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Volumn 44, Issue 9, 1996, Pages 1669-1675

Chilianthins A-F, six triterpene esters having dimeric structures from Rhoiptelea chiliantha diels et HAND.-MAZZ.

Author keywords

acid ester; chilianthin; Rhoiptelea chiliantha; Rhoipteleaceae; triterpene caffeate; triterpene lignan ester; triterpene naphthalene carboxylic

Indexed keywords

CAFFEIC ACID DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; CHILIANTHIN A; CHILIANTHIN B; CHILIANTHIN C; CHILIANTHIN D; CHILIANTHIN E; CHILIANTHIN F; DIMER; LIGNAN DERIVATIVE; MYRICERIC ACID B; TRITERPENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0029830259     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.44.1669     Document Type: Article
Times cited : (24)

References (20)
  • 1
    • 10244231061 scopus 로고
    • Zhang Z., Zhiwu Fenlei Xuebao, 19, 168-177 (1981); Liu C., Yunnan Zhiwu Yanjiu, 9, 181-186 (1987); Lu A., Li J., Xu K., Zhiwu Fenlei Xuebao, 29, 481-193 (1991).
    • (1981) Zhiwu Fenlei Xuebao , vol.19 , pp. 168-177
    • Zhang, Z.1
  • 2
    • 84962721273 scopus 로고
    • Zhang Z., Zhiwu Fenlei Xuebao, 19, 168-177 (1981); Liu C., Yunnan Zhiwu Yanjiu, 9, 181-186 (1987); Lu A., Li J., Xu K., Zhiwu Fenlei Xuebao, 29, 481-193 (1991).
    • (1987) Yunnan Zhiwu Yanjiu , vol.9 , pp. 181-186
    • Liu, C.1
  • 3
    • 10244254039 scopus 로고
    • Zhang Z., Zhiwu Fenlei Xuebao, 19, 168-177 (1981); Liu C., Yunnan Zhiwu Yanjiu, 9, 181-186 (1987); Lu A., Li J., Xu K., Zhiwu Fenlei Xuebao, 29, 481-193 (1991).
    • (1991) Zhiwu Fenlei Xuebao , vol.29 , pp. 481-1193
    • Lu, A.1    Li, J.2    Xu, K.3
  • 7
    • 10244235435 scopus 로고
    • A preliminary communication on the structure elucidation of 1, 2 and 3: Jiang Z., Tanaka T., Kouno I., Tetrahedron Lett., 35, 2131-2134 (1994). Compounds 2 and 3 were originally named rhoipteleic acids A and B, respectively, in the communication; however, they are renamed chilianthins A and B, respectively, in order to avoid confusion with rhoiptelic acid, which is a rearranged ursane triterpene acid isolated from the same plant source as described in reference 2.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 2131-2134
    • Jiang, Z.1    Tanaka, T.2    Kouno, I.3
  • 8
    • 0001427147 scopus 로고
    • Maillard M., Adewunmi C. O., Hostettmann K., Phytochemistry, 31, 1321-1323 (1992); Kashiwada K., Zhang D. C., Chen Y. P., Cheng C. M., Chen H. T., Chang H. C., Chang J. J., Lee K. H., J. Nat. Prod., 56, 2077-2082 (1993).
    • (1992) Phytochemistry , vol.31 , pp. 1321-1323
    • Maillard, M.1    Adewunmi, C.O.2    Hostettmann, K.3
  • 11
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    • Koekemoer J. M., Vermeulen N. M. J., Anderson L. A. P., J. S. Afr. Chem. Inst., 27, 131-136 (1974) [Chem. Abstr., 82, 140328f (1974)].
    • (1974) Chem. Abstr. , vol.82
  • 15
    • 0008978868 scopus 로고
    • Anderson G. W., Callahan, F. M., J. Am. Chem. Soc., 82, 3359-3363 (1960). The ester linkages of 2a and 3a could not be cleaved by alkaline treatment.
    • (1960) J. Am. Chem. Soc. , vol.82 , pp. 3359-3363
    • Anderson, G.W.1    Callahan, F.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.