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11.85,12.76,14.14,15.15,18.92,21.01,21.09,21.38,22.93,26.64,27.98,28.03,28.62,29.70,30.98,34.85,35.93,36.58,37.00,39.55,40.26,43.38,46.66,49.65,54.96,56.02,116.48,117.47,139.14,145.85
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gujinwang: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-04-07 18:34:06
1 .     Citrostadienol
    ÏàËÆ¶È:96.6%
Korean Journal of Pharmacognosy          2009          40(4)          319-325
Phytochemical Studies on Lonicera Caulis (1) - Sterols and Triterpenoids
Kim, Ju-Sun; Yean, Min-Hye; Lee, So-Young; Lee, Je-Hyun; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     citrostadienol
C30H50O     ÏàËÆ¶È:96.6%
Pharmaceutical Biology          1997          35          358-363
ANTICOMPLEMENTARY ACTIVITY AND COMPLETE 13C NMR ASSIGNMENT OF CITROSTADIENOL FROM SCHIZANDRA C'HINENSIS
Im Sean Lee, Sei Ryang Oh, Keun Young Jung, Dong Sean Kim, lung Hee Kim and Hyeong-Kyu Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     14-methyl-stigmasta-7,24(28)-dien-3-ol
C30H50O     ÏàËÆ¶È:93.3%
China Journal of Chinese Materia Medica          2001          26          610-612
Studies on Chemical Constituents of Fragaria ananassa Duch
RUAN Jinlan, CHEN Jingbo, ZHAO Xiaoya, SUN Nanjun, John M Cassady, Gary D Stoner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     citrostadienol
    ÏàËÆ¶È:86.6%
Archives of Pharmacal Research          2015          38          186−192
Terpenes and sterols from the fruits of Prunus mume and their inhibitory effects on osteoclast differentiation by suppressing tartrate-resistant acid phosphatase activity
Xi-Tao Yan, Sang-Hyun Lee, Wei Li , Hae-Dong Jang, Young-Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     4-methyl stigmast-7-en-3-ol
    ÏàËÆ¶È:83.3%
China Journal of Chinese Materia Medica          2007          32          403-406
Study on chemical constituents of Myricaria paniculata I
Li Shuai, CHENG Ruoyun, YU Dequan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Erianol
    ÏàËÆ¶È:83.3%
Chemistry of Natural Compounds          2012          48          168-169
CHEMICAL CONSTITUENTS OF Eria spicata
Liqin Wang,Mingmei Wu,Jian Huang,Jihua Wang,Yegao Chen,and Benlin Yin1
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 6M
    ÏàËÆ¶È:83.3%
Phytochemistry          1989          28          629-631
Sterols and fatty acids of the freshwater Myriophyllum verticillatum
Marina Della Greca,Pietro Monaco,Lucio Previtera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     erianol
C30H50O     ÏàËÆ¶È:83.3%
Phytochemistry          1989          28          1487-1490
Erianol,a 4¦Á-methylsterol from the orchid Eria convallarioides
P.L. Majumder,Amita Kar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     24-ethyl-lophenol
    ÏàËÆ¶È:83.3%
Archives of Pharmacal Research          2015          38          186−192
Terpenes and sterols from the fruits of Prunus mume and their inhibitory effects on osteoclast differentiation by suppressing tartrate-resistant acid phosphatase activity
Xi-Tao Yan, Sang-Hyun Lee, Wei Li , Hae-Dong Jang, Young-Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Cholest-4¦Á-methyl-7-en-3¦Á-ethinyl-3¦Â-ol
C30H48O     ÏàËÆ¶È:80%
Steroids          2006          71          476-483
Synthesis and antitumor activity of cholest-4¦Á-methyl-7-en-3¦Â-ol derivatives
Lan He, Yumei Liu, Jiangong Shi, Qiang Pei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     fungisterol
C28H48O     ÏàËÆ¶È:80%
Natural Product Sciences          2008          14          1-11
Peroxynitrite scavengers from Phellinus linteus
Jeong, Da-Mi; Jung, Hyun-Ah; Kang, Hye-Sook; Choi, Jae-Sue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Gramisterol
    ÏàËÆ¶È:80%
Korean Journal of Pharmacognosy          2009          40(4)          319-325
Phytochemical Studies on Lonicera Caulis (1) - Sterols and Triterpenoids
