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CDCl3 206.2,172.4,135.5,134.6,133.4,132.6,130.1,129.2,128.5,126.2,86.1,82.9,72.0,43.5,38.6,31.1,28.4,24.3,23.2,23.0,21.3,21.1,17.0,15.6,15.4 [ Last edited by icaszzx on 2013-4-25 at 16:44 ] |
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1 . 4-O-acetyl-5-O-benzoyl-3¦Â-hydroxy-20-deoxyingenol C29H36O6 ÏàËÆ¶È:92.5% Journal of Asian Natural Products Research 2008 10 101-104 A new diterpene from the processed roots of Euphorbia Kansui CHUN-FA LI, JIN-HUI WANG, YUE CONG and XIAN LI Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . kansuiphorin D C27H30O4 ÏàËÆ¶È:92.3% Chinese Traditional and Herbal Drugs 2012 43 1891-1895 Study on antitumor constituents of Euphorbia lunulata WANG Jue; LI Xiao-fan; XIE Pu; WANG Tie-jie Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . kansuiphorin C C29H34O6 ÏàËÆ¶È:89.2% Chinese Traditional and Herbal Drugs 2003 34 489-492 Studies on ingenol-type diterpene esters in root tuber of Euphorbia kansui PAN Qin; MIN Zhi-da Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ingenol triacetate ÏàËÆ¶È:76.9% Planta Medica 1989 55 271-272 An Antitumor Principle from Euphorbia lath yris Hideji Itokawa, Yoshitatsu Ichihara, Kinzo Watanabe, and Koichi Talceya Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3,5,20-O-triacetylingenol ÏàËÆ¶È:76.9% Zeitschrift f¨¹r Naturforschung C 2008 63 59-65 Antinematodal Activities of Ingenane Diterpenes from Euphorbia kansui and their Derivatives against the Pine Wood Nematode (Bursaphelenchus xylophilus) J. Shi, Z. Li, T. Nitoda, M. Izumi, H. Kanzaki, N. Baba, K. Kawazu, and S. Nakajima Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ingenol ester 5 ÏàËÆ¶È:72% Phytochemistry 1997 45 563-570 Ingenane and lathyrane diterpenes from the latex of Euphorbia canariensis J. Alberto Marco, Juan F. Sanz-Cervera, Alberto Yuste Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-O-[N-(2-aminobenzoyl)]anthraniloyl-5-O-acetyl-20-O-angelylingenol C41H48N2O9 ÏàËÆ¶È:72% European Journal of Medicinal Chemistry 2009 44 3188-3194 Bio-active compounds from Euphorbia cornigera Boiss Imam Bakhsh Baloch, Musa Kaleem Baloch, Ahmad Khan Baloch Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3,20-O-diacetyl-5-O-[N-(2-aminobenzoyl)]anthraniloylingenol C38H44N2O9 ÏàËÆ¶È:72% European Journal of Medicinal Chemistry 2009 44 3188-3194 Bio-active compounds from Euphorbia cornigera Boiss Imam Bakhsh Baloch, Musa Kaleem Baloch, Ahmad Khan Baloch Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 5,20-O-diacetyl-3-O-[N-(2-aminobenzoyl)]anthraniloylingenol C38H44N2O9 ÏàËÆ¶È:72% European Journal of Medicinal Chemistry 2009 44 3188-3194 Bio-active compounds from Euphorbia cornigera Boiss Imam Bakhsh Baloch, Musa Kaleem Baloch, Ahmad Khan Baloch Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ingenol ester 1 ÏàËÆ¶È:70.3% Phytochemistry 1997 45 563-570 Ingenane and lathyrane diterpenes from the latex of Euphorbia canariensis J. Alberto Marco, Juan F. Sanz-Cervera, Alberto Yuste Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 17-O-acetyl-3-[(Z)-2-methyl-2-butenoyl]-20-deoxy-17-hydroxyingenol C27H36O7 ÏàËÆ¶È:70.3% Agricultural and Biological Chemistry 1989 53 425-430 Toxic Diterpernes from Euphorbia trigona (Saiunkaku: an Indoor Foliage Plant in Japan) Masahiro TADA, Hiromichi SEKI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 20-O-acetyl-3-O-(Z)-2-methyl-2-butenoyl]ingenol ÏàËÆ¶È:70.3% Agricultural and Biological Chemistry 1989 53 425-430 Toxic Diterpernes from Euphorbia trigona (Saiunkaku: an Indoor Foliage Plant in Japan) Masahiro TADA, Hiromichi