| ²é¿´: 482 | »Ø¸´: 2 | |||
yetta_he½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
»¯ºÏÎï1: CDCL3 12.07,12.20,18.99,19.25,19.61,20.04,21.30,23.28,24.52,31.85,32.11,36.36,36.72,37.46,39.99,42.53,46.04,50.34,56.98,72.03,121,94,140.96 »¯ºÏÎï2: CDCL3 11.74,11.87,18.66,18.93,19.30,19.71,20.93,24.16,29.00,31.44,31.77,35.99,36.40,37.19,39.64,42.15,42.17,45.66,50.00,56.62,71.14,121.18,141.01 |
» ²ÂÄãϲ»¶
ÓÐûÓÐѧУ²ÄÁÏרҵÊÕ¿çµ÷(Ò»Ö¾Ô¸085410)
ÒѾÓÐ7È˻ظ´
311Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
268·Ö085602»¯Ñ§¹¤³Ìµ÷¼Á
ÒѾÓÐ9È˻ظ´
³õÊÔ·Ö332£¬Ò»Ö¾Ô¸±¨¿¼Î÷±±¹¤Òµ´óѧ£¬
ÒѾÓÐ5È˻ظ´
085801 ×Ü·Ö275 ±¾¿ÆÐÂÄÜÔ´ Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸¿ó´ó£¬²ÄÁϹ¤³Ìר˶314·Ö£¬0856¿Éµ÷¶¼¿ÉÒÔ
ÒѾÓÐ4È˻ظ´
288Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁÏר˶³õÊÔ·Ö332Ò»Ö¾Ô¸Î÷±±¹¤Òµ´óѧ£¬
ÒѾÓÐ4È˻ظ´
²ÄÁÏר˶(0856) 339·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
»¯Ñ§¹¤³ÌÓë¼¼Êõרҵһ־Ը¹þ¹¤³Ì 291·ÖBÇø ¹ú¼Ò¼¶´ó´´¸ºÔðÈË ÓÐÒ»×÷ÂÛÎÄ
ÒѾÓÐ11È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯ½á¹û£º¹²²éµ½602¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:81.4% Chemical & Pharmaceutical Bulletin 1993 41 2007-2009 Constituents of Prunus zippeliana Leaves and Branches Junichi KITAJIMA and Yasuko TANAKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:81.4% Steroids 2005 70 886-895 Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Â-sitosterol ÏàËÆ¶È:81.4% Korean Journal of Pharmacognosy 2005 36(2) 145-150 Phytochemical Constituents of Cirsium nipponicum (MAX.) Makino Lee, Jong-Hwa; Lee, Kang-Ro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Â-sitosterol ÏàËÆ¶È:81.4% Korean Journal of Pharmacognosy 2010 41 238-244 Constituents of Cynanchum auriculatum and their Inhibitory Effect on Melanogenesis in B16 Mouse Melanoma Cell Lines Choi, Hyun-Gyu; Jiang, Yanfu; Roh, Eun-Mi-Ri; Kim, Young-Soo; Xu, Guang-Hua; Na, Min-Kyun; Lee, Seung-Ho Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-sitosterol ÏàËÆ¶È:81.4% Journal of Agricultural and Food Chemistry 2002 50 4709-4712 Sphingolipid and Other Constituents from Almond Nuts (Prunus amygdalus Batsch) Shengmin Sang, Hiroe Kikuzaki, Karen Lapsley, Robert T. Rosen, Nobuji Nakatani, and Chi-Tang Ho Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-sitosterol C29H58O ÏàËÆ¶È:81.4% Journal of Agricultural and Food Chemistry 1989 37 1363-1367 Isolation of compounds with antimutagenic activity from Savoy Chieftain cabbage Terence Lawson, Janet Nunnally, Betty Walker, Edward Bresnick, Desmond Wheeler, Maureen Wheeler Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-sitosterol ÏàËÆ¶È:81.4% Journal of Wood Science 2013 59 155-159 Antibacterial compounds from shoot skins of moso bamboo (Phyllostachys pubescens) Akinobu Tanaka, Kuniyoshi Shimizu, Ryuichiro Kondo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . sitosterol C29H50O ÏàËÆ¶È:81.4% Asian Journal of Chemistry 2014 26 8019-8021 Constituents from the Root of Lantana camara AMMAR A. AL-FADHLI, * and JAMAL A. NASSER Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:80.7% Chemical & Pharmaceutical Bulletin 1993 41 1238-1243 Two New 2-Arylbenzofuran Derivatives from Hypoglycemic Activity-Bearing Fractions of Morus insignis Purusotam BASNET,Shigetoshi KADOTA,Satoshi TERASHIMA,Mineo SHIMIZU and Tsuneo