Blebbistatin S enantiomer

CAS No. 856925-71-8

Blebbistatin S enantiomer( S)-(-)-Blebbistatin )

Catalog No. M16215 CAS No. 856925-71-8

Blebbistatin S enantiomer ((S)-(-)-Blebbistatin) is the S enantiomer of blebbistatin.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 33 In Stock
5MG 54 In Stock
10MG 92 In Stock
25MG 180 In Stock
50MG 276 In Stock
100MG 445 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Blebbistatin S enantiomer
  • Note
    Research use only, not for human use.
  • Brief Description
    Blebbistatin S enantiomer ((S)-(-)-Blebbistatin) is the S enantiomer of blebbistatin.
  • Description
    Blebbistatin S enantiomer ((S)-(-)-Blebbistatin) is the S enantiomer of blebbistatin, which is a potent and selective myosin II inhibitor with IC50 of 0.5-5 uM; inhibits contraction of the cleavage furrow without disrupting mitosis or contractile ring assembly, inhibits pancreatic adenocarcinoma cellular invasiveness; inhibits some myosin II-independent processes and that blebbistatin inhibits other activities in the absence of myosin II.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    S)-(-)-Blebbistatin
  • Pathway
    Cytoskeleton/Cell Adhesion Molecules
  • Target
    Myosin
  • Recptor
    non-musclemyosinIIATPases
  • Research Area
    Other Indications
  • Indication
    ——

Chemical Information

  • CAS Number
    856925-71-8
  • Formula Weight
    292.3318
  • Molecular Formula
    C18H16N2O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 5.2 mg/mL (Need ultrasonic and warming)
  • SMILES
    CC1=CC2=C(C=C1)N=C3[C@](C2=O)(CCN3C4=CC=CC=C4)O
  • Chemical Name
    4H-Pyrrolo[2,3-b]quinolin-4-one, 1,2,3,3a-tetrahydro-3a-hydroxy-6-methyl-1-phenyl-, (3aS)-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Straight AF, et al. Science. 2003 Mar 14;299(5613):1743-7. 2. Abe M, et al. J Biol Chem. 2003 Nov 28;278(48):47707-12. 3. Duxbury MS, et al. Biochem Biophys Res Commun. 2004 Jan 23;313(4):992-7. 4. Shu S, et al. Proc Natl Acad Sci U S A. 2005 Feb 1;102(5):1472-7.
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