Pim
Pim(皮姆)
Pim protein kinases are a family of serine/threonine kinases consisting of three members of Ca2+/calmodulin-dependent protein kinases, including PIM1, PIM2 and PIM3, that are responsible for cell cycle regulation and antiapoptotic activity as well as homing and migration of receptor tyrosine kinases mediated through the JAK/STAT pathway. All three pim protein kinases share high homology at the amino acid level and hence exhibit greatly overlapping functions, in which 71% and 61% identical amino acids have been found between PIM1/PIM3 and between PIM1/PIM2 respectively. PIM1 comprises two isoforms of 34 and 44 kDa respectively; while PIM2 comprises three isoforms of 34, 37 and 40 kDa respectively. However, PIM3 comprises only one protein.
Pim 相关产品(30)
- GC13154Pim1/AKK1-IN-1CAS: 1093222-27-5纯度: >98.00%
Pim1/AKK1-IN-1是一种有效的多靶点抑制剂,对Pim1、AKK1(AAK1)、LKB1和MST2等激酶具有抑制作用。
- GC16497SGI-1776 free baseCAS: 1025065-69-3纯度: >99.00%
SGI-1776 free base是一种ATP竞争性的Pim激酶抑制剂,可抑制Pim-1(IC 50 =7nM)、Pim-2(IC 50 =363nM)和Pim-3(IC 50 =69nM)的活性。
- GC19419PIM inhibitor 1 phosphateCAS: 2088852-47-3纯度: >98.00%
Uzansertib (INCB053914) phosphate 是一种具有口服活性的 ATP 竞争性泛 PIM 激酶抑制剂,对 PIM1、PIM2、PIM3 的 IC50 分别为 0.24 nM、30 nM、0.12 nM。 PIM inhibitor 1 phosphate 对多种血液肿瘤细胞系具有广泛的抗增殖活性。
- GC34964(1S,3R,5R)-PIM447 dihydrochloride纯度: >98.00%
(1S,3R,5R)-PIM447 (dihydrochloride)是PIM的抑制剂,来自专利US 20100056576 A1化合物实例72。对Pim1,Pim2和Pim3的IC50分别为0.095,0.522和0.369 μM。
- GC36918PIM-447 dihydrochlorideCAS: 1820565-69-2纯度: >99.00%
PIM447是泛PIM激酶抑制剂,对PIM1,PIM2,PIM3的 Ki 分别为6,18,9 nM。
- GC64774SEL24-B489CAS: 1616359-00-2纯度: >98.00%
SEL24-B489 是有效的、I 型的、口服有效的、PIM 和 FLT3-ITD 的双抑制剂,其对PIM1、PIM2 和 PIM3 的 Kd 值分别为 2 nM、2 nM、和 3 nM。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC12660 | AZD1208 | 1204144-28-4 | >98.00% | |
AZD1208 是一种有效、高选择性且可口服的 Pim 激酶抑制剂,对 PIM1、PIM2 和 PIM3 的 IC50 值分别为 0.4、5 和 1.9nM。 | ||||
| GC13056 | CX-6258 | 1202916-90-2 | >99.50% | |
A pan-Pim kinase inhibitor | ||||
| GC13154 | Pim1/AKK1-IN-1 | 1093222-27-5 | >98.00% | |
Pim1/AKK1-IN-1是一种有效的多靶点抑制剂,对Pim1、AKK1(AAK1)、LKB1和MST2等激酶具有抑制作用。 | ||||
| GC13488 | R8-T198wt | 2305815-72-7 | - | |
R8-T198wt 是一种细胞可渗透的羧基末端 p27Kip1 肽,通过抑制 Pim-1 激酶表现出抗肿瘤活性。 | ||||
| GC13558 | PIM-1 Inhibitor 2 | 477845-12-8 | - | |