NAMBA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-Sitosterol ÏàËÆ¶È:80.7% Korean Journal of Pharmacognosy 2007 38(1) 67-70 Isolation of Isoprenoidal Compounds from the Stems of Acer tegmentosum Max Hur, Jong-Moon; Jun, Mi-Ra; Yang, Eun-Ju; Choi, Sun-Ha; Park, Jong-Cheol; Song, Kyung-Sik Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Â-sitosterol ÏàËÆ¶È:80.7% Korean Journal of Pharmacognosy 2004 35(1) 80-87 The Chemical Structures and Their Antioxidant Activity of the Components Isolated from the Heartwood of Hemiptelea davidii Chang, Bok-Sim; Kwon, Yong-Soo; Kim, Chang-Min Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . sitosterol C29H50O ÏàËÆ¶È:80.7% Phytochemistry 1987 26 753-754 Iridoid glycosides from Penstemon richardsonii Birgit Gering,Peter Junior,Max Wichtl Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . ¦Â-sitosterol ÏàËÆ¶È:80% Industrial Crops and Products 2014 59 189−196 Antimicrobial and cytotoxic activities of Alnus rugosa L. aerial parts and identification of the bioactive components Khaled Rashed, Ana Ćirić, Jasmina Glamočlija, Ricardo C. Calhelha, Isabel C.F.R. Ferreira, Marina Soković Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 5¦Á-stigmast-9(11)-en-3¦Â-ol C29H50O ÏàËÆ¶È:78.5% China Journal of Chinese Materia Medica 1996 21 666-667 Studies on Chemical Components of Cynomorium songaricum Rupr. Xu Xiuzhi, Zhang Chengzhong and Li Chong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Â-sistosterol C29H50O ÏàËÆ¶È:78.5% Natural Product Sciences 2007 13 220-224 Antioxidant Activity of Cholesterol Derived from Silkworm Pupae Heo, Jung-Eun; Ryu, Jae-Ha; Jeong, Hye-Kyoung; Chung, Wan-Tae; Ahn, Mi-Young Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-sitosterol ÏàËÆ¶È:78.5% Chinese Pharmaceutical Journal 2009 44 1372-1374 Chemical Constituents of the Roots of Uritca fissa E.Pritz. JI Bao-quan, FENG Bao-min, SHI Li-ying, TANG Ling, WANG Yong-qi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . ¦Â-sitosterol ÏàËÆ¶È:78.5% Modern Chinese Medicine 2007 9(12) 11-13 Studies on the chemical Constituents of Ampelopsis grossedentata He Guixia, Pei Gang, Du Fanglu, OU Yangwen, Li Bin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . ¦Â-sitosterol ÏàËÆ¶È:78.5% Journal of Shenyang Pharmaceutical University 2011 28 364-367 Isolation and identification of chemical constituents of root of Girardinia suborbiculata C. J. Chen subsp. Triloba FENG Bao-min, LIU Jing-yan, WANG Hui-guo, SHI Li-ying, TANG Ling, WANG Yong-qi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . ¦Â-sitosterol ÏàËÆ¶È:78.5% Natural Product Research and Development 2004 16 213-214 STUDIES ON LIPOSOLUBLE CONSTITUENTS OF HUPERZIA CRISPATE CHING PEI Gang;; ZHOU Pu-hua; HE Gui-xia; DU Fang-lu; JIANG Dao-song Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-sitosterol ÏàËÆ¶È:78.5% Zeitschrift f¨¹r Naturforschung C 2003 58 441-445 Feeding Stimulative Activity of Steroidal and Secoiridoid Glucosides and Their Hydrolysed Derivatives toward the Olive Weevil (Dyscerus perforatus) E. Kadowaki, Y. Yoshida, N. Baba, and S. Nakajima Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:78.5% Molecules 2013 18 1325-1336 Chemical Constituents of Caesalpinia decapetala (Roth) Alston Xiao-Hua Wei, Sheng-Jie Yang, Na Liang, De-Yu Hu, Lin-Hong Jin, Wei Xue and