SCOPUS 정보 검색 플랫폼

Volumn 45, Issue 16, 2002, Pages 3482-3490

Synthesis of potent leukotriene A4 hydrolase inhibitors. Identification of 3-[methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic acid

(19) Penning, Thomas D a Russell, Mark A a Chen, Barbara B a Chen, Helen Y a Liang, Chi Dean a Mahoney, Matthew W a Malecha, James W a Miyashiro, Julie M a Yu, Stella S a Askonas, Leslie J a Gierse, James K a Harding, Elizabeth I a Highkin, Maureen K a Kachur, James F a Kim, Suzanne H a Villani Price, Doreen a Pyla, E Yvonne a Ghoreishi Haack, Nayereh S a Smith, Walter G a

a PFIZER INC (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 [METHYL [3 [4 (PHENYLMETHYL)PHENOXY]PROPYL]AMINO]PROPANOIC ACID; [2 (4 PHENYLPHENOXY)ETHYL]PYRROLIDINE; LEUKOTRIENE A4 HYDROLASE; LEUKOTRIENE A4 HYDROLASE INHIBITOR; LEUKOTRIENE B4; PYRROLIDINE DERIVATIVE; SC 22716; SC 57461A; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIINFLAMMATORY ACTIVITY; ARTICLE; ASTHMA; CONTROLLED STUDY; CYTOKINE PRODUCTION; DRUG IDENTIFICATION; DRUG MECHANISM; DRUG POTENCY; DRUG SYNTHESIS; ENTERITIS; ENZYME ACTIVITY; IMMUNOMODULATION; MOUSE; NONHUMAN; PATHOGENESIS; PSORIASIS; RHEUMATOID ARTHRITIS; STRUCTURE ACTIVITY RELATION;

ADMINISTRATION, ORAL; ANIMALS; BETA-ALANINE; ENZYME INHIBITORS; EPOXIDE HYDROLASES; HUMANS; LEUKOTRIENE A4; MICE; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0036682429 PISSN: 00222623 EISSN: None Source Type: Journal
DOI: 10.1021/jm0200916 Document Type: Article

Times cited : (34)

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