A potent PIM-1 kinase inhibitor | ||||
| GC16497 | SGI-1776 free base | 1025065-69-3 | >99.00% | |
SGI-1776 free base是一种ATP竞争性的Pim激酶抑制剂,可抑制Pim-1(IC 50 =7nM)、Pim-2(IC 50 =363nM)和Pim-3(IC 50 =69nM)的活性。 | ||||
| GC17178 | TCS PIM-1 1 | 491871-58-0 | >98.00% | |
A Pim-1 kinase inhibitor | ||||
| GC11104 | SMI-4a | 438190-29-5 | >99.50% | |
A Pim kinase inhibitor | ||||
| GC12359 | Hispidulin | 1447-88-7 | >99.00% | |
A flavonoid with diverse biological activities | ||||
| GC19361 | TP-3654 | 1361951-15-6 | >99.50% | |
A Pim kinase inhibitor | ||||
| GC19398 | PIM447 | 1210608-43-7 | - | |
PIM447 (LGH447) 是一种有效的、口服的、选择性的泛 PIM 激酶抑制剂,对 PIM1、PIM2 和 PIM3 的 Ki 值分别为 6、18 和 9 pM。 PIM447 具有双重抗骨髓瘤和骨保护作用。 PIM447 诱导细胞凋亡。 | ||||
| GC19419 | PIM inhibitor 1 phosphate | 2088852-47-3 | >98.00% | |
Uzansertib (INCB053914) phosphate 是一种具有口服活性的 ATP 竞争性泛 PIM 激酶抑制剂,对 PIM1、PIM2、PIM3 的 IC50 分别为 0.24 nM、30 nM、0.12 nM。 PIM inhibitor 1 phosphate 对多种血液肿瘤细胞系具有广泛的抗增殖活性。 | ||||
| GC19747 | CX-6258 HCl | 1353859-00-3 | >99.00% | |
A pan-Pim kinase inhibitor | ||||
| GC32958 | GDC-0339 | 1428569-85-0 | >99.50% | |
GDC-0339是Pim激酶抑制剂,作用于BaF3PIM1时,IC50为43.6nM。 | ||||
| GC33253 | GNE-955 | 1527523-39-2 | - | |
GNE-955是有效的泛Pim激酶抑制剂,Ki分别为18,110,8nM。 | ||||
| GC34138 | M-110 | 1395048-49-3 | >98.50% | |
M-110是Pim激酶抑制剂,抑制前列腺癌细胞系增殖IC50为0.6-0.9uM。 | ||||
| GC34964 | (1S,3R,5R)-PIM447 dihydrochloride | - | >98.00% | |
(1S,3R,5R)-PIM447 (dihydrochloride)是PIM的抑制剂,来自专利US 20100056576 A1化合物实例72。对Pim1,Pim2和Pim3的IC50分别为0.095,0.522和0.369 μM。 | ||||
| GC35447 | AZD1208 hydrochloride | 1621866-96-3 | - | |
A pan-Pim kinase inhibitor | ||||
| GC35762 | CX-6258 hydrochloride hydrate | 1353858-99-7 | >98.50% | |
A pan-Pim kinase inhibitor | ||||
| GC36918 | PIM-447 dihydrochloride | 1820565-69-2 | >99.00% | |
PIM447是泛PIM激酶抑制剂,对PIM1,PIM2,PIM3的 Ki 分别为6,18,9 nM。 | ||||
| GC37651 | SMI-16a | 587852-28-6 | >99.50% | |
A Pim-1 kinase inhibitor | ||||
| GC39485 | CK2/ERK8-IN-1 | 1085822-09-8 | >99.00% | |
A dual inhibitor of CK2 and ERK8 | ||||
| GC64774 | SEL24-B489 | 1616359-00-2 | >98.00% | |
SEL24-B489 是有效的、I 型的、口服有效的、PIM 和 FLT3-ITD 的双抑制剂,其对PIM1、PIM2 和 PIM3 的 Kd 值分别为 2 nM、2 nM、和 3 nM。 | ||||
| GC65201 | Quercetagetin | 90-18-6 | >99.00% | |
A selective Pim-1 inhibitor | ||||
