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

By Targets:	ADC Cytotoxin (3) ADC Linker (12) Amino Acid Derivatives (1) Amyloid-β (2) Apoptosis (4) Autophagy (2) Bacterial (1) Biochemical Assay Reagents (1) Cathepsin (1) DNA/RNA Synthesis (2) Drug Metabolite (1) Drug-Linker Conjugates for ADC (3) E3 Ligase Ligand-Linker Conjugates (4) Endogenous Metabolite (2) Fluorescent Dye (4) HIF/HIF Prolyl-Hydroxylase (1) HIV (1) IAP (1) Isotope-Labeled Compounds (3) Ligands for E3 Ligase (4) Ligands for Target Protein for PROTAC (2) Opioid Receptor (1) PKC (1) PROTAC Linkers (7) Protease Activated Receptor (PAR) (11) STAT (2) STING (2) Survivin (1) Topoisomerase (2) Virus Protease (1)
By Research Areas:	Cancer (49) Cardiovascular Disease (3) Endocrinology (1) Infection (3) Inflammation/Immunology (9) Metabolic Disease (7) Neurological Disease (8)

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-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-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-161022S

FL118-C3-O-C-amide-C-NH2-d5

Isotope-Labeled Compounds ADC Linker Others

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-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 .

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)..

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

**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) .

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

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

Others Others

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

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

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

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

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

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) .

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-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

Others Cancer

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

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

HY-145399

*Mal-PEG8-amide-Val-Ala-(4-NH2)-Exatecan* SG 3932	Drug-Linker Conjugates for ADC Topoisomerase	Cancer
Mal-PEG8-amide-Val-Ala-(4-NH2)-Exatecan is a Drug-Linker Conjugates for ADC, which comprises a topoisomerase inhibitor and a linker for ligand unit connecting. Mal-PEG8-amide-Val-Ala-(4-NH2)-Exatecan can be used to synthesis antibody-drug conjugate (ADC) .

HY-139085B

XL388-C2-amide-PEG9-NH2 TFA

Others Cancer

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

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

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].

*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-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 .

**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-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-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-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-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-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-148872

Thalidomide-5-NH2-C8-NH2 TFA

Biochemical Assay Reagents Others

Thalidomide-5-NH2-C8-NH2 TFA can be used for compound synthesis .

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

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-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-P10065

RKLLW-NH2

Cathepsin Inflammation/Immunology

RKLLW-NH2 is a Cathepsin L inhibitor .

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 .

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-P1309A

*PAR-4 Agonist Peptide, amide* TFA** 1 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 1 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-D2098

TAMRA-PEG2-NH2	Fluorescent Dye	Others
TAMRA-PEG2-NH2 是含有 4 个 PEG 单元的 TAMRA (HY-135640) 染料衍生物。TAMRA-PEG2-NH2 含有 NH2 团，可以与羧基发生缩合反应形成共价键。

HY-D2101

TAMRA-PEG3-NH2	Fluorescent Dye	Others
TAMRA-PEG3-NH2 是含有 3 个 PEG 单元的 TAMRA (HY-135640) 染料衍生物。TAMRA-PEG3-NH2 含有 NH2 团，可以与羧基发生缩合反应形成共价键。

HY-D2102

TAMRA-PEG7-NH2	Fluorescent Dye	Others
TAMRA-PEG7-NH2 是含有 7 个 PEG 单元的 TAMRA (HY-135640) 染料衍生物。TAMRA-PEG7-NH2 含有 NH2 团，可以与羧基发生缩合反应形成共价键。

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 .

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-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-103684

RT-NH2 Real Thiol-NH2	Fluorescent Dye	Neurological Disease
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-P5360

TFLLRN-NH2

Protease Activated Receptor (PAR) Others

TFLLRN-NH2 is a biological active peptide. (PAR-1 Agonist)

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

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-136008A

*(S,R,S)-AHPC-PEG1-NH2* dihydrochloride** VH032-PEG1-NH2 dihydrochloride	E3 Ligase Ligand-Linker Conjugates	Cancer
(S,R,S)-AHPC-PEG1-NH2 (VH032-PEG1-NH2) dihydrochloride incorporates a VHL ligand for the E3 ubiquitin ligase and a PROTAC linker. (S,R,S)-AHPC-PEG1-NH2 dihydrochloride can be used to design PROTACs .

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-145397

*(4-NH2)-Exatecan*	ADC Cytotoxin Topoisomerase	Cancer
(4-NH2)-Exatecan, a topoisomerase inhibitor, is a derivative of Exatecan. (4-NH2)-Exatecan can be used in the synthesis of antibody-drug conjugates (ADCs) (US20200306243A1, compound A) .

