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1786438-30-9

中文名稱(chēng) (R)-CR8 (trihydrochloride)
英文名稱(chēng) (R)-CR8 (trihydrochloride)
CAS 1786438-30-9
更新日期 2023/03/20 15:41:25
分子式 C24H30ClN7O
分子量 468
MOL 文件 1786438-30-9.mol
1786438-30-9 結(jié)構(gòu)式 1786438-30-9 結(jié)構(gòu)式

基本信息

中文別名
化合物 T12617
(R)-CR8 3HCL
(2R)-2-[[9-(甲基乙基)-6-[[4-(2-吡啶基)苯基]甲基]氨基]-9H-嘌呤-2-基]氨基]-1-丁醇三鹽酸鹽
英文別名
(R)?-?CR8 (trihydrochloride)
CR8, (R)-Isomer trihydrochloride

物理化學(xué)性質(zhì)

儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMSO: 62.5 mg/mL (115.54 mM)
形態(tài)Solid
顏色White to off-white
(R)-CR8 (trihydrochloride)價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱(chēng)CAS號(hào)包裝價(jià)格
2024/08/19HY-18340A(R)-CR8 (trihydrochloride)
(R)-CR8 trihydrochloride
1786438-30-95mg900元
2024/08/19HY-18340A(R)-CR8 (trihydrochloride)
(R)-CR8 trihydrochloride
1786438-30-910mM * 1mLin DMSO1071元
2024/08/19HY-18340A(R)-CR8 (trihydrochloride)
(R)-CR8 trihydrochloride
1786438-30-910mg1450元

常見(jiàn)問(wèn)題列表

生物活性
(R)-CR8 (CR8) trihydrochloride 是 Roscovitine 的第二代類(lèi)似物,是一種有效的 CDK1/2/5/7/9 抑制劑。(R)-CR8 trihydrochloride 抑制 CDK1/cyclin B (IC50=0.09 μM)、CDK2/cyclin A (0.072 μM)、CDK2/cyclin E (0.041 μM)、CDK5/p25 (0.11 μM)、CDK7/cyclin H (1.1 μM)、CDK9/cyclin T (0.18 μM) 和 CK1δ/ε (0.4 μM)。(R)-CR8 trihydrochloride 誘導(dǎo)細(xì)胞凋亡并具有神經(jīng)保護(hù)作用。(R)-CR8 trihydrochloride 作為一種分子膠降解劑來(lái)消耗細(xì)胞周期蛋白 K。
靶點(diǎn)

CDK1/cyclinB1

0.09 μM (IC 50 )

cdk2/cyclin A

0.072 μM (IC 50 )

CDK2/cyclinE

0.041 μM (IC 50 )

Cdk5/p25

0.11 μM (IC 50 )

CDK7/cyclin H

1.1 μM (IC 50 )

CDK9/Cyclin T

0.18 μM (IC 50 )

CK1δ/ε

0.4 μM (IC 50 )

體外研究

(R)-CR8 (CR8) trihydrochloride (0.1-100 μM; 48 hours) is a potent inducer of apoptotic cell death with an IC 50 of 0.49 μM for SH-SY5Y cell line.
(R)-CR8 trihydrochloride (0.25-10 μM) induces a dose-dependent induction of poly-(ADP-ribose)polymerase (PARP) cleavage.
The CDK-bound form of (R)-CR8 trihydrochloride has a solvent-exposed pyridyl moiety that induces the formation of a complex between CDK12-cyclin K and the CUL4 adaptor protein DDB1, bypassing the requirement for a substrate receptor and presenting cyclin K for ubiquitination and degradation

Apoptosis Analysis

Cell Line: SH-SY5Y cell line
Concentration: 0.1, 1, 10, 100 μM
Incubation Time: 24 hours
Result: Reduced cell survival in a dose-dependent manner.
體內(nèi)研究

(R)-CR8 trihydrochloride (5?mg/Kg; i.p.) results in a significant reduction in lesion size at 28 days in histological assessment.

Animal Model: Adult (10 to 12 weeks old) male Sprague-Dawley rats (310 to 330?g)
Dosage: 5?mg/Kg
Administration: i.p.
Result: Resulted in a significant reduction in lesion size.
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