产品详情
Targets
Target | Value |
---|---|
CDK9/CyclinT | IC50: <10nM |
CDK5/p35 | IC50: 13nM |
CDK2/CyclinA | IC50: 47nM |
GSK-3β | IC50: 89nM |
CDK4/CyclinD1 | IC50: 100nM |
CDK6/CyclinD3 | IC50: 170nM |
CDK1/CyclinB | IC50: 210nM |
CDK3/CyclinE | IC50: 360nM |
PI3Kβ | IC50: >1μM |
PLK3 | IC50: >1μM |
RET | IC50: >1μM |
SGK | IC50: >1μM |
TrkB | IC50: >1μM |
JAK2 | IC50: >1μM |
CDK7/CyclinH/MAT1 | IC50: 2.4μM |
SAPK2A(p38α) | IC50: >10μM |
p70S6K | IC50: >10μM |
PDGFR | IC50: >10μM |
PDK-1 | IC50: >10μM |
PKBβ | IC50: >10μM |
VEGFR1 | IC50: >10μM |
AuroraA | IC50: >10μM |
c-Abl | IC50: >10μM |
c-Src | IC50: >10μM |
Chk1 | IC50: >10μM |
EGFR | IC50: >10μM |
FGFR3 | IC50: >10μM |
IR | IC50: >10μM |
JNK2 | IC50: >10μM |
MAPK1 | IC50: >10μM |
MEK1 | IC50: >10μM |
Met | IC50: >10μM |
In vitro (25°C) | DMSO | 9 mg/mL (23.54 mM) | |
Water | Insoluble | ||
Ethanol | Insoluble | ||
In vivo | 2% DMSO+30% PEG 300+2% Tween 80+ddH2O | 1 mg/mL | |
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.1 mM | 26.16 mL | 130.82 mL | 261.64 mL |
0.5 mM | 5.23 mL | 26.16 mL | 52.33 mL |
1 mM | 2.62 mL | 13.08 mL | 26.16 mL |
5 mM | 0.52 mL | 2.62 mL | 5.23 mL |
*The above data is based on the productmolecular weight 382.2. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
目录号 | A10093 |
---|---|
作用机制 | Inhibitor (抑制剂) |
M. Wt | 382.2 |
Formula | C16H17Cl2N5O2 |
Purity | >99% |
Storage | Store lyophilized at -20ºC, keep desiccated. |
CAS No. | 844442-38-2 |
Synonyms | AT-7519 |
SMILES | C1CNCCC1NC(=O)C2=C(C=NN2)NC(=O)C3=C(C=CC=C3Cl)Cl |
产品标签
Product Questions
Product Questions
Flavopiridol HCl
Flavopiridol HCl是细胞周期蛋白依赖性激酶的抑制剂。(-)-顺式形式诱导特定肿瘤细胞的凋亡。
Dinaciclib (SCH 727965)
Dinaciclib (SCH 727965)是一种有效且选择性的细胞周期蛋白依赖性激酶(CDK)抑制剂,选择性抑制CDK1,CDK2,CDK5…
LY2835219 (abemaciclib)
LY2835219 (abemaciclib)是一种细胞周期蛋白依赖性激酶(CDK)抑制剂,靶向CDK4(cyclin D1)和CDK6(cyclin D3)细胞…
PHA-793887
PHA-793887是一种新型有效的CDK2,CDK5和CDK7抑制剂,IC50分别为8 nM,5 nM 和10 nM,作用于CDK2,5,和7比作用于CDK1…
PHA-767491
PHA-767491是一种有效的,具有ATP竞争性的双重cdc7/cdk9抑制剂 (IC50值分别为10和34 nM),可防止DNA复制的启动。