CGP 77675; CGP-77675

英文名称:CGP77675
CAS号:234772-64-6
分子式:C26H29N5O2
分子量:443.54
EINECS号:
Mol文件:234772-64-6.mol
CGP 77675; CGP-77675 结构式

CGP 77675; CGP-77675 性质

储存条件 2-8°C
溶解度 二甲基亚砜:>10mg/mL
形态 粉末
颜色 白色至米色
InChIKey WUPXZZWTHIZICK-UHFFFAOYSA-N
SMILES COc1cccc(c1)-c2cn(-c3ccc(CCN4CCC(O)CC4)cc3)c5ncnc(N)c25

CGP 77675; CGP-77675 用途与合成方法

CGP77675 是一种有效的 Src 家族激酶抑制剂。CGP77675 抑制 Src,EGFR,KDR,v-Abl 和 Lck,IC50 分别为 0.02、0.15、1.0、0.31 和 0.29 μM。具有抗肿瘤活性。

IC50: 0.02 μM (Src), 0.15 μM (EGFR), 1.0 μM (KDR), 0.31 μM (v-Abl), 0.29 μM (Lck)

CGP77675 inhibits phosphorylation of peptide substrates and autophosphorylation of purified Src (IC 50 s of 5-20 and 40 nM, respectively) .
CGP77675 dose dependently inhibits phosphorylation of poly-Glu-Tyr with an IC 50 value of 5.5 nM, and of the optimal Src substrate (OSS) peptide with an IC 50 value of 16.7 nM. These IC 50 values are similar to the value obtained with chicken Src (20 nM).
CGP77675 inhibits the parathyroid hormone-induced bone resorption in rat fetal long bone cultures with an IC 50 of 0.8 μM.
CGP77675 (0.04-10 μM; 2 hours) potently inhibits tyrosine phosphorylation of the Src substrates Fak and paxillin, but has much less effect on Src (IC 50 values 0.2, 0.5, and 5.7μM) in IC8.1 cells.

Cell Viability Assay

Cell Line: MC3T3-E1 cells
Concentration: 0.2, 1, and 5 μM
Incubation Time: 3 days
Result: Did not influence cell viability for up to 3 days of treatment.

Western Blot Analysis

Cell Line: Src-overexpressing IC8.1 cells
Concentration: 0.04, 0.2, 1, 5, and 10 μM
Incubation Time: 2 hours
Result: Dose dependently inhibited phosphorylation of Fak and paxillin, but not of Src.

CGP77675 (1, 5, and 25 mg/kg; injected s.c.; twice a day) inhibits IL-1β-induced hypercalcemia in Mice.
CGP77675 (10 and 50 mg/kg; administered orally; twice a day for 6 weeks) partially prevents bone loss and rescues bone microarchitectural features in young ovx rats.

Animal Model: Male mice (Tif:MAGf; Novartis Animal Farm) of 25-30 g body
Dosage: 1, 5, and 25 mg/kg
Administration: Injected s.c.; twice a day
Result: Prevented IL-1β-induced hypercalcemia in mice without affecting serum amyloid protein levels.
Animal Model: Eight-week-old (175-209 g) female rats of the Sprague-Dawley-derived strain Tif:RAlf
Dosage: 10 and 50 mg/kg
Administration: Administered orally; twice a day for 6 weeks
Result: Partly prevented bone loss.

安全信息

WGK Germany3
存储类别11 - 可燃固体

CGP 77675; CGP-77675 价格(试剂级)

更新日期 产品编号 产品名称 CAS号 包装 价格
2026-09-15 HY-W062835 234772-64-6 1 mg 636
2026-09-15 HY-W062835 CGP 77675; CGP-77675 234772-64-6 5mg 1400

CGP 77675; CGP-77675供应商 更多

南京百鑫德诺生物科技有限公司
联系电话:025-58849295
产品介绍:
英文名称:CGP77675
CAS:234772-64-6
纯度:0.98
包装信息:1mg;5mg;10mg;25mg;50mg;100mg
备注:试剂
Sigma-Aldrich西格玛奥德里奇(上海)贸易有限公司
联系电话:021-61415566 800-8193336
产品介绍:
英文名称:CGP77675
CAS:234772-64-6
纯度:>=98% (HPLC)
包装信息:25MG
备注:SML0314-25MG
成都创科诚生物科技有限公司
联系电话:028-028-0000000 13008177686
产品介绍:
英文名称:1-(4-(4-Amino-5-(3-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)phenethyl)piperidin-4-ol
CAS:234772-64-6
纯度:95%min
包装信息:1g、10g、50g
上海一飞生物科技有限公司
联系电话:021-65675885 18964387627
产品介绍:
英文名称:CGP 77675
CAS:234772-64-6
纯度:98%
包装信息:1mg;2mg;5mg
备注:试剂级
ChemeGen 中国
联系电话: 18818260767
产品介绍:
英文名称:CGP 77675
CAS:234772-64-6
纯度:98%
包装信息:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
备注:品牌:ChemeGen

最新发布供应信息

化合物 CGP77675|T30855|TargetMol
TargetMol中国(陶术生物) 2026-09-26

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