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oyf8888

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[求助] 跪求微谱数据,衷心感谢! 已有1人参与

氘代氯仿
11.697,21.214,21.775,23.028,26.746,29.865,34.973,37.651,39.442,40.672,46.219,70.959,79.891,116.060,141.893
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oyf8888: 金币+12, ★★★很有帮助, 非常感谢!祝您一切顺利! 2013-12-27 16:52:36
查询模式:模糊查询
碳谱数据输入:
按从小到大顺序输入,数字间用英文半角逗号(,)分隔例如:
21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

溶剂选项:
匹配容差: (数字格式,可自行设定)
相似度:   %(相似度>=50%)



查询结果:共查到440个化合物(查询结果仅供参考)
1 .     oplodiol
    相似度:100%
Korean Journal of Pharmacognosy          2004          35(2)          152-156
Isolation of Melanin Biosynthesis Inhibitory Compounds from the Flowers of Magnolia denudata
Xu, Guang-Hua; Kim, Jeong-Ah; Park, Sung-Hee; Son, Ae-Ryang; Chang, Tae-Soo; Chang, Hyun-Wook; Chung, See-Ryun; Lee, Seung-Ho
Structure      13C NMR   碳谱模拟图
2 .     compound 12
    相似度:100%
Phytochemistry          1989          28          2717-2721
Sesquiterpenoids and phenolics of Pulicaria paludosa
Arturo San Feliciano,Manuel Medarde,Marina Gordaliza,Esther Del Olmo,José M. Miguel del Corral
Structure      13C NMR   碳谱模拟图
3 .     oplodiol
    相似度:100%
Phytochemistry          1983          22          1457-1459
Sesquiterpene alcohols and triterpenoids from Liatris microcephala
Werner Herz, Kinzo Watanabe
Structure      13C NMR   碳谱模拟图
4 .     oplodiol
    相似度:100%
Archives of Pharmacal Research          1997          20          363-367
Sesquiterpene components from the flower buds of Magnolia fargesii
Keun Young Jung, Dong Seon Kim, Sei Ryang Oh, Im Seon Lee and Jung Joon Lee, et al.
Structure      13C NMR   碳谱模拟图
5 .     Oplodiol
    相似度:100%
Archives of Pharmacal Research          2001          24          194-197
Phytochemical constituents of Artemisia japonica ssp. Littoricola
Hak Cheol Kwon and Kang Ro Lee
Structure      13C NMR   碳谱模拟图
6 .     oplodiol
C15H26O2     相似度:100%
Chemistry of Natural Compounds          2011          47          850-851
Sesquiterpenoids from Petasites tatewakianus
Wei-Dong Xie, Yan-Li Miao, Peng-Xiang Lai and Kyung-Ho Row
Structure      13C NMR   碳谱模拟图
7 .     oplodiol
    相似度:100%
Journal of the Chinese Chemical Society          2002          49          427-431
Cytotoxic Components from the Leaves of Schefflera taiwaniana
Yueh-Hsiung Kuo*, Jir-Mehng Lo and Yih-Fwu Chan
Structure      13C NMR   碳谱模拟图
8 .     eudesm-5-ene-1β,4α-diol
C15H26O2     相似度:93.3%
Indian Journal of Chemistry Section B          1999          38B          828-830
New sesquiterpene and other constituents from Artemissia arenaria
Wei Guo, Ri-Xia Zhu, Yan-Ping Shi& Zhong-Jian Jia
Structure      13C NMR   碳谱模拟图
9 .     oplodiol
    相似度:93.3%
Chinese Traditional and Herbal Drugs          2012          43          51-54
Chemical constituents in stems and leaves of Illicium simonsii
LIU Ji-feng; ZHANG Xue-mei; SHI Yao; ZHANG Quan; MA Yun-bao; CHEN Ji-jun
Structure      13C NMR   碳谱模拟图
10 .     6-Eudesmene-1β,4β-diol
    相似度:73.3%
Phytochemistry          1995          39          603-607
Sesquiterpenes from leaves of Cryptomeria japonica
Wen-Chiung Su, Jim-Min Fang, Yu-Shia Cheng