SEKI Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-O-[N-(2-aminobenzoyl)]anthraniloyl-5-O-acetyl-20-O-angelylingenol C41H48N2O9 ÏàËÆ¶È:68% European Journal of Medicinal Chemistry 2009 44 3188-3194 Bio-active compounds from Euphorbia cornigera Boiss Imam Bakhsh Baloch, Musa Kaleem Baloch, Ahmad Khan Baloch Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-O-angelyl-5-O-[N-(2-aminobenzoyl)]anthraniloyl-20-O-acetylingenol C38H44N2O9 ÏàËÆ¶È:68% European Journal of Medicinal Chemistry 2009 44 3188-3194 Bio-active compounds from Euphorbia cornigera Boiss Imam Bakhsh Baloch, Musa Kaleem Baloch, Ahmad Khan Baloch Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ingenol ester 4 ÏàËÆ¶È:67.8% Phytochemistry 1997 45 563-570 Ingenane and lathyrane diterpenes from the latex of Euphorbia canariensis J. Alberto Marco, Juan F. Sanz-Cervera, Alberto Yuste Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ingenol ester 2 ÏàËÆ¶È:66.6% Phytochemistry 1997 45 563-570 Ingenane and lathyrane diterpenes from the latex of Euphorbia canariensis J. Alberto Marco, Juan F. Sanz-Cervera, Alberto Yuste Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3-O-acetyl-5-O-[N-(2-aminobenzoyl)]anthraniloyl-20-O-angelyingenol C41H48N2O9 ÏàËÆ¶È:64% European Journal of Medicinal Chemistry 2009 44 3188-3194 Bio-active compounds from Euphorbia cornigera Boiss Imam Bakhsh Baloch, Musa Kaleem Baloch, Ahmad Khan Baloch Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 3-O-acetyl-5-O-angelyl-20-[N-(2-aminobenzoyl)]anthranilylingenol C41H48N2O9 ÏàËÆ¶È:64% European Journal of Medicinal Chemistry 2009 44 3188-3194 Bio-active compounds from Euphorbia cornigera Boiss Imam Bakhsh Baloch, Musa Kaleem Baloch, Ahmad Khan Baloch Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3-O-angelyl-5-O-acetyl-20-O-[N-(2-aminobenzoyl)]anthraniloylingenol C41H48N2O9 ÏàËÆ¶È:64% European Journal of Medicinal Chemistry 2009 44 3188-3194 Bio-active compounds from Euphorbia cornigera Boiss Imam Bakhsh Baloch, Musa Kaleem Baloch, Ahmad Khan Baloch Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Ingenol-3-N-methylanthranilate C28H35NO6 ÏàËÆ¶È:62.9% Natural Product Communications 2007 2 375-379 Synthesis of Sapintoxin D and N-Methylanthranilate-BasedFluorescent Bioprobes Francesco Mainieri, Alberto Pagani, Abdellah Ech-Chahad and Giovanni Appendino Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ingenol-3-angelate-5,20-diacetate ÏàËÆ¶È:62.0% Phytochemistry 1997 45 563-570 Ingenane and lathyrane diterpenes from the latex of Euphorbia canariensis J. Alberto Marco, Juan F. Sanz-Cervera, Alberto Yuste Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 3-O-(2E,4Z-Decadienoyl)-20-deoxyingenol C30H42O5 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2003 51(8) 935-941 Diterpenes from the Roots of Euphorbia kansui and Their in Vitro Effects on the Cell Division of Xenopus(2) Li-Yan WANG,Nai-Li WANG,Xin-Sheng YAO,Syohei MIYATA,and Susumu KITANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 3-O-(2E,4E-Decadienoyl)-20-deoxyingenol C30H42O5 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2003 51(8) 935-941 Diterpenes from the Roots of Euphorbia kansui and Their in Vitro Effects on the Cell Division of Xenopus(2) Li-Yan WANG,Nai-Li WANG,Xin-Sheng YAO,Syohei MIYATA,and Susumu KITANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (2Z,6Z,10E)-cericerene-15,24-diol C25H42O2 ÏàËÆ¶È:60% Journal of Natural Products 1999 62 1504-1509 Sesterterpenoids and Diterpenoids of the Wax Excreted by a Scale Insect, Ceroplastes pseudoceriferus Masahiko Toki, Takashi Ooi, and Takenori Kusumi Structure 13C NMR ̼Æ×Ä£Äâͼ |

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