按首字母搜索

Cas号索引 9

• 938435-69-9 | Flobetair (Catalog# : 102904)Coming soon!
• 939055-18-2 | FIPI (Catalog# : 102617)FIPI is a derivative of halopemide which potently inhibits both PLD1 (IC50 = 25 nM) a
• 942206-85-1 | GSK1016790A (Catalog# : 2071511)GSK1016790A, also known as GSK101, is a TRPV4 agonist that elicits calcium influx in
• 901245-65-6 | GSK-5959 (Catalog# : 1811266)GSK-5959是一种有效的选择性BRPF1溴域抑制剂(IC50 = 80 nM)。
• 937174-76-0 | GSK-690693 (Catalog# : 161009019)Pan-AKT kinase inhibitor GSK-690693 binds to and inhibits Akt kinases 1, 2, and 3, wh
• 929095-18-1 | GSK-461364 (Catalog# : 16071032)GSK-461364 is a Polo-like kinase 1 inhibitor, is also a small molecule Polo-like kina
• 936694-12-1 | Glesatinib(MGCD-265) (Catalog# : 012001)Glesatinib is a potent tyrosine kinase inhibitor with potential antineoplastic activi
• 937812-80-1 | Gamma-Secretase Modulators (Catalog# : 011909)Coming soon!
• 957054-30-7 | GDC-0941 (Catalog# : 120115)GDC-0941 is a potent inhibitor of PI3K/ with IC50 of 3 nM, with modest selectivity ag
• 942918-07-2 | GSK-1070916 (Catalog# : 111011)GSK1070916 is a reversible and ATP-competitive inhibitor of Aurora B/C with IC50 of 3
• 958852-01-2 | GSK1059615 (Catalog# : 52628)GSK1059615 is a dual inhibitor of PI3K/// (reversible) and mTOR with IC50 of 0.4 nM/0
• 928037-13-2 | Golvatinib (E7050) (Catalog# : 52020)Golvatinib (E7050) is a dualc-MetandVEGFR-2inhibitor with IC50 of 14 nM and 16 nM, do
• 924296-39-9 | HBX-41108 (Catalog# : 19317)HBX 41108是泛素特异性蛋白酶(USP) 7的抑制剂。HBX 41108通过IC(50)在亚
• 941987-60-6 | H 151 (Catalog# : 1811022)H 151是一种诱捕拮抗剂，共价结合在Cys91上，阻断棕榈酰化和防止
• 934343-74-5 | HSP990 (NVP-HSP990) (Catalog# : 52015)NVP-HSP990 (HSP990) is a novel, potent and selectiveHSP90inhibitor for HSP90/ withIC5
• 942123-43-5 | Inarigivir soproxil (Catalog# : 186277)Inarigivir soproxil，也被称为SB 9200，是一种抗病毒药物。
• 901751-47-1 | iCRT3 (Catalog# : 18492)iCRT3是Wnt/β-catenin信号的拮抗剂，在Wnt responsive STF16-luc reporter assay
• 945526-43-2 | ISCK03 (Catalog# : 1791118)ISCK03是一种有效的c-kit抑制剂。ISCK03抑制在501mel人黑素瘤细胞的SC
• 914638-30-5 | IDO-IN-1 (Catalog# : 16122822)IDO-IN-1 is a potent and selective indoleamine-2,3-dioxygenase (IDO) inhibitor with I
• 937263-43-9 | Irbinitinib (Catalog# : 011310)Irbinitinib is a potent and selective HER2 inhibitor with IC50 of 8 nM, equipotent ag
• 914471-09-3 | IDO-IN-2 (Catalog# : 123002)IDO-IN-2 is a potent IDO1 inhibitor(IC50=10 nM) with desirable pharmaceutical propert
• 99059-64-0 | 3-iodo-4-isopropylbenzoic acid (Catalog# : 80313)Coming soon!
• 931398-72-0 | IOX2 (Catalog# : 52527)IOX2 is a selective inhibitor of the Hypoxia Inducible Factor (HIF) Prolyl-Hydroxylas
• 943540-74-7 | JNJ-38877618 (Catalog# : 204307)JNJ-38877618 is a hepatocyte growth factor receptor (HGFR; MET; c-Met) inhibitor pote
• 900573-88-8 | JI-101 (Catalog# : 16122823)JI-101 is an orally active inhibitor of vascular endothelial growth factor receptor 2
• 952849-76-2 | KKL-10 (Catalog# : 184217)KKL-10是一种抗菌药物。KKL-10在体外和体外感染中均表现出了对弱毒
• 927822-86-4 | KC7F2 (Catalog# : 16122827)KC7F2 is a potent HIF-1 pathway inhibitor with potential anticancer activity. KC7F2 i
• 938440-64-3 | Ku-0063794 (Catalog# : 121424)KU-0063794 is a selective inhibitor of mammalian target of rapamycin (mTOR) (IC50 ~10
• 925701-49-1 | KU-60019 (Catalog# : 52576)KU-60019 is an improved analogue of KU-55933, with IC50 of 6.3 nM for ATM
• 924835-67-6 | LP-184 (Catalog# : 24121)LP-184 is an acylfulvene-derived prodrug activated by the oxidoreductase PTGR1 that a