±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 329  |  »Ø¸´: 1

swaucq

½ð³æ (ÕýʽдÊÖ)

[ÇóÖú] ΢Æ×ÇóÖú»¯ºÏÎï½á¹¹

18.4,19.4,30.7,31.4,31.4,35.3,38.8,55.6,66.5,66.7,74.1,99.4,106.0,107.0,144.5,161.9,163.8,164.3
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

²»±°²»¿º
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

ÌìÏÂÎÞË«ts

ľ³æ (ÕýʽдÊÖ)

¡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
swaucq: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-07-06 20:21:31
²éѯģʽ£ºÄ£ºý²éѯ
̼Æ×Êý¾ÝÊäÈ룺
°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺
21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

ÈܼÁÑ¡Ï
Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨)
ÏàËÆ¶È£º   %(ÏàËÆ¶È>=50%)



²éѯ½á¹û£º¹²²éµ½24¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     asperentin-8-O-methyl ether
C17H22O5     ÏàËÆ¶È:88.8%
Zeitschrift f¨¹r Naturforschung C          2012          67c          587-593
Plant Growth Activities of Aspyran, Asperentin,and its Analogues Produced by the Fungus Aspergillus sp.
Yasuo Kimura, Naomi Shimomura, Fumiaki Tanigawa, Shozo Fujioka, and Atsumi Shimad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     MT-5
    ÏàËÆ¶È:83.3%
Chemical & Pharmaceutical Bulletin          1999          47          1426-1432
Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens
Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     MT-5
    ÏàËÆ¶È:61.1%
Chemical & Pharmaceutical Bulletin          1999          47          1426-1432
Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens
Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     MT-4
    ÏàËÆ¶È:55.5%
Chemical & Pharmaceutical Bulletin          1999          47          1426-1432
Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens
Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     asperentin-6-O-methyl ether
C17H22O5     ÏàËÆ¶È:55.5%
Zeitschrift f¨¹r Naturforschung C          2012          67c          587-593
Plant Growth Activities of Aspyran, Asperentin,and its Analogues Produced by the Fungus Aspergillus sp.
Yasuo Kimura, Naomi Shimomura, Fumiaki Tanigawa, Shozo Fujioka, and Atsumi Shimad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Paecilomycin L
C19H26O7     ÏàËÆ¶È:52.6%
Tetrahedron Letters          2013          54          2648-2650
Paecilomycins J¨CM, four new ¦Â-resorcylic acid lactones from Paecilomyces sp. SC0924
Liang-Xiong Xu, Ping Wu, Huan-Huan Wei, Jing-Hua Xue, Xiao-Peng Hu, Xiao-Yi Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (7'R)-7-hydroxyspirolaxine
C23H32O7;     ÏàËÆ¶È:52.1%
Chemistry & Biodiversity          2007          Vol. 4          2772
Microbial Transformation of Spirolaxine, a Bioactive Undecaketide Fungal Metabolite from the Basidiomycete Sporotrichum laxum
Gianluca Nasini, Adriana Bava, Giovanni Fronza, and Giuseppe Giannini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (¡À)-2-(4-Hydroxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)-7-methyl-4-phenyl-3,4-dihydro-2Hpyrano-[3,2-c]pyridin-5(6H)-one
C21H20N2O4     ÏàËÆ¶È:50%
Molecules          2009          14          4973-4986
Synthesis and Phytotoxic Activity of New Pyridones Derived from 4-Hydroxy-6-Methylpyridin-2(1H)-one
Antonio Jacinto Demuner, Vania Maria Moreira Valente, Luiz Cl¨¢udio Almeida Barbosa, Akshat Rathi, Timothy J. Donohoe and Amber L. Thompson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     MT-4
    ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1999          47          1426-1432
Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens
Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     11¦Â-hydroxy-11¦Â,1-dihydromedicarpin
C16H16O5     ÏàËÆ¶È:50%
Phytochemistry          1998          48          187-190
Pterocarpans from Ononis viscosa subsp. breviflora
