modulates the electrical activity of brainstem neurons ^[2] .

HY-P3592

YLPLRF-NH2	Peptides	Others
YLPLRF-NH2 is a synthetic peptide.

HY-P4671

*Nle-Arg-Phe-NH2* acetate**	Drug Derivative	Others
Nle-Arg-Phe-NH2 (acetate) is a tripeptide compound, usually in the form of acetate .

HY-P3421

NH2-SSK-COOH	Peptides	Cancer
NH2-SSK-COOH is a oligopeptide compoused of Ser-Ser-Lys.

HY-P3420

NH2-ASK-COOH	Peptides	Cancer
NH2-ASK-COOH is a oligopeptide compoused of Ala-Ser-Lys.

HY-P3423

NH2-KAA-COOH	Peptides	Cancer
NH2-KAA-COOH is a oligopeptide compoused of Lys-Ala-Ala.

Cat. No.	Product Name

HY-K0226

CHO Magnetic Beads (200 nm, 10 mg/mL)
MCE CHO Magnetic Beads (200 nm, 10 mg/mL) contain CHO functional groups, which react with primary amines on proteins or other molecules to form stable amide linkages，can covalently immobilize proteins for the affinity purification of antibodies, antigens and other biomolecules.

HY-K0227

NHS Magnetic Beads (200nm, 10 mg/mL)
MCE NHS Magnetic Beads (200 nm, 10 mg/mL) contain N-hydroxysuccinimide (NHS) functional groups, which react with primary amines on proteins or other molecules to form stable amide linkages，can covalently immobilize proteins for the affinity purification of antibodies, antigens and other biomolecules.

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-N11886

*5-NH2-Baicalein*	Structural Classification Flavonoids Classification of Application Fields Animals Flavones Source classification Other Diseases Endogenous metabolite Disease Research Fields	Drug Metabolite
5-NH2-Baicalein is an aminated metabolite of Baicalein (HY-N0196). 5-NH2-Baicalein can be used for research of ammonia and ammonia-associated chronic diseases .

HY-134313

*8-NH2-ATP* 8-Aminoadenosine-5'-O-triphosphate	Structural Classification Natural Products Classification of Application Fields Source classification Metabolic Disease Endogenous metabolite Disease Research Fields	DNA/RNA Synthesis Endogenous Metabolite
8-NH2-ATP, an inactive form of ATP, is produced by 8-NH2-Ado. 8-NH2-Ado is reported to be potent as shown by induction of apoptosis-related cleavage of poly (ADP-ribose) polymerase ^[2].

Species:	Human (12) Bovine (1)
Tag:	GFP (1) His (13) Tag Free (2) Strep (5) GST (1) Trx (1) Flag (7)
Source:	HEK293 (8) E. coli (9)

Cat. No.	Compare	Product Name	Species	Source

HY-P74650

	*PC4/SUB1 Protein, Human (His)* Activated RNA polymerase II transcriptional coactivator p15; PC4; p14; sub1; RPO2TC1	Human	E. coli
	The PC4/SUB1 protein acts as a multifunctional coactivator that cooperates with TAF to promote functional interactions between upstream activators and the general transcription machinery. Its role extends to the potential stability of multiprotein transcription complexes. PC4/SUB1 Protein, Human (His) is the recombinant human-derived PC4/SUB1 protein, expressed by E. coli , with N-His labeled tag. The total length of PC4/SUB1 Protein, Human (His) is 127 a.a., with molecular weight of ~19 kDa.

HY-P702119

	FDH1 Protein, Candida boidinii FDH1; formate dehydrogenase; FDH; NAD-dependent formate dehydrogenase	Others	E. coli
	FDH1 protein serves as a catalyst in the NAD(+)-dependent oxidation of formate to carbon dioxide. This enzymatic activity represents the conclusive step in the methanol oxidation pathway within methylotrophic microorganisms. Beyond its involvement in methylotrophic organisms, FDH1 also plays a crucial role in non-methylotrophic organisms, where it contributes to the detoxification of exogenous formate. FDH1 Protein, Candida boidinii is the recombinant FDH1 protein, expressed by E. coli , with tag free. The total length of FDH1 Protein, Candida boidinii is 364 a.a., .

