Chlorozotocin

Title: Chlorozotocin
CAS Registry Number: 54749-90-5
CAS Name: 2-[[[(2-Chloroethyl)nitrosoamino]carbonyl]amino]-2-deoxy-D-glucose
Additional Names: 2-[3-(2-chloroethyl)-3-nitrosoureido]-2-deoxy-D-glucopyranose; 1-(2-chloroethyl)-1-nitroso-3-(D-glucos-2-yl)urea; DCNU
Manufacturers' Codes: NSC-178248
Molecular Formula: C9H16ClN3O7
Molecular Weight: 313.69
Percent Composition: C 34.46%, H 5.14%, Cl 11.30%, N 13.40%, O 35.70%
Literature References: Chloroethylnitrosourea derivative with antitumor activity. Similar to carmustine, lomustine, nimustine, ranimustine, q.q.v; 2-chloroethyl analog of streptozotocin, q.v. Synthesis: H. D. Burns et al., Org. Prep. Proced. Int. 6, 259 (1974); T. P. Johnston et al., J. Med. Chem. 18, 104 (1975). Pharmacology: T. Anderson et al., Cancer Res. 35, 761 (1975); P. S. Schein et al., Cancer Treat. Rep. 60, 801 (1976). Decomposition in aqueous media: J. A. Montgomery et al., J. Med. Chem. 18, 568 (1975).
Properties: Ivory colored crystals, mp 147-148° (dec with the evolution of gas), (Burns, Heindel). Also reported as mp 140-141° (dec), (Johnston). Sol in water.
Melting point: mp 147-148° (dec with the evolution of gas); mp 140-141° (dec)
CAUTION: This substance is reasonably anticipated to be a human carcinogen: Report on Carcinogens, Eleventh Edition (PB2005-104914, 2004) p III-62.
Therap-Cat: Antineoplastic.
Keywords: Antineoplastic; Alkylating Agents; Nitrosoureas.
Chlorphenesin Chlorphenesin Carbamate Chlorpheniramine Chlorphenoxamide Chlorphenoxamine

Chlorozotocin
Chlorozotocin.png
Systematic (IUPAC) name
1-(2-Chloroethyl)-1-nitroso-3-[(2R,3R,4S,5R)-3,4,5,6-tetrahydroxy-1-oxohexan-2-yl]urea
Clinical data
Legal status  ?
Identifiers
CAS number 54749-90-5 YesY
ATC code None
PubChem CID 451706
ChemSpider 397854 N
UNII 3053LTY75Z N
KEGG C19170 N
ChEMBL CHEMBL499699 N
Chemical data
Formula C9H16ClN3O7 
Mol. mass 313.69 g/mol
 N (what is this?)  (verify)

Chlorozotocin is a nitrosourea. It is used for cancer therapy.[citation needed]

It is an analogue of streptozotocin.[1]