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Volumn 16, Issue 9, 2006, Pages 2475-2478

Substrate specificity of strictosidine synthase

Author keywords

Alkaloids; Biosynthesis; Enzyme catalysis; Glycosidase; Pictet Spengler

Indexed keywords

4 FLUOROTRYPTAMINE; 5 FLUOROTRYPTAMINE; 6 FLUOROTRYPTAMINE; 7 FLUOROTRYPTAMINE; ALDEHYDE DERIVATIVE; AMINE; BENZOFURAN DERIVATIVE; INDOLE ALKALOID; SECOLOGANIN; STRICTOSIDINE; STRICTOSIDINE SYNTHASE; SYNTHETASE; TERPENE DERIVATIVE; TRYPTAMINE; UNCLASSIFIED DRUG;

EID: 33644990230     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2006.01.098     Document Type: Article
Times cited : (79)

References (30)
  • 17
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    • note
    • + expect. 557.2, obsd 557.2). Synthesis of authentic standards (diastereomeric mixtures) and evaluation of chemical reaction rates was performed by reacting amine and aldehyde substrates (20 mM concentration) under aqueous conditions (150 mM maleic acid, pH 2).
  • 20
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    • Benzofuran (4) and benzothiophene (5) derivatives were generated from reduction of the commercially available nitrile compounds. (Shafiee, A.; Mohamadpour, M. J. Heterocycl. Chem. 1978, 15, 481.)
    • (1978) J. Heterocycl. Chem. , vol.15 , pp. 481
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  • 21
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    • The pyrrole ethanamine compound (16) was synthesized as described. (Wasley, J. W. F.; Hamdan, A. Synth. Commun. 1985, 15, 71.) All other tryptamine analogs were commercially available.
    • (1985) Synth. Commun. , vol.15 , pp. 71
    • Wasley, J.W.F.1    Hamdan, A.2
  • 25
    • 84982076728 scopus 로고
    • 3OH, 7:3) to yield purified secologanin (1 g). NMR and mass spectral data matched previously reported values
    • (1976) Chem. Ber. , vol.109 , pp. 3640
    • Kinast, G.1    Tietze, L.F.2
  • 30
    • 33644988101 scopus 로고    scopus 로고
    • note
    • + expect. 365.4, obsd 365.5).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.