HY-P702120

	FDH1 Protein, Candida boidinii (His) FDH1; formate dehydrogenase; FDH; NAD-dependent formate dehydrogenase	Others	E. coli
	FDH1 protein serves as a catalyst in the NAD(+)-dependent oxidation of formate to carbon dioxide. This enzymatic activity represents the conclusive step in the methanol oxidation pathway within methylotrophic microorganisms. Beyond its involvement in methylotrophic organisms, FDH1 also plays a crucial role in non-methylotrophic organisms, where it contributes to the detoxification of exogenous formate. FDH1 Protein, Candida boidinii (His) is the recombinant FDH1 protein, expressed by E. coli , with N-6*His labeled tag. The total length of FDH1 Protein, Candida boidinii (His) is 364 a.a., .

HY-P703500

	FDH Protein, Pseudomonas sp. formate dehydrogenase; NAD-dependent formate dehydrogenase; Pseudomonas sp. (strain 101); Achromobacter parvulus T1; Oxidoreductase; 1.17.1.9	Others	E. coli
	FDH Protein, Pseudomonas sp. is the recombinant FDH, expressed by E. coli , with tag Free labeled tag. The total length of FDH Protein, Pseudomonas sp. is 400 a.a., .

HY-P703501

	FDH Protein, Pseudomonas sp. (His, Strep) formate dehydrogenase; NAD-dependent formate dehydrogenase; Pseudomonas sp. (strain 101); Achromobacter parvulus T1; Oxidoreductase; 1.17.1.9	Human	E. coli
	FDH Protein, Pseudomonas sp. (His, Strep) is the recombinant human-derived FDH, expressed by E. coli , with Strep, His labeled tag. The total length of FDH Protein, Pseudomonas sp. (His, Strep) is 400 a.a.,

HY-P703502

	FDH Protein, Pseudomonas sp. (His, Strep) formate dehydrogenase; NAD-dependent formate dehydrogenase; Pseudomonas sp. (strain 101); Achromobacter parvulus T1; Oxidoreductase; 1.17.1.9	Others	E. coli
	FDH Protein, Pseudomonas sp. (His, Strep) is the recombinant FDH, expressed by E. coli , with Strep, His labeled tag. The total length of FDH Protein, Pseudomonas sp. (His, Strep) is 400 a.a., .

HY-P71174

	NTAQ1 Protein, Human (GST) Protein N-terminal glutamine amidohydrolase; WDYHV1; Protein NH2-terminal glutamine deamidase; N-terminal Gln amidase; Nt(Q)-amidase; C8orf32; NTAQ1	Human	E. coli
	NTAQ1 Protein is a monomeric globular protein with alpha-beta-alpha three-layer sandwich architecture. NTAQ1 converts N-terminal glutamine to glutamate by eliminating the amine group and plays an essential role in the N-end rule pathway for protein degradation. The active site and catalytic mechanism of NTAQ1 are similar to those of transglutaminases. NTAQ1 Protein, Human (GST) is the recombinant human-derived NTAQ1 protein, expressed by E. coli , with N-GST labeled tag.

HY-P703334

	ABCF3 Protein, Human (HEK293, His, Strep, Flag) ATP-binding cassette sub-family F member 3; ABCF3; Homo sapiens; Human	Human	HEK293
	ABCF3 Protein, Human (HEK293, His, Strep, Flag) is the recombinant human-derived ABCF3, expressed by HEK293 , with Strep, His, Flag labeled tag. The total length of ABCF3 Protein, Human (HEK293, His, Strep, Flag) is 708 a.a.,

HY-P7621

	ABCB5 Protein, Human (Trx) rHuABCB5, N-Trx; ATP-binding cassette sub-family B member 5; P-glycoprotein ABCB5; ABCB5	Human	E. coli
	ABCB5, N-Trx Protein, Human is a plasma membrane-spanning protein that in humans is encoded by the ABCB5 gene. ABCB5 is an ABC transporter and P-glycoprotein family member principally expressed in physiological skin and human malignant melanoma.

HY-P703309

	ABCA6 Protein, Human (HEK293, His, Strep, Flag) ATP-binding cassette sub-family A member 6; ABCA6; Homo sapiens; Human; Translocase	Human	HEK293
	ABCA6 Protein, Human (HEK293, His, Strep, Flag) is the recombinant human-derived ABCA6, expressed by HEK293 , with Strep, His, Flag labeled tag. The total length of ABCA6 Protein, Human (HEK293, His, Strep, Flag) is 1616 a.a.,

