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1.
A New Asterosaponin from the Starfish Culcita novaeguineae 总被引:1,自引:0,他引:1
HaiFengTANG YangHuaYI LingLI PengSUN DaZhengZHOU BaoShuLIU 《中国化学快报》2005,16(5):619-622
A new asterosaponin named novaeguinoside A, along with a known saponin, asteronyl pentaglycoside sulfate, was isolated from the starfish Culcita novaeguineae. The new compound was identitied to be sodium 6α-O-{β-D-fucopyranosyl-(1→2)-β-D-fucopyranosyl-(1→4)-[β-D-quinovopyranosyl-(1→2)]-β-D-xylopyranosyl-(1→3)-[β-D-quinovopyranosyl}-5α-pregn-9(11)-en-20-one-3β-yl-sulfate by extensive spectral analysis and chemical evidence. 相似文献
2.
STUDIES OF ELECTRON SPIN RESONANCE ON BILIRUBIN FREE RADICALS 总被引:1,自引:0,他引:1
The nature of ESR signals derived from bilirubin-Ⅸα has been studied by focusing onthe samples treated with free radical generating and inhibiting systems, i.e. X-XOD, Fe/EDTA, SOD, mannitol/ascorbate, CO, KCN, etc. In all the cases, the stable signals comprisethose originated from semiquinone radical (g = 2.0012) and superoxide free radical (g_∥=2.041, g_⊥= 2.0040). The superoxide is shown binding with certain metal ions chelated bybilirubin. The free radical scavengers are able to destroy these radicals. The kinetic curveof the regeneration of bilirubin radicals has been determined and the reaction follows azero order mechanism. It is likely that both the physiological and toxic actions of bilirubinare related to the characters of its free radicals. Bilirubin is discussed as "active oxygensink" in mammalians. 相似文献
3.
Yun Long ZHANG Liang Ren ZHANG* Zhen Jun YANG Ji Mei MIN Li He ZHANG* Yang LU Ning Bo GONG Qi Tai ZHENG National Research Laboratory of Natural Biomimetic Drugs Peking University Beijing Institue of Materia Medica Chinese 《中国化学快报》2001,(5)
Tubercidin (4-amino-7--D-riobofuranosyl-7-H-pyrrolo[2,3-d]pyrimidine) 1, an antibio-tic substance produced in the culture broth of Streptomyces tubericidus1, is an adenosine analog in which N-7 is replaced by a carbon atom. It has attracted much attention due to the biological activities for the growth inhibition of certain tumors, and many derivatives of tubercidin have been synthesized2-5.For the synthesis of tubercidin analogs, 4-chloro-7-H-pyrrolo[2,3-d]pyrimidine-2,3,5-tri-O-acetyl--D-r… 相似文献
4.
GuoQiangLI XiangLI ZhiWeiDENG HuaShiGUAN WenHanLIN 《中国化学快报》2005,16(4):494-496
Two new compounds, namely 7α, 10α-dimethyl-3β-isopropene-1, 2-ene-octahydro-naphthalene (1) and ethyl 5Z,8Z, 11Z, 14Z-nonadecatetraenoate (2) were isolated from the soft coralNephthea hainansis. Compound 1 was a pseutosesquiterpene and 2 was a polyunsaturated fattyacid ethylate. Their structures were established on the basis of spectroscopic methods. 相似文献
5.
SHI Lei FENG Xiu-e LIN Wen-han FANG Lian-hua DU Guan-hua LI Qing-shan . School of Pharmaceutical Science Shanxi Medical University Taiyuan P. R. China . State Key Laboratory of Natural Biomimetic Drugs Peking University Beijing 《高等学校化学研究》2011,(2):237-240
A series of new flavanone derivatives of farrerol was designed and synthesized as a potent inhibitor of vascular smooth muscle cells(VSMCs) vegetation according to a convenient method. The structures of all the synthesized compounds were confirmed by 1H NMR, 13C NMR and EIHR-MS. The biological activities of these compounds against VSMCs in vitro were evaluated. The assay results indicate that two compounds, 5,7-dihydroxy-6,8-dimethyl- 2-(2-nitrophenyl)chroman-4-one(7f) and 2,3-dibromo-4,5-dihydroxydiphenylm... 相似文献
6.
A New Cyclic Bisdesmoside from Tubers of Bolbostemma paniculatum 总被引:2,自引:0,他引:2
HaiFengTANG YangHuaYI ShuYuZHANG PengSUN LingLI DaZhengZHOU 《中国化学快报》2005,16(4):479-482
The structure of tubeimoside V (1), a new cyclic bisdesmoside, isolated from tubers of Bolbostemma paniculatum (Tu Bei Mu), was established by means of 2D NMR spectral and chemical methods. Compound 1 has inter-saccharide chain bridging by a dicrotalic acid to form aunique macrocyclic structure. 相似文献
7.
<正>Eudistalbin A was isolated from marine tunicate eudistoma album and possess cytotoxic activity(ED_(50)3.2μg/mL) in vitro against the growth of KB human buccal carinoma cells.The synthetic eudistalbin A showed potent inhibitory activity against the breast carcinoma cell line MDA-231 with an IC_(50) value of 2.1μmol/L using the metabolic assay MTT.All structures of new compounds were confirmed by ~1H NMR,~(13)C NMR,HRMS and optical rotation. 相似文献
8.
Wen Han LIN* Jun LI Hong Zheng FU Peter PROKSCH National Research Laboratories of Natural Biomimetic Drugs Peking University Beijing Institut fuer Pharmazeutische Biologie Heinrich-Heine Universitat Duesseldorf D- 《中国化学快报》2001,(5)
In the previous report on bioactive secondary metabolites from the sponge-associated fungus Aspergillus versicolor (Vuill) Tirab, the bioassay guiding fractionation led to isolation of six new compounds with unusual skeleton based on chromone ring system from the inculated fungus which was isolated from fresh samples of marine sponge Xestospongia exigua, collected along coast line of Bali, Indonesia in 19971. In the continuation of our chemical investigation on the marine fungus, four compou… 相似文献
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10.
Li Jun HUANG Yan PANG Ji Mei MIN Li He ZHANG* National Research Laboratory of Natural Biomimetic Drugs Peking University Beijing 《中国化学快报》2001,(7)
Cyclic ADP-ribose (cADPR) 1 (Figure 1), a intracellular Ca2+-mobilizing messenger, is of great interest because of its significant importance in the signal transduction1. However, the biological as well as chemical instability of cADPR limits the studies of its physiological role, at least in some aspect2. Recently, Shuto et.al.3 constructed a mimic of cADPR, cyclic IDP-carbocyclic-ribose 2, in which the 4'-oxo in furanose is substituted by a methylene group and the stability of 2 is i… 相似文献