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Current Pharmaceutical Design

Volumn 8, Issue 15, 2002, Pages 1335-1347

Tumour cytochrome P450 and drug activation

(2) Patterson, L H a Murray, G I a

a UNIVERSITY OF LONDON (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

1,4 BIS[[2 (DIMETHYLAMINO N OXIDE)ETHYL]AMINO] 5,8 DIHYDROXYANTHRAQUINONE; 4 HYDROXYTAMOXIFEN; ACROLEIN; ALKYLATING AGENT; ANTIESTROGEN; BENZOTHIAZOLE DERIVATIVE; CHLORMETHINE; CYCLOPHOSPHAMIDE; CYTOCHROME P450; CYTOCHROME P450 1A1; CYTOCHROME P450 1B1; CYTOCHROME P450 2B6; CYTOCHROME P450 2C9; CYTOCHROME P450 2D6; CYTOCHROME P450 3A; CYTOCHROME P450 3A4; DACARBAZINE; DRUG METABOLIZING ENZYME; FLUOROURACIL; FLUTAMIDE; IFOSFAMIDE; MESSENGER RNA; NEMORUBICIN; OXAZAPHOSPHORINE DERIVATIVE; PROCARBAZINE; PRODRUG; TAMOXIFEN; TEGAFUR; TROLEANDOMYCIN; ANTINEOPLASTIC AGENT; ISOENZYME;

ANTINEOPLASTIC ACTIVITY; ARTICLE; BLADDER CANCER; BREAST CANCER; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DIGESTIVE SYSTEM CANCER; DRUG ACTIVATION; DRUG HALF LIFE; DRUG HYDROXYLATION; DRUG MECHANISM; DRUG STRUCTURE; DRUG SYNTHESIS; HUMAN; IMMUNOREACTIVITY; LIVER CANCER; LUNG CANCER; PHASE 1 CLINICAL TRIAL; PRIORITY JOURNAL; PROSTATE CANCER; PROTEIN EXPRESSION; RETROSPECTIVE STUDY; STRUCTURE ACTIVITY RELATION; BIOSYNTHESIS; CHEMISTRY; DRUG DESIGN; ENZYME SPECIFICITY; METABOLISM; NEOPLASM; OXIDATION REDUCTION REACTION; REVIEW;

ANTINEOPLASTIC AGENTS; CYTOCHROME P-450 ENZYME SYSTEM; DRUG DESIGN; HUMAN; ISOENZYMES; NEOPLASMS; OXIDATION-REDUCTION; PRODRUGS; SUBSTRATE SPECIFICITY; HUMANS;

EID: 0036015562 PISSN: 13816128 EISSN: None Source Type: Journal
DOI: 10.2174/1381612023394502 Document Type: Article

Times cited : (145)

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