HY-P72069

	ABCC1 Protein, Human (His) ABC 29; ABC29; ABCC 1; ABCC; Abcc1; ATP binding cassette sub family C CFTR/MRP; member 1; ATP binding cassette sub-family C member 1; ATP binding cassette subfamily C member 1; ATP binding cassette transporter variant ABCC1delta ex13; ATP binding cassette transporter variant ABCC1delta ex13&14; ATP binding cassette transporter variant ABCC1delta ex25; ATP binding cassette transporter variant ABCC1delta ex25&26; ATP binding cassette, sub-family C CFTR/MRP; , member 1; ATP-binding cassette sub-family C member 1; DKFZp686N04233; DKFZp781G125; GS X; GSX; Leukotriene C4; transporter; LTC4 transporter; MRP 1; MRP; MRP1; MRP1_HUMAN; Multidrug resistance associated protein 1; Multidrug resistance protein; Multidrug resistance-associated protein 1; Multiple drug resistance associated protein; Multiple drug resistance protein 1	Human	E. coli
	ABCC1, Human (His) is a multitasking ATP-binding cassette (ABC) transporter. ABCC1, Human plays a part in inflammatory and other immunological diseases, age-related macular degeneration, cardiovascular disease, and certain neurological disorders as well as tumor progression.

HY-P701355

	bABCC1 Protein, Bovine (HEK293, GFP, StrepⅡ, His) ABCC1; Multidrug resistance-associated protein 1; ATP-binding cassette sub-family C member 1; Glutathione-S-conjugate-translocating ATPase ABCC1; Leukotriene C(4) transporter; LTC4 transporter	Bovine	HEK293
	The bABCC1 protein plays a key role in cellular physiology, mediating the ATP-dependent export of a variety of substrates, including drugs and organic anions. Notably, it confers resistance to anticancer drugs, actively reducing their intracellular accumulation. bABCC1 Protein, Bovine (HEK293, GFP, Strep, His) is the recombinant human-derived bABCC1 protein, expressed by HEK293 , with C-10*His, C-GFP, C-Strep labeled tag. The total length of bABCC1 Protein, Bovine (HEK293, GFP, Strep, His) is 1530 a.a., .

HY-P703304

	ABCB10 Protein, Human (HEK293, Flag, His, E659Q) ATP-binding cassette sub-family B member 10, mitochondrial; ABC-mitochondrial erythroid protein; ABC-me protein; ATP-binding cassette transporter 10; ABC transporter 10 protein; Mitochondrial ATP-binding cassette 2; M-ABC2; ABCB10; Homo sapiens; Human; ABC transporter 10 protein	Human	HEK293
	ABCB10 Protein, Human (HEK293, Flag, His, E659Q) is the recombinant human-derived ABCB10, expressed by HEK293 , with His, Flag labeled tag. ,

HY-P703305

	ABCB10 Protein, Human (HEK293, Flag, His, N229A) ATP-binding cassette sub-family B member 10, mitochondrial; ABC-mitochondrial erythroid protein; ABC-me protein; ATP-binding cassette transporter 10; ABC transporter 10 protein; Mitochondrial ATP-binding cassette 2; M-ABC2; ABCB10; Homo sapiens; Human; ABC transporter 10 protein	Human	HEK293
	ABCB10 Protein, Human (HEK293, Flag, His, N229A) is the recombinant human-derived ABCB10, expressed by HEK293 , with His, Flag labeled tag. ,

HY-P703306

	ABCB10 Protein, Human (HEK293, Flag, His, N407A) ATP-binding cassette sub-family B member 10, mitochondrial; ABC-mitochondrial erythroid protein; ABC-me protein; ATP-binding cassette transporter 10; ABC transporter 10 protein; Mitochondrial ATP-binding cassette 2; M-ABC2; ABCB10; Homo sapiens; Human; ABC transporter 10 protein	Human	HEK293
	ABCB10 Protein, Human (HEK293, Flag, His, N407A) is the recombinant human-derived ABCB10, expressed by HEK293 , with His, Flag labeled tag. ,

HY-P703307

	ABCB10 Protein, Human (HEK293, Flag, His, N229A, F398A) ATP-binding cassette sub-family B member 10, mitochondrial; ABC-mitochondrial erythroid protein; ABC-me protein; ATP-binding cassette transporter 10; ABC transporter 10 protein; Mitochondrial ATP-binding cassette 2; M-ABC2; ABCB10; Homo sapiens; Human; ABC transporter 10 protein	Human	HEK293
	ABCB10 Protein, Human (HEK293, Flag, His, N229A, F398A) is the recombinant human-derived ABCB10, expressed by HEK293 , with His, Flag labeled tag. ,

