
SB-431542
CAS No. 301836-41-9
SB-431542 ( SB 431542 | SB431542 )
产品货号. M13943 CAS No. 301836-41-9
SB-431542 是一种有效的、特异性的 TGF-β I 型受体 (ALK5) 抑制剂,IC50 为 94 nM。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥405 | 有现货 |
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10MG | ¥656 | 有现货 |
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25MG | ¥1320 | 有现货 |
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50MG | ¥2398 | 有现货 |
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100MG | ¥4439 | 有现货 |
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200MG | ¥4496 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称SB-431542
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述SB-431542 是一种有效的、特异性的 TGF-β I 型受体 (ALK5) 抑制剂,IC50 为 94 nM。
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产品描述SB-431542 is a potent, specific TGF-β type I receptor (ALK5) inhibitor with IC50 of 94 nM; also substantially inhibits ALK4 and 7, but not other ALKs; efficiently inhibits the ability of activated ALK4, ALK5, and ALK7 to phosphorylate Smad2; a selective inhibitor of endogenous activin and TGF-beta signaling but has no effect on BMP signaling, and has no effect on components of the ERK, JNK, or p38 MAP kinase pathways.(In Vitro):SB-431542 can inhibit the activity for ALK4, ALK5 and ALK7 with IC50 values of 1 μM, 0.75 μM and 2 μM, respectively.SB-431542 (0- 10 μM; 24 h) inhibits ALK5 and also the activin type I receptor ALK4 and the nodal type I receptor ALK7, which are very highly related to ALK5 in their kinase domains.SB-431542 (0.1, 0.5, 1, 5, or 10 μM; 30 min) efficiently inhibits Smad phosphorylation induced by TGF-β and activin but not BMP4.SB-431542 (0-10 μM) inhibits TGF-beta-induced transcription, gene expression, apoptosis, and growth suppression.(In Vivo):SB-431542 (subconjunctival; 0.5 and 2 mM; on days 1, 2, 3, and 7) inhibits scar formation after glaucoma filtration surgery in New Zealand rabbits.
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体外实验SB-431542 (GMP) (10 μM; 10 days) induces human pluripotent stem cells (hPSCs) to post-mitotic cortical neurons differentiation.SB-431542 (GMP) (10 μM) facilitates directed differentiation into midbrain dopamine neurons (mDA).SB-431542 (GMP) (3.8 μM) promotes differentiation of hPSCs to multipotent hematopoietic progenitors that arise from SOX17+ hemogenic endothelium in vitro. RT-PCRCell Line:Human pluripotent stem cells (hPSCs)Concentration:10 μM Incubation Time:10 days Result:Showed downregulation of the pluripotency marker OCT4 and induction of neural and neuronal markers PAX6, FOXG1 and DCX, as well as markers of early born cortical neurons, including TBR1 (preplate, subplate and layer VI) and REELIN, in LSB+X/P/S/D conditions.
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体内实验——
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同义词SB 431542 | SB431542
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通路TGF-beta/Smad
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靶点TGFBR
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受体ALK5|ALK4
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研究领域Cancer
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适应症——
化学信息
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CAS Number301836-41-9
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分子量384.3875
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分子式C22H16N4O3
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纯度>98% (HPLC)
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溶解度DMSO: ≥ 40 mg/mL; Ethanol: 11.17 mg/mL (Need ultrasonic and warming)
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SMILESO=C(N)C1=CC=C(C2=NC(C3=CC=C(OCO4)C4=C3)=C(C5=NC=CC=C5)N2)C=C1
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化学全称Benzamide, 4-[4-(1,3-benzodioxol-5-yl)-5-(2-pyridinyl)-1H-imidazol-2-yl]-
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Callahan JF, et al. J Med Chem. 2002 Feb 28;45(5):999-1001.
2. Inman GJ, et al. Mol Pharmacol. 2002 Jul;62(1):65-74.
3. Matsuyama S, et al. Cancer Res. 2003 Nov 15;63(22):7791-8.
4. Hjelmeland MD, et al. Mol Cancer Ther. 2004 Jun;3(6):737-45.
产品手册




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