Pyrroles
Sigma Aldrich Fine Chemicals Biosciences Nicergoline for peak identification European Pharmacopoeia (EP) Reference Standard | 27848-84-6 | MFCD00869626 |
Nicergoline for peak identification European Pharmacopoeia (EP) Reference Standard | Mol Wt: 484.39 | 27848-84-6 | MFCD00869626 |
Sigma Aldrich Fine Chemicals Biosciences R-Ketorolac >=95% (HPLC) | 66635-93-6 | MFCD00871492 | 25MG
R-Ketorolac >=95% (HPLC) | Purity: >=95% (HPLC) | Mol Wt: 255.27 | 66635-93-6 | MFCD00871492 | 25MG
Medchemexpress LLC Pha-665752 | 477575-56-7 | MFCD18632554; MFCD07772270 | 99.9% | 641.61 g/mol | C32H34Cl2N4O4S | 5 MG
PHA-665752 is a selective, ATP-competitive inhibitor of the c-Met (HGFR) receptor tyrosine kinase used in preclinical research to induce apoptosis, cause cell-cycle arrest, and reduce tumor growth in vitro and in vivo. It demonstrates high potency and selectivity versus other kinases and is supplied for research use only.
- Selective ATP-competitive c-Met inhibitor with Ki ≈ 4 nM and IC50 ≈ 9 nM.
- High purity solid (approximately 99.9%) suitable for biochemical assays.
- Molecular formula C32H34Cl2N4O4S; molecular weight 641.61 g/mol.
- Storage: powder at -20°C for long term; in solution store at -80°C when possible.
- Supplied in small preweighed milligram quantities for laboratory research.
Medchemexpress LLC Midostaurin | 120685-11-2 | MFCD00871372 | 5 mg
Midostaurin | Purity: 99.89% | Mol Wt: 570.65 | 120685-11-2 | MFCD00871372 | 5 mg
Medchemexpress LLC HY-112769 10mg Medchemexpress, EX229 CAS:1219739-36-2 Purity:>98%
Medchemexpress, HY-112769 10mg EX229 CAS:1219739-36-2 EX229, a Benzimidazole derivative, is a potent and allosteric activator of AMP-activated protein kinase (AMPK), with Kds of 0.06 μM, 0.06 μM and 0.51 μM for α1β1γ1, α2β1γ1 and α1β2γ1 in biolayer interferometry, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Selleck Chemical LLC Atorvastatin
Atorvastatin is a lipid lowering agent It is a competitive inhibitor of hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase the rate-determining enzyme in cholesterol biosynthesis via the mevalonate pathway Atorvastatin activates autophagy
Selleck Chemical LLC Sunitinib malate S1042-500mg
Sunitinib malate is a multi-targeted RTK inhibitor targeting VEGFR2 (Flk-1) and PDGFR with IC50 of 80 nM and 2 nM in cell-free assays and also inhibits c-Kit Sunitinib Malate effectively inhibits autophosphorylation of Ire1 Sunitinib Malate increases both death receptor and mitochondrial-dependent apoptosis
Sigma Aldrich Fine Chemicals Biosciences JNJ-40418677 >=98% (HPLC) | 1146594-87-7 | 25MG
JNJ-40418677 >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 480.44 | 1146594-87-7 | 25MG
Sigma Aldrich Fine Chemicals Biosciences Ondansetron for LC system suitability European Pharmacopoeia (EP) Reference Standard | 103639-04-9 | MFCD00374371 |
Ondansetron for LC system suitability European Pharmacopoeia (EP) Reference Standard | Mol Wt: 365.85 | 103639-04-9 | MFCD00374371 |
Cayman Chemical RBromoenol lactone
A selective iPLA2γ inhibitor (IC50 = ~0.6 µM); selective for iPLA2γ over iPLA2β at 20-30 µM
Cayman Chemical SBromoenol lactone
A selective iPLA2β inhibitor; inhibits vasopressin-induced release of arachidonate from cultured rat aortic smooth muscle (A10) cells (IC50 = 2 µM); >1,000-fold selective for iPLA2 versus cPLA2 and 10-fold selective for iPLA2β versus iPLA2γ
Aobchem (3-Fluoro-5-iodophenyl)boronic acid | 97% | CAS 3068071-30-4 | C6H5BFIO2 | 1g
(3-Fluoro-5-iodophenyl)boronic acid | 97% | CAS 3068071-30-4 | C6H5BFIO2 | 1g