Kim, Ju-Sun; Yean, Min-Hye; Lee, So-Young; Lee, Je-Hyun; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 1
C29H48O     ÏàËÆ¶È:80%
Phytochemistry          1987          26          2644-2645
Identification of 24-methylenelophenol from heartwood of Azadirachta indica
R. Banerji,Gopal Misra,S.K. Nigam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 1a
C31H50O2     ÏàËÆ¶È:77.4%
Phytochemistry          1987          26          2644-2645
Identification of 24-methylenelophenol from heartwood of Azadirachta indica
R. Banerji,Gopal Misra,S.K. Nigam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     sterol ether
C30H52O2     ÏàËÆ¶È:76.6%
Journal of Natural Products          1996          59          161-162
A New Cytotoxic Sterol Methoxymethyl Ether from a Deep Water Marine Sponge Scleritoderma sp. cf. paccardi
Sarath P. Gunasekera, Michelle Kelly-Borges, and Ross E. Longley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ergosta-7-en-3¦Â-ol
    ÏàËÆ¶È:76.6%
Chemical & Pharmaceutical Bulletin          1991          39          1958-1961
New Toxic Metabolites from a Mushroom, Hebeloma vinosophyllum. III. Isolation and Structures of Three New Glycosides, Hebevinosides XII, XIII and XIV, and Productivity of the Hebevinosides at Three Growth Stages of the Mushroom
Haruhiro FUJIMOTO,Kaijiro MAEDA and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     4 -methyl-ergost-7,24(28)-diene-3¦Â-ol-23-one
C29H46O2     ÏàËÆ¶È:76.6%
Steroids          2007          72          901-907
New 4¦Á-methyl steroids from a Chinese soft coral Nephthea sp.
Ke Ma, Wei Li, Hongwei Fu, Kazuo Koike, Wenhan Lin, Leen van Ofwegen, Hongzheng Fu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     4-methyl-cholesta-7-ene-3¦Â-ol
    ÏàËÆ¶È:76.6%
China Journal of Chinese Materia Medica          2009          34          1805-1808
Chemical constituents from herb of Solanum lyratum
YANG Li , FENG Feng, GAO Yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     4¦Á,24S-dimethyl-5¦Á-cholest-7-en-3¦Â-ol
    ÏàËÆ¶È:76.6%
Phytochemistry          1989          28          629-631
Sterols and fatty acids of the freshwater Myriophyllum verticillatum
Marina Della Greca,Pietro Monaco,Lucio Previtera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     stigmast-7-en-3¦Â-ol
    ÏàËÆ¶È:76.6%
Phytochemistry          1990          29          2351-2355
Sterol glucosides from Prunella vulgaris
Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     24(R)-ethyllophenol
    ÏàËÆ¶È:76.6%
Phytochemistry          1980          19          2491-2492
24(R)-ethyllophenol from Solanum melongena seeds
Toshihiro Itoh, Tsutomu Tamura, Masakazu Sagawa, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     compound 2
    ÏàËÆ¶È:76.6%
Phytochemistry          1980          19          2491-2492
24(R)-ethyllophenol from Solanum melongena seeds
Toshihiro Itoh, Tsutomu Tamura, Masakazu Sagawa, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     compound 4
    ÏàËÆ¶È:76.6%
Phytochemistry          1980          19          2491-2492
24(R)-ethyllophenol from Solanum melongena seeds
Toshihiro Itoh, Tsutomu Tamura, Masakazu Sagawa, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     stigmast-7-en-3¦Â-ol
    ÏàËÆ¶È:76.6%
Chinese Traditional and Herbal Drugs          2009          40          1039-1042
ɽ·¯µÄ»¯Ñ§³É·ÖÑо¿
»ô³¤ºç;Áººè;ÕÅÇìÓ¢;Íõß“;ÕÔÓñÓ¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     (3¦Â,5¦Á,20R,24S)-stigmasta-7-en-3-ol
    ÏàËÆ¶È:76.6%
Chinese Traditional and Herbal Drugs          2001          32          199-201
Two new sterols in the husk of Xanthoceras sorbifolia
CHENG Wen ming; YANG Bai zhen; LI Chun ru
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     4-¼×»ùµ¨çÞ-7-Ï©-3¦Â-´¼
    ÏàËÆ¶È:76.6%
Chinese Journal of Medicinal Chemistry          2005          15          100-102
Study of the chemical constituents from Asterias rollentias Bell.
