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Volumn 44, Issue 2, 2001, Pages 208-214

Nucleosides and nucleotides. 200. Reinvestigation of 5′-N-ethylcarboxamidoadenosine derivatives: Structure-activity relationships for P3 purinoceptor-like proteins

Author keywords

[No Author keywords available]

Indexed keywords

1 (ADENIN 9 YL) 1 DEOXY N CYCLOHEXYL BETA DEXTRO RIBOFURANURONAMIDE; 1 (ADENIN 9 YL) 1 DEOXY N ETHYL BETA DEXTRO RIBOFURANURONAMIDE; 1 (ADENIN 9 YL) 1 DEOXY N N PENTYL BETA DEXTRO RIBOFURANURONAMIDE; 9 (6,7 DIDEOXY BETA DEXTRO ALLOHEPT 5 YNOFURANOSYL)ADENINE; ADENOSINE 5' (N ETHYLCARBOXAMIDE); ADENOSINE A1 RECEPTOR; ADENOSINE A2A RECEPTOR; ADENOSINE A2B RECEPTOR; ADENOSINE A3 RECEPTOR; ADENOSINE RECEPTOR; ALKYL GROUP; AMIDE; BINDING PROTEIN; HAK 2701; LIGAND; NITROGEN; NUCLEOSIDE; NUCLEOTIDE; P3 PURINORECEPTOR LIKE PROTEIN; PURINE P2 RECEPTOR; RECEPTOR SUBTYPE; UNCLASSIFIED DRUG;

EID: 0035905865     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm000150k     Document Type: Article
Times cited : (8)

References (26)
  • 1
    • 0034612038 scopus 로고    scopus 로고
    • Synthesis of a 1′α-phenylselenouridine derivative as a synthetic precursor for various 1′-modified nucleosides, via enolization at the 1′-position of 3′,5′-O-TIPDS-2′-ketouridine
    • (2000) Tetrahedron Lett. , vol.41 , pp. 3643-3646
    • Kodama, T.1    Shuto, S.2    Nomura, M.3    Matsuda, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.