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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H16N2O2
Molecular Weight 292.3318
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BLEBBISTATIN, (+)-

SMILES

CC1=CC=C2N=C3N(CC[C@]3(O)C(=O)C2=C1)C4=CC=CC=C4

InChI

InChIKey=LZAXPYOBKSJSEX-SFHVURJKSA-N
InChI=1S/C18H16N2O2/c1-12-7-8-15-14(11-12)16(21)18(22)9-10-20(17(18)19-15)13-5-3-2-4-6-13/h2-8,11,22H,9-10H2,1H3/t18-/m0/s1

HIDE SMILES / InChI

Molecular Formula C18H16N2O2
Molecular Weight 292.3318
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Blebbistatin is a small molecule inhibitor discovered in a screen for inhibitors of nonmuscle myosin IIA. Blebbistatin is a specific inhibitor of nonmuscle myosin II, it inhibited contraction of the cleavage furrow without disrupting mitosis or contractile ring assembly. (+)-blebbistatin is an inactive enantiomer of (±)-Blebbistatin. (–)-blebbistatin is the active species, with an inhibitory concentration for 50% inhibition (IC50) of 2 uM, whereas (+)-blebbistatin is inactive. (+)-blebbistatin is useful as a negative control for the active enantiomer, (-)-Blebbistatin.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
(+)-blebbistatin didn`t inhibit Dictyostelium myosin II in the 0-200 uM concentration range
Substance Class Chemical
Created
by admin
on Sat Dec 16 11:00:17 GMT 2023
Edited
by admin
on Sat Dec 16 11:00:17 GMT 2023
Record UNII
XWG1958E8I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BLEBBISTATIN, (+)-
Common Name English
4H-PYRROLO(2,3-B)QUINOLIN-4-ONE, 1,2,3,3A-TETRAHYDRO-3A-HYDROXY-6-METHYL-1-PHENYL-, (3AR)-
Systematic Name English
(+)-BLEBBISTATIN
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID10424990
Created by admin on Sat Dec 16 11:00:17 GMT 2023 , Edited by admin on Sat Dec 16 11:00:17 GMT 2023
PRIMARY
CAS
1177356-70-5
Created by admin on Sat Dec 16 11:00:17 GMT 2023 , Edited by admin on Sat Dec 16 11:00:17 GMT 2023
PRIMARY
PUBCHEM
6604910
Created by admin on Sat Dec 16 11:00:17 GMT 2023 , Edited by admin on Sat Dec 16 11:00:17 GMT 2023
PRIMARY
FDA UNII
XWG1958E8I
Created by admin on Sat Dec 16 11:00:17 GMT 2023 , Edited by admin on Sat Dec 16 11:00:17 GMT 2023
PRIMARY