28 Results for "

human DPP4

" in MedChemExpress (MCE) Product Catalog:
Products (28)

28 Results for "human DPP4" in MCE Product Catalog:

6
6 Publications Verification
Cat. No.: HY-14806
CAS No.: 760937-92-6
Purity:  99.79%
Synonyms: MP-513
Teneligliptin (MP-513) hydrobromide hydrate is an orally active and selective dipeptidyl peptidase 4 (DPP-4) inhibitor (IC50s: 0.37 and 0.29 nM for the human and rat DPP-4, respectively). Teneligliptin hydrobromide hydrate improves blood glucose levels and can be used in researches related to type 2 diabetes mellitus .
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6
6 Publications Verification
Cat. No.: HY-14806A
CAS No.: 906093-29-6
Purity:  99.99%
Synonyms: MP-513 hydrobromide
Teneligliptin (MP-513) hydrobromide is an orally active and selective dipeptidyl peptidase 4 (DPP-4) inhibitor (IC50s: 0.37 and 0.29 nM for the human and rat DPP-4, respectively). Teneligliptin hydrobromide improves blood glucose levels and can be used in researches related to type 2 diabetes mellitus .
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6
6 Publications Verification
Cat. No.: HY-14806B
CAS No.: 1572583-29-9
Purity:  99.00%
Synonyms: MP-513 hydrobromide hydrate
Teneligliptin (MP-513) hydrobromide hydrate is an orally active and selective dipeptidyl peptidase 4 (DPP-4) inhibitor (IC50s: 0.37 and 0.29 nM for the human and rat DPP-4, respectively). Teneligliptin hydrobromide hydrate improves blood glucose levels and can be used in researches related to type 2 diabetes mellitus .
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4
4 Cited Publications
Cat. No.: HY-P72975
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: Dipeptidyl peptidase 4; ADABP; ADCP-2; DPP IV; TP103; CD26; DPP4
Species:  
Source:  
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Cat. No.: HY-14892A
CAS No.: 1374639-74-3
Purity:  98.17%
Synonyms: LC15-0444 tartrate
Target:  

Dipeptidyl Peptidase

연구분야:  

Metabolic Disease

Gemigliptin tartrate (LC15-0444 tartrate) is a highly selective, reversible and competitive dipeptidyl peptidase-4 (DPP-4) inhibitor, with an IC50 of 10.3 nM for human recombinant DPP-4. Gemigliptin tartrate exhibits potent anti-glycation properties. Gemigliptin tartrate can be used for the research of advanced glycation end products (AGE)-related diabetic complications .
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Cat. No.: HY-P1141
CAS No.: 161748-29-4
Target:  

GCGR

연구분야:  

Metabolic Disease

GLP-1(9-36)amide is a major metabolite of glucagon-like peptide-1-(7-36) amide formed by the enzyme dipeptidyl peptidase-4 (DPP-4). GLP-1(9-36)amide acts as an antagonist to the human pancreatic GLP-1 receptor .
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Cat. No.: HY-14892
CAS No.: 911637-19-9
Synonyms: LC15-0444
Target:  

Dipeptidyl Peptidase

연구분야:  

Metabolic Disease Cancer

Gemigliptin (LC15-0444 ) is a highly selective, reversible and competitive dipeptidyl peptidase-4 (DPP-4) inhibitor, with an IC50 of 10.3 nM for human recombinant DPP-4. Gemigliptin exhibits potent anti-glycation properties. Gemigliptin can be used for the research of advanced glycation end products (AGE)-related diabetic complications .
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Cat. No.: HY-P4344
CAS No.: 1926163-52-1
Met-Gly-Pro-AMC is a fluorescent peptide substrate active against *Caenorhabditis elegans* DPF-3, hDPP4, and methionyl aminopeptidase 2 (MetAP2). Met-Gly-Pro-AMC undergoes cleavage via tripeptidyl peptidase activity to release a fluorescent product. Met-Gly-Pro-AMC is used to detect the activities of tripeptidyl peptidases and MetAP2 peptidases in in vitro enzyme activity assays .
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Cat. No.: HY-P1141A
Target:  

GCGR

연구분야:  

Metabolic Disease

GLP-1(9-36)amide TFA is a major metabolite of glucagon-like peptide-1-(7-36) amide formed by the enzyme dipeptidyl peptidase-4 (DPP-4). GLP-1(9-36)amide TFA acts as an antagonist to the human pancreatic GLP-1 receptor .
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Cat. No.: HY-108795
CAS No.: 224638-84-0
Purity:  98.79%
Synonyms: GLP-1-Gly8; GLP-1 (7-36) analog
Target:  

GLP Receptor

연구분야:  

Metabolic Disease

Albiglutide fragment (GLP-1 (7-36) analog) is an active fragment of Albiglutide (7-36) and a glucagon-like peptide-1 (GLP-1) analog (a long-acting GLP-1 receptor agonist). Albiglutide is produced by the fusion of DPP-4 resistant GLP-1 dimer with the human albumin gene. Moreover, Albiglutide fragment significantly reduces glycosylated hemoglobin (A1C) and is used in type 2 diabetes (T2D) studies .
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Cat. No.: HY-RS03963
연구분야:  