ZHAN Yong-cheng, DONG Zhen-min, LIU Tao, PEI Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     4-¼×»ùµ¨çÞ-7,24-¶þÏ©-3¦Â-´¼
    ÏàËÆ¶È:76.6%
Chinese Journal of Medicinal Chemistry          2005          15          100-102
Study of the chemical constituents from Asterias rollentias Bell.
ZHAN Yong-cheng, DONG Zhen-min, LIU Tao, PEI Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     24,26,26-trimethyl cholest-7en-3¦Â-ol
C30H52O     ÏàËÆ¶È:76.6%
Tetrahedron Letters          1999          40          2955-2956
Thymosiosterol and ¦¤24 thymosiosterol, new sterols from the sponge Thymosiopsis sp.
Val¨¦rie Bultel-Ponc¨¦, Jean-Paul Brouard, Jean Vacelet, Mich¨¨le Guyot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     24¦Â-ethyl-25-dehydrolophenol
    ÏàËÆ¶È:76.6%
Journal of the Chemical Society, Perkin Transactions 1          1989                   1969-1974
Biosynthesis of 24¦Â-ethylsterols in cultured cells of Trichosanthes kirilowii(cucurbitaceae) fed with [1,2-13C2]- and [2-13C2H3]-acetate: reinvestigation of the stereochemistry at C-25
Shujiro Seo, Atsuku Uomori, Yohko Yoshimura, Ken'ichi Takeda, Haruo Seto, Yutaka Ebizuka, Hiroshi Noguchi and Ushio Sankawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     22-dihydrochondrillasterol
    ÏàËÆ¶È:76.6%
Journal of the Chemical Society, Perkin Transactions 1          1989                   1969-1974
Biosynthesis of 24¦Â-ethylsterols in cultured cells of Trichosanthes kirilowii(cucurbitaceae) fed with [1,2-13C2]- and [2-13C2H3]-acetate: reinvestigation of the stereochemistry at C-25
Shujiro Seo, Atsuku Uomori, Yohko Yoshimura, Ken'ichi Takeda, Haruo Seto, Yutaka Ebizuka, Hiroshi Noguchi and Ushio Sankawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     (3S,20S)-20-[(N-butyl-N-methyl-amino)-methyl]-pregn-7-en-3-ol
    ÏàËÆ¶È:76.6%
Bioorganic & Medicinal Chemistry          2009          17          8123-8137
Side chain azasteroids and thiasteroids as sterol methyltransferase inhibitors in ergosterol biosynthesis
Delphine Renard, Johann Perruchon, Martin Giera, Jörg M¨¹ller, Franz Bracher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     compound 5
    ÏàËÆ¶È:76.6%
Journal of the Chinese Chemical Society          1993          40          305-307
The 4¦Á-Methylsterol Violasterol A from Viola formosana Hayata
ÀîÊçÍñ(Shwu-Woan Lee);ê?˜s²Å(Zong-Tsi Chen);ê?ÇïÃ÷(Chiu-Ming Chen)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     5¦Á-sitgmasta-7-en-3¦Â-ol
    ÏàËÆ¶È:76.6%
Journal of the Chinese Chemical Society          2000          47          1131-1136
The Low Polar Constituents from Bidens Pilosa L. var. minor (Blume) Sherff
Ming-Huey Chang, Guei-Jane Wang,Yueh-Hsiung Kuo and Ching-Kuo Lee*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     stigmast-7-en-3¦Â-ol
    ÏàËÆ¶È:76.6%
Modern Chinese Medicine          2012          14          7-11
Separation and Identification of Chemical Constituents from Agriophyllum squarrosum( L. ) Moq.