Song Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . ¦Â-sitosterol ÏàËÆ¶È:78.5% Chemistry and Industry of Forest Products 2013 33 133-136 Chemical Constituents from the Branch of Litsea cubeba ( Lour. ) Pers. CHEN Zhan-juan, BI He-ping, FAN Chao-jun, BAO Chang-yu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:78.5% Natural Product Research and Development 2013 25 1367-1369 Study on the Chemical Constituents of Fruticosa potentilla L. XU Xiao-jie, WANG Wei, WANG Yu-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . ¦Â-Sitosterol ÏàËÆ¶È:78.5% Guihaia 2014 34 155-159 Study on the chemical constituents of Peristrophe roxburghiana GE Li, LAN Liu-Feng, BAO Hui-Bin, YANG Ke-Di Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-04-02 19:57:37
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
yetta_he: ½ð±Ò+20, ¡ïÓаïÖú 2015-04-02 20:15:44
yetta_he: ½ð±Ò+20, ¡ïÓаïÖú 2015-04-02 20:15:44
|
²éѯ½á¹û£º¹²²éµ½785¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-sitosterol C29H58O ÏàËÆ¶È:85.1% Journal of Agricultural and Food Chemistry 1989 37 1363-1367 Isolation of compounds with antimutagenic activity from Savoy Chieftain cabbage Terence Lawson, Janet Nunnally, Betty Walker, Edward Bresnick, Desmond Wheeler, Maureen Wheeler Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 24-oxochol-5-en-3¦Â-ol C27H44O2 ÏàËÆ¶È:83.3% Steroids 2009 74 81-87 A facile synthesis of C-24 and C-25 oxysterols by in situ generated ethyl(trifluoromethyl)dioxirane Shoujiro Ogawa, Genta Kakiyama, Akina Muto, Atsuko Hosoda, Kuniko Mitamura, Shigeo Ikegawa, Alan F. Hofmann, Takashi Iida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 23-Iodo-24-norchol-5-en-3¦Â-ol C23H37OI ÏàËÆ¶È:82.6% Steroids 2005 70 551-562 Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Alexey V. Antonchick, Andrey P. Antonchick, Bernd Schneider Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . N-Methyl-3¦Â-hydroxy-¡÷5-cholenamide C25H41NO2 ÏàËÆ¶È:82.6% Bioorganic & Medicinal Chemistry 2013 21 5297-5309 Structure¨Cactivity relationship studies of Niemann-Pick type C1-like 1 (NPC1L1) ligands identified by screening assay monitoring pharmacological chaperone effect Fumika Karaki, Kenji Ohgane, Kosuke Dodo, Yuichi Hashimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-sistosterol C29H50O ÏàËÆ¶È:82.1% Natural Product Sciences 2007 13 220-224 Antioxidant Activity of Cholesterol Derived from Silkworm Pupae Heo, Jung-Eun; Ryu, Jae-Ha; Jeong, Hye-Kyoung; Chung, Wan-Tae; Ahn, Mi-Young Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . [28-pro-R-2H]-clionasterol ÏàËÆ¶È:82.1% Tetrahedron Letters 2002 43 5479-5481 Mechanism of clerosterol biosynthesis in Ajuga hairy roots: stereochemistry of C-28 methylation of 24-methylene sterol Takeshi Koami, Kiyoshi Ohyama, Yoshinori Fujimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . [28-pro-S-2H]-clionasterol ÏàËÆ¶È:82.1% Tetrahedron Letters 2002 43 5479-5481 Mechanism of clerosterol biosynthesis in Ajuga hairy roots: stereochemistry of C-28 methylation of 24-methylene sterol Takeshi Koami, Kiyoshi Ohyama, Yoshinori Fujimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-sitosterol ÏàËÆ¶È:82.1% Zeitschrift f¨¹r Naturforschung C 2003 58 441-445 Feeding Stimulative Activity of Steroidal and Secoiridoid Glucosides and Their Hydrolysed Derivatives