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Volumn 10, Issue 4, 2000, Pages 315-317

4-Aza-2,3-dehydro-4-deoxypodophyllotoxins: Simple Aza-podophyllotoxin analogues possessing potent cytotoxicity

Author keywords

[No Author keywords available]

Indexed keywords

4 AZA 2,3 DEHYDRO 4 DEOXYPODOPHYLLOTOXIN; DEOXYPODOPHYLLOTOXIN; DRUG ANALOG; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034696048     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(99)00693-9     Document Type: Article
Times cited : (80)

References (15)
  • 8
    • 0030683597 scopus 로고    scopus 로고
    • New compounds 2b, 2g and 2h were prepared according to the method described therein. 2b: Y. 68%, mp 284-286 °C; 2g: Y. 96%, mp 280-282 °C; 2h: Y. 95%, mp >300 °C
    • Hitotsuyanagi, Y.; Kobayashi, M.; Fukuyo, M.; Takeya, K.; Itokawa, H. Tetrahedron Lett. 1997, 38, 8295. New compounds 2b, 2g and 2h were prepared according to the method described therein. 2b: Y. 68%, mp 284-286 °C; 2g: Y. 96%, mp 280-282 °C; 2h: Y. 95%, mp >300 °C.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 8295
    • Hitotsuyanagi, Y.1    Kobayashi, M.2    Fukuyo, M.3    Takeya, K.4    Itokawa, H.5
  • 13
    • 0017656951 scopus 로고
    • A similar tendency in activity was also observed for related compounds. Deoxypodophyllotoxin cyclic ether, where the lactone carbonyl group of 4-deoxypodophyllotoxin was substituted by a methylene unit, was 8-11 times more cytotoxic than the 4-deoxypodophyllotoxin analogue having a cyclopentane ring D structure
    • A similar tendency in activity was also observed for related compounds. Deoxypodophyllotoxin cyclic ether, where the lactone carbonyl group of 4-deoxypodophyllotoxin was substituted by a methylene unit, was 8-11 times more cytotoxic than the 4-deoxypodophyllotoxin analogue having a cyclopentane ring D structure. Gensler, W. J.; Murthy, C. D.; Trammel, M. H. J. Med. Chem. 1977, 20, 635; Loike, J. D.; Brewer, C. F.; Sternlicht, H.; Gensler, W. J.; Horwitz, S. B. Cancer Res. 1978, 38, 2688.
    • (1977) J. Med. Chem. , vol.20 , pp. 635
    • Gensler, W.J.1    Murthy, C.D.2    Trammel, M.H.3
  • 14
    • 0018083128 scopus 로고
    • A similar tendency in activity was also observed for related compounds. Deoxypodophyllotoxin cyclic ether, where the lactone carbonyl group of 4-deoxypodophyllotoxin was substituted by a methylene unit, was 8-11 times more cytotoxic than the 4-deoxypodophyllotoxin analogue having a cyclopentane ring D structure. Gensler, W. J.; Murthy, C. D.; Trammel, M. H. J. Med. Chem. 1977, 20, 635; Loike, J. D.; Brewer, C. F.; Sternlicht, H.; Gensler, W. J.; Horwitz, S. B. Cancer Res. 1978, 38, 2688.
    • (1978) Cancer Res. , vol.38 , pp. 2688
    • Loike, J.D.1    Brewer, C.F.2    Sternlicht, H.3    Gensler, W.J.4    Horwitz, S.B.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.