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
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
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.
CNS Activity
Originator
Approval Year
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15671182
(+)-blebbistatin didn`t inhibit Dictyostelium myosin II in the 0-200 uM concentration range
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:00:17 GMT 2023
by
admin
on
Sat Dec 16 11:00:17 GMT 2023
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Record UNII |
XWG1958E8I
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Record Status |
Validated (UNII)
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Record Version |
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-
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DTXSID10424990
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1177356-70-5
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6604910
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XWG1958E8I
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admin on Sat Dec 16 11:00:17 GMT 2023 , Edited by admin on Sat Dec 16 11:00:17 GMT 2023
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