±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 1797  |  »Ø¸´: 6

tianxinyan

Òø³æ (СÓÐÃûÆø)

[ÇóÖú] ÇóÖúÒ»¸ö»¯ºÏÎïάÆÕÊý¾Ý

13C NMR (101 MHz, CDCL3)    14.108,22.688£¬28.842,29,671,30.730,30.944£¬31.897,61.227,61.341,68.058, 103.391, 108.787,114.264,130.303,130.978,146.551, 154.619,155.334,183.494, 184.062
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

»ð¼ý´©Æ¨Æ¨

ľ³æ (ÕýʽдÊÖ)

µØÇòÇò³¤

ÔõôÓÖÊÇÕâÑù ÓÖÓÐÖÐÎıêµãÓÖÓÐÓ¢Îıêµã Öмä¿ÕµÄ¸ñ´óСҲ²»Ò»Ñù
ÉþÃüÊÇÈë´ÎµÄ¾®²Â
2Â¥2012-10-06 08:02:48
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

»ð¼ý´©Æ¨Æ¨

ľ³æ (ÕýʽдÊÖ)

µØÇòÇò³¤

14.1,22.6,28.8,29,6,30.7,30.9,31.8,61.2,61.3,68.0,103.3,108.7,114.2,130.3,130.9,146.5,154.6,155.3,183.4,184.1

Ï´ÎÒª¸Ä³ÉÕâÑù£¡£¡
ÉþÃüÊÇÈë´ÎµÄ¾®²Â
3Â¥2012-10-06 08:05:33
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

»ð¼ý´©Æ¨Æ¨

ľ³æ (ÕýʽдÊÖ)

µØÇòÇò³¤

¡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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
tianxinyan: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú, лл 2012-10-06 10:45:51
²éѯ½á¹û£º¹²²éµ½28¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
--------------------------------------------------------------------------------

1 .     (3R)-Astragaluquinone
C17H16O6     ÏàËÆ¶È:66.6%
Phytochemistry          1994          36          1387-1389
Antimicrobial isoflavans from Astragalus species
Nadia A. El-Sebakhy, Aya M. Asaad, Rokia M. Abdallah, Soad M. Toaima, Maged S. Abdel-Kader, Frank R. Stermitz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     Pendulone
    ÏàËÆ¶È:66.6%
Journal of China Pharmaceutical University          2002          33          274-276
Isoflavans and Isoflavone from Astragalus hoantchy
ZHAO Ming; DUAN Jin Ao; HUANG Wen Zhe; ZHOU Rong Han; CHE Chun Tao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     (3R)-7-Hydroxy-3',4'-dimethoxyisoflavan-2',5'-quinone
C17H16O6     ÏàËÆ¶È:66.6%
Natural Product Communications          2008          3          1491-1494
Isoflavonoids from an Egyptian Collection of Colutea istria
Mohamed M. Radwan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     pendulone
C17H16O6     ÏàËÆ¶È:66.6%
Natural Product Communications          2011          6          1645-1650
Antiparasitic and Antimicrobial Isoflavanquinones from Abrus schimperi
Aziz A. Rahman, Volodymyr Samoylenko, Surendra K. Jain, Babu L. Tekwani, Shabana I. Khan, Melissa R. Jacob, Jacob O. Midiwo, John P. Hester, Larry A. Walker and Ilias Muhamma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     kiritiquinone dimethyl ether
C30H50O4     ÏàËÆ¶È:59.0%
Indian Journal of Chemistry          2010          49B          1637-1641
A new quinone from Maesa indica (roxb.)A.dc,(myrsinaceae)
Gina R Kuruvilla,M Neeraja,A Srikrishna* G S R Subba Rao,A V S Sudhakar &Padma Venkatasubramanian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     compound 8
    ÏàËÆ¶È:57.1%
Phytochemistry          2003                   855-862
Benzoquinone derivatives of Myrsine africana and Maesa lanceolata
Lawrence O. Arot Manguro, Jacob O. Midiwo, Wolfgang Kraus, Ivar Ugi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

7 .     compound 2a
    ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          1987          35          3016-3020
Antitumor Principles from Ginkgo biloba L.
HIDER ITOKAWA,NOBUO TOTSUKA,KEISUKE NAKAHARA,KOICHI TAKEYA,JEAN-PIERRE LEPOITTEVIN and YOSHINORI ASAKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

8 .     secundiflorol G
    ÏàËÆ¶È:57.1%
Phytochemistry          1998          48          1187-1193
Isoflavonoids from Sophora secundiflora, S. arizonica and S. gypsophila
Toshiyuki Tanaka, Masayosi Ohyama, Munekazu Iinuma, Yoshiaki Shirataki, Manki Komatsu, Charles L. Burandt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

