菅属植物的地理分布

菅属(Themeda Forssk.)是禾本科高粱族(Poaceae:Andropogoneae)中佛焰苞物种的代表类群之一,在高粱族占据关键的系统演化位置,具有高度的形态和生态多样性。通过野外调查和查阅标本及文献,菅属约有27种植物,旧世界均有分布,新世界3种隶属于菅组。中国有13种,分布在西南至华南各省(区),云南干热河谷地区有10种。研究表明中国云南及印度北部是菅属的分布中心和多样性中心,中国云南及印度北部是否为菅属的起源地尚需确证。     

值得注意的中国南部植物

该文续报道胡麻科、桑寄生科等科7个分类单位。胡麻科的茶菱属和茶菱均为广东新记录。云南槲寄生、锈毛钝果寄生和枫香钝果寄生均为海南新记录。《海南植物志》第二卷记载的五蕊桑寄生(产于琼中),现订正琼中的标本应为枫香钝果寄生,海南不产五蕊寄生属植物。大戟科的子弹枫现已成为广西和广东的归化种。无患子科的雅旗是我国新引种的经济植物。     

杯菊精油成分的研究

杯菊〔(Cyathocline purpurea(Buch-Ham.)O.Ktze)又名(C.lyrata Cass.)〕属菊科杯菊属植物。广佈于热带亚洲和热带非洲,在我国南方的广西、贵州、云南均有野生分布。我国民间用于杀虫、清热解毒、消炎止血、除湿利尿等,在一些地方性的本草图册中均有记载。印度学者对印度索加尔产的杯菊精油化学成份进行过研究,其主要成份为倍半萜醇-杯菊醇(cyathoclol)及其乙酯,约占精油的50％。本文报道云南南部产杯菊的精油化学成份,其主要成份为百里香氢醌二甲醚(thymo-hydroquinonedimethyl(ther)(约70％)及异丁酸百里香酯(thymyl iso-butyrate)(约19％),后者     

《植物分类与资源学报》征订启事

(原刊名《云南植物研究》)《植物分类与资源学报》(原刊名《云南植物研究》)创刊于1979年,是由中国科学院主管、中国科学院昆明植物研究所及中国植物学会承办的全国性自然科学学术期刊。经过30多年的努力,现已成为我国与植物科学研究相关的主要学术性期刊之一,已成为中国自然科学核心期刊,中国     

《植物分类与资源学报》征订启事

(原刊名《云南植物研究》)《植物分类与资源学报》(原刊名《云南植物研究》)创刊于1979年,是由中国科学院主管、中国科学院昆明植物研究所及中国植物学会承办的全国性自然科学学术期刊。经过30多年的努力,现已成为我国与植物科学研究相关的主要学术性     

中国蚜科新纪录,4

在调查云南森林昆虫中发现下述种类为我国首次纪录。 大尾小长管蚜Macrosiphoniella grandicauda Takahashi et Kuwana, 1963,中国新纪录。采自云南丽江(林科所1980.V.23),各型孤雌蚜。寄主为艾蒿,盖满3—4寸嫩梢。活体叶绿色,体稍扁。不易从植物上坠落。国外分布于朝鲜、日本和印度。     

中药胡黄连的研究进展

胡黄连为我国传统中药,一向依赖进口,原植物为印度胡黄连（ＰｃｒｏｒｈｉｚａｋｕｒｒｏｏａＲｏｙｌｅｅｘＢｅｎｔｈ）。本世纪６０年代,在西藏和云南发现西藏胡黄连（Ｐ．ｓｃｒｏｐｈｕｌａｒｉｆｌｏｒａＰｅｎｎｅｌ）并栽培作为印度胡黄连的代用品。近年来,国外研究发现印度胡黄连根茎中环烯醚萜甙类成分具有显著抗乙肝病毒活性、保肝降酶等作用,引起了人们关注。本文对胡黄连研究作了系统回顾,为西藏胡黄连进一步开发利用提供参考     