Alejandro F. Barrero, Eduardo Cabrera, Ignacio Rodriguez Garcia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3,4-dihydro-6,8-dimethoxxy-3-(2-hydroxypentyl)isocoumarin
C16H22O5     ÏàËÆ¶È:50%
Journal of Natural Products          2010          73          75-78
An Antimycobacterial Cyclodepsipeptide from the Entomopathogenic Fungus Ophiocordyceps communis BCC 16475
Rachada Haritakun, Malipan Sappan, Rapheephat Suvannakad, Kanoksri Tasanathai and Masahiko Isaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     capillofuranocarboxylate
C18H24O5     ÏàËÆ¶È:50%
Journal of Natural Products          2010          73          771-775
Antiviral and Anti-inflammatory Metabolites from the Soft Coral Sinularia capillosa
Shi-Yie Cheng, Ki-Jhih Huang, Shang-Kwei Wang, Zhi-Horng Wen, Pei-Wen Chen and Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     tomentonone
    ÏàËÆ¶È:50%
Phytochemistry          1997          46          1423-1429
Prenylated xanthonoids from Calophyllum apetalum
Munekazu Iinuma, Tetsuro Ito, Hideki Tosa, Toshiyuki Tanaka, Ryoko Miyake, Veliah Chelladurai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     cladosporin
    ÏàËÆ¶È:50%
Journal of Natural Products          1993          Vol 56          1397
Isocladosporin, a Biologically Active Isomer of Cladosporin from Cladosporium cladosporioides
John M. Jacyno, John S. Harwood, Horace G. Cutler, Mee-Kyoung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (10'R)-5-(10-hydroxytridecyl)-1-O-methylresorcinol
C20H34O3     ÏàËÆ¶È:50%
Phytochemistry          1994          36          189-194
Resorcinol derivatives and other components from Ononis viscosa subsp. breviflora
Alejandro.F. Barrero, Eduardo Cabrera, Ignacio Rodr¨ªguez, Eva M. Fern¨¢ndez-Gallego
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (20S)-16-Ene-22-thia-24-nor-26,27-dimethyl-8-ol
C18H32O2S     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2008          16          1796-1815
Synthesis and structure¨Cactivity relationships of 16-ene-22-thia-1¦Á,25-dihydroxy-26,27-dimethyl-19-norvitamin D3 analogs having side chains of different sizes
Hajime Takaku, Yukiko Miyamoto, Shiori Asami, Mika Shimazaki, Sachiko Yamada, Keiko Yamamoto, Nobuyuki Udagawa, Hector F. DeLuca, Masato Shimizu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     10¦Â-hydroxymonocillin II
C18H22O5     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2009          17          4622-4635
Synthesis and structure¨Cactivity relationships of radicicol derivatives and WNT-5A expression inhibitory activity
Hideki Shinonaga, Toshiya Noguchi, Akiko Ikeda, Mari Aoki, Natsuko Fujimoto, Akira Kawashima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     cladosporin
C16H20O5     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2012          48          467-469
Secondary metabolites of the marine fungus Aspergillus ustus KMM 4640
G. K. Oleinikova, V. A. Denisenko, N. N. Slinkina and Sh. Sh. Afiyatullov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     2-((4S,6S)-6-(2-((R,Z)-3-methoxy-2-methylbut-1-enyl)oxazol-4-yl)-2,2-dimethyl-1,3-dioxan-4-yl)ethanol
C17H27NO5     ÏàËÆ¶È:50%
Journal of the American Chemical Society          2010          132          10286-10292
Total Synthesis of Enigmazole A from Cinachyrella enigmatica. Bidirectional Bond Constructions with an Ambident 2,4-Disubstituted Oxazole Synthon
Colin K. Skepper, Tim Quach and Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     4-((4S,6R)-6-(2-iodoethyl)-2,2-dimethyl-1,3-dioxan-4-yl)-2-((R,Z)-3-methoxy-2-methylbut-1-enyl)oxazole
C17H26NO4I     ÏàËÆ¶È:50%
Journal of the American Chemical Society          2010          132          10286-10292
Total Synthesis of Enigmazole A from Cinachyrella enigmatica. Bidirectional Bond Constructions with an Ambident 2,4-Disubstituted Oxazole Synthon
