Chemical structures of constituents from the flowers of Osmanthus fragrans var. aurantiacus

被引：32

作者：

Liu, Jiang ^{[1
]}

Nakamura, Seikou ^{[2
]}

Xu, Bin ^{[2
]}

Matsumoto, Takahiro ^{[2
]}

Ohta, Tomoe ^{[2
]}

Fujimoto, Katsuyoshi ^{[2
]}

Ogawa, Keiko ^{[2
]}

Fukaya, Masashi ^{[2
]}

Miyake, Shiori ^{[2
]}

Yoshikawa, Masayuki ^{[2
]}

Matsuda, Hisashi ^{[2
]}

机构：

[1] Sichuan Agr Univ, Minist Agr, Key Lab Crop Ecophysiol & Farming Syst Southwest, Chengdu 611130, Peoples R China

[2] Kyoto Pharmaceut Univ, Dept Pharmacognosy, Yamashina Ku, Kyoto 6078412, Japan

来源：

JOURNAL OF NATURAL MEDICINES | 2015年 / 69卷 / 01期

关键词：

Osmanthus fragrans var. aurantiacus; Floraosmanoside; Floraosmanolactone; Megastigmane; gamma-Decalactone; Medicinal flower; NITRIC-OXIDE PRODUCTION; ACYLATED SUCROSES; PRUNUS-MUME; FRAXINUS-EXCELSIOR; PHENOLIC-COMPOUNDS; CAMELLIA-JAPONICA; ALDOSE REDUCTASE; CANANGA-ODORATA; BUDS; MELANOGENESIS;

D O I：

10.1007/s11418-014-0869-1

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

Three new megastigmane glycosides named floraosmanosides I-III and a new gamma-decalactone named floraosmanolactone I together with 16 known constituents were isolated from the flowers of Osmanthus fragrans var. aurantiacus cultivated in Guangxi Zhuang Autonomous Region, China. The chemical structures of the new compounds were elucidated on the basis of chemical and physicochemical evidence. Among them, ligustroside and (+)-pinoresinol significantly inhibited nitric oxide production in lipopolysaccharide-activated RAW264.7 macrophages.

引用

页码：135 / 141

页数：7

共 35 条

[1] Bai NS, 2013, ACS SYM SER, V1127, P115
[2] Iridoids from Fraxinus excelsior with Adipocyte Differentiation-Inhibitory and PPARα Activation Activity
Bai, Naisheng
He, Kan
Ibarra, Alvin
Bily, Antoine
Roller, Marc
Chen, Xiaozhuo
Ruehl, Ralph
[J]. JOURNAL OF NATURAL PRODUCTS, 2010, 73 (01): : 2 - 6
[3] DEYAMA T, 1987, CHEM PHARM BULL, V35, P1785
[4] Bu4N[Fe(CO)3(NO)]-Catalyzed Hydrosilylation of Aldehydes and Ketones
Dieskau, Andre P.
Begouin, Jeanne-Marie
Plietker, Bernd
[J]. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2011, 2011 (27) : 5291 - 5296
[5] ENANTIOSELECTIVE LACTONIZATION OF SODIUM 4-HYDROXYPIMELATE UNDER ABIOLOGICAL CONDITIONS
FUJI, K
NODE, M
TERADA, S
MURATA, M
NAGASAWA, H
TAGA, T
MACHIDA, K
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (22) : 6404 - 6406
[6] Structures of acylated sucroses from the flower buds of Prunus mume
Fujimoto, Katsuyoshi
Nakamura, Seikou
Matsumoto, Takahiro
Ohta, Tomoe
Yoshikawa, Masayuki
Ogawa, Keiko
Kashiwazaki, Eri
Matsuda, Hisashi
[J]. JOURNAL OF NATURAL MEDICINES, 2014, 68 (03) : 481 - 487
[7] GERANYL 6-O-BETA-D-XYLOPYRANOSYL-BETA-D-GLUCOPYRANOSIDE ISOLATED AS AN AROMA PRECURSOR FROM TEA LEAVES FOR OOLONG TEA
GUO, WF
SAKATA, K
WATANABE, N
NAKAJIMA, R
YAGI, A
INA, K
LUO, SJ
[J]. PHYTOCHEMISTRY, 1993, 33 (06) : 1373 - 1375
[8] Sesquiterpenes from an Egyptian Herbal Medicine, Pulicaria undulate, with Inhibitory Effects on Nitric Oxide Production in RAW264.7 Macrophage Cells
Hegazy, Mohamed-Elamir F.
Matsuda, Hisashi
Nakamura, Seikou
Yabe, Mikuko
Matsumoto, Tomoko
Yoshikawa, Masayuki
[J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2012, 60 (03) : 363 - 370
[9] A new lignan from Balanophora abbreviata and inhibition of lipopolysaccharide (LPS)-induced inducible nitric oxide synthase (iNOS) expression
Hosokawa, A
Sumino, M
Nakamura, T
Yano, S
Sekine, T
Ruangrungsi, N
Watanabe, K
Ikegami, F
[J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2004, 52 (10) : 1265 - 1267
[10] STUDIES ON MONOTERPENE GLUCOSIDES AND RELATED NATURAL-PRODUCTS .29. 2 NEW IRIDOID GLUCOSIDES FROM OSMANTHUS-FRAGRANS
INOUYE, H
INOUE, K
NISHIOKA, T
KANIWA, M
[J]. PHYTOCHEMISTRY, 1975, 14 (09) : 2029 - 2032

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