秦岭产珠子参根茎的皂甙成分

从陕西省秦岭产珠子参（Panax japonicus C.A.Meyer var.major(Burk.)Wu et Feng)的根茎中分离得到7个皂甙,经13CNMR快速原子轰击质谱（FAB－MS）等测定,并与标准品对照,其中6个分别鉴定为已知竹节参甙（chikusetsusa ponin)V(即人参甙Rg),IVa,齐墩果酸－28－O－β－D－葡萄哟喃糖甙（oleanolic acid 28-O-β－glucopyranoside),人参甙（ginsenoside)Rg2,Re以及三七甙（notoginsenoside)R2.另一皂甙为竹节参甙IV,甲酯（chikusetsusa ponin IVa methyl ester),即齐墩果酸－（3－O－β－D－葡萄吡喃糖醛酸甲酯）－28－O－β－D－葡萄吡喃糖甙（oleanolie acid-(3-O-β－D－glucorunopyranosyl-methylate)-28-O-β-D-glucopyranoside),系首次从植物中分离得到,对陕西省秦岭产和云南丽江产的珠子参根茎的皂甙成分进行了比较和讨论。     

兔耳兰

<正> 兔耳兰(Cymbidium lancifolium),又名宽叶兰,为英国学者虎克于1823年发表在《外来植物志》(Exot.F1.1:t.51)上 分布于广东、广西、四川、云南、贵州、台湾和西藏等省区、日本、越南、尼泊尔、印度及马来西亚亦产。兔耳兰为地生或半附生草本,一般见于海拔2200米以下的林内,或附生于树上,岩石上。属名Cymbidium源自希腊文 引喻该属植物具舟形的唇瓣,种加词lancifolium意为“具     

滇西香茅挥发油的化学成分

滇西香茅(Cymbopogon khasiamus(Hack.)Stapf ex Bor)为禾本科植物,分布于印度及缅甸,该植物过去在中国无分布记载,作者在云南首次发现。其挥发油为主要有效成分,当地与芸香草(Cymbopogon distans(Steud)Wats.)混用。为合理开发和利用该种植物,对挥发油的化学成分进行了分析。     

Metabolic pathways from 1 alpha,25-dihydroxyvitamin D3 to 1 alpha,25-dihydroxyvitamin D3-26,23-lactone. Stereo-retained and stereo-selective lactonization

The present study was carried out in order to elucidate the metabolic pathway from 1 alpha,25-(OH)2D3 to 1 alpha,25-(OH)2D3-26,23-lactone. For that purpose, we stereospecifically synthesized the vitamin D3 derivatives 1 alpha,23(S),25-(OH)3D3, 1 alpha,23(S),25(R),26-tetrahydroxyvitamin D3, and 23(S),25(R)-1 alpha,25-dihydroxyvitamin D3-lactol. The in vitro metabolism of these compounds was examined in kidney homogenates and intestinal mucosa homogenates from 1 alpha,25-(OH)2D3-supplemented chicks. The naturally occurring 23(S),25(R)-1 alpha,25-dihydroxyvitamin D3-26,23-lactone was produced (in increasing amounts) from 1 alpha,25-(OH)2D3, 1 alpha,25(R),26-(OH)3D3, 1 alpha,23(S),25-(OH),D3, 1 alpha,23(S),25(R),26-(OH)4D3, and 23(S),25(R)-1 alpha,25-(OH)2D3-26,23-lactol. These results indicated that there are two possible metabolic pathways from 1 alpha,25-(OH)2D3 to 1 alpha,23(S),25(R),26-(OH)4D3: the major one is by way of 1 alpha,23(S),25-(OH)3D3 and the minor one is by way of 1 alpha,25(R),26-(OH)3D3. 1 alpha,23(S),25(R),26-Tetrahydroxyvitamin D3 is further metabolized to 23(S),25(R)-1 alpha,25-dihydroxyvitamin D3-26,23-lactone via 23(S),25(R)-1 alpha,25-dihydroxyvitamin D3-26,23-lactol. In the course of our studies, a new biosynthetic vitamin D3 metabolite was isolated in pure form. This metabolite was identified as 23(S),25(R)-1 alpha,25-(OH)2D3-26,23-lactol by UV spectrophotometry and mass spectrometry. Furthermore, we establish in this report that the lactonization of 1 alpha,23,25,26-(OH)4D3 and 1 alpha,25-(OH)2D3-26,23-lactol occurs in a stereo-retained and stereo-selective fashion.     

