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Volumn 34, Issue 8, 2004, Pages 1489-1497

Synthesis of a piceatannol analog: Replacement of hydroxy group with amide functionality

Author keywords

Amido group; Piceatannol; Protein tyrosine kinase; Stilbene derivatives

Indexed keywords

AMIDE; PICEATANNOL DERIVATIVE; PROTEIN TYROSINE KINASE; STILBENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 2442689080     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120030700     Document Type: Article
Times cited : (5)

References (12)
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    • Natürliche polyhydroxystilbene. Die synthese von oxyresveratrol, piceatannol und rhapontigenin
    • Reimann, E. Natürliche polyhydroxystilbene. Die synthese von oxyresveratrol, piceatannol und rhapontigenin. Tetrahedron Lett. 1970, 11 (47), 4051-4053.
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    • Reimann, E.1
  • 7
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    • Synthesis and protein-tyrosine kinase inhibitory activity of polyhydroxylated stilbene analogues of piceatannol
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    • Yamada, K.; Ikezaki, M.; Umino, N.; Ohtsuka, H.; Itoh, N.; Ikezawa, K.; Kiyomoto, A.; Iwakuma, T. Studies on 1,2,3,4-tetrahydroisoquinoline derivatives. I. Syntheses and beta-adrenoceptor activities of positional isomers of trimetoquinol with respect to its 6,7-dihydroxyl groups. Chem. Pharm. Bull. (Tokyo) 1981, 29 (3), 744-753.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.