487929-M

Nocodazole

≥97% (HPLC), Mitosis inhibitor, liquid

• Synonim(y): InSolution Nocodazole, Methyl-(5-(2-thienylcarbonyl)-1H-benzimidazol-2-yl)-carbamate, Methyl-5-(thiophene-2-carbonyl)-1H-benzo[d]imidazol-2-ylcarbamate, R17934, R17934, Methyl-(5-(2-thienylcarbonyl)-1H-benzimidazol-2-yl)-carbamate, Methyl-5-(thiophene-2-carbonyl)-1H-benzo[d]imidazol-2-ylcarbamate
• Wzór empiryczny (zapis Hilla): C₁₄H₁₁N₃O₃S
• Numer CAS: 31430-18-9
• Masa cząsteczkowa: 301.32
• UNSPSC Code: 12352200
• MDL number: MFCD00005588
• NACRES: NA.77
• Assay: ≥97% (HPLC)
• Form: liquid
• Quality level: 100
• Storage condition: OK to freeze, avoid repeated freeze/thaw cycles, desiccated (hygroscopic), protect from light

Właściwości

• Nazwa produktu: Nocodazole, InSolution, ≥97%, 50 mM in DMSO, Inhibitor of mammalian cell mitosis via a highly aspecific antimicrotubular activity
• Quality Level: 100
• assay: ≥97% (HPLC)
• form: liquid
• manufacturer/tradename: Calbiochem^®
• storage condition: OK to freeze, avoid repeated freeze/thaw cycles, desiccated (hygroscopic), protect from light
• storage temp.: −70°C
• SMILES string: [s]1c(ccc1)C(=O)c2cc3nc([nH]c3cc2)NC(=O)OC
• InChI: 1S/C14H11N3O3S/c1-20-14(19)17-13-15-9-5-4-8(7-10(9)16-13)12(18)11-3-2-6-21-11/h2-7H,1H3,(H2,15,16,17,19)
• InChI key: KYRVNWMVYQXFEU-UHFFFAOYSA-N

Opis

General description

Inhibitor of mitosis. Has highly specific antimicrotubular activity for mammalian cells in culture. Promotes tubulin depolymerization. Also acts as a high-affinity ligand for the cancer-related kinases ABL, c-KIT, BRAF, and MEK (K_d<2 M). The solid form of this compound (Cat. No. 487928) is also available.

Biochem/physiol Actions

Primary Target
Microtubules

Secondary Target
Certain kinases

Physical form

A 50 mM (10 mg/664 µL) solution of Nocodazole (Cat. No. 487928) in DMSO.

Preparation Note

Following initial thaw, aliquot and freeze (-70°C). Aliquots are stable for up to 1 year at -70°C.

Other Notes

Park, H., et al. 2012. Chem. Med. Chem.7, 53.
Bunz, F., et al. 1998. Science282, 1497.
Fleischman, L.F., et al. 1993. Oncogene8, 771.Pomies, P., and Block, M.R. 1992. Biochem. Biophys. Res. Commun.189, 1429.
Rennison, M.E., et al. 1992. J. Cell Sci.102, 239.
Thyberg, J., and Moskalewski, S. 1992. J. Cell Sci.103, 1167.

Legal Information

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

Disclaimer

Toxicity: Irritant (B)

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Informacja o środkach bezpieczeństwa

• pictograms: GHS08
• signalword: Warning
• hcodes: H341
• pcodes: P201 - P202 - P280 - P308 + P313 - P405 - P501
• Hazard Classifications: Muta. 2
• Klasa składowania: 10 - Combustible liquids
• wgk: WGK 2
• flash_point_f: 188.6 °F - closed cup - (refers to pure substance)
• flash_point_c: 87 °C - closed cup - (refers to pure substance)