所有产品分类
所有产品
信号通路
- Angiogenesis/Protein Tyrosine Kinase
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-
GPCR/G Protein
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Neuro Signaling Pathway
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Protease/Metabolic Enzyme
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研究领域
- Metabolic Disease
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- Infection
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天然产物
抗体
多肽
催化剂
杂质对照品
医药中间体
基础原料
Pim
结构式 | 货号 | 产品名称 | CAS号 |
---|
BCP43782 | PIM1-IN-1 新 | 1417630-95-5 | |
PIM1-IN-1 is a potent and highly selective inhibitor of PIM1/3(IC50s of 7, 5530 and 70 nM for PIM1, PIM2, and PIM3, respectively),with Antiproliferative and anti-cancer activity.
|
BCP42656 | Parsaclisib hydrochloride 新 | 1995889-48-9 | |
Parsaclisib, also known as INCB050465, is a novel PI3Kδ inhibitor which synergizes with PIM protein kinase inhibition to cause tumor regression in a model of DLBCL.
|
BCP32632 | NSC31205 新 | 6320-51-0 | |
NSC 31205 is a PIM2/1 inhibitor.
|
BCP15861 | TCS PIM-1 1 新 | 491871-58-0 | |
TCS PIM-1 1 is a potent and selective ATP-competitive Pim-1 kianse inhibitor with IC50 of 50 nM, displays good selectivity over Pim-2 and MEK1/MEK2(IC50s >20,000 nM).
|
BCP21212 | SMI-4a 新 | 327033-36-3 | |
SMI-4a, also called as TCS-PIM-1-4a, a thiazolidinedione compound, is a potent, selective ATP-competitive inhibitor against Pim protein kinase (IC50 = 24 nM against Pim-1 and 100 nM against Pim-2) with little or no activity against a panel of 58 other kinase.
|
BCP31128 | PIM447 dihydrochloride 新 | 1820565-69-2 | |
PIM447 is a pan-PIM kinase ihibitor with Kis of 6, 18, 9 nM for PIM1, PIM2 and PIM3, respectively.
|
BCP27625 | Pim1/AKK1-IN-1 新 | 1093222-27-5 | |
Pim1/AKK1-IN-1 is a potent multi-kinase inhibitor with Kd values of 35 nM/53 nM/75 nM/380 nM for Pim1/AKK1/MST2/LKB1 respectively, and also inhibits MPSK1 and TNIK.
|
BCP13641 | LGB321 新 | 1210415-88-5 | |
LGB-321 is a potent and selective ATP-competitive small molecule inhibitor of PIM kinases (Pan-PIM kinase inhibitor).
|
BCP30070 | TP-3654 新 | 1361951-15-6 | |
TP-3654 is a second-generation Pim kinase inhibitor with Ki values of 5 and 42 nM for Pim-1 and Pim-3, respectively.
|
BCP24206 | LGH447 Hydrochloride | 1210416-52-6 | |
LGH447 Hydrochloride is Potent and specific pan-PIM inhibitor, inhibiting proliferation of several AML cell lines, showing dual antitumoral and bone antiresorptive effects.
|