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Merck
CN

203392

(+)-Blebbistatin

The inactive enantiomer of (±)-Blebbistatin.

别名:

(+)-Blebbistatin

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关于此项目

经验公式（希尔记法）:
C18H16N2O2
化学文摘社编号:
1177356-70-5
分子量:
292.33
MDL number:
MFCD08460906
UNSPSC Code:
12352200
NACRES:
NA.77

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SMILES string

N2(CC[C@]3(C2=Nc4c(cc(cc4)C)C3=O)O)c1ccccc1

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

InChI key

LZAXPYOBKSJSEX-SFHVURJKSA-N

assay

≥98% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, protect from light

color

yellow

solubility

methanol: 1.5 mg/mL, 100% DMSO: 100 mg/mL, 90% DMSO: 75 mg/mL

shipped in

wet ice

storage temp.

−20°C

Quality Level

100

相关类别

General description

The inactive enantiomer of (±)-Blebbistatin (Cat. No. 203390). Useful as a negative control for the active enantiomer (Cat. No. 203391).

Biochem/physiol Actions

Cell permeable: no
Primary Target
Inactive enantiomer of (±)-Blebbistatin
Product does not compete with ATP.
Reversible: no

Packaging

Packaged under inert gas

Preparation Note

Following reconstitution in methanol, aliquot and freeze (-20°C). Stock solutions in 90% DMSO or methanol are stable for up to 1 month at -20°C. Stock solutions in 100% DMSO are unstable; reconstitute just prior to use.

Other Notes

Shu, S., et al. 2005. Proc. Natl. Acad. Sci. USA102, 1472.
Jacobelli, J., et al. 2004. Nat. Immunol.5, 531.
Kovacs, M., et al. 2004. J. Biol. Chem.279, 35557.
Straight, A.F., et al. 2003. Science299, 1743.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Harmful & Carcinogenic / Teratogenic (E)

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

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Ying Liu et al.
Kidney diseases (Basel, Switzerland), 6(6), 422-433 (2020-12-15)
Levels of urinary microvesicles, which are increased during various kidney injuries, have diagnostic potential for renal diseases. However, the significance of urinary microvesicles as a renal disease indicator is dampened by the difficulty to ascertain their cell source. The aim

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