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Revision as of 20:20, 29 July 2010 editPotatoBot (talk | contribs)Bots51,239 editsm Stub sorting and placement of stub template(s): antineoplastic-drug-stub← Previous edit Latest revision as of 23:01, 1 April 2023 edit undoEntranced98 (talk | contribs)Extended confirmed users, Pending changes reviewers, Rollbackers172,956 edits Importing Wikidata short description: "Chemical compound"Tag: Shortdesc helper 
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{{Short description|Chemical compound}}
{{Drugbox {{Drugbox
| Verifiedfields = changed
| IUPAC_name = 3-(2-chloroethyl)-4-oxo-3,4-dihydroimidazotetrazine-8-carboxamide
| Watchedfields = changed
| image = Mitozolomide.svg
| verifiedrevid = 376147382
| CAS_number = 85622-95-3
| IUPAC_name = 3-(2-chloroethyl)-4-oxo-3,4-dihydroimidazotetrazine-8-carboxamide
| ATC_prefix = none
| image = Mitozolomide.svg
| ATC_suffix =
| width = 210
| PubChem = 71766

| DrugBank =
<!--Clinical data-->
| C=7|H=7|Cl=1|N=6|O=2
| tradename =
| molecular_weight = 242.622 g/mol
| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X -->
| smiles = NC(=O)c1ncn2C(=O)N(CCCl)\N=N/c12
| pregnancy_US = <!-- A / B / C / D / X -->
| bioavailability =
| pregnancy_category =
| protein_bound =
| legal_AU = <!-- S2, S3, S4, S5, S6, S7, S8, S9 or Unscheduled-->
| metabolism =
| legal_CA = <!-- Schedule I, II, III, IV, V, VI, VII, VIII -->
| elimination_half-life =
| excretion = | legal_UK = <!-- GSL, P, POM, CD, or Class A, B, C -->
| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> | legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V -->
| legal_status =
| pregnancy_US = <!-- A / B / C / D / X -->
| routes_of_administration =
| pregnancy_category=

| legal_AU = <!-- S2, S3, S4, S5, S6, S7, S8, S9 or Unscheduled-->
<!--Pharmacokinetic data-->
| legal_CA = <!-- Schedule I, II, III, IV, V, VI, VII, VIII -->
| bioavailability =
| legal_UK = <!-- GSL, P, POM, CD, or Class A, B, C -->
| protein_bound =
| legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V -->
| legal_status = | metabolism =
| elimination_half-life =
| routes_of_administration =
| excretion =

<!--Identifiers-->
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 85622-95-3
| ATC_prefix = none
| ATC_suffix =
| PubChem = 71766
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank =
| UNII_Ref = {{fdacite|changed|FDA}}
| UNII = E3U7286V3W
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 435951
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 64805

<!--Chemical data-->
| C=7 | H=7 | Cl=1 | N=6 | O=2
| smiles = NC(=O)c1ncn2C(=O)N(CCCl)\N=N/c12
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C7H7ClN6O2/c8-1-2-14-7(16)13-3-10-4(5(9)15)6(13)11-12-14/h3H,1-2H2,(H2,9,15)
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = QXYYYPFGTSJXNS-UHFFFAOYSA-N
}} }}
'''Mitozolomide''' (]) is an ]. It is an ] derivative. '''Mitozolomide''' (]) is an ]. It is an ] derivative.


Development of mitozolomide was discontinued during ] ]s after it was found to cause severe and unpredictable ].<ref>{{cite journal |author=Fairbairn LJ, Chinnasamy N, Lashford LS, Chinnasamy D, Rafferty JA |title=Enhancing hemopoietic drug resistance: a rationale for reconsidering the clinical use of mitozolomide |journal=Cancer Gene Ther |volume=7 |issue=2 |pages=233–9 |year=2000 |month=February |pmid=10770631 |url=http://www.nature.com/cgt/journal/v7/n2/pdf/7700120a.pdf |doi=10.1038/sj.cgt.7700120}}</ref> ], which has been in clinical use since 1999, is a less toxic ] of mitozolomide.<ref>{{cite journal |author=Newlands ES, Blackledge GR, Slack JA, ''et al.'' |title=Phase I trial of temozolomide (CCRG 81045: M&B 39831: NSC 362856) |journal=Br J Cancer |volume=65 |issue=2 |pages=287–91 |year=1992 |month=February |pmid=1739631 |pmc=1977719}}</ref> Development of mitozolomide was discontinued during ] ]s after it was found to cause severe and unpredictable ].<ref>{{cite journal |vauthors=Fairbairn LJ, Chinnasamy N, Lashford LS, Chinnasamy D, Rafferty JA |title=Enhancing hemopoietic drug resistance: a rationale for reconsidering the clinical use of mitozolomide |journal=Cancer Gene Ther |volume=7 |issue=2 |pages=233–9 |date=February 2000 |pmid=10770631 |url=http://www.nature.com/cgt/journal/v7/n2/pdf/7700120a.pdf |doi=10.1038/sj.cgt.7700120|s2cid=2597751 |doi-access=free }}</ref> ], which has been in clinical use since 1999, is a less toxic ] of mitozolomide.<ref>{{cite journal |vauthors=Newlands ES, Blackledge GR, Slack JA, etal |title=Phase I trial of temozolomide (CCRG 81045: M&B 39831: NSC 362856) |journal=Br J Cancer |volume=65 |issue=2 |pages=287–91 |date=February 1992 |pmid=1739631 |pmc=1977719 |doi=10.1038/bjc.1992.57}}</ref>


==References== ==References==
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{{Chemotherapeutic agents}} {{Chemotherapeutic agents}}


] ]
]

]
]


{{antineoplastic-drug-stub}} {{antineoplastic-drug-stub}}