Structure      13C NMR   碳谱模拟图
11 .     compound 12a
    相似度:70.5%
Phytochemistry          1989          28          2717-2721
Sesquiterpenoids and phenolics of Pulicaria paludosa
Arturo San Feliciano,Manuel Medarde,Marina Gordaliza,Esther Del Olmo,José M. Miguel del Corral
Structure      13C NMR   碳谱模拟图
12 .     Caryolane-1,7α-diol
C15H26O2     相似度:66.6%
Chemical & Pharmaceutical Bulletin          2011          59          1430-1433
Sesquiterpenes from the Secondary Metabolites of Streptomyces sp.(YIM 56130)
Zhi YANG, Yabin YANG, Xueqiong YANG, Yong ZHANG, Lixing ZHAO, Lihua XU, and Zhongtao DING
Structure      13C NMR   碳谱模拟图
13 .     compound 20
C25H47NO4     相似度:66.6%
Journal of the American Chemical Society          1987          109          4940-4948
Stereorational total synthesis of (.+-.)-porantherine
David M. Ryckman, Robert V. Stevens
Structure      13C NMR   碳谱模拟图
14 .     (-)-(1R,2R,4R,6R,7S,9S)-4-acetyl-1,5,5,6,7-pentamethyltricyclo[4.3.0.02,9]nonan-8-one
C16H24O2     相似度:62.5%
Indian Journal of Chemistry Section B          2005          44B          1029-1039
Enantiospecific synthesis of sesquiterpenes from (R)-carvone. Synthesis of 3-thapsenol
Srikrishna,A; Anebouselvy,K
Structure      13C NMR   碳谱模拟图
15 .     (1S,3R,3aR,6S,7S,9aR)-decahydro-1-(hydroxymethyl)-1,7-dimethyl-3a,7-methano-3aH-cyclopentacyclooctene
C15H26O3     相似度:60%
Chemistry & Biodiversity          2006          Vol. 3          791
Four New Compounds from the Leaves of Acer truncatum
Lang-Ping Dong, Hai-Yang Liu, Wei Ni, Jun-Zhu Li, and Chang-Xiang Chen
Structure      13C NMR   碳谱模拟图
16 .     longifolene epoxide
    相似度:60%
Helvetica Chimica Acta          2003          Vol. 86          106
The Ozonolysis of Longifolene: A Tool for the Preparation of Useful Chiral Compounds. Configuration Determination of New StereogenicCenters by NMR Spectroscopy and X-Ray Crystallography
Vladimir Dimitrov, Gudrun Hopp Rentsch, Anthony Linden, and Manfred Hesse
Structure      13C NMR   碳谱模拟图
17 .     (-)-α-Chamipinene, (1S,6S,7S)-2,2,6,8-tetramethyltricyclo[5.3.1.01,6]undec-8-ene
C15H24     相似度:60%
Phytochemistry          2005          66          249-260
Sesquiterpenes from Cupressus macrocarpa foliage
Laurence G. Cool
Structure      13C NMR   碳谱模拟图
18 .     1β-Hydroxy-eudesma-5,11-diene
    相似度:60%
Phytochemistry          2004          65          127-137
ent-Clerodane diterpenes and other constituents from the liverwort Adelanthus lindenbergianus (Lehm.) Mitt.
Barbara Blä s, Josef Zapp, Hans Becker
Structure      13C NMR   碳谱模拟图
19 .     (1R,5R,6S,7S,9S,10S,11R)-1,9-Dihydroxyeudesm-3-en-12,6-olide
C15H22O4     相似度:60%
Phytochemistry          2003                   479-484
Sesquiterpene lactone glucosides and alkyl glycosides from the fruit of cumin
Tomomi Takayanagi, Toru Ishikawa, Junichi Kitajima
Structure      13C NMR   碳谱模拟图
20 .     deschloroelatol
    相似度:60%
Journal of Natural Products          1997          60          967-970
Laurencia rigida: Chemical Investigations of Its Antifouling Dichloromethane Extract
Gabriele M. König and Anthony D. Wright
Structure      13C NMR   碳谱模拟图
Domyallbesttohaveahappylife.
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