Biochemical and immunological demonstration of prostaglandin D2, E2, and F2 alpha formation from prostaglandin H2 by various rat glutathione S-transferase isozymes

Glutathione S-transferase isozymes purified from normal rat liver (1-1, 1-2, 2-2, 3-3, 3-4, and 4-4), liver with hyperplastic nodules (7-7), brain (Yn1Yn1), and testis (Yn1Yn2) all had prostaglandin H2-converting activity. The prostaglandin H2 E-isomerase activity was high in 1-1 (1400 nmol/min/mg protein), 1-2 (1170), and 2-2 (420), moderate in 3-3, 3-4, 4-4, Yn1Yn1, and Yn1Yn2 (52-100), and weak but significant in 7-7 (33). The prostaglandin H2 D-isomerase activity was relatively high in 1-1 (170) and 1-2 (200), moderate in 2-2 (60) and Yn1Yn2 (43), and weak but marked in 3-3 (16), 4-4 (16), and 7-7 (14). The prostaglandin H2 F-reductase activity was remarkable in 1-1 (1250), 1-2 (920), and 2-2 (390), and weakly detected in 3-3 (24), 4-4 (28), and 7-7 (14). Glutathione was absolutely required for these prostaglandin H2-converting reactions, and its stoichiometric consumption was associated with F-reductase activity but not E- and D-isomerase activities. The Km values for glutathione and prostaglandin H2 were about 200 and 10-40 microM, respectively. By immunoabsorption analyses with various antibodies specific for each isozyme, we examined its contribution to the formation of prostaglandins D2, E2, and F2 alpha from prostaglandin H2 in 100,000g supernatants of rat liver, kidney, and testis. In the liver, about 90% of the F-reductase activity (9.8 nmol/min/mg protein) was shown to be catalyzed by the 1-2 group of isozymes. The E-isomerase activity (16.5) was catalyzed about 60 and 40% by the 1-2 and 3-4 groups, respectively; and the D-isomerase activity (3.7) was catalyzed by the 1-2 group (50%) and the 3-4 group and Yn1Yn2 (15-25%). In the kidney, the E-isomerase activity (9.4) was catalyzed by 1-1, 1-2 (40%), 2-2, 3-4 group, and 7-7 (10-20%). The F-reductase activity (3.3) was mostly catalyzed by the 1-2 group (75%). In the testis, the E-isomerase activity (3.9) was catalyzed by the 1-2 group (20-30%), the 3-4 group, and Yn1Yn2 (30-60%).     

Biotransformation of bufadienolides by cell suspension cultures of Saussurea involucrata

The biotransformation of three bioactive bufadienolides, namely, bufotalin (1), telocinobufagin (2), and gamabufotalin (3) by cell suspension cultures of Saussurea involucrata yielded 11 products. Bufotalin yielded 3-epi-bufotalin (1a), 3-epi-desacetylbufotalin (1b), 3-epi-bufotalin 3-O-β-D-glucoside (1c), 1β-hydroxybufotalin (1d), and 5β-hydroxybufotalin (1e); telocinobufagin yielded 3-dehydroscillarenin (2a), 3-dehydrobufalin (2b), and 3-epi-telocinobufagin (2c); and gamabufotalin yielded 3-epi-gamabufotalin (3a), 3-dehydrogamabufotalin (3b), and 3-dehydro-Δ1-gamabufotalin (3c), respectively. Among these 11 products, 1a, 1b, 1c, 1d, 3a and 3c are previously unreported. The structures of these metabolites were elucidated based on NMR spectroscopic analyses and mass spectrometry. Most metabolites showed significant cytotoxic activities against human hepatoma (HepG2) and breast cancer (MCF-7) cell lines. In addition, the time course for the biotransformation of 3 was investigated.     

广东土牛膝的化学成分

广东土牛膝为菊科泽兰属植物华泽兰（Eupatorium chinense）的干燥根。从其甲醇提取物中共分离得到11个化合物,其中eupatorinA（1）为一新化合物,经波谱学方法鉴定为（threo）-3-O-acetyl-1-（4-hydroxy-3-methoxyphenyl）-2-[4-（3-hydroxy-1-（E）-propenyl）-2,6-dimethoxyphenoxy]propyl-β-D-glucopy-ranoside。已知化合物分别鉴定为（threo）-3-hydroxy-1-（4-hydroxy-3-methoxyphenyl）-2-[4-（3-hydroxy-1-（E）-propenyl）-2,6-dimethoxyphenox-y]-propyl-β-D-glucopyranoside（2）,ardisiacrispinA（3）,ardisiac-rispinB（4）,euparone（5）,3-（2,3-dihydroxy-isopen-tyl）-4-hydroxyacetophenone（6）,12,13-di-hydroxy-euparin（7）,gymnastone（8）,N-（2′-hydroxy-tetracosanosyl）-2-amino-1,3,4-trihydroxy-octa-dec-8-（E）-ene（9）,stigmasterol（10）和stigmasterol-3-O-β-D-glucopyranoside（11）。化合物2-4为首次从菊科植物,5-8为首次从泽兰属植物中分离得到。     

Synthesis of two phosphate-containing "heptasaccharide" fragments of the capsular polysaccharides of Streptococcus pneumoniae types 6A and 6B.

