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Cdk1/2阻害剤III

Cdk1/2阻害剤III 化學(xué)構(gòu)造式
443798-55-8
CAS番號(hào).
443798-55-8
化學(xué)名:
Cdk1/2阻害剤III
別名:
5-アミノ-N-(2,6-ジフルオロフェニル)-3-[(4-スルファモイルフェニル)アミノ]-1H-1,2,4-トリアゾール-1-カルボチオアミド;Cdk1/2阻害剤III;cdk1/2インヒビトルIII;4-[[1-[(2,6-ジフルオロアニリノ)カルボノチオイル]-5-アミノ-1H-1,2,4-トリアゾール-3-イル]アミノ]ベンゼンスルホンアミド
英語名:
CDK1/2InhibitorIII
英語別名:
2 Inhibitor III;CDK1/2InhibitorIII;Cdk-1/2 Inhibitor III,Cdk1/2 Inhibitor III;5-amino-N-(2,6-difluorophenyl)-3-(4-sulfamoylanilino)-1,2,4-triazole-1-carbothioamide;1H-1,2,4-Triazole-1-carbothioamide, 3-amino-5-[[4-(aminosulfonyl)phenyl]amino]-N-(2,6-difluorophenyl)-
CBNumber:
CB11113964
化學(xué)式:
C15H13F2N7O2S2
分子量:
425.44
MOL File:
443798-55-8.mol
MSDS File:
SDS

Cdk1/2阻害剤III 物理性質(zhì)

沸點(diǎn) :
649.1±65.0 °C(Predicted)
比重(密度) :
1.72±0.1 g/cm3(Predicted)
貯蔵溫度 :
+2C to +8C
溶解性:
DMSO: 10mg/mL
THF: soluble
acetone: soluble
外見 :
白い固體
酸解離定數(shù)(Pka):
6.61±0.70(Predicted)
色:
white
InChI:
1S/C15H13F2N7O2S2/c16-10-2-1-3-11(17)12(10)21-15(27)24-13(18)22-14(23-24)20-8-4-6-9(7-5-8)28(19,25)26/h1-7H,(H,21,27)(H2,19,25,26)(H3,18,20,22,23)
InChIKey:
ARIOBGGRZJITQX-UHFFFAOYSA-N
SMILES:
Fc1c(c(ccc1)F)NC(=S)[n]2nc(nc2N)Nc3ccc(cc3)[S](=O)(=O)N

安全性情報(bào)

WGK Germany  WGK 1
ストレージクラス 11 - Combustible Solids

Cdk1/2阻害剤III 価格

メーカー 製品番號(hào) 製品説明 CAS番號(hào) 包裝 価格 更新時(shí)間 購入

Cdk1/2阻害剤III 化學(xué)特性,用途語,生産方法

使用

Cyclin-dependent kinases (Cdks) are key regulators of cell cycle progression and are therefore promising targets for cancer therapy. Cdk1/2 Inhibitor III is a cell-permeable inhibitor of Cdk1/cyclin B and Cdk2/cyclin A (IC50s = 0.6 and 0.5 nM, respectively). It less potently inhibits CDC2-like kinases 1 and 3, VEGFR2, and GSK-3β (IC50s = 8.9, 29, 32, and 140 nM, respectively) and is without effect against a panel of other kinases. Cdk1/2 Inhibitor III blocks the growth of several cancer cell lines (IC50 values range from 20 to 92 nM).

一般的な説明

A cell-permeable triazolo-diamine compound that displays anti-proliferative properties in various human cancer cells (IC50 = 20 nM, 35 nM and 92 nM in HCT-116, HeLa, and A375 cells, respectively). Acts as a highly potent, reversible, ATP-competitive inhibitor of Cdk1/cyclin B and Cdk2/cyclin A (IC50 = 600 pM and 500 pM, respectively) with selectivity over VEGF-R2 (IC50 = 32 nM), GSK-3β (IC50 = 140 nM), and a panel of eight other kinases (IC50 ≥ 1 μM).

Biochem/physiol Actions

Cell permeable: yes

Cdk1/2阻害剤III 上流と下流の製品情報(bào)

原材料

準(zhǔn)備製品


Cdk1/2阻害剤III 生産企業(yè)

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Cdk1/2阻害剤III  スペクトルデータ(1HNMR)



  • 443798-55-8
  • CDK1/2InhibitorIII
  • 5-amino-N-(2,6-difluorophenyl)-3-(4-sulfamoylanilino)-1,2,4-triazole-1-carbothioamide
  • 2 Inhibitor III
  • Cdk-1/2 Inhibitor III,Cdk1/2 Inhibitor III
  • 1H-1,2,4-Triazole-1-carbothioamide, 3-amino-5-[[4-(aminosulfonyl)phenyl]amino]-N-(2,6-difluorophenyl)-
  • 5-アミノ-N-(2,6-ジフルオロフェニル)-3-[(4-スルファモイルフェニル)アミノ]-1H-1,2,4-トリアゾール-1-カルボチオアミド
  • Cdk1/2阻害剤III
  • cdk1/2インヒビトルIII
  • 4-[[1-[(2,6-ジフルオロアニリノ)カルボノチオイル]-5-アミノ-1H-1,2,4-トリアゾール-3-イル]アミノ]ベンゼンスルホンアミド
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