Home > Compound List > Product Information
Mizoribine_Molecular_structure_CAS_50924-49-7)
Click picture or here to close

Mizoribine

Catalog No. M3047 Name Sigma Aldrich
CAS Number 50924-49-7 Website http://www.sigmaaldrich.com
M. F. C9H13N3O6 Telephone 1-800-521-8956
M. W. 259.21602 Fax
Purity ≥98% (TLC) Email
Storage Chembase ID: 72651

SYNONYMS

IUPAC name
1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-hydroxy-1H-imidazole-4-carboxamide
IUPAC Traditional name
bredinin
Synonyms
N′-(β-D-Ribofuranosyl)-5-hydroxy-imida-zole-4-carboxamide

DATABASE IDS

MDL Number MFCD00057221
CAS Number 50924-49-7
PubChem SID 24278546

PROPERTIES

Purity ≥98% (TLC)
GHS Pictograms GHS07
GHS Pictograms GHS08
GHS Signal Word Danger
GHS Hazard statements H315-H319-H335-H360
European Hazard Symbols Toxic Toxic (T)
Personal Protective Equipment Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
GHS Precautionary statements P201-P261-P305 + P351 + P338-P308 + P313
Risk Statements 46-60-61-36/37/38
RTECS NI3980000
Safety Statements 53-22-26-36/37/39-45
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Mizoribine is an imidazole nucleoside possessing strong immunosuppressive properties. Selectively blocks T-cell proliferation response to mitogenic and allo-antigenic stimulation. Mizoribine blocks the movement of T cells from G to S phase. In addition, it significantly decreases the number of B cells at the S, G, and M phases. Mizoribine inhibits de novo synthesis of nucleotides by inhibition of inosine monophosphate dehydrogenase. The resulting nucleotide depletion inhibits DNA synthesis.

REFERENCES