CAS 856925-71-8|(-)-Blebbistatin

Introduction:Basic information about CAS 856925-71-8|(-)-Blebbistatin, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name(-)-Blebbistatin
CAS Number856925-71-8Molecular Weight292.33
Density1.3±0.1 g/cm3Boiling Point486.7±55.0 °C at 760 mmHg
Molecular FormulaC18H16N2O2Melting Point210-212ºC
MSDSChineseUSAFlash Point248.1±31.5 °C
Symbol
GHS07
Signal WordWarning

Names

Name(S)-(-)-Blebbistatin
SynonymMore Synonyms

(-)-Blebbistatin BiologicalActivity

Description(-)-Blebbistatin is an S enantiomer of blebbistatin. Blebbistatin is a potent and selective myosin II inhibitor with IC50s ranging from 0.5 to 5 μM.
Related CatalogSignaling Pathways >>Cytoskeleton >>MyosinResearch Areas >>Cardiovascular Disease
Target

IC50: 0.5 to 5 μM (myosin II)[1]

In VitroBlebbistatin potently inhibits several striated muscle myosins as well as vertebrate nonmuscle myosin IIA and IIB with IC50 values ranging from 0.5 to 5 μM. Smooth muscle myosin is only poorly inhibited (IC50=80 μM)[1]. Blebbistatin does not compete with nucleotide binding to the skeletal muscle myosin subfragment-1. The inhibitor preferentially binds to the ATPase intermediate with ADP and phosphate bound at the active site, and it slows down phosphate release. It blocks the myosin heads in a products complex with low actin affinity[2]. In culture-activated hepatic stellate cells, blebbistatin is found to change both cell morphology and function. Stellate cells become smaller, acquire a dendritic morphology and have less myosin IIA-containing stress fibres and vinculin-containing focal adhesions. Blebbistatin impairs silicone wrinkle formation, reduces collagen gel contraction and blocks endothelin-1-induced intracellular Ca2+ release. It promotes wound-induced cell migration[3].
In VivoBlebbistatin dose-dependently and completely relax both KCl- and carbachol-induced rat detrusor and endothelin-1-induced human bladder contraction. Pre-incubation with 10 μM blebbistatin attenuates carbachol responsiveness by 65% while blocking electrical field stimulation-induced bladder contraction reaching 50% inhibition at 32 Hz[4].
Cell AssayFreshly isolated HSCs are replated on 96-well plate. At day 3, medium is replaced by serum-free medium and cells are starved overnight, treated with or without blebbistatin (25 μM) for 2 h followed by stimulation with platelet-derived growth factor-BB (20 ng/mL). After an overnight incubation, the WST-1 cell proliferation assay are performed[3].
References

[1]. Limouze J, et al. Specificity of blebbistatin, an inhibitor of myosin II. J Muscle Res Cell Motil. 2004;25(4-5):337-41.

[2]. Kovács M, et al. Mechanism of blebbistatin inhibition of myosin II. J Biol Chem. 2004 Aug 20;279(34):35557-63.

[3]. Liu Z, et al. Blebbistatin inhibits contraction and accelerates migration in mouse hepatic stellate cells. Br J Pharmacol. 2010 Jan 1;159(2):304-15.

[4]. Zhang X, et al. In vitro and in vivo relaxation of urinary bladder smooth muscle by the selective myosin IIinhibitor, blebbistatin. BJU Int. 2011 Jan;107(2):310-7.

Chemical & Physical Properties

Density1.3±0.1 g/cm3
Boiling Point486.7±55.0 °C at 760 mmHg
Melting Point210-212ºC
Molecular FormulaC18H16N2O2
Molecular Weight292.33
Flash Point248.1±31.5 °C
PSA52.90000
LogP0.93
Vapour Pressure0.0±1.3 mmHg at 25°C
Index of Refraction1.681
InChIKeyLZAXPYOBKSJSEX-GOSISDBHSA-N
SMILESCc1ccc2c(c1)C(=O)C1(O)CCN(c3ccccc3)C1=N2
Storage conditionDesiccate at +4°C
Water SolubilityDMSO: soluble5mg/mL

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH302-H312-H315-H317-H319-H332-H335
Precautionary StatementsP261-P280-P305 + P351 + P338
Personal Protective Equipmentdust mask type N95 (US);Eyeshields;Faceshields;Gloves
Hazard CodesXn
Risk Phrases20/21/22-36/37/38
Safety Phrases26-36/37
RIDADRNONH for all modes of transport

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Synonyms

(3aS)-3a-Hydroxy-6-methyl-1-phenyl-1,2,3,3a,4a,8a-hexahydro-4H-pyrrolo[2,3-b]quinolin-4-one
4H-Pyrrolo[2,3-b]quinolin-4-one, 1,2,3,3a,4a,8a-hexahydro-3a-hydroxy-6-methyl-1-phenyl-, (3aS)-
(3aS)-3a-hydroxy-6-methyl-1-phenyl-2,3-dihydropyrrolo[2,3-b]quinolin-4-one
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