SCOPUS 정보 검색 플랫폼

Archiv der Pharmazie

Volumn 341, Issue 9, 2008, Pages 536-547

Thalidomide as a multi-template for development of biologically active compounds

(1) Hashimoto, Yuichi a

a UNIVERSITY OF TOKYO (Japan)

Author keywords

Biological response modifier; Enzyme inhibitor; Metabolites; Nuclear receptor ligand; Thalidomide

Indexed keywords

1 DEOXYNOJIRIMYCIN; 2 (2,6 DIISOPROPYLPHENYL) 5 HYDROXY 1H ISOINDOLE 1,3 DIONE; 3 [3 [[2 CHLORO 3 (TRIFLUOROMETHYL)BENZYL](2 DIPHENYLETHYL)AMINO]PROPOXY]PHENYLACETIC ACID; 5 HYDROXYTHALIDOMIDE; ALPHA GLUCOSIDASE INHIBITOR; AMINOPEPTIDASE INHIBITOR; ANGIOGENESIS INHIBITOR; ANTIANDROGEN; ANTIGESTAGEN; CALPASTATIN; ENZYME INHIBITOR; HISTONE DEACETYLASE INHIBITOR; HORMONE INHIBITOR; HYDROLASE INHIBITOR; LENALIDOMIDE; LIVER X RECEPTOR ANTAGONIST; LIVER X RECEPTOR INHIBITOR; N HYDROXYTHALIDOMIDE; NITRIC OXIDE SYNTHASE INHIBITOR; PROSTAGLANDIN SYNTHASE INHIBITOR; RETINOID DERIVATIVE; RHIZOXIN; RICCARDIN C; THALIDOMIDE; THALIDOMIDE DERIVATIVE; THYMIDINE PHOSPHORYLASE INHIBITOR; TRANSFERASE INHIBITOR; TUMOR NECROSIS FACTOR ALPHA; TUMOR NECROSIS FACTOR ALPHA INHIBITOR; UNCLASSIFIED DRUG;

ACQUIRED IMMUNE DEFICIENCY SYNDROME; BIOLOGICAL ACTIVITY; CELL DIFFERENTIATION; DRUG ACTIVITY; DRUG MECHANISM; DRUG STRUCTURE; ENZYME INHIBITION; HEPATITIS B; HEPATITIS C; HUMAN; MICROTUBULE ASSEMBLY; MULTIPLE MYELOMA; PRIORITY JOURNAL; REVIEW;

ALPHA-GLUCOSIDASES; ANIMALS; DNA-BINDING PROTEINS; DRUG DESIGN; HUMANS; RECEPTORS, CYTOPLASMIC AND NUCLEAR; THALIDOMIDE; TUBULIN;

EID: 53549098210 PISSN: 03656233 EISSN: 15214184 Source Type: Journal
DOI: 10.1002/ardp.200700217 Document Type: Review

Times cited : (79)

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