3-(4-Pyridyl)

  Cat. No.:  DC8567   Featured
Chemical Structure
7272-84-6
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Field of application
3-(4-Pyridyl)indole is a ROCK-I inhibitor (IC50 = 25 µM) that promotes cell spreading, inhibits membrane blebbing, and induces dissolution of actin stress fibers in a wound healing assay
Cas No.: 7272-84-6
Chemical Name: 3-(4-pyridinyl)-1H-Indole
Synonyms: 3-(4-pyridinyl)-1H-Indole;3-(4-Pyridyl)indole;rockout;4-(3-indolyl)-pyridine;3--indol;3-(PYRIDIN-4-YL)INDOLE;3-(pyridin-4-yl)-1H-indole;3-(4-Pyridyl)-1H-indole
SMILES: N1C=CC(C2C3C(=CC=CC=3)NC=2)=CC=1
Formula: C13H10N2
M.Wt: 194.231902599335
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: 3-(4-Pyridyl)indole is a ROCK-I inhibitor (IC50 = 25 µM) that promotes cell spreading, inhibits membrane blebbing, and induces dissolution of actin stress fibers in a wound healing assay.It also inhibits ROCK-II and PRK2, another Rho-dependent kinase, with similar potency, while inhibiting MSK-1 and PKA with relatively weaker potency.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
DC72592 Zelasudil Zelasudil is a Rho-associated (ROCK) kinase inhibitor. Zelasudil has a ROCK2 binding affinity.
DC45762 Y-27632 Y-27632 is a selective ROCK1 (p160ROCK) inhibitor with Ki of 140 nM in a cell-free assay, exhibits >200-fold selectivity over other kinases, including PKC, cAMP-dependent protein kinase, MLCK and PAK.
DC8567 3-(4-Pyridyl) 3-(4-Pyridyl)indole is a ROCK-I inhibitor (IC50 = 25 µM) that promotes cell spreading, inhibits membrane blebbing, and induces dissolution of actin stress fibers in a wound healing assay
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