9 .     (3R)-colutequinone
C18H18O6     ÏàËÆ¶È:57.1%
Phytochemistry          1996          43          377-380
Colutequinone and colutehydroquinone, antifungal isoflavonoids from Colutea arborescens
Paul W. Grosvenor, David O. Gray
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

10 .     5-(8'Z-Ê®Îå̼ϩ)¼ä±½¶þ·Ó
C21H34O2     ÏàËÆ¶È:57.1%
Chinese Traditional and Herbal Drugs          2004          35          18-20
ÒøÐÓÍâÖÖÆ¤Ìþ»ù·Ó¼°Ìþ»ù·ÓËáÀà³É·ÖÑо¿
ÀîºéÇì,ºÎÕÕ·¶,ÕÅÓÂÃñ,SINAŸ Pierre
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

11 .     lanneaquinol
C23H38O2     ÏàËÆ¶È:52.3%
Journal of Natural Products          1997          60          116-121
Novel Cytotoxic, Alkylated Hydroquinones from Lannea welwitschii
Amiram Groweiss, John H. Cardellina II, Lewis K. Pannell, Duangchan Uyakul, Yoel Kashman, and Michael R. Boyd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

12 .     abruquinone F
C19H20O8     ÏàËÆ¶È:52.3%
Planta Medica          1995          61          307-312
Potent Antiplatelet, Anti-Inflammatory and Antiallergic Isoflavanquinones from the Roots of Abrus precatorius
Sheng-ChuKuo ,Sheng-Chih Chen .Lin-HuiChen ,Jin-BinWa Jih-Pyang Wang andChe-MingTeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

13 .     (4Z,8E)-1-[(Tetrahydropyran-2-yl)oxy]tetradeca-4,8-diene
    ÏàËÆ¶È:52.3%
Chemistry & Biodiversity          2009          6          1388-1403
Syntheses, Characterizations, and Biological Activities of Tetradeca-4,8-dien-1-yl Acetates as Sex Attractants of Leaf-Mining Moth of the Genus Phyllonorycter (Lepidoptera: Gracillariidae)
Ilme Liblikas, Raimondas Moz¨¹raitis, Ellen M. Santangelo, Remigijus Noreika, and Anna-Karin Borg-Karlson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

14 .     5-(Z-heptadec-8-enyl) resorcinol
    ÏàËÆ¶È:52.3%
Journal of Asian Natural Products Research          2007          9          545-549
Resorcinol derivatives from Ardisia maculosa
YING ZHENG and FENG-E WU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

15 .     5-[1'-(docosa-2'E,5'E-dienyl)]-1,4-dioxin-2,3-dione
C26H44O4     ÏàËÆ¶È:52.3%
Natural Product Research          2009          23          1740-1745
Two new dioxin derivatives from the aerial parts of Lawsonia alba
Bina S. Siddiqui; Nizam Uddin; Sabira Begum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

16 .     AR17:1
C23H38O2     ÏàËÆ¶È:52.3%
Phytochemistry          1996          41          1485-1489
Isolation of 5-(8'Z-heptadecenyl)-resorcinol from etiolated rice seedlings as an antifungal agent
Yoshikatsu Suzuki, Yasuaki Esumi, Hiroshi Hyakutake, Yoshiki Kono, Akira Sakurai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

17 .     trilinoleyl glyceride
    ÏàËÆ¶È:52.3%
Phytochemistry          1991          30          3369-3377
Fern constituents: Triterpenoids isolated from Polypodium vulgare, P. fauriei and P. virginianum
YŌko Arai, Motoko Yamaide, Sachiko Yamazaki, Hiroyuki Ageta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

18 .     4-(4-(Hexadecyloxy)benzyl)phenol
C29H44O2     ÏàËÆ¶È:52.3%
Canadian Journal of Chemistry          2010          88          1003-1008
Deoxygenation of diarylmethanols with dilute mineral acid
Kyle A. Hope-Ross and John F. Kadla
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

19 .     (3-Chloro-5-hexyl-2,6-dimethoxyphenyl)(4,5-dichloropyrrol-3-yl)methanone
C19H22O3NCl3     ÏàËÆ¶È:52.3%
Organic Letters          2009          Vol.11,No.8          1693-1695
Revised Structure and Synthesis of Celastramycin A, A Potent Innate Immune Suppressor
Haruhisa Kikuchi, Mizuki Sekiya, Yasuhiro Katou, Kazunori Ueda,Takahiro Kabeya, Shoichiro Kurata, and Yoshiteru Oshima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

