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Volumn 7, Issue 3, 1997, Pages 347-350

Studies on the active conformation of NK1 antagonist CGP 49823. Part 1. Synthesis of conformationally restricted analogs

Author keywords

[No Author keywords available]

Indexed keywords

2 BENZYL 1 (3,5 DIMETHYLBENZOYL) 4 (4 QUINOLINYLMETHYLAMINO)PIPERIDINE; 8 AZABICYCLO[3.2.1]OCTANE DERIVATIVE; BICYCLO[3.2.1]OCTANE DERIVATIVE; NEUROKININ 1 RECEPTOR; NEUROKININ 1 RECEPTOR ANTAGONIST; PIPERIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0031552082     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(96)00623-3     Document Type: Article
Times cited : (9)

References (16)
  • 5
    • 0011478440 scopus 로고    scopus 로고
    • Detailed X-ray crystallographic data for 10 have been deposited at the Cambridge Crystallographic Data Centre
    • (4) Detailed X-ray crystallographic data for 10 have been deposited at the Cambridge Crystallographic Data Centre.
  • 13
    • 0011488353 scopus 로고    scopus 로고
    • 3 was used for reduction of the azide functionality in the preparation of 5
    • 3 was used for reduction of the azide functionality in the preparation of 5.
  • 14
    • 0003020201 scopus 로고
    • 3H-Substance P binding sites
    • Skrabanek, P.; Powell, D., Eds.; Boole Press Ltd.; Dublin, 1983
    • 3H-Substance P binding sites", in Substance P - Dublin 1983, Proc. Int. Symp. (1983), pp. 198-199, Skrabanek, P.; Powell, D., Eds.; Boole Press Ltd.; Dublin, 1983.
    • (1983) Substance P - Dublin 1983, Proc. Int. Symp. , pp. 198-199
    • Bittiger, H.1    Heid, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.