Cat. No. | 製品名 | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T76810 | Ganitumab | 905703-97-1 | 98% |
Ganitumab
|
Ganitumab (AMG 479) is a highly potent monoclonal antibody to type 1 insulin-like growth factor receptor (IGF1R). Ganitumab is recognized to bind to IGF1R at low... | ||||
T76727 | Teprotumumab | 1036734-93-6 | 98% |
Teprotumumab
|
Teprotumumab is a human monoclonal antibody that blocks the IGF-1 receptor (IGF-1R). Teprotumumab binds to the extracellular α-subunit domain ligand of IGF-1R. T... | ||||
T9980 | AVJ16 | 98% |
|
|
AVJ16 as a member of the insulin growth factor 2 mRNA-binding protein family, binds to the mRNA of certain genes to regulate protein translation. | ||||
TN7108 | Urolithin C | 165393-06-6 |
|
|
Urolithin C is a gut metabolite of ellagic acid. Urolithin C induces apoptosis in PC12 cells through a mitochondria-mediated pathway. | ||||
T6S1487 | Ginsenoside Rg5 | 186763-78-0 |
|
|
1. Ginsenoside Rg5 could be a beneficial agent for the treatment of Alzheimer's disease. 2. Ginsenoside Rg5 suppresses LPS-induced nitric oxide (NO) production a... | ||||
TP1125 | Insulin(cattle) | 11070-73-8 |
|
|
Insulin bovine (Insulin from bovine pancreas) is a biologically derived two-chain polypeptide hormone, synthesized in vivo by pancreatic β cells. It is frequentl... | ||||
T9030 | SU4984 | 186610-89-9 | 100% |
|
SU4984 is a cell-permeable, ATP-competitive and reversible inhibitor of the fibroblast growth factor receptor 1 (FGFR1). | ||||
T3621 | Brigatinib | 1197953-54-0 | 100% |
|
Brigatinib (AP-26113) is a highly potent and selective ALK inhibitor. | ||||
T76795 | Xentuzumab | 1417158-65-6 | 95.21% |
|
Xentuzumab (BI836845) is a recombinant monoclonal antibody to humanised IGF ligand that inhibits IGF1 and IGF2 growth-promoting signalling and inhibits AKT activ... | ||||
TP2209L | Xenin 8 acetate | TP2209L | 95.54% |
|
Xenin 8 acetate is a biologically active fragment of Xenin in the neurotensin/xenopsin family. Xenin 8 acetate augments Arginine-induced insulin release (by 40%)... | ||||
T11593 | I-OMe-Tyrphostin AG 538 | 1094048-77-7 | 96.66% |
|
I-OMe-Tyrphostin AG 538 is a specific IGF-1R inhibitor and ATP-competitive inhibitor of PI5P4Kα (IC50: 1 µM).I-OMe-Tyrphostin AG 538 inhibits IGF-1R-mediated sig... | ||||
T13564L | AZ7550 hydrochloride | 2309762-40-9 | 97.07% |
|
AZ7550 hydrochloride (AZ7550 hydrochloride ), an active metabolite of AZD9291, inhibits the activity of IGF1R (IC50: 1.6 μM). | ||||
T13564 | AZ7550 | 1421373-99-0 | 97.07% |
|
AZ7550, an active metabolite of AZD9291, inhibits the activity of IGF1R (IC50: 1.6 μM). | ||||
T4605 | NT157 | 1384426-12-3 | 97.55% |
|
NT157 is a small molecule tyrphostin targeting IRS protein and has the potential to inhibit IGF-1R and STAT3 signaling pathways in TME cancer cells and stromal c... | ||||
T3059 | ALK-IN-1 | 1197958-12-5 | 97.66% |
|
ALK-IN-1 (AP26113) is a potent ALK inhibitor with IC50 of 0.62 nM in a cell-free assay, demonstrated ability overcome Crizotinib resistance mediated by a L1196M ... | ||||
T1918 | NVP-TAE 226 | 761437-28-9 | 98.07% |
|
NVP-TAE 226 (TAE226) is an effective FAK inhibitor (IC50: 5.5 nM) and most effective to Pyk2(IC50: 3.5 nM); 10- to 100-fold less effective against IGF-1R, InsR, ... | ||||
T2642 | PD173074 | 219580-11-7 | 98.15% |
|
PD173074 is an effective FGFR1 inhibitor (IC50: 25 nM) and also inhibits VEGFR2 (IC50: 100-200 nM) in cell-free assays. The selectivity is higher ~1000-fold for ... | ||||
T37588L | GIP (1-30) amide, porcine acetate | 98.50% |
|
|
GIP (1-30) amide, porcine acetate is an agonist of fully glucose-dependent insulinotropic polypeptide (GIP) receptor. GIP (1-30) amide, porcine acetate can weakl... | ||||
T10285 | ALK inhibitor 1 | 761436-81-1 | 98.55% |
|
ALK inhibitor 1 is a selective ALK kinase inhibitor. | ||||
TP2018L | GIP (human) acetate | TP2018L | 98.65% |
|
GIP (human) acetate is a stimulator of glucose-dependent insulin secretion and a weak inhibitor of gastric acid secretion. GIP (human) acetate plays a vital role... |