Colin K. Skepper, Tim Quach and Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     3-(2-methoxy-1-methyl-vinyl)-4,6,6-trimethyl-5-methylene-3-vinyl-bicyclo[2.2.2]octan-2-one
C18H26O2     ÏàËÆ¶È:50%
Canadian Journal of Chemistry          2004          82          227-239
Part 2: Efficient strategies for the construction of variably substituted bicyclo[5.3.1]undecenones (AB-taxane ring systems) and their conversion to tricyclo[9.3.1.03,8]pentadecenones (ABC taxane ring systems) and bicyclo[2.2.2]octanones
Nidia P Villalva-Serv¨ªn, Alain Laurent, Alex G Fallis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     E-1-(Tetrahydro-2-pyranyloxy)-8-dodecen-3,6-diyne
    ÏàËÆ¶È:50%
Journal of the Brazilian Chemical Society          2004          15          372-377
Electroantennographic Responses of Heterotermes tenuis (Isoptera: Rhinotermitidae) to Synthetic (3Z,6Z,8E)-Dodecatrien-1-ol
Luciane G. Batista-Pereira, M¨¢rcio G. dos Santos, Arlene G. Corr¨ºa, João B. Fernandes, C¨¦lia R. R. C. Dietrich, Dilmar A. Pereira, Odair C. Bueno and Ana Maria Costa-Leonardo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     9-methylene-9,11-secopodocarp-11-ene
C18H30     ÏàËÆ¶È:50%
Australian Journal of Chemistry          1981          34          1959-1973
Structure odour studies with some diterpene derived acetals
PK Grant and DD Rowan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     N-(L-Valyl-L-methionyl)-8-amino-2,6-anhydro-3,8-dideoxy-8-glycero-D-talo-octonic Acid
    ÏàËÆ¶È:50%
Journal of Medicinal Chemistry          1987          30          2309-2313
Design and synthesis of peptide derivatives of a 3-deoxy-D-manno-2-octulosonic acid (KDO) analog as novel antibacterial agents acting upon lipopolysaccharide biosynthesis
Alf Claesson, Anita M. Jansson, Brian G. Pring, Stephen M. Hammond, Bertil Ekstroem
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-07-06 14:57:06
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ swaucq µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 085600£¬×¨Òµ¿Î»¯¹¤Ô­Àí£¬321·ÖÇóµ÷¼Á +6 ´ó²öС×Ó 2026-03-28 6/300 2026-04-03 22:38 by JimmyQAQ
[¿¼ÑÐ] Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤085600£¬Çóµ÷¼Á +17 ³ÔµÄ²»ÉÙ 2026-04-02 17/850 2026-04-03 21:48 by qlm5820
[¿¼ÑÐ] 0856£¬269·ÖÇóµ÷¼Á +15 ÓÐѧÉϾÍÐÐÇóÇóÁ 2026-03-30 18/900 2026-04-03 16:50 by melodiousnow
[¿¼ÑÐ] Çóµ÷¼Á²»Ìôרҵ +3 xrh030412 2026-04-01 3/150 2026-04-03 14:40 by µªÆøÆøÆø
[¿¼ÑÐ] 289-Çóµ÷¼Á +4 ÕâÀïÊÇ_ 2026-04-03 4/200 2026-04-03 14:23 by 1753564080
[¿¼ÑÐ] 273Çóµ÷¼Á +20 ÀîÜÆÐÂ1 2026-03-31 20/1000 2026-04-03 09:58 by linyelide
[¿¼ÑÐ] ÍÁľ304Çóµ÷¼Á +4 ÍÃͻͻͻ£¬ 2026-04-02 5/250 2026-04-02 21:16 by ÍÃͻͻͻ£¬
[¿¼ÑÐ] Ò»Ö¾Ô¸±±¾©¿Æ¼¼²ÄÁÏ¿ÆÑ§Ó빤³Ì288·Ö£¬Çóµ÷¼Á +14 Êdz½°¡ 2026-04-02 14/700 2026-04-02 21:10 by dongzh2009
[¿¼ÑÐ] 279Çóµ÷¼Á +5 ¸µÎÄÇï 2026-04-02 5/250 2026-04-02 18:10 by ±ÊÂä½õÖÝ
[¿¼ÑÐ] 348Çóµ÷¼Á +11 zzzzyk123 2026-04-01 11/550 2026-04-02 16:52 by Wang200018
[¿¼ÑÐ] 26¿¼Ñе÷¼Á +4 Wnz.20030617 2026-04-01 5/250 2026-04-02 16:11 by 1939136013¹·×³
[¿¼ÑÐ] 267Çóµ÷¼Á +13 uiybh 2026-03-31 13/650 2026-04-01 10:25 by ̽123
[¿¼ÑÐ] Çóµ÷¼Á ÉúÎïѧ 377·Ö +6 zzll03 2026-03-31 6/300 2026-03-31 17:33 by ÌÆãå¶ù
[¿¼ÑÐ] ÎïÀíѧµ÷¼Á +4 СÑò36 2026-03-30 4/200 2026-03-31 16:16 by lishahe
[¿¼ÑÐ] 353Çóµ÷¼Á +3 ½­ÉÏ·ã_26 2026-03-28 3/150 2026-03-31 15:53 by jp9609
[¿¼ÑÐ] 085601 329·Öµ÷¼Á +6 yzsa12 2026-03-31 6/300 2026-03-31 15:23 by yanflower7133
[¿¼ÑÐ] 297 µØÀíѧ070500 ¸´ÊÔÇóµ÷¼Á +3 СԲȦȦooo 2026-03-30 3/150 2026-03-30 21:05 by ÓàÕðyz
[¿¼ÑÐ] µ÷¼Á +4 GK72 2026-03-30 4/200 2026-03-30 20:32 by dick_runner
[¿¼ÑÐ] 293Çóµ÷¼Á +3 ĩδmm 2026-03-30 5/250 2026-03-30 17:23 by Íõ±£½Ü33
[¿¼ÑÐ] 291Çóµ÷¼Á +5 Y-cap 2026-03-29 6/300 2026-03-29 13:18 by mumin1990
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û