Five new nortriterpenoid glycosides from the bulbs of Scilla scilloides

Chemical and Pharmaceutical Bulletin

Volumn 61, Issue 5, 2013, Pages 592-598

  Ono, Masateru ^a   Ochiai, Tetsuya ^a   Yasuda, Shin ^a   Nishida, Yoichiro ^b   Tanaka, Toshiharu ^a   Okawa, Masafumi ^c   Kinjo, Junei ^c   Yoshimitsu, Hitoshi ^d   Nohara, Toshihiro ^d  

^a TOKAI UNIVERSITY   (Japan)

^b Aso Pharmaceutical Co Ltd   (Japan)

^c FUKUOKA UNIVERSITY   (Japan)

^d SOJO UNIVERSITY   (Japan)

Author keywords

Glycoside; Liliaceae; Norlanostane; Scilla scilloides; Triterpenoid

Indexed keywords

15 DEOXYEUCOSTEROL 3 O BETA DEXTRO APIOFURANOSYL (1-2) O BETA DEXTRO GLUCOPYRANOSYL (1-2) O ALPHA LEVO ARABINOPYRANOSYL (1-6) BETA DEXTRO GLUCOPYRANOSIDE; 15 DEOXYEUCOSTEROL 3 O BETA DEXTRO GLUCOPYRANOSYL (1-2) O ALPHA LEVO ARABINOPYRANOSYL (1-6) BETA DEXTRO GLUCOPYRANOSIDE; 17ALPHA,23 EPOXY 3BETA,16BETA,29 TRIHYDROXY 27 NOR LANOST 8 ENE 24 ONE 3 O BETA DEXTRO APIOFURANOSYL (1-2) O BETA DEXTRO GLUCOPYRANOSYL (1-2) O ALPHA LEVO ARABINOPYRANOSYL (1-6) BETA DEXTRO GLUCOPYRANOSIDE; 17ALPHA,23 EPOXY 3BETA,29 DIHYDROXY 27 NOR LANOST 8 ENE 15,24 DIONE 3 O ALPHA LEVO RHAMNOPYRANOSYL (1-2) O BETA DEXTRO GLUCOPYRANOSYL (1-2) O ALPHA LEVO ARABINOPYRANOSYL (1-6) BETA DEXTRO GLUCOPYRANOSIDE; ACETOXY 15 DEOXYEUCOSTEROL 3 O BETA DEXTRO GLUCOPYRANOSYL (1-2) O ALPHA LEVO ARABINOPYRANOSYL (1-6) BETA DEXTRO GLUCOPYRANOSIDE; GLYCOSIDE; TRITERPENOID; UNCLASSIFIED DRUG;

ARTICLE; DRUG ISOLATION; DRUG STRUCTURE; MEDICINAL PLANT; PLANT BULB; SCILLA SCILLOIDES; SPECTROSCOPY;

GLYCOSIDES; MOLECULAR STRUCTURE; PLANT ROOTS; SCILLA; STEREOISOMERISM; TRITERPENES;

EID: 84878772083     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.c13-00116     Document Type: Article

References (16)

1. "Chuyaku Daijiten," ed. by Koso Shin Igakuin, Shanghai Kagaku Gijutsu Shuppansha, 1978, p. 2270.
2. Kouno I., Komori T., Kawasaki T., Tetrahedron Lett., 14, 4569-4572 (1973).
3. Kouno I., Noda N., Ida I., Sholichin M., Miyahara K., Komori T., Kawasaki T., Liebigs Ann. Chem., 1982, 306-314 (1982).
4. Sholichin M., Miyahara K., Kawasaki T., Heterocycles, 17, 251-257 (1982).
5. Sholichin M., Miyahara K., Kawasaki T., Chem. Pharm. Bull., 33, 1756-1759 (1985).
6. Lee S.-M., Chun H.-K., Lee C.-H., Min B.-S., Lee E.-S., Kho Y.-H., Chem. Pharm. Bull., 50, 1245-1249 (2002).
7. Nishida Y., Eto M., Miyashita H., Ikeda T., Yamaguchi K., Yoshimitsu H., Nohara T., Ono M., Chem. Pharm. Bull., 56, 1022-1025 (2008).
8. Ono M., Toyohisa D., Morishita T., Horita H., Yasuda S., Nishida Y., Tanaka T., Okawa M., Kinjo J., Yoshimitsu H., Nohara T., Chem. Pharm. Bull., 59, 1348-1354 (2011).
9. Ono M., Takatsu Y., Ochiai T., Yasuda S., Nishida Y., Tanaka T., Okawa M., Kinjo J., Yoshimitsu H., Nohara T., Chem. Pharm. Bull., 60, 1314-1319 (2012).
10. Ono M., Sugita F., Shigematsu S., Takamura C., Yoshimitsu H., Miyashita H., Ikeda T., Nohara T., Chem. Pharm. Bull., 55, 1093-1096 (2007).
11. Kuroda M., Mimaki Y., Ori K., Sakagami H., Sashida Y., J. Nat. Prod., 67, 2099-2103 (2004).
12. Seo S., Tomita Y., Tori K., Yoshimura Y., J. Am. Chem. Soc., 100, 3331-3339 (1978).
13. Kasai R., Suzuo M., Asakawa J., Tanaka O., Tetrahedron Lett., 18, 175-178 (1977).
14. Tori K., Seo S., Yoshimura Y., Arita H., Tomita Y., Tetrahedron Lett., 18, 179-182 (1977).
15. Amschler G., Frahm A. W., Müller-Doblies D., Müller-Doblies U., Phytochemistry, 47, 429-436 (1998).
16. Takigawa A., Muto H., Kabata K., Okawa M., Kinjo J., Yoshimitsu H., Nohara T., Ono M., J. Nat. Prod., 74, 2414-2419 (2011).