GONG Bang, ZHAN Kai-xuan, ZHOU Yu-hua, ZHANG Lan, HUI Ye-qian, LI Yu-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     24-Ethyl-cholest-5¦Á-7-en-3-¦Â-ol
C29H50O     ÏàËÆ¶È:76.6%
Bioorganic & Medicinal Chemistry          2007          15          6834-6845
Marine natural products from the Turkish sponge Agelas oroides that inhibit the enoyl reductases from Plasmodium falciparum, Mycobacterium tuberculosis and Escherichia coli
Deniz Tasdemir, B¨¹lent Topaloglu, Remo Perozzo, Reto Brun, Rosann O¡¯Neill, N¨¦stor M. Carballeira, Xujie Zhang, Peter J. Tonge, Anthony Linden, Peter R¨¹edi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     3¦Â-¼×Ñõ»ù-¶¹çÞ-7-Ï©
    ÏàËÆ¶È:76.6%
Journal of Chinese Medicinal Materials          2010          33          1725-1727
Studies on the Chemical Constituents of Toricellia angulata var. intermedia
ZHANG Jin-wen, GUO Jie-ru, TANG Fei, ZHANG Xiao-qiong, XU Jiang-tao, YAO Guang-min, ZHANG Yong-hui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     4-methyl-cholesta-7-ene-3¦Â-ol
    ÏàËÆ¶È:76.6%
Natural Product Research and Development          2013          25          631-633
Study on the Chemical Constituents of Dregea sinensis Hemsl
JIA Shao-hua, LIU Feng-liang, LV Fang, CHEN Yan, DAI Rong-ji, MENG Wei-wei, DENG Yu-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     22,23-dihydrospinasterol
    ÏàËÆ¶È:76.6%
West China Journal of Pharmaceutical Sciences          2013          28          004-005
Study on the chemical constituents from Arenaria polytrichoides (I)
WUXian-xue, XIEJian-xin, LI De-liang, BAI Hong-mei, CHENGLi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     ergosta-7-en-3¦Â-ol
C28H48O     ÏàËÆ¶È:76.6%
Journal of the Chilean Chemical Society          2002          47          511-516
ESTEROLES, ¨¢CIDOS GRASOS E HIDROCARBUROS DE LOS CUERPOS FRUCT¨ªFEROS DE GANODERMA AUSTRALE
IVONNE J. NIETO*, MEISER A. VALENCIA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     stigmast-7-en-3¦Â-ol
    ÏàËÆ¶È:76.6%
Chinese Joumal of Experimental Traditional Medical Fomulae          2012          18          107-109
Study on Chemical Constituents from Prunella vulgaris
YU Qian, QI Jin, LIU Shou-jin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     24¦Á-ethyl-5¦Á-cholesta-7-en-3¦Â-ol
C29H48O     ÏàËÆ¶È:76.6%
Acta Botanica Yunnanica          1988          10          475-479
THE CHEMICAI CONSTITUENTS FROM ROOTS OF CUCUBITA FOETIDISSIMA
Fan Juan, Feng Baoshu, Qiu Minhua, Nie Ruilin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     ¦¤7-sitosterol
    ÏàËÆ¶È:76.6%
Bulletin of the Korean Chemical Society          2014          35          2335-2341
Steroids from the Cold Water Starfish Ctenodiscus crispatus with Cytotoxic and Apoptotic Effects on Human Hepatocellular Carcinoma and Glioblastoma Cells
Tran Hong Quang, Dong-Sung Lee, Se Jong Han, Il Chan Kim, Joung Han Yim, Youn-Chul Kim*, Hyuncheol Oh*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     compound 3
    ÏàËÆ¶È:75%
Phytochemistry          1980          19          2491-2492
24(R)-ethyllophenol from Solanum melongena seeds
Toshihiro Itoh, Tsutomu Tamura, Masakazu Sagawa, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     24 ¦Î -ethyl-25(27)-dehydrolophenol acetate
    ÏàËÆ¶È:75%
Phytochemistry          1981          20          1929-1933
24¦Â-Ethyl-31-norlanosta-8,25(27)-dien-3¦Â-ol and 24¦Â-ethyl-25(27)-dehydrolophenol in seeds of three cucurbitaceae species
T. Itoh, Y. Kikuchi, N. Shimizu, T. Tamura, T. Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     24-ethyllophenol acetate
    ÏàËÆ¶È:75%
Phytochemistry          1981          20          1929-1933
24¦Â-Ethyl-31-norlanosta-8,25(27)-dien-3¦Â-ol and 24¦Â-ethyl-25(27)-dehydrolophenol in seeds of three cucurbitaceae species
T. Itoh, Y. Kikuchi, N. Shimizu, T. Tamura, T. Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     24¦Á-ethyllophenol acetate
