Home   >  
TGF beta/Smad
  • Wnt/Stem Cell
TGF β/Smad

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products






Raw Materials


Chemical Structure Cat. No. Product Name CAS No.
Halofuginone Hydrobromide Chemical Structure
BCP19376 Halofuginone Hydrobromide 64924-67-0
Halofuginone Hydrobromide is a potent prolyl-tRNA synthetase inhibitor.
Chebulinic acid Chemical Structure
BCP09990 Chebulinic acid 18942-26-2
Chebulinic acid is a potent natural inhibitor of M. tuberculosis DNA gyrase, also can inhibit SMAD-3 phosphorylation, inhibit H+ K+-ATPase activity.
Halofuginone Chemical Structure
BCP07016 Halofuginone 55837-20-2
Halofuginone is a plant derivative that has been shown to inhibit Th17 differentiation, and recently tested as a potential immunosuppressant.
Halofuginone lactate Chemical Structure
BCP18878 Halofuginone lactate 82186-71-8
Halofuginone is the competitively inhibitor of prolyl-tRNA synthetase with Ki of 18.3 nM.
Halofuginone Hydrochloride Chemical Structure
BCP19375 Halofuginone Hydrochloride 1217623-74-9
Halofuginone is the competitively inhibitor of prolyl-tRNA synthetase with Ki of 18.3 nM.
Kartogenin Chemical Structure
BCP09135 Kartogenin 4727-31-5
Kartogenin(KGN) is a small molecule stimulator of chondrogenesis; promotes chondrocyte differentiation(EC50=100 nM) and binds to filamin A.
SIS3 Chemical Structure
BCP19304 SIS3 521984-48-5
SIS3 is a potent and selective inhibitor of Smad3. a potent regulator of the human Nox4 promoter.
Pirfenidone Chemical Structure
BCP04473 Pirfenidone 53179-13-8
Pirfenidone leads to a reduction of TGF-β2 mRNA levels and of the mature TGF-β2 protein due to decreased expression and direct inhibition of the TGF-β pro-protein convertase furin.
GW788388 Chemical Structure
BCP04559 GW788388 452342-67-5
GW788388 is a potent and selective inhibitor of ALK5 with IC50 of 18 nM, also inhibits TGF-β type II receptor and activin type II receptor activities, but does not inhibit BMP type II receptor.
SB-431542 Chemical Structure
BCP01765 SB-431542 301836-41-9
SB-431542 is potent and selective inhibitor of the transforming growth factor-β (TGF-β) type I receptor activin receptor-like kinase ALK5 (IC50 = 94 nM) and its relatives ALK4 and ALK7.
12下一頁共 16 條記錄 1 / 2 頁 
福建36选7奖金 大庆52麻将群 北京快三销售时间 北京快乐8开奖软件 赚钱 烟台麻将规则 终于知道四方河南麻将一直赢 北京赛车微信群 福彩3d走势图-综合版 欢乐麻将怎么开房间 紫金岛长沙麻将打不开 pc蛋蛋高级自动投注 山西体育彩票十一选五 福建快三走势图 山东群英会任选单式 俩人玩扑克的新玩法 攒劲甘肃麻将能作弊吗