HY-N11886

*5-NH2-Baicalein*	Drug Metabolite	Others
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-P1260

FSLLRY-NH2

1 Publications Verification

Protease Activated Receptor (PAR) Neurological Disease

FSLLRY-NH2 is a protease-activated receptor 2 (PAR2) inhibitor .

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-D2098

TAMRA-PEG2-NH2	Fluorescent Dyes/Probes
TAMRA-PEG2-NH2 是含有 4 个 PEG 单元的 TAMRA (HY-135640) 染料衍生物。TAMRA-PEG2-NH2 含有 NH2 团，可以与羧基发生缩合反应形成共价键。

HY-D2101

TAMRA-PEG3-NH2	Fluorescent Dyes/Probes
TAMRA-PEG3-NH2 是含有 3 个 PEG 单元的 TAMRA (HY-135640) 染料衍生物。TAMRA-PEG3-NH2 含有 NH2 团，可以与羧基发生缩合反应形成共价键。

HY-D2102

TAMRA-PEG7-NH2	Fluorescent Dyes/Probes
TAMRA-PEG7-NH2 是含有 7 个 PEG 单元的 TAMRA (HY-135640) 染料衍生物。TAMRA-PEG7-NH2 含有 NH2 团，可以与羧基发生缩合反应形成共价键。

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-P4701

*pTH-Related Protein (1-34) amide* (human, mouse, rat)** Human PTHrP-(1-34)NH2	Peptides	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-P10215

Ac-{Cpg}-Thr-Ala-{Ala(CO)}-Asp-{Cpg}-NH2	Peptides	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-P1311

RLLFT-NH2

Peptides Others

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

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-P1311A

RLLFT-NH2 TFA

Peptides Others

RLLFT-NH2 TFA is a reversed amino acid sequence negative control peptide for TFLLR-NH2 .

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-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-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-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-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-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-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-P1309A

*PAR-4 Agonist Peptide, amide* TFA** 1 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 1 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-P1312

LRGILS-NH2

Peptides 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	Peptides	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-P3591

YMRF-NH2

Peptides Neurological Disease

YMRF-NH2 is a neuropeptide. YMRF-NH2 binds to FMRFa-R with an EC₅₀ value of 31 nM ^[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-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

Peptides 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-P5360

TFLLRN-NH2

Protease Activated Receptor (PAR) Others

TFLLRN-NH2 is a biological active peptide. (PAR-1 Agonist)
HY-P5456

KRPpSQRHGSKY-NH2

Peptides 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

1 Publications Verification

Protease Activated Receptor (PAR) Neurological Disease

FSLLRY-NH2 is a protease-activated receptor 2 (PAR2) inhibitor .

HY-P4487

H-Pro-Pro-Asp-NH2	Peptides	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-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-P5245

Ac-KLKKTETQ-NH2

Peptides Metabolic Disease

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

HY-P3975

Glp-His-Pro-Gly-NH2 pGlu-His-Pro-Gly-NH2	Peptides	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	Peptides	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-P3437

Dabcyl-KTSAVLQSGFRKM-Glu(Edans)-NH2	Virus Protease	Others
Dabcyl-KTSAVLQSGFRKM-Glu(Edans)-NH2 is a fluorogenic peptide, as the substrate to measure the enzymatic activities of protease forms. Dabcyl-KTSAVLQSGFRKM-Glu(Edans)-NH2 can be used for researching 2019-nCoV (COVID-19) infection.

HY-P4671

Nle-Arg-Phe-NH2 acetate

Peptides Others

Nle-Arg-Phe-NH2 (acetate) is a tripeptide compound, usually in the form of acetate .
HY-P3422

NH2-AKA-COOH

Peptides Cancer

NH2-AKA-COOH is a oligopeptide compoused of Ala-Lys-Ala.
HY-P3423

NH2-KAA-COOH

Peptides Cancer

NH2-KAA-COOH is a oligopeptide compoused of Lys-Ala-Ala.
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-P1060

LPYFD-NH2	Amyloid-β	Neurological Disease
LPYFD-NH2, a pentapeptide, exerts some inhibitory effect on the aggregation of Aβ(1-42). LPYFD-NH2 can be used for the research of Alzheimer’s disease .

HY-P1260A

FSLLRY-NH2 TFA

1 Publications Verification

Protease Activated Receptor (PAR) Neurological Disease

FSLLRY-NH2 TFA is a protease-activated receptor 2 (PAR2) inhibitor .

HY-P2708

H-Gly-Pro-Arg-Pro-NH2	Peptides	Cardiovascular Disease
H-Gly-Pro-Arg-Pro-NH2 is a peptide that mimics the N-terminal Gly-Pro-Arg region in the a chain of fibrin protein. H-Gly-Pro-Arg-Pro-NH2 prevents fibrin polymerization .