Others

DPP4 Human Pre-designed siRNA Set A contains three designed siRNAs for DPP4 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-14892C
CAS No.: 1523530-62-2
Synonyms: LC15-0444 hydrochloride
Target:  

Dipeptidyl Peptidase

연구분야:  

Metabolic Disease Cancer

Gemigliptin hydrochloride is the hydrochloride salt of Gemigliptin (HY-14892). Gemigliptin hydrochloride is a highly selective, reversible and competitive dipeptidyl peptidase-4 (DPP-4) inhibitor, with an IC50 of 10.3 nM for human recombinant DPP-4. Gemigliptin hydrochloride exhibits potent anti-glycation properties. Gemigliptin hydrochloride can be used for the research of advanced glycation end products (AGE)-related diabetic complications .
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Cat. No.: HY-14806R
CAS No.: 760937-92-6
Synonyms: MP-513 (Standard)
Teneligliptin (Standard) is the analytical standard of Teneligliptin. This product is intended for research and analytical applications. Teneligliptin (MP-513) is a potent, orally available, competitive, and long-lasting DPP-4 inhibitor. Teneligliptin competitively inhibits human plasma, rat plasma, and human recombinant DPP-4 in vitro, with IC50s of approximately 1 nM .
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Cat. No.: HY-14892B
CAS No.: 1375415-82-9
Synonyms: LC15-0444 tartrate hydrate
Target:  

Dipeptidyl Peptidase

연구분야:  

Metabolic Disease

Gemigliptin (LC15-0444 ) tartrate hydrate is a selective, reversible and competitive dipeptidyl peptidase-4 (DPP-4) inhibitor, with an IC50 of 10.3 nM for human recombinant DPP-4. Gemigliptin tartrate hydrate exhibits potent anti-glycation properties. Gemigliptin tartrate hydrate can be used for the research of advanced glycation end products (AGE)-related diabetic complications .
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Cat. No.: HY-W741755A
Target:  

Dipeptidyl Peptidase

연구분야:  

Metabolic Disease

5-Hydroxy saxagliptin hydrochloride is an active metabolite of Saxagliptin (HY-10285) and a potent and selective DPP-4 inhibitor. 5-Hydroxy saxagliptin hydrochloride has Ki values of 2.6 nM and 2.9 nM for humans and cynomolgus monkeys, respectively. 5-Hydroxy saxagliptin hydrochloride can be used in the research of type 2 diabetes mellitus .
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Cat. No.: HY-P9806
Synonyms: MERS-D12; MERS Antibody-D12

Target:  

SARS-CoV

연구분야:  

Infection

Anti-MERS-D12 mAb (MERS-D12; MERS Antibody-D12) is a human monoclonal IgG1. Anti-MERS-D12 mAb binds directly to the DPP4 interacting region of the MERS-CoV Spike receptor binding domain (RBD) and effect neutralization by directly blocking receptor binding .
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Cat. No.: HY-14806S1
Synonyms: MP-513-d4
Teneligliptin-d4 is deuterium labeled Teneligliptin. Teneligliptin (MP-513) is a potent, orally available, competitive, and long-lasting DPP-4 inhibitor. Teneligliptin competitively inhibits human plasma, rat plasma, and human recombinant DPP-4 in vitro, with IC50s of approximately 1 nM .
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Cat. No.: HY-111294
CAS No.: 851389-35-0
Target:  

Dipeptidyl Peptidase

연구분야:  

Metabolic Disease

ASP4000 hydrochloride is a potent, competitive, selective, orally active DPP4 inhibitor with an IC50 value of 2.25 nM against human recombinant DPP4. ASP4000 hydrochloride shows antihyperglycemic activity. ASP4000 hydrochloride can be used in the research of type 2 diabetes .
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Cat. No.: HY-14806S2
Synonyms: MP-513-d5
Teneligliptin-d5 (MP-513-d5) is deuterium labeled Teneligliptin. Teneligliptin (MP-513) hydrobromide hydrate is an orally active and selective dipeptidyl peptidase 4 (DPP-4) inhibitor (IC50s: 0.37 and 0.29 nM for the human and rat DPP-4, respectively). Teneligliptin hydrobromide hydrate improves blood glucose levels and can be used in researches related to type 2 diabetes mellitus .
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Cat. No.: HY-109060
CAS No.: 1601479-87-1
Synonyms: ZYDPLA1
Target:  

Dipeptidyl Peptidase

연구분야:  

Metabolic Disease

Garvagliptin (ZYDPLA1) is an orally active, competitive and long acting DPP4 Inhibitor, with an IC50 of 2.99 nM against human recombinant DPP IV. Garvagliptin (ZYDPLA1) exhibits antihyperglycemic effect .
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