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Details

Stereochemistry ACHIRAL
Molecular Formula C16H16N2OS
Molecular Weight 284.376
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-(2-(2-METHYLINDOL-3-YL)ETHYL)-2-THIENYLCARBOXAMIDE

SMILES

CC1=C(CCNC(=O)C2=CC=CS2)C3=C(N1)C=CC=C3

InChI

InChIKey=ACAKNPKRLPMONU-UHFFFAOYSA-N
InChI=1S/C16H16N2OS/c1-11-12(13-5-2-3-6-14(13)18-11)8-9-17-16(19)15-7-4-10-20-15/h2-7,10,18H,8-9H2,1H3,(H,17,19)

HIDE SMILES / InChI

Molecular Formula C16H16N2OS
Molecular Weight 284.376
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

CK-636 is an Arp2/3 complex inhibitor with IC50 of 4 μM, 24 μM and 32 μM for inhibition of actin polymerization induced by human, fission yeast and bovine Arp2/3 complex, respectively. CK-636 binds between Arp2 and Arp3, where it appears to block movement of Arp2 and Arp3 into their active conformation. CK-636 inhibits actin polymerization mediated by Arp2/3 complex in live cells, and reduces the formation of actin filament comet tails by Listeria in infected SKOV3 cells. CK-636 inhibits lamellipodia formation at the leading edges of migrating T cells, and causes reduced velocity. In addition, a substantial fraction of CK-636-treated T cells on zigzag patterns with an acute turning angle are trapped near the interfaces formed by the turning points of zigzag patterns.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Characterization of two classes of small molecule inhibitors of Arp2/3 complex.
2009-08-20
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
Effects of CK-636 on actin fluorescence around Listeria was evaluated in SKOV3 cells. Infected cells were treated with CK-636 (up to 100 mkM) for 60 min followed by a 60 min washout. CK-636 reduced the formation of actin filament comet tails by Listeria in infected SKOV3 cells
Substance Class Chemical
Created
by admin
on Wed Apr 02 05:17:14 GMT 2025
Edited
by admin
on Wed Apr 02 05:17:14 GMT 2025
Record UNII
82XC8RSD8V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-(2-(2-METHYLINDOL-3-YL)ETHYL)-2-THIENYLCARBOXAMIDE
Systematic Name English
CK-636
Preferred Name English
N-(2-(2-METHYL-1H-INDOL-3-YL)ETHYL)THIOPHENE-2-CARBOXAMIDE
Systematic Name English
2-THIOPHENECARBOXAMIDE, N-(2-(2-METHYL-1H-INDOL-3-YL)ETHYL)-
Systematic Name English
Code System Code Type Description
DRUG BANK
DB08235
Created by admin on Wed Apr 02 05:17:14 GMT 2025 , Edited by admin on Wed Apr 02 05:17:14 GMT 2025
PRIMARY
CAS
442632-72-6
Created by admin on Wed Apr 02 05:17:14 GMT 2025 , Edited by admin on Wed Apr 02 05:17:14 GMT 2025
PRIMARY
PUBCHEM
588963
Created by admin on Wed Apr 02 05:17:14 GMT 2025 , Edited by admin on Wed Apr 02 05:17:14 GMT 2025
PRIMARY
FDA UNII
82XC8RSD8V
Created by admin on Wed Apr 02 05:17:14 GMT 2025 , Edited by admin on Wed Apr 02 05:17:14 GMT 2025
PRIMARY