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Volumn 57, Issue 2, 2001, Pages 283-296

Synthesis and biological evaluation of deoxypreussomerin A and palmarumycin CP1 and related naphthoquinone spiroketals

(4) Wipf, Peter a Jung, Jae Kyu a Rodríguez, Sonia a Lazo, John S a

a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE (United States)

Author keywords

Breast cancer cell line; Cytotoxicity; Deoxypreussomerin; Iodobenzenediacetate; Naphthoquinone; Palmarumycin; Phenol oxidation; Polymer bound reagent; Spirocyclization; Total synthesis

Indexed keywords

1,4 NAPHTHOQUINONE DERIVATIVE; 5 HYDROXY 8 METHOXY 1 TETRALONE; ANTINEOPLASTIC AGENT; BIS HYDROXYNAPHTHYL ETHER; DEOXYPREUSSOMERIN A; DEOXYPREUSSOMERIN B; ETHER DERIVATIVE; KETONE DERIVATIVE; PALMARUMYCIN C1; PALMARUMYCIN C3; PALMARUMYCIN C4; PALMARUMYCIN C5; PALMARUMYCIN C6; PALMARUMYCIN C7; PALMARUMYCIN C8; PALMARUMYCIN CP1; PALMARUMYCIN CP2; PALMARUMYCIN CP3; PALMARUMYCIN CP4; PALMARUMYCIN CP5; PREUSSOMERIN A; PREUSSOMERIN B; PREUSSOMERIN C; PREUSSOMERIN D; PREUSSOMERIN E; PREUSSOMERIN F; PREUSSOMERIN G; PREUSSOMERIN I; SPIRO COMPOUND; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ARTICLE; BREAST CARCINOMA; CANCER CELL CULTURE; CELL STRAIN MCF 7; CHEMICAL REACTION; CONCENTRATION RESPONSE; CONTROLLED STUDY; CYCLIZATION; DRUG STRUCTURE; HUMAN; HUMAN CELL; IC 50; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY;

MINK CELL FOCUS-FORMING VIRUS;

EID: 0035819338 PISSN: 00404020 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4020(00)00936-4 Document Type: Article

Times cited : (53)

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