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Volumn 57, Issue 2, 2004, Pages 89-96

SF2809 compounds, novel chymase inhibitors from Dactylosporangium sp. 2. Strucutural elucidation

Author keywords

[No Author keywords available]

Indexed keywords

CARBENE; CARBON; CATHEPSIN; CHYMASE; CHYMASE INHIBITOR; CHYMOTRYPSIN; ENZYME INHIBITOR; INDOLE; N METHYL 4 HYDROXY 2 QUINOLINONE; PHENYL GROUP; SF 2809 I; SF 2809 II; SF 2809 III; SF 2809 IV; SF 2809 V; SF 2809 VI; UNCLASSIFIED DRUG;

EID: 1642523734     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.7164/antibiotics.57.89     Document Type: Article
Times cited : (14)

References (11)
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    • Tani, M.; Y. Gyobu, T. Sasaki, O. Takenouchi, T. Kawamura, T. Kamimura & T. Harada: SF2809 compounds, novel chymase inhibitors produced by an actinomycete. 1. Taxonomy, fermentation, isolation and biological properties. J. Antibiotics 57: 83-88, 2004
    • (2004) J. Antibiotics , vol.57 , pp. 83-88
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  • 2
    • 2442704009 scopus 로고    scopus 로고
    • Synthesis of SF2809-V, chymase inhibitor, and its analogues by three component condensation: Model study for high throughput synthesis of a chymase inhibitor library
    • in press
    • Yamamoto, Y. & K. Harimaya: Synthesis of SF2809-V, chymase inhibitor, and its analogues by three component condensation: Model study for high throughput synthesis of a chymase inhibitor library. Chem. Lett. in press
    • Chem. Lett.
    • Yamamoto, Y.1    Harimaya, K.2
  • 3
    • 9244225633 scopus 로고
    • Quinoline, quinazoline, and acridone alkaloids
    • Grundon, M. F.: Quinoline, quinazoline, and acridone alkaloids. Natl. Prod. Rep. 7: 131-138, 1990
    • (1990) Natl. Prod. Rep. , vol.7 , pp. 131-138
    • Grundon, M.F.1
  • 4
    • 0025317821 scopus 로고
    • A new alkaloid, montanine, from Ruta Montana
    • Ulubelen, A.: A new alkaloid, montanine, from Ruta Montana. J. Nat. Prod. 53: 207-209, 1990
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  • 6
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    • 0038663069 scopus 로고    scopus 로고
    • Nonpeptidic chymase inhibitors: Design and structure-activity relationships of pyrimidinone derivatives based on the predicted binding mode of a peptidic inhibitor
    • Akahoshi, F.: Nonpeptidic Dhymase inhibitors: design and structure-activity relationships of pyrimidinone derivatives based on the predicted binding mode of a peptidic inhibitor. Curr. Pharm. Des. 9: 1191-1199, 2003
    • (2003) Curr. Pharm. Des. , vol.9 , pp. 1191-1199
    • Akahoshi, F.1
  • 9
    • 0035085173 scopus 로고    scopus 로고
    • Non-peptidic inhibitors of human chymase. Synthesis, structure-activity relationships, and pharmacokinetic profiles of a series of 5-amino-6-oxo-1,6-dihydropyrimidine-containing trifluoromethyl ketones
    • Akahoshi, F.; A. AShimori, T. Yoshimura, T. Imada, M. Nakajima, N. Mitsutomi, S. Kuwahara, T. Ohtsuka, C. Fukaya, M. Miyazaki & N. Nakamura: Non-peptidic inhibitors of human chymase. Synthesis, structure-activity relationships, and pharmacokinetic profiles of a series of 5-amino-6-oxo-1,6-dihydropyrimidine-containing trifluoromethyl ketones. Bioorg. Med. Chem. 9: 301-315, 2001
    • (2001) Bioorg. Med. Chem. , vol.9 , pp. 301-315
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  • 10
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    • Thiobenzimidazole derivatives
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.