Description
Thiazovivin is an inhibitor of ROCK that stabilizes E-cadherin and induces stem cell differentiation.
Product Unit Size | Cost | Quantity | Stock |
---|
Thiazovivin is an inhibitor of ROCK that stabilizes E-cadherin and induces stem cell differentiation.
Cas No. | 1226056-71-8 |
---|---|
Purity | ≥98% |
Formula | C15H13N5OS |
Formula Wt. | 311.36 |
Chemical Name | N-Benzyl-2-(pyrimidin-4-ylamino)thiazole-4-carboxamide |
IUPAC Name | N-benzyl-2-(pyrimidin-4-ylamino)-1,3-thiazole-4-carboxamide |
Synonym | N-Benzyl-2-(pyrimidin-4-ylamino)-thiazole-4-carboxamide; N-(PHENYLMETHYL)-2-(4-PYRIMIDINYLAMINO)-4-THIAZOLECARBOXAMIDE; SR-01000650935; PubChem24336; cc-22 |
Solubility | DMSO 15 mg/mL (48.17 mM) Water Insoluble Ethanol Insoluble |
Appearance | Light tan solid |
Store Temp | -20°C |
---|---|
Ship Temp | Ambient |
MSDS | |
---|---|
Info Sheet |
Wang F, Scoville D, He XC, et al. Isolation and characterization of intestinal stem cells based on surface marker combinations and colony-formation assay. Gastroenterology. 2013 Aug;145(2):383-95.e1-21. PMID: 23644405.
Groß B, Sgodda M, Rasche M, et al. Improved generation of patient-specific induced pluripotent stem cells using a chemically-defined and matrigel-based approach. Curr Mol Med. 2013 Jun;13(5):765-76. PMID: 23642058.
Zhu J, Pang D, Zhou Y, et al. Direct conversion of porcine embryonic fibroblasts into adipocytes by chemical molecules. Cell Reprogram. 2012 Apr;14(2):99-105. PMID: 22372576.
Steroid; glucocorticoid agonist.
Bufanolide steroid found in Bufo arenarum;VEGFR...
ASK1 inhibitor.
Mycotoxin produced by species of Fusarium; pote...
Triterpene found in Centella, prevents melanoge...
Triterpene saponin found in Bupleurum.
Tenoxicam impurity
Tyrosine kinase inhibitor.
Flavanol originally found in Camilla (green tea...
MEK1/2 inhibitor.
Mycotoxin produced by Fusarium; ER agonist.
PAK4 inhibitor.
Endogenous peptide, involved in water/Na+ homeo...
Mycotoxin that has structural similarity to est...
MEK inhibitor.
AhR antagonist.
Bactericidal
Casein kinase 2 inhibitor.
PARP inhibitor; potential Pim1 inhibitor.
NMDA NR1/NR2B antagonist.