37 Results for "

InsR

" in MedChemExpress (MCE) Product Catalog:
Products (37)

37 Results for "InsR" in MCE Product Catalog:

43
43 Publications Verification
Cat. No.: HY-15656
CAS No.: 1032900-25-6
Purity:  99.98%
Synonyms: LDK378
Ceritinib (LDK378) is a selective, orally bioavailable, and ATP-competitive ALK tyrosine kinase inhibitor with an IC50 of 200 pM. Ceritinib also inhibits IGF-1R, InsR, and STK22D with IC50 values of 8, 7, and 23 nM, respectively. Ceritinib shows great antitumor potency .
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43
43 Publications Verification
Cat. No.: HY-15656A
CAS No.: 1380575-43-8
Purity:  99.90%
Synonyms: LDK378 dihydrochloride
Ceritinib (LDK378) dihydrochloride is a selective, orally bioavailable and ATP-competitive ALK tyrosine kinase inhibitor with an IC50 of 200 pM. Ceritinib dihydrochloride also inhibits IGF-1R, InsR, and STK22D with IC50 values of 8, 7, and 23 nM, respectively. Ceritinib dihydrochloride shows great antitumor potency .
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13
13 Cited Publications
Cat. No.: HY-50866
CAS No.: 475489-16-8
Synonyms: AEW541
Research Areas:  

Endocrinology Cancer

NVP-AEW541 (AEW541 ) is an orally active inhibitor of the insulin-like growth factor 1 receptor (IGF-1R) with an IC50 value of 0.15 μM. NVP-AEW541 also inhibits InsR, IC50 with a value of 0.14 μM. NVP-AEW541 has antitumor activity .
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11
11 Cited Publications
Cat. No.: HY-13203
CAS No.: 761437-28-9
Purity:  99.77%
Synonyms: TAE226
Research Areas:  

Endocrinology Cancer

NVP-TAE 226 (TAE226) is a potent and ATP-competitive dual FAK and IGF-1R inhibitor with IC50s of 5.5 nM and 140 nM, respectively. NVP-TAE 226 (TAE226) also effectively inhibits Pyk2 and insulin receptor (InsR) with IC50s of 3.5 nM and 44 nM, respectively .
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3
3 Cited Publications
Cat. No.: HY-10252
CAS No.: 475488-23-4
Purity:  99.30%
Synonyms: ADW742; GSK 552602A; ADW
Research Areas:  

Endocrinology Cancer

NVP-ADW742 (ADW742) is an orally active, selective IGF-1R tyrosine kinase inhibitor with an IC50 of 0.17 μM. NVP-ADW742 inhibits insulin receptor (InsR) with an IC50 of 2.8 μM. NVP-ADW742 induces pleiotropic antiproliferative/proapoptotic biologic sequelae in tumor cells .
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Cat. No.: HY-P991290
IRAB-B is a human monoclonal antibody targeting INSR. IRAB-B is an insulin receptor (IR) antagonist and can be used in the study of insulin resistance and diabetes .
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Cat. No.: HY-P990712
CAS No.: 2410976-61-1
Synonyms: RZ-358; XOMA 358

Target:  

Insulin Receptor

Research Areas:  

Inflammation/Immunology

Ersodetug is an anti-INSR (insulin receptor) human IgG2 κ monoclonal antibody . Recommend Isotype Controls: Human IgG2 kappa, Isotype Control (HY-P99002).
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Cat. No.: HY-RS06847
Research Areas:  

Others

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

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Cat. No.: HY-E70730
Target:  

IGF-1R

Research Areas:  

Metabolic Disease

The whole IGF axis constitutes an interactive network composed of the peptide-ligands IGF1, IGF2 and insulin, and the receptors IGF1R, IGF2R and insulin receptor (INSR) as IGF binding proteins (IGFBPs). The INSR itself appears in two isoforms, INSRA and INSRB differing in 12 amino acids encoded by exon 11. INSR Recombinant Human Active Protein Kinase is a recombinant INSR protein that can be used to study INSR-related functions .
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Cat. No.: HY-169066
Target:  

Insulin Receptor

Research Areas:  