toward the Olive Weevil (Dyscerus perforatus) E. Kadowaki, Y. Yoshida, N. Baba, and S. Nakajima Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:82.1% Molecules 2013 18 1325-1336 Chemical Constituents of Caesalpinia decapetala (Roth) Alston Xiao-Hua Wei, Sheng-Jie Yang, Na Liang, De-Yu Hu, Lin-Hong Jin, Wei Xue and Song Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-sitosterol ÏàËÆ¶È:82.1% Chemistry and Industry of Forest Products 2013 33 133-136 Chemical Constituents from the Branch of Litsea cubeba ( Lour. ) Pers. CHEN Zhan-juan, BI He-ping, FAN Chao-jun, BAO Chang-yu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Â-Sitosterol ÏàËÆ¶È:82.1% Guihaia 2014 34 155-159 Study on the chemical constituents of Peristrophe roxburghiana GE Li, LAN Liu-Feng, BAO Hui-Bin, YANG Ke-Di Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . ¦Â-sitosterol ÏàËÆ¶È:82.1% Chinese Journal of Modern Applied Pharmacy 2009 26 460-462 Studies on the Chemical Constituents in Ranunculus muricatus L WANG Ling-jie, GAO Xiao-zhong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . campesterol ÏàËÆ¶È:82.1% Chinese Pharmaceutical Journal 2012 47 500-503 Study on Chemical Constituents of Rosa chinensis Jacq. Flower WANG Xiao-yan; WANG Wen-wen; ZHOU Yong-hui; JIANG Xin-ke; JING Lin-lin; JIA Lu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Â-sitosterol ÏàËÆ¶È:82.1% Korean Journal of Pharmacognosy 2013 44 1-5 Isolation of Compounds having Inhibitory Activity toward Tyrosinase from Receptaculum Nelumbinis Hyun Woo Cho, Won Seok Jung, Byeong Gwan An, Jung Hee Cho and Su Young Jung Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Â-sitosterol ÏàËÆ¶È:82.1% Northwest Pharmaceutical Journal 2013 28 241-244 Study on chemical constituents of Arenaria kansuensis Maxim. ¢ô LEI Ning, L¨¹ Yali, DU Shushan, DENG Zhiwei, MA Ping Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-sitosterol ÏàËÆ¶È:82.1% Chinese Joumal of Experimental Traditional Medical Fomulae 2011 17 118-120 Research on Chemical Constituents of Ethyl Acetate Fraction from Li Nationality Medicine Elaeagnus gonyanthes Caulis et Folium WEI Na, WANG Yong, LI Pei-pei, LI Hong-fu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:81.4% Chemical & Pharmaceutical Bulletin 1993 41 2007-2009 Constituents of Prunus zippeliana Leaves and Branches Junichi KITAJIMA and Yasuko TANAKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . ¦Â-sitosterol ÏàËÆ¶È:81.4% Acta Botanica Boreali-Occidentalia Sinica 2004 24 1093-1095 Studies on chemical constituents from tibetan medioine Elsholtzia ianthina DNG Chen-xu, ZHOU Ling-yun, JILAN-JU, JIWEN-he, MA Yu-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:81.4% Steroids 2005 70 886-895 Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-sitosterol ÏàËÆ¶È:81.4% China Journal of Chinese Materia Medica 2003 28 237-239 Studies on Chemical Constituents in the Peels of Citrus changshan-huyou (I) ZHAO Xxuemei, YE Xingqian, XI Yufang, ZHU Dayuan, JIANG Shanhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . ¦Â-sitosterol ÏàËÆ¶È:81.4% Korean Journal of Pharmacognosy 2005 36(2) 145-150 Phytochemical Constituents of Cirsium nipponicum (MAX.) Makino Lee, Jong-Hwa; Lee, Kang-Ro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2015-04-02 20:01:29













»Ø¸´´ËÂ¥