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Nocodazole

Catalog No. M1404 Name Sigma Aldrich
CAS Number 31430-18-9 Website http://www.sigmaaldrich.com
M. F. C14H11N3O3S Telephone 1-800-521-8956
M. W. 301.32044 Fax
Purity ≥99% (TLC) Email
Storage Chembase ID: 5936

SYNONYMS

IUPAC name
methyl N-[5-(thiophene-2-carbonyl)-1H-1,3-benzodiazol-2-yl]carbamate
IUPAC Traditional name
nocodazol
Synonyms
R 17934
Methyl N-(5-thenoyl-2-benzimidazolyl)carbamate
[5-(2-Thienylcarbonyl)-1H-benzimidazol-2-yl]-carbamic acid methyl ester
Methyl [5-(2-thienylcarbonyl)-1H-benzimidazol-2-yl]carbamate
Oncodazole

DATABASE IDS

CAS Number 31430-18-9
MDL Number MFCD00005588
PubChem SID 24278535
Beilstein Number 1085978
EC Number 250-626-5

PROPERTIES

Purity ≥99% (TLC)
Quality Level PREMIUM
Gene Information human ... TUBB(203068)
Apperance white powder
Melting Point 300 °C (dec.)
Solubility DMSO: soluble10 mg/mL (may require heating)
Solubility H2O: insoluble
GHS Pictograms GHS08
GHS Signal Word Warning
GHS Hazard statements H341-H361d
European Hazard Symbols Harmful Harmful (Xn)
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
GHS Precautionary statements P281
Risk Statements 63-68
RTECS DD6521000
Safety Statements 36/37
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Antimitotic agent that disrupts microtubules by binding to β?tubulin and preventing formation of one of the two interchain disulfide linkages, thus inhibiting microtubule dynamics, disruption of mitotic spindle function, and fragmentation of the Golgi complex. Arrests the cell cycle at G2/M phase. Prevents phosphorylation of the T cell antigen receptor and inhibits its activity. Stimulates the intrinsic GTPase activity of tubulin. Activates the JNK/SAPK signaling pathway and induces apoptosis in several normal and tumor cell lines.

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