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bb864448334: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-05-13 14:48:44
1 .     3¦Â,20R,24-trihydroxypropakisnordammaran-12-one
C27H46O4     ÏàËÆ¶È:70.3%
Journal of Natural Products          1997          60          1236-1241
Microbial Transformation of Protopanaxadiol and Protopanaxatriol Derivatives with Mycobacterium sp. (NRRL B-3805)
K. C. Wang, Perng-Haur Wang, and Shoei-Sheng Lee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     lup-12-en-3¦Â-ol
    ÏàËÆ¶È:66.6%
Journal of Chemistry          2008          46          456-461
Isolation and structural characterization of triterpenes from Celastrus hindii Benth
Trịnh Thị Thủy Quyen, Nguyễn Huy Cường, Phạm Thị Ninh, Trần Văn Sung
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     zizyphulanostan-21-oic acid
C30H50O3     ÏàËÆ¶È:66.6%
Pharmaceutical Biology          2004          42          508-511
New Compounds from Zizyphus vulgaris
Hayat M. Mukhtar, S. H. Ansari, M. Ali, T. Naved
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     3¦Â,20S-dihydroxytaraxastane
C30H52O2     ÏàËÆ¶È:65.5%
Fitoterapia          2001          72          709-711
Triterpenes from the resin of Protium heptaphyllum
G.S. Susunaga, A.C. Siania, M.G. Pizzolatti,R.A. Yunes, F. Delle Monache
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     halistanol sulfate E
    ÏàËÆ¶È:65.5%
Tetrahedron          1992          48          5467-5472
Halistanol Sulfates A-E, New Steroid Sulfates, from a Marine Sponge, Epipolasis sp.
Satoshi Kanazawa, Nobuhiro Fusetani, Shigeki Matsunaga
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     15-O-Pivalate
C25H44O5     ÏàËÆ¶È:65.3%
Phytochemistry          2010          71          675-681
Microtropiosides A¨CF: ent-Labdane diterpenoid glucosides from the leaves of Microtropis japonica (Celastraceae)
Yuka Koyama, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     8¦Â-hydroxy-3-O-¦Â-D-glucopyranosyl-ent-labda-13-en-15,16-diol
C26H46O9     ÏàËÆ¶È:65.3%
Phytochemistry Letters          2012          5          500-505
Isolation of three new ent-labdane diterpenes from Dodonaea viscosa Jacquin (Sapindaceae): Preliminary evaluation of antiherpes activity
Simone Quintana de Oliveira, Maria Tereza Rojo de Almeida, Flora Maraslis, Izabella Tha¨ªs Silva, Thais Cristine Marques Sincero, Jorge Alejandro Palermo, Gabriela Myriam Cabrera, Miguel Soriano Balparda Caro, Cl¨¢udia Maria Oliveira Simões, Eloir Paulo Sch
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     forticine
C27H45O2N     ÏàËÆ¶È:62.9%
Chemical & Pharmaceutical Bulletin          2002          50(8)          1013-1016
New Steroidal Alkaloids from Fritillaria imperialis and Their Cholinesterase Inhibiting Activities
ATTA-UR-RAHMAN,Muhammad Nadeem AKHTAR, Muhammad Iqbal CHOUDHARY, Yoshisuke TSUDA,Bilge SENER,Assad KHALID, and Masood PARVEZ
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     9¦Á,11¦Á-