The "heptasaccharides" O-alpha-D-galactopyranosyl-(1----3)- O-alpha-D-glucopyranosyl-(1----3)-alpha, beta-L-rhamnopyranose 2'-[O-alpha-D-galactopyranosyl-(1----3)-O-alpha-D-glucopyranosyl- (1----3)-O-alpha-L-rhamnopyranosyl-(1----3)-D-ribit-5-yl sodium phosphate] (25) and O-alpha-D-galactopyranosyl- (1----3)-O-alpha-D-glucopyranosyl-(1----3)-alpha, beta-L-rhamnopyranose 2'-[O-alpha-D-galactopyranosyl-(1----3)-O-alpha-D-glucopyranosyl- (1----3)-O-alpha-L-rhamnopyranosyl-(1----4)-D-ribit-5-yl sodium phosphate] (27), which are structural elements of the capsular polysaccharides of Streptococcus pneumoniae types 6A and 6B ([----2)- -alpha-D-Galp-(1----3)-alpha-D-Glcp-(1----3)-alpha-L-Rhap- (1----X)-D-RibOH-(5-P----]n; 6A X = 3, 6B X = 4), respectively, have been synthesized. 2,4-Di-O-acetyl- 3-O-[2,4,6-tri-O-acetyl-3-O-(2,3,4,6-tetra-O-acetyl-alpha-D- galactopyranosyl)-alpha-D-glucopyranosyl]-alpha-L-rhamnopyranosyl trichloroacetimidate (13) was coupled with 5-O-allyloxycarbonyl-1,2,4-tri-O- benzyl-D-ribitol (10), using trimethylsilyl triflate as a promotor (----14), and deallyloxycarbonylation (----15) and conversion into the corresponding triethylammonium phosphonate then gave 16. Condensation of 16 with 4-methoxybenzyl 2,4-di-O-benzyl-3-O-[2,4,6-tri-O-benzyl-3-O-(3,4,6-tri-O-benzyl-alpha-D- galactopyranosyl)-alpha-D-glucopyranosyl]- alpha-L-rhamnopyranoside (22) followed by oxidation and deprotection afforded 25. 5-O-Allyl-1-O-allyloxycarbonyl-2,3-di-O-benzyl-D-ribitol (12) was coupled with 13, using trimethylsilyl triflate as a promoter, the resulting tetrasaccharide-alditol derivative 17 was deallyloxycarbonylated (----18), acetylated (----19), and deallylated (----20), and the product was converted into the triethylammonium phosphonate derivative 21. Condensation of 21 with 22 followed by oxidation and deprotection afforded 27.     

Chemical Constituents of Guangdong Tu Niu Xi (Eupatorium chinense,Compositae)

One new compound, namely eupatorin A (1), was isolated from the methanolic extract of Guangdong Tu Niu Xi, the dried roots of Eupatorium chinense (Compositae). Its structure was determined to be (threo) 3 O acetyl 1 (4 hydroxy 3 methoxyphenyl) 2 \[4 (3 hydroxy 1 (E) propenyl) 2, 6 dimethoxyphenoxy\]propyl β D gluco pyranoside on the basis of detailed spectroscopic analysis. In addition, ten known compounds, including (threo) 3 hydroxy 1 (4 hydroxy 3 methoxyphenyl) 2 \[4 (3 hydroxy 1 (E) propenyl) 2, 6 dimethoxyphenoxy\]propyl β D glucopyranoside (2), ardisiacrispin A (3), ardisiacrispin B (4), euparone (5), 3 (2, 3 dihydroxy isopentyl) 4 hydroxy acetophenone (6), 12,13 dihydroxy euparin (7), gymnastone (8), N (2′ hydroxy tetracosanosyl) 2 amino 1, 3, 4 trihydroxy octadec 8 (E) ene (9), stigmasterol (10) and stigmasterol 3 O β D glucopyranoside (11) were also obtained. This was the first time that compounds 2-4 were reported from Compositae family, while 5-8 were isolated from the genus Eupatorium.     

