• 13585831301
  • 021-59541103 021-60443211
  • 3004967995

RGB-286638

  • 產(chǎn)品貨號(hào):CS-01Y67168
  • 產(chǎn)品價(jià)格:電議
  • 產(chǎn)品產(chǎn)地:進(jìn)口、國(guó)產(chǎn)
  • 包裝類型:2mg 5mg 10mg 50mg 100mg
  • 采購(gòu)熱度:226
  • 庫(kù)存:100
  • CAS號(hào):784210-87-3
  • 方法:
  • 含量:>98.00%
  • 品牌名稱:莼試
  • 分子式:C29H37Cl2N7O4
  • 分子量:618.55

簡(jiǎn)介內(nèi)容:質(zhì)量保證、價(jià)格優(yōu)惠

在線訂購(gòu)  免費(fèi)訂購(gòu)熱線:021-59541103 021-60443211

標(biāo)簽:RGB-286638 

產(chǎn)品目錄

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聯(lián)系人:高小姐

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商品詳情購(gòu)物流程代測(cè)服務(wù)付款方式常見問(wèn)題

化學(xué)性質(zhì):                                                                                                             

規(guī)格

2mg 5mg 10mg 50mg 100mg

CAS

784210-87-3

別名

N/A

化學(xué)名

N/A

分子式

C29H37Cl2N7O4

分子量

618.55

溶解度

DMSO: 150 mg/mL (242.50 mM)

儲(chǔ)存條件

Store at -20°C

General tips

For obtaining a higher solubility , please warm the tube at 37 and shake it in the ultrasonic bath for a while.

Shipping Condition

Evaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request

 

產(chǎn)品描述:                                                                                                             

RGB-286638 is a CDK inhibitor that inhibits the kinase activity of cyclin T1-CDK9, cyclin B1-CDK1, cyclin E-CDK2, cyclin D1-CDK4, cyclin E-CDK3, and p35-CDK5 with IC50s of 1, 2, 3, 4, 5 and 5 nM, respectively; also inhibits GSK-3β, TAK1, Jak2 and MEK1, with IC50s of 3, 5, 50, and 54 nM. T1-CDK9|1 nM (IC50)|cyclin B1-CDK1|2 nM (IC50)|cyclin E-CDK2|3 nM (IC50)|cyclin D1-CDK4|4 nM (IC50)|cyclin E-CDK3|5 nM (IC50)|p35-CDK5|5 nM (IC50)|cyclin H-CDK7|44 nM (IC50)|cyclin D3-CDK6|55 nM (IC50)|GSK-3β|3 nM (IC50)|JAK2|50 nM (IC50)|MEK1|54 nM (IC50)|Fms|1 nM (IC50)|TAK1|5 nM (IC50)|JNK1a1|17 nM (IC50)|JNK1a2|40 nM (IC50)|C-src|25 nM (IC50)|AMPK|41 nM (IC50)

RGB-286638 is an indenopyrazole-derived CDK inhibitor (CDKI) with Ki-nanomolar activity against transcriptional CDKs. RGB-286638 inhibits several tyrosine and serine/threonine non-CDK enzymes, i.e. GSK-3β, TAK1, AMPK, Jak2, MEK1. The dose- and time-dependent effect of treatment with RGB-286638 (12.5-100nM) is investigated on the growth of human p53-wt (MM.1S, MM.1R, and H929) and p53-mutant (U266, OPM1, and RPMI) MM cells by MTT assay, assessing viability at 24 and 48 hours. The half-maximally effective concentrations (EC50) range between 20 and 70 nM at 48 hours. Dose-dependent differences in growth among p53-wt and -mutant cells are observed after 50nM treatment, with p53-wt MM.1S, MM.1R and H929 being slightly more sensitive to RGB-286638 treatment at 48h[1].

Dose-finding studies with RGB-286638 identify 40 mg/kg/day IV treatment as the maximum tolerated dose in SCID mice. Five days IV treatment with RGB-286638 significantly suppresses MM tumor growth, with maximum TGI (%) noted at day 14 following end of treatment at 85.06% and 86.34% in the 30 mg/kg and 40 mg/kg treated cohorts respectively. The log10 cell kill (LCK Td: 4.5 days) is 1.6 for both treated groups. RGB-286638 treatment is also associated with improved survival, evidenced by first death at day 24 in controls versus day 43 in both treated groups. No toxic deaths occurred during this study: maximum percentage of body weight (BW) loss is observed on day 5 (8.4%) at 30 mg/kg dosage schedule, and on day 15 (9.9%) after 40 mg/kg dosing, with weight recovery in the following two weeks[1].

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原創(chuàng)作者:上海莼試生物技術(shù)有限公司

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