HY-P703308

	ABCB10 Protein, Human (HEK293, Flag, His, N229A, N407A) ATP-binding cassette sub-family B member 10, mitochondrial; ABC-mitochondrial erythroid protein; ABC-me protein; ATP-binding cassette transporter 10; ABC transporter 10 protein; Mitochondrial ATP-binding cassette 2; M-ABC2; ABCB10; Homo sapiens; Human; ABC transporter 10 protein	Human	HEK293
	ABCB10 Protein, Human (HEK293, Flag, His, N229A, N407A) is the recombinant human-derived ABCB10, expressed by HEK293 , with His, Flag labeled tag. ,

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Cat. No.	Product Name	Chemical Structure

HY-161022S1

**FL118-C3-O-C-amide-C-NH2-d5 formate**
FL118-C3-O-C-amide-C-NH2-d5 formate is a deuterium labeled FL118-C3-O-C-amide-C-NH2 formate. FL118-C3-O-C-amide-C-NH2 formate is an ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .

HY-W007497S

*H-β-Ala-NH2.-d4HCl*
H-β-Ala-NH2.-d₄ HCl is the deuterium labeled H-β-Ala-NH2.HCl[1].

HY-145397S

*(4-NH2)-Exatecan-d5*
(4-NH2)-Exatecan-d5 is a deuterated labeled (4-NH2)-Exatecan . (4-NH2)-Exatecan (compound A), a topoisomerase inhibitor, is a derivative of Exatecan. (4-NH2)-Exatecan can be used in the synthesis of antibody-drug conjugates (ADCs) ^[2].

HY-161022S

FL118-C3-O-C-amide-C-NH2-d5
FL118-C3-O-C-amide-C-NH2-d₅ is a deuterium labeled FL118-C3-O-C-amide-C-NH2 .

HY-40171S

NH2-C2-NH-Boc-d4
NH2-C2-NH-Boc-d₄ is the deuterium labeled NH2-C2-NH-Boc[1]. NH2-C2-NH-Boc (PROTAC Linker 22) is a alkyl chain-based PROTAC linker can be used in the synthesis of PROTACs[2].

Cat. No.	Compare	Product Name	Application	Reactivity

HY-P80527

	ABCB5 Antibody (YA836) ABCB5 P-gp; ATP binding cassette sub family B (MDR/TAP) member 5; P glycoprotein ABCB5	WB, ICC/IF	Human
	ABCB5 Antibody (YA836) is a non-conjugated and Mouse origined monoclonal antibody about 139 kDa, targeting to ABCB5 (8D2). It can be used for WB,ICC/IF assays with tag free, in the background of Human.

HY-P80772

	P Glycoprotein Antibody 2 Publications Verification p-pg; PGP; ABCB1; MDR1; PGY1; Multidrug resistance protein 1; ATP-binding cassette sub-family B member 1; P-glycoprotein 1; CD antigen CD243	WB	Human
	P Glycoprotein Antibody is a non-conjugated and Rabbit origined monoclonal antibody about 141 kDa, targeting to P Glycoprotein. It can be used for WB assays with tag free, in the background of Human.

HY-P81118

	MRP2 Antibody ABC30 antibody; abcC2 antibody; ATP binding cassette sub family C (CFTR/MRP) member 2 antibody; ATP binding cassette subfamily C member 2 antibody; ATP-binding cassette sub-family C member 2 antibody; Canalicular multidrug resistance protein antibody; Canalicular multispecific organic anion transporter 1 antibody; CMOAT antibody; CMOAT1 antibody; cMRP antibody; DJS antibody; KIAA1010 antibody; MRP 2 antibody; MRP2_HUMAN antibody; Multidrug resistance associated protein 2 antibody; Multidrug resistance-associated protein 2 antibody;	WB, ICC/IF, FC	Human
	MRP2/ABCC2 Antibody is an unconjugated, approximately 174 kDa, rabbit-derived, anti-MRP2/ABCC2 monoclonal antibody. MRP2/ABCC2 Antibody can be used for: WB, ICC/IF, FC expriments in human background without labeling.

HY-P83773

	CFTR Antibody(YA3569) ABC 35 antibody ABC35 antibody ABCC 7 antibody ABCC7 antibody ATP binding cassette sub family C member 7 antibody; cAMP dependent chloride channel antibody; cAMP-dependent chloride channel antibody; CF antibody; CFTR antibody; CFTR/MRP antibody; CFTR_HUMAN antibody; Channel conductance controlling ATPase antibody; Channel conductance-controlling ATPase antibody; Cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub family C, member 7) antibody; Cystic fibrosis transmembrane conductance regulator antibody; Cystic Fibrosis Transmembrane Regulator antibody; dJ760C5.1 antibody; MRP 7 antibody; MRP7 antibody; TNR CFTR antibody	WB, IP	Human