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3-(4-Pyridyl)indole ROCK-I inhibitor

Catalog No.C4254
Size Price Stock Qty
10mg
$61.00
In stock
25mg
$144.00
In stock
50mg
$255.00
In stock

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Sample solution is provided at 25 µL, 10mM.

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Chemical structure

3-(4-Pyridyl)indole

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Chemical Properties

Cas No. 7272-84-6 SDF Download SDF
Synonyms Rho Kinase Inhibitor III,ROCK Inhibitor III,Rockout
Chemical Name 3-(4-pyridinyl)-1H-indole
Canonical SMILES C12=CC=CC=C1NC=C2C3=CC=NC=C3
Formula C13H10N2 M.Wt 194.2
Solubility Soluble in DMSO Storage Store at -20°C
Shipping Condition Evaluation sample solution : ship with blue ice.All other available size: ship with RT , or blue ice upon request
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.

Background

3-(4-pyridyl)indole (Rockout) is a Rho-kinase inhibitor [1].

Rho-associated protein kinase (ROCK) belongs to a family of serine-threonine kinases mainly involved in regulating the shape and movement of cells by acting on the cytoskeleton [2].

Rockout caused decreased migration and aberrant morphology. Rockout showed no effect on phagocytosis, listeria motility or actin polymerization in permeabilized yeast. In a human melanoma cell line M2 cells that blebs constitutively in a manner that is sensitive to actin cytoskeletal perturbation, Rockout (50 μM) stopped the cell blebbing within 2 min and with washout blebbing returned to normal levels within 3 min. The IC50 of Rockout was 12 μM and it inhibited blebbing in nearly all cells at 50 μM. In B3T3 cells, treatment with 50 μM Rockout resulted in significant morphological change within 10 min [1]. At an ATP concentration of 100 μM, Rockout inhibited ROCK activity with an approximate IC50 of 25 μM. Rockout (25 μM) inhibited ROCK-II and PRK to a similar degree, and MSK-1 and PKA to a lesser extent. Rockout showed no inhibitory effect on PKCα or SAPK2a [1].

References:
[1] Yarrow J C, Totsukawa G, Charras G T, et al.  Screening for cell migration inhibitors via automated microscopy reveals a Rho-kinase inhibitor[J]. Chemistry & biology, 2005, 12(3): 385-395.
[2] Amano M, Fukata Y, Kaibuchi K.  Regulation and functions of Rho-associated kinase[J]. Experimental cell research, 2000, 261(1): 44-51.