HY-P4014

HSDAVFTDNYTRLRRQLAVRRYLNSILN-NH2

Peptides Inflammation/Immunology

HSDAVFTDNYTRLRRQLAVRRYLNSILN-NH2 is an anti-inflammatory peptide .

HY-P5915

FAM-DEALA-Hyp-YIPMDDDFQLRSF-NH2	HIF/HIF Prolyl-Hydroxylase	Cancer
FAM-DEALA-Hyp-YIPMDDDFQLRSF-NH2, a 5-FAM labeled HIF-1α peptide, is a substrate of VHL. FAM-DEALA-Hyp-YIPMDDDFQLRSF-NH2 binds to VHL protein with a K_D of 3 nM. Ex/Em (λ) = 485/520 nm .

HY-P6028

GSNKSKPK-NH2

Peptides Others

GSNKSKPK-NH2 is a model peptide based on a c-Src N-terminal peptide that can be used as NMT substrate .

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-134313A

*8-NH2-ATP tetrasodium* 8-Aminoadenosine-5'-O-triphosphate tetrasodium	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 tetrasodium, an inactive form of ATP, is produced by 8-NH2-Ado. 8-NH2-Ado tetrasodium induces apoptosis-related cleavage of poly (ADP-ribose) polymerase ^[2].

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)
Tag:	GFP (3) His (10) SUMO (1) Strep (3) GST (1) Trx (1)
Source:	HEK293 (3) E. coli Cell-free (5) E. coli (4)

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-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. The total length of NTAQ1 Protein, Human (GST) is 205 a.a., with molecular weight of 45-50 kDa.

HY-P702276

	FAAH2 Protein, Human (Cell-Free, His) Fatty-acid amide hydrolase 2; Amidase domain-containing protein; Anandamide amidohydrolase 2; Oleamide hydrolase 2	Human	E. coli Cell-free
	FAAH2 proteins play a central role in cellular processes by catalyzing the hydrolysis of endogenous amidated lipids, including the sleep-inducing lipid oleamide ((9Z)-octadecylamide) and the endocannabinoid anandamide (N-(5Z) , 8Z, 11Z, 14Z-eicosate tetraenoyl)))-ethanolamine) and other fatty amides. FAAH2 Protein, Human (Cell-Free, His) is the recombinant human-derived FAAH2 protein, expressed by E. coli Cell-free , with N-10*His labeled tag. The total length of FAAH2 Protein, Human (Cell-Free, His) is 532 a.a., with molecular weight of 59.8 kDa.

HY-P702197

	ABCD3 Protein, Human (Cell-Free, His) ATP-binding cassette sub-family D member 3; 70 kDa peroxisomal membrane protein; PMP70	Human	E. coli Cell-free
	ABCD3 is a member of the ATP-binding cassette (ABC) family. ABCD3 Protein, Human (Cell-Free, His) is the recombinant human-derived ABCD3 protein, expressed by E. coli Cell-free , with N-10*His labeled tag. The total length of ABCD3 Protein, Human (Cell-Free, His) is 659 a.a., with molecular weight of 81.5 kDa.

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-P72012

	ABCD1 Protein, Human (Cell-Free, His) ABC42; Abcd1; ABCD1_HUMAN; Adrenoleukodystrophy protein; ALD; Aldgh; ALDP; AMN; ATP binding cassette; sub family D ALD; ; member 1; ATP-binding cassette sub-family D member 1; OTTHUMP00000025960; OTTMUSP00000019283; RGD1562128; RP23 373N8.2; X linked adrenoleukodystrophy ALD; gene homolog	Human	E. coli Cell-free
	ABCD1, Human (His) is one of the four ATP-binding cassette (ABC) proteins in subfamily D. Dysfunction of ABCD1 causes neurodegenerative disorder X-linked adrenoleukodystrophy (X-ALD).

HY-P702196

	ABCD2 Protein, Human (Cell-Free, His) ATP-binding cassette sub-family D member 2; Adrenoleukodystrophy-like 1; Adrenoleukodystrophy-related protein; hALDR	Human	E. coli Cell-free
	ABCD2 protein is an ATP-dependent transporter in the ABC family that promotes the transport of very long chain fatty acids (VLCFA)-CoA into peroxisomes and exhibits fatty acyl-CoA thioesterase (ACOT) and ATPase activities. Its substrate specificity overlaps with ABCD1, including a clear preference for shorter VLCFA (C22:0) and polyunsaturated fatty acids (PUFA) such as C22:6-CoA and C24:6-CoA. ABCD2 Protein, Human (Cell-Free, His) is the recombinant human-derived ABCD2 protein, expressed by E. coli Cell-free , with N-10*His labeled tag. The total length of ABCD2 Protein, Human (Cell-Free, His) is 740 a.a., with molecular weight of 89.3 kDa.