20 .     (3-Chloro-5-hexyl-2,6-dimethoxyphenyl)pyrrol-2-ylmethanone
C19H24O3NCl     ÏàËÆ¶È:52.3%
Organic Letters          2009          Vol.11,No.8          1693-1695
Revised Structure and Synthesis of Celastramycin A, A Potent Innate Immune Suppressor
Haruhisa Kikuchi, Mizuki Sekiya, Yasuhiro Katou, Kazunori Ueda,Takahiro Kabeya, Shoichiro Kurata, and Yoshiteru Oshima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

21 .     monoene
    ÏàËÆ¶È:52.3%
Phytochemistry          1989          28          161-164
Resorcinol derivatives and other components of Ononis speciosa
Alejandro F. Barrero,Juan F. Sanchez,Antonio Barr¨®n,Fernando Corrales,Ignacio Rodriguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

22 .     3-(4-nitrophenyl)-5-pentadecyl-1,3-benzoxazine-2,4-dione
C29H38N2O5     ÏàËÆ¶È:52.3%
Heterocycles          2005          65          311-318
New Application of Triphosgene in a Convenient Synthesis of 3-Aryl-1,3-benzoxazine-2,4-diones from Anacardic Acids
In¨ºs Sabioni Resck,* Maria Lucilia dos Santos, and Luiz Antonio Soares Romeiro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

23 .     compound 6
    ÏàËÆ¶È:52.3%
Heterocycles          2005          65          823-841
Yb(OTf)3-catalyzed Vinylogous Mannich Reaction of Trialkylsilyloxyfuran
Sylvain Oudeyer, Bruno Dudot, and Jacques Royer*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

24 .     5-(8-pentadecenyl)-1,3-benzenediol
    ÏàËÆ¶È:52.3%
Chinese Traditional and Herbal Drugs          2006          37          818-821
Phenolic constituents in Embelia ribes
LIN Peng-cheng; LI Shuai; WANG Su-juan; YANG Yong-chun; SHI Jian-gong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

25 .     dilinolein
    ÏàËÆ¶È:52.3%
Chinese Traditional and Herbal Drugs          2001          32          291-293
Isolation and identification of lipide from Setaria italica ¢ñ
WANG Hai tang; SHI Qing liang; YIN Wei ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

26 .     (+)-Isomucronulatol
    ÏàËÆ¶È:52.3%
Pharmazie          2002          57          75-76
Isoflavans from Sphaerophysa salsula
Zhong-Jun Ma - Bai-Ling Hou - Jin-Hui Wang - Xian Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

27 .     compound 27
C57H74F2O4     ÏàËÆ¶È:50%
European Journal of Organic Chemistry          2010                   3049-3067
Synthesis of Fluorine-Containing Molecular Rotors and Their Assembly on Gold Nanoparticles
Dominic Thibeault, Mich¨¨le Auger and Jean-François Morin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

28 .     (Z)-2-(Icos-11-enoyloxy)propane-1,3-diyl dibutyrate
C31H56O6     ÏàËÆ¶È:50%
Tetrahedron          2012          68          5422-5428
Application of chemoenzymatic hydrolysis in the synthesis of 2-monoacylglycerols
Kyle M. Whitten, Alexandros Makriyannis, Subramanian K. Vadivel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------
ÉþÃüÊÇÈë´ÎµÄ¾®²Â
4Â¥2012-10-06 08:05:46
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

xiaohu918

½û³æ (ÕýʽдÊÖ)

±¾ÌûÄÚÈݱ»ÆÁ±Î

5Â¥2012-10-06 08:29:01
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

tianxinyan

Òø³æ (СÓÐÃûÆø)

ÒýÓûØÌû:
3Â¥: Originally posted by »ð¼ý´©Æ¨Æ¨ at 2012-10-06 08:05:33
14.1,22.6,28.8,29,6,30.7,30.9,31.8,61.2,61.3,68.0,103.3,108.7,114.2,130.3,130.9,146.5,154.6,155.3,183.4,184.1

Ï´ÎÒª¸Ä³ÉÕâÑù£¡£¡

лл£¬Ï´ÎÒ»¶¨×¢Ò⣡
6Â¥2012-10-06 10:46:26
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

»ð¼ý´©Æ¨Æ¨

ľ³æ (ÕýʽдÊÖ)

µØÇòÇò³¤

ÒýÓûØÌû:
5Â¥: Originally posted by xiaohu918 at 2012-10-06 08:29:01
ÇëÎÊÕâ¸öÊÇÔÚÄÄÀï²éµ½µÄ°¡£¿...

