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ГУ 6656

ГУ 6656 структура
330161-87-0
CAS №
330161-87-0
Химическое название:
ГУ 6656
английское имя:
SU 6656
Синонимы:
CS-1672;SU 6656;SU-6656;SU6656 - CAS 330161-87-0 - Calbiochem;N,N-diMethyl-2-oxo-3-((4,5,6,7-tetrahydro-1H-indol-2-yl)Methyl)indoline-5-sulfonaMide;N,N-Dimethyl-2-oxo-3-((4,5,6,7-tetrahydro-1H-indol-2-yl)methylene)indoline-5-sulfonamide;2,3-dihydro-n,n-dimethyl-2-oxo-3-[(4,5,6,7-tetrahydro-1h-indol-2-yl)methylene]-1h-indole-5-sulfonamide;1H-Indole-5-sulfonamide, 2,3-dihydro-N,N-dimethyl-2-oxo-3-[(4,5,6,7-tetrahydro-1H-indol-2-yl)methylene]-;PTK2 protein tyrosine kinase 2,Focal adhesion kinase,FAK,Akt,SU-6656,PTK2,Inhibitor,Protein kinase B,SU 6656,SU6656,Src,PKB,inhibit
CBNumber:
CB0504775
Формула:
C19H21N3O3S
молекулярный вес:
371.45
MOL File:
330161-87-0.mol

ГУ 6656 атрибут

плотность: 1.378±0.06 g/cm3(Predicted)
температура хранения: -20°C
растворимость: ДМСО: раствор апельсина 12 мг/мл
пка: 11.87±0.20(Predicted)
форма: пудра
цвет: Оранжево-коричневый
ИнЧИКей: LOGJQOUIVKBFGH-YBEGLDIGSA-N

Заявления о рисках и безопасности

WGK Германия 3

ГУ 6656 химические свойства, назначение, производство

Описание

The Src family of proto-oncogenic kinases include nine mammalian non-receptor tyrosine kinases that are involved in intracellular signaling and are often relevant to carcinogenesis. SU6656 is a selective inhibitor of Src kinases, Including Src, Yes, Lyn, and Fyn (IC50 = 280, 20, 130, 170 nM, respectively). It weakly inhibits some other kinases when used at >10 μM. SU6656 has been used to study the role of Src kinases in cell growth and development in diverse processes, including nervous system development, fibrosis, and cancer.

Использование

SU 6656 is a small molecule selective inhibitor of the Src kinase family and induces caspase-independant cancer cell death.

Общее описание

A potent, cell-permeable, reversible, and ATP-competitive inhibitor of Src-family protein tyrosine kinases. Inhibits Src (IC50 = 280 nM) as well as closely related kinases Fyn (IC50 = 170 nM), Yes (IC50 = 20 nM) and Lyn (IC50 = 130 nM). The inhibition is competitive with respect to ATP. Has only a trivial effect on Lck (IC50 = 6.88 μM). Does not affect the activity of PDGF-β receptor kinase (IC50 ≥10 μM) and IGF-1 receptor kinase (IC50 ≥20 μM).

ГУ 6656 препаратная продукция и сырье

сырьё

препарат


ГУ 6656 поставщик

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