Metabolic Disease

INSR agonist 1 is an insulin receptor (INSR) agonist. INSR agonist 1 can increase INSR pY1355/1361 levels and works synergistically with insulin .
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Cat. No.: HY-15656R
CAS No.: 1032900-25-6
Synonyms: LDK378 (Standard)
Ceritinib (Standard) is the analytical standard of Ceritinib (HY-15656). This product is intended for research and analytical applications. Ceritinib is a selective, orally bioavailable, and ATP-competitive ALK tyrosine kinase inhibitor with an IC50 of 200 pM. Ceritinib also inhibits IGF-1R, InsR, and STK22D with IC50 values of 8, 7, and 23 nM, respectively. Ceritinib shows great antitumor potency .
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Cat. No.: HY-15656S
CAS No.: 1632484-77-5
Purity:  98.00%
Synonyms: LDK378 d7
Ceritinib (LDK378)-d7 is a deuterium labeled Ceritinib (HY-15656). Ceritinib is a selective, orally bioavailable and ATP-competitive ALK tyrosine kinase inhibitor . Ceritinib is a selective, orally bioavailable, and ATP-competitive ALK tyrosine kinase inhibitor with an IC50 of 200 pM. Ceritinib also inhibits IGF-1R, InsR, and STK22D with IC50 values of 8, 7, and 23 nM, respectively. Ceritinib shows great antitumor potency .
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Cat. No.: HY-10252A
CAS No.: 475489-15-7
Synonyms: cis-ADW742; cis-GSK 552602A; cis-ADW
Research Areas:  

Inflammation/Immunology

cis-NVP-ADW742 (cis-ADW742) is a cis isomer of NVP-ADW742 (HY-10252). NVP-ADW742 is an orally active, selective IGF-1R tyrosine kinase inhibitor with an IC50 of 0.17 μM. NVP-ADW742 inhibits insulin receptor (InsR) with an IC50 of 2.8 μM. NVP-ADW742 induces pleiotropic antiproliferative/proapoptotic biologic sequelae in tumor cells .
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Cat. No.: HY-RS06846
Research Areas:  

Others

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

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Cat. No.: HY-RS06848
Research Areas:  

Others

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

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Cat. No.: HY-P991291

Target:  

Insulin Receptor

Research Areas:  

Endocrinology

XOMA 129 is a human monoclonal antibody targeting INSR. XOMA 129 is an insulin receptor (IR) antagonist that inhibits the drop in blood glucose. XOMA 129 can be used in the study of hypoglycemia .
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Cat. No.: HY-108230
CAS No.: 1197958-53-4
Research Areas:  

Cancer

ALK-IN-12 is a potent and orally active ALK inhibitor with an IC50 of 0.18 nM. ALK-IN-12 also inhibits IGF1R and InsR (IC50=20.3 and 90.6 nM). Antitumor activities .
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Cat. No.: HY-50866B
CAS No.: 2320261-63-8
Synonyms: AEW541 dihydrochloride
Research Areas:  

Cancer

NVP-AEW541 dihydrochloride (AEW541 dihydrochloride) is an orally active inhibitor of the insulin-like growth factor 1 receptor (IGF-1R) with an IC50 value of 0.15 μM. NVP-AEW541 dihydrochloride also inhibits InsR, IC50 with a value of 0.14 μM. NVP-AEW541 dihydrochloride has antitumor activity .
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Cat. No.: HY-15656AR
CAS No.: 1380575-43-8
Synonyms: LDK378 dihydrochloride (Standard)
Ceritinib (LDK378) dihydrochloride (Standard) is the analytical standard of Ceritinib dihydrochloride (HY-15656A). This product is intended for research and analytical applications. Ceritinib dihydrochloride is a selective, orally bioavailable, and ATP-competitive ALK tyrosine kinase inhibitor with an IC50 of 200 pM. Ceritinib dihydrochloride also inhibits IGF-1R, InsR, and STK22D with IC50 values of 8, 7, and 23 nM, respectively. Ceritinib shows great antitumor potency .
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Cat. No.: HY-13203R
CAS No.: 761437-28-9
Synonyms: TAE226 (Standard)
NVP-TAE 226 (Standard) is the analytical standard of NVP-TAE 226. This product is intended for research and analytical applications. NVP-TAE 226 (TAE226) is a potent and ATP-competitive dual FAK and IGF-1R inhibitor with IC50s of 5.5 nM and 140 nM, respectively. NVP-TAE 226 (TAE226) also effectively inhibits Pyk2 and insulin receptor (InsR) with IC50s of 3.5 nM and 44 nM, respectively .
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