Analysis of flavonoids in flower petals of soybean near-isogenic lines for flower and pubescence color genes

W1, W3, W4, and Wm genes control flower color, whereas T and Td genes control pubescence color in soybean. W1, W3, Wm, and T are presumed to encode flavonoid 3'5'-hydroxylase (EC 1.14.13.88), dihydroflavonol 4-reductase (EC 1.1.1.219), flavonol synthase (EC 1.14.11.23), and flavonoid 3'-hydroxylase (EC 1.14.13.21), respectively. The objective of this study was to determine the structure of the primary anthocyanin, flavonol, and dihydroflavonol in flower petals. Primary component of anthocyanin in purple flower cultivars Clark (W1W1 w3w3 W4W4 WmWm TT TdTd) and Harosoy (W1W1 w3w3 W4W4 WmWm tt TdTd) was malvidin 3,5-di-O-glucoside with delphinidin 3,5-di-O-glucoside as a minor compound. Primary flavonol and dihydroflavonol were kaempferol 3-O-gentiobioside and aromadendrin 3-O-glucoside, respectively. Quantitative analysis of near-isogenic lines (NILs) for flower or pubescence color genes, Clark-w1 (white flower), Clark-w4 (near-white flower), Clark-W3w4 (dilute purple flower), Clark-t (gray pubescence), Clark-td (near-gray pubescence), Harosoy-wm (magenta flower), and Harosoy-T (tawny pubescence) was carried out. No anthocyanins were detected in Clark-w1 and Clark-w4, whereas a trace amount was detected in Clark-W3w4. Amount of flavonols and dihydroflavonol in NILs with w1 or w4 were largely similar to the NILs with purple flower suggesting that W1 and W4 affect only anthocyanin biosynthesis. Amount of flavonol glycosides was substantially reduced and dihydroflavonol was increased in Harosoy-wm suggesting that Wm is responsible for the production of flavonol from dihydroflavonol. The recessive wm allele reduces flavonol amount and inhibits co-pigmentation between anthocyanins and flavonols resulting in less bluer (magenta) flower color. Pubescence color genes, T or Td, had no apparent effect on flavonoid biosynthesis in flower petals.     

广东土牛膝的化学成分(英文)

广东土牛膝为菊科泽兰属植物华泽兰(Eupatorium chinense)的干燥根。从其甲醇提取物中共分离得到11个化合物,其中eupatorinA(1)为一新化合物,经波谱学方法鉴定为(threo)-3-O-acetyl-1-(4-hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxy-1-(E)-propenyl)-2,6-dimethoxyphenoxy]propyl-β-D-glucopy-ranoside。已知化合物分别鉴定为(threo)-3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxy-1-(E)-propenyl)-2,6-dimethoxyphenox-y]-propyl-β-D-glucopyranoside(2),ardisiacrispinA(3),ardisiac-rispinB(4),euparone(5),3-(2,3-dihydroxy-isopen-tyl)-4-hydroxyacetophenone(6),12,13-di-hydroxy-euparin(7),gymnastone(8),N-(2′-hydroxy-tetracosanosyl)-2-amino-1,3,4-trihydroxy-octa-dec-8-(E)-ene(9),stigmasterol(10)和stigmasterol-3-O-β-D-glucopyranoside(11)。化合物2-4为首次从菊科植物,5-8为首次从泽兰属植物中分离得到。     

Isolation and comparative analysis of multiple isoenzymes of glutathione-S-transferase from the liver of intact rats and rats administered phenobarbital, 3-methylcholanthrene and butylhydroxytoluene

Seven glutathione-S-transferase (GST) isozymes were purified from liver cytosol of intact male Wistar rats: 1-1(A), 1-1(B), 1-2, 2-2, 3-3, 3-4, 4-4. Treatment of rats with butylated hydroxytoluene (BHT) led to the induction of isozymes GST 1-1(A), 1-1(B) (2-fold), 3-3 (3.5-fold) as well as to the appearance of two new isozymes--1-3 and 4-4(A). Phenobarbital (PB) induced isozymes GST 1-1(A), 1-1(B) (2-fold) and 3-3 (1.5-fold). BHT and PB caused an increase in the specific activity of isozymes 1-1(A), 1-1(B), 3-3, 3-4 towards 1-chloro-2.4-dinitrobenzene and 1.2-dichloro-4-nitrobenzene. 3-Methylcholanthrene (MC) induced isozymes 1-2 (1.5-fold), 2-2 (2-fold) and 4-4 (3-fold). A conclusion was drawn that BHT and PB induced the GST subunits 1 and 3, whereas MC--subunits 2 and 4.