΢Æ×Êý¾Ý
ÉþÃüÊÇÈë´ÎµÄ¾®²Â
7Â¥2012-10-07 07:57:16
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ tianxinyan µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] Çóµ÷¼Á +4 QiMing7 2026-03-25 5/250 2026-03-29 21:10 by ÌÆãå¶ù
[¿¼ÑÐ] 279Çóµ÷¼Á +4 µûÎèÇáÈÆ 2026-03-29 4/200 2026-03-29 09:45 by laoshidan
[¿¼ÑÐ] 329Çóµ÷¼Á +7 ÐÇÒ°? 2026-03-26 7/350 2026-03-29 06:43 by 544594351
[¿¼ÑÐ] 321Çóµ÷¼Á +7 è±Óñ~~ 2026-03-25 8/400 2026-03-29 06:41 by 544594351
[¿¼ÑÐ] 315Çóµ÷¼Á +4 akie... 2026-03-28 5/250 2026-03-28 21:05 by zhq0425
[¿¼ÑÐ] 332Çóµ÷¼Á +4 @MZB382400 2026-03-28 4/200 2026-03-28 21:02 by ÌÆãå¶ù
[¿¼ÑÐ] Ò»Ö¾Ô¸»ªÀí£¬ÊýÒ»Ó¢Ò»285ÇóAÇøµ÷¼Á +8 AZMK 2026-03-25 12/600 2026-03-28 18:15 by AZMK
[¿¼ÑÐ] ѹ¹ú¼ÒÒ»ÇøÏߣ¬Çóµ¼Ê¦ÊÕÁô£¬Óж÷±ØÐ»£¡ +7 ÃÔÈ˵Ĺþ¹þ 2026-03-28 7/350 2026-03-28 16:47 by ´ß»¯´ó°×
[¿¼ÑÐ] 283Çóµ÷¼Á +3 A child 2026-03-28 3/150 2026-03-28 15:41 by ms629
[¿¼ÑÐ] 312£¬ÉúÎïѧÇóµ÷¼Á +3 СÒëͬѧabc 2026-03-28 3/150 2026-03-28 15:32 by ÂäÉ˼
[¿¼ÑÐ] Ò»Ö¾Ô¸ÏÃÃÅ´óѧ»¯Ñ§Ñ§Ë¶307Çóµ÷¼Á +10 y7czhao 2026-03-26 10/500 2026-03-28 14:23 by ÌÆãå¶ù
[¿¼ÑÐ] 0703»¯Ñ§/290Çóµ÷¼Á/±¾¿Æ¾­Àú·á¸»/¹¤¿ÆÒ²¿É +9 µ¤ÇàÄÌ¸Ç 2026-03-26 10/500 2026-03-28 07:45 by barnett0632
[¿¼ÑÐ] 315µ÷¼Á +4 0860Çóµ÷¼Á 2026-03-26 5/250 2026-03-27 11:23 by wangjy2002
[¿¼ÑÐ] Çóµ÷¼Á Ò»Ö¾Ô¸ ±¾¿Æ ±±¿Æ´ó »¯Ñ§ 343 +6 13831862839 2026-03-24 7/350 2026-03-26 22:57 by ²»³Ôô~µÄ؈
[¿¼ÑÐ] µ÷¼Á +4 èÖèÖyoyo 2026-03-26 4/200 2026-03-26 20:43 by fmesaito
[¿¼ÑÐ] ¡¾2026¿¼Ñе÷¼Á¡¿ÖÆÒ©¹¤³Ì 284·Ö ÇóÏà¹Ø×¨Òµµ÷¼ÁÃû¶î +4 Ô¬Û¼Û¼ 2026-03-25 8/400 2026-03-25 14:32 by lbsjt
[¿¼ÑÐ] 347Çóµ÷¼Á +4 L when 2026-03-25 4/200 2026-03-25 13:37 by cocolv
[¿¼ÑÐ] 292Çóµ÷¼Á +4 ¶ì¶ì¶ì¶î¶î¶î¶î¶ 2026-03-24 4/200 2026-03-24 16:41 by peike
[¿¼ÑÐ] 344Çóµ÷¼Á +3 desto 2026-03-24 3/150 2026-03-24 10:09 by ²«»÷518
[¿¼ÑÐ] 269Çóµ÷¼Á +4 ÎÒÏë¶ÁÑÐ11 2026-03-23 4/200 2026-03-23 21:25 by pswait
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û