USD $2.00-10.00 / Kilogram
USD $2.00-10.00 / Kilogram
USD $1.00-1.00 / Kilogram
USD $1.00-1.00 / Kilogram
USD $1.00-10.00 / Kilogram
USD $96.00-98.00 / Kilogram
USD $1.00-1.00 / Kilogram
our company was built in 2009 with an iso certificate.in the past 5 years, we have grown up as a famous fine chemicals supplier in china and we had established stable business relationships with samsung,lg,merck,thermo fisher scientific and so on.our main business covers the fields below:
1.noble metal catalysts (pt.pd...)
2.organic phosphine ligands (tert-butyl-phosphine.cyclohexyl-phosphine...)
3.oled intermediates (fluorene,carbazole,boric acid...)
4.customs synthesis
our advantage:
1. higest quality and good package
2.fast delivery
3.better payment term
4.fast response to customer within 6 hours
5.good business credit in europe ,us ,japan ,korea
anyway ,if you need any chemicals from china ,henan tianfu can help you
a-83-01 basic information |
product name: | a-83-01 |
synonyms: | 3-(6-methyl-2-pyridinyl)-n-phenyl-4-(4-quinolinyl)-1h-pyrazole-1-carbothioamide;a 83-01, >=98%;tgf inhibitor a-83-01;3-(6-methylpyridin-2-yl)-n-phenyl-4-(quinolin-4-yl)-1h-pyrazole-1-carbothioamide |
cas: | 909910-43-6 |
mf: | c25h19n5s |
mw: | 421.526 |
einecs: | |
product categories: | protein kinase;tgf-beta/smad;inhibitors |
mol file: | 909910-43-6.mol |
a-83-01 chemical properties |
mp | 111℃ |
storage temp. | store at -20°c |
safety information |
hazard codes | xn |
risk statements | 22-36/37/38 |
safety statements | 26-36 |
a-83-01 usage and synthesis |
usage | a 83-01 is a selective inhibitor of tgf-β type i receptor. a 83-01 treatment increases tumor permeability. |
biological activity | selective inhibitor of tgf- β type i receptor alk5 kinase, type i activin/nodal receptor alk4 and type i nodal receptor alk7 (ic 50 values are 12, 45 and 7.5 nm respectively). blocks phosphorylation of smad2 and inhibits tgf- β -induced epithelial-to-mesenchymal transition. only weakly inhibits alk-1, -2, -3, -6 and mapk activity. more potent than sb 431542 (4-[4-(1,3-benzodioxol-5-yl)-5-(2-pyridinyl)-1h-imidazol -2-yl]benzamide). inhibits differentiation of rat induced pluripotent stem cells (ripscs) and increases clonal expansion efficiency. helps maintain homogeneity and long-term in vitro self-renewal of human ipscs. |