HY-P702195

	ABCB8 Protein, Human (Cell-Free, His, SUMO) Mitochondrial potassium channel ATP-binding subunit; ATP-binding cassette sub-family B member 8, mitochondrial; ABCB8; Mitochondrial ATP-binding cassette 1; M-ABC1; Mitochondrial sulfonylurea-receptor; MITOSUR	Human	E. coli Cell-free
	ABCB8 is the ATP-binding subunit of mitochondrial potassium channels and cooperates with CCDC51/MITOK to form mitoK (ATP) channels in the inner mitochondrial membrane. This complex promotes ATP-dependent potassium currents. ABCB8 Protein, Human (Cell-Free, His, SUMO) is the recombinant human-derived ABCB8 protein, expressed by E. coli Cell-free , with N-6*His, N-SUMO labeled tag. The total length of ABCB8 Protein, Human (Cell-Free, His, SUMO) is 656 a.a., with molecular weight of 87 kDa.

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-P701354

	ABCC4 Protein, Human (HEK293, GFP, Strep, His) ABCC4; ATP-binding cassette sub-family C member 4; MRP/cMOAT-related ABC transporter; Multi-specific organic anion transporter B; MOAT-B; Multidrug resistance-associated protein 4	Human	HEK293
	ABCC4 Protein, an ATP-binding cassette (ABC) family member, actively transports endogenous compounds (cAMP, cGMP, bile acids) and xenobiotics from cells. Its versatility extends to glutathione conjugates (LTC4, LTB4) and drug metabolites, mediating cotransport of bile acids with reduced glutathione. ABCC4's function includes resistance to anticancer agents like methotrexate, highlighting its role in cellular communication and drug transport. ABCC4 Protein, Human (HEK293, GFP, Strep, His) is the recombinant human-derived ABCC4 protein, expressed by HEK293 , with C-10*His, C-GFP, C-Strep labeled tag. The total length of ABCC4 Protein, Human (HEK293, GFP, Strep, His) is 1325 a.a., .

HY-P701355

	bABCC1 Protein, Human (HEK293, GFP, Strep, 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	Human	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, Human (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, Human (HEK293, GFP, Strep, His) is 1530 a.a., .

HY-P701356

	bABCC1 Protein, Human (HEK293, E1454Q, GFP, Strep, 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	Human	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, Human (HEK293, E1454Q, GFP, Strep, His) is the recombinant human-derived bABCC1 protein, expressed by HEK293 , with C-10*His, C-GFP, C-Strep labeled tag and E1454Q, , , , mutation. The total length of bABCC1 Protein, Human (HEK293, E1454Q, GFP, Strep, His) is 1530 a.a., .

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-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.	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 p-pg; 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/ABCC2 Antibody multidrug resistance-associated protein2; ABC30; ABCC2; ATP binding cassette sub family C (CFTR/MRP) member 2; ATP binding cassette subfamily C member 2; Canalicular multidrug resistance protein; Canalicular multispecific organic anion transporter 1; CMOAT; CMOAT1; cMRP; DJS; KIAA1010; MRP 2; MRP-2; MRP2; Multidrug resistance associated protein 2; MRP2_HUMAN; ATP-binding cassette sub-family C member 2; Multidrug resistance-associated protein 2.	WB; ELISA; IHC-P; IHC-F; IF	Human, Mouse, Rat,
MRP2/ABCC2 Antibody is an unconjugated, approximately 174 kDa, rabbit-derived, anti-MRP2/ABCC2 polyclonal antibody. MRP2/ABCC2 Antibody can be used for: WB, ELISA, IHC-P, IHC-F, IF expriments in human, mouse, rat, background without labeling.


Products	In-stock - + Add to Cart
Cat. No.
Species
Source
Tag
Accession
Gene ID
Molecular Weight
Purity
Endotoxin Level
Biological Activity
Appearance
Formulation
Storage & Stability
Shipping
Free Sample	Yes No
Size	* This product has been "discontinued". Optimized version of product available: / In-stock - + Add to Cart Get quote

MCE Japan Authorized Agent ナミキ商事株式会社コスモ・バイオ株式会社
Salutation			Country or Region *
Applicant Name *			Organization Name *
Department *
Email Address *			Product Name *
Cat. No.			Requested quantity *
Phone Number *
Remarks

Inhibitors & Agonists

Fluorescent Dye

Peptides

MCE Kits

Natural
Products

Recombinant Proteins

Isotope-Labeled Compounds

Antibodies

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

Inhibitors & Agonists

Fluorescent Dye

Peptides

MCE Kits

NaturalProducts

Recombinant Proteins

Isotope-Labeled Compounds

Antibodies

Natural
Products