    ÏàËÆ¶È:75%
Phytochemistry          1981          20          1929-1933
24¦Â-Ethyl-31-norlanosta-8,25(27)-dien-3¦Â-ol and 24¦Â-ethyl-25(27)-dehydrolophenol in seeds of three cucurbitaceae species
T. Itoh, Y. Kikuchi, N. Shimizu, T. Tamura, T. Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     compound 5a
    ÏàËÆ¶È:75%
Journal of the Chinese Chemical Society          1993          40          305-307
The 4¦Á-Methylsterol Violasterol A from Viola formosana Hayata
ÀîÊçÍñ(Shwu-Woan Lee);ê?˜s²Å(Zong-Tsi Chen);ê?ÇïÃ÷(Chiu-Ming Chen)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     Cholest-4¦Á-methyl-7-en-3¦Â-ol-hemisuccinate
C32H52O4     ÏàËÆ¶È:74.1%
Steroids          2006          71          476-483
Synthesis and antitumor activity of cholest-4¦Á-methyl-7-en-3¦Â-ol derivatives
Lan He, Yumei Liu, Jiangong Shi, Qiang Pei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     22-dihydrochondrillasterol
    ÏàËÆ¶È:74.1%
Phytochemistry          1981          20          761-764
Co-occurrence of chondrillasterol and spinasterol in two cucurbitaceae seeds as shown by 13C NMR
Toshihiro Itoh, Yoshinori Kikuchi, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     22-dihydrospinasterol
    ÏàËÆ¶È:74.1%
Phytochemistry          1981          20          761-764
Co-occurrence of chondrillasterol and spinasterol in two cucurbitaceae seeds as shown by 13C NMR
Toshihiro Itoh, Yoshinori Kikuchi, Toshitake Tamura, Taro Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     22-dihydrospinasterol
    ÏàËÆ¶È:74.1%
Phytochemistry          1982          21          727-730
Co-occurrence of c-24 epimeric 24-ethyl-¦¤7 -sterols in the roots of Trichosanthes japonica
T. Itoh, K. Yoshida, T. Tamura, T. Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     22-dihydrochondrillasterol
    ÏàËÆ¶È:74.1%
Phytochemistry          1982          21          727-730
Co-occurrence of c-24 epimeric 24-ethyl-¦¤7 -sterols in the roots of Trichosanthes japonica
T. Itoh, K. Yoshida, T. Tamura, T. Matsumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     24,24-Dimethyl-5¦Á-cholesta-7,25-dien-22-yn-30-ol (6) acetate
C31H46O2     ÏàËÆ¶È:74.1%
The Journal of Organic Chemistry          1989          54          606-610
Isolation of acetylenic sterols from a higher plant. Further evidence that marine sterols are not unique
Toshihiro Akihisa, Toshitake Tamura, Taro Matsumoto, W. C. M. C. Kokke, Takao Yokota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     24,24-Dimethyl-5¦Á-cholest-7-en-33-ol (10) acetate
    ÏàËÆ¶È:74.1%
The Journal of Organic Chemistry          1989          54          606-610
Isolation of acetylenic sterols from a higher plant. Further evidence that marine sterols are not unique
Toshihiro Akihisa, Toshitake Tamura, Taro Matsumoto, W. C. M. C. Kokke, Takao Yokota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     (24S)-5¦Á-Stigmast-7-en-3¦Â-ol (4) acetate
    ÏàËÆ¶È:74.1%
The Journal of Organic Chemistry          1989          54          606-610
Isolation of acetylenic sterols from a higher plant. Further evidence that marine sterols are not unique
Toshihiro Akihisa, Toshitake Tamura, Taro Matsumoto, W. C. M. C. Kokke, Takao Yokota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     22,23-Dihydrospinasterol
    ÏàËÆ¶È:73.3%
Acta Botanica Yunnanica          1995          17(1)          103-108
CHEMICAL CONSTITUENTS FROM CLERODENDRUM JAPONICUM
TIAN Jun, SUN Han-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     (22E,24Z)-5¦Á-stigmasta-7,22,24(241)-trien-3¦Â-yl acetate
C31H48O2     ÏàËÆ¶È:73.3%
Chemical & Pharmaceutical Bulletin          1996          44          1202-1207
Eight Novel Sterols from the Roots of Bryonia dioica JACQ.
Toshihiro AKIHISA,Yumiko KIMURA,Wilhelmus C. M. C. KOKKE,Takashi ITOH and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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