SCOPUS 정보 검색 플랫폼

Volumn 1, Issue 21, 2003, Pages 3656-3662

Synthesis of potent CXCR4 inhibitors possessing low cytotoxicity and improved biostability based on T140 derivatives

(11) Tamamura, Hirokazu a Hiramatsu, Kenichi a Kusano, Shuichi b Terakubo, Shigemi b Yamamoto, Naoki c Trent, John O d Wang, Zixuan e Peiper, Stephen C e Nakashima, Hideki b Otaka, Akira a Fujii, Nobutaka a

a KYOTO UNIVERSITY (Japan)

b ST MARIANNA UNIVERSITY SCHOOL OF MEDICINE (Japan)

c TOKYO MEDICAL AND DENTAL UNIVERSITY (Japan)

d UNIVERSITY OF LOUISVILLE (United States)

e MEDICAL COLLEGE OF GEORGIA (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLATION; CYTOLOGY; DRUG PRODUCTS; LEAD COMPOUNDS; POLYPEPTIDES; SYNTHESIS (CHEMICAL); TOXICITY;

BIOSTABILITY; CYTOTOXICITY; INHIBITORS; MOUSE SERUM; NAPHTHYLALANINE; RAT LIVER HOMOGENATE;

AMINO ACIDS;

HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS 1;

CHEMOKINE RECEPTOR CXCR4; OLIGOPEPTIDE; T 140;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; CELL LINE; CHEMISTRY; DRUG ANTAGONISM; DRUG EFFECT; HUMAN; METABOLISM; MOLECULAR GENETICS; MOUSE; T LYMPHOCYTE;

AMINO ACID SEQUENCE; ANIMALS; CELL LINE; HUMANS; MICE; MOLECULAR SEQUENCE DATA; OLIGOPEPTIDES; RECEPTORS, CXCR4; T-LYMPHOCYTES;

EID: 0142096799 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/b306473p Document Type: Article

Times cited : (66)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.