本栏目报道了中国学者最新从天然产物中分离鉴定,且在中国期刊发表的新化合物,有的结构新颖, 有的具有生物活性,本栏目对于候选药物发现、先导化合物的结构修饰与改造和天然有效活性成分 的构效关系研究具有一定启发与借鉴作用。Sesquiterpenes(倍半萜类)5-hydroxy-6,6,9-trimethyl-4,8a-e-poxy-2,3,4a,5,6,7,8a,9-octa-hy dro-4H-naphtho<2,3-b>furan-8-oneStereumsp·8954ChinChem Lett,2005,16(12):1615-1617LI Guo-Hong,ZHANG Ke-Qin*Yunnan University*C15H20O4=264<α>2D2+112°
Data:IR,MS,NMReupalinolide BEupatoriumlindleyanumChin J Nat Med,2005,3(4):224-227YANG Nian-Yun*,TIAN Li-Juan,QIANShi-HuiJiangsu Provincial Academy of TraditionalChinese Medicine*C24H30O9=462<α>2D0-93°Data:M S,NMR10-hydroxyepiaplysinLaurenciatristichaChinChemLett,2005,16(12):1611-1614SUNJie,HANLi-Jun*,SHI Da-YongInstitute of Oceanology,Chinese Academyof Sciences*C15H19BrO2=312/310<α>2D0-8·1° Data:IR,MS,NMR10-hydroxyaplysinLaurenciatristichaChinChemLett,2005,16(12):1611-1614SUNJie,HANLi-Jun*,SHI Da-YongInstitute of Oceanology,Chinese Academyof Sciences*C15H19BrO2=312/310<α>2D0-50·1°mp 48~50℃Data:IR,MS,NMR1β-angeloyloxy-6β,10α-di hydroxy-8α-methoxyeremophila-7(11)en-8β,12-olideLigulariamyriocephalaChin ChemLett,2005,16(12):1618-1620LIUJun-Xi,WEI Xiao-Ning,SHI Yan-Ping*Lanzhou Institute of Chemical Physics;Chinese Academy of Sciences*C21H30O7=394<α>2D0-11°mp 170~171℃Data:UV,IR,MS,NMR1β-angeloyloxy-6β,1 0β-dihydroxy-8β-methoxyeremophila-7(11)en-8α,12-olideLigulariamyriocephalaChin ChemLett,2005,16(12):1618-1620LIUJun-Xi,WEI Xiao-Ning,SHI Yan-Ping*Lanzhou Institute of Chemical Physics;Chinese Academy of Sciences*C21H30O7=394<α>2D0+186°mp 180~181℃Data:UV,IR,MS,NMRDiterpenes(二萜类)sinomontanine GAconitumsinomontanumChin J Org Chem,2005,25(10):1235-1239PENG Chong-Sheng,CHEN Dong-Lin,WANGFeng-Peng*Sichuan University*C22H34NO7=423<α>1D7-32·0°D ata:IR,MS,NMRingenol-20-myristinateEuphorbiawallichiiChin Tradit Herb Drugs,2005,36(12):1763-1767LI Yu-Lin,SUO You-Rui*Northwest Institute Plateau Biology*C34H54O6=558<α>2D0-14·0°Data:IR,MS,NMRingenol-3-myristinateEuphorbia wallichiiChin Tradit Herb Drugs,2005,36(12):1763-1767LI Yu-Lin,SUO You-Rui*Northwest Institute Plateau Biology*C34H54O6=558<α>2D0+22°Data:IR,MS,NMRsinomontanine FAconitumsinomontanumChin J Org Chem,2005,25(10):1235-1239PENG Chong-Sheng,CHEN Dong-Lin,WANGFeng-Peng*Sichuan University*C30H40N2O9=572<α>1D7+44·4°Data:IR,MS,NMRsinomontanine HAconitumsinomontanumChin J Org Chem,2005,25(10):1235-1239PENG Chong-Sheng,CHEN Dong-Lin,WANGFeng-Peng*Sichuan University*C32H44N2O9=600<α>1D7-28·8°Data:IR,MS,NMRsinomontanine IAconitumsinomontanumChin J Org Chem,2005,25(10):1235-1239PENG Chong-Sheng,CHEN Dong-Lin,WANGFeng-Peng*Sichuan University*C34H45N2O10=640<α>1D7-9·8°Data:IR,MS,NMRTriterpenes(三萜类)12β-acetoxycimigenol-3-O-β-D-xylopy-ranosideCimicifugafoetidaActa Bot Yunnan,2005,27(3):331-336SUN Li-Rong,YAN Jian,QIU Ming-Hua*KunmingInstitute of Botany*C37H58O11=678<α>2D4-141°mp 185~187℃Data:IR,MS,NMRcapilliposide D2Lysimachia capillipesChin ChemLett,2005,16(12):1607-1610TIAN Jing-Kui*,XIE Chen,ZOUZhong-MeiZhejiang University*C58H96O28=1240<α>2D0-5·0°mp 208~210℃Data:MS,NMRcapilliposide C1Lysimachia capillipesChin ChemLett,2005,16(12):1607-1610TIAN Jing-Kui*,XIE Chen,ZOUZhong-MeiZhejiang University*C57H94O24=1262<α>2D0-10·0°mp 239~241℃Data:MS,NMR,ACTjulibroside J25AlbiziajulibrissinChin J Org Chem,2005,25(6):654-659ZOU Kun,CUI Jing-Rong,ZHAO Yu-Ying*Peking University*C85H136O43=1844<α>DData:IR,MS,NMR,ACTFlavonoids(黄酮类)crenatosideRhamnus crenatusActa PharmSin,2005,40(12):1127-1130WUXiao-Ming,PEI Yue-Hu,ZHOUJin-Yun*CAMS and PUMC*C30H28O11=564<α>2D0-44·5°mp>300℃D ata:UV,IR,MS,NMRAlkaloids(生物碱)evodiaxinineEvodiarutaecarpaJ China Pharm Univ,2005,36(6):520-522WANG Qi-Zhi,LIANG Jing-Yu*,CHENJunChina Pharmaceutical University*C20H15N3O=313<α>2D3 0°mp 175~176℃Data:UV,IR,MS,NMRSteroids(甾体类)(3E)-cholest-4-en-3,6-dione-3-oxi meCinachyrella australiensisChin J Org Chem,2005,25(12):1606-1609XIAO Ding-Jun,PENG Xue-Dong,DENGSong-Zhi*Shanghai Institute of
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