(-)-Blebbistatin structure
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Common Name | (-)-Blebbistatin | ||
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CAS Number | 856925-71-8 | Molecular Weight | 292.33 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 486.7±55.0 °C at 760 mmHg | |
Molecular Formula | C18H16N2O2 | Melting Point | 210-212ºC | |
MSDS | Chinese USA | Flash Point | 248.1±31.5 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of (-)-Blebbistatin(-)-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. |
Name | (S)-(-)-Blebbistatin |
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Synonym | More Synonyms |
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. |
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Related Catalog | |
Target |
IC50: 0.5 to 5 μM (myosin II)[1] |
In Vitro | Blebbistatin 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 Vivo | Blebbistatin 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 Assay | Freshly 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 |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 486.7±55.0 °C at 760 mmHg |
Melting Point | 210-212ºC |
Molecular Formula | C18H16N2O2 |
Molecular Weight | 292.33 |
Flash Point | 248.1±31.5 °C |
PSA | 52.90000 |
LogP | 0.93 |
Vapour Pressure | 0.0±1.3 mmHg at 25°C |
Index of Refraction | 1.681 |
Storage condition | Desiccate at +4°C |
Water Solubility | DMSO: soluble5mg/mL |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H312-H315-H317-H319-H332-H335 |
Precautionary Statements | P261-P280-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
Hazard Codes | Xn |
Risk Phrases | 20/21/22-36/37/38 |
Safety Phrases | 26-36/37 |
RIDADR | NONH for all modes of transport |
Stretch-stimulated glucose transport in skeletal muscle is regulated by Rac1.
J. Physiol. 593(3) , 645-56, (2015) Rac1 regulates stretch-stimulated (i.e. mechanical stress) glucose transport in muscle. Actin depolymerization decreases stretch-induced glucose transport in skeletal muscle. Rac1 is a required part o... |
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Formation of contractile networks and fibers in the medial cell cortex through myosin-II turnover, contraction, and stress-stabilization.
Cytoskeleton (Hoboken.) 72(1) , 29-46, (2015) The morphology of adhered cells depends crucially on the formation of a contractile meshwork of parallel and cross-linked fibers along the contacting surface. The motor activity and minifilament assem... |
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Intramolecular loop/tail interactions are essential for connexin 43-hemichannel activity.
FASEB J. 24 , 4378-95, (2010) Connexin-assembled gap junctions (GJs) and hemichannels coordinate intercellular signaling processes. Although the regulation of connexins in GJs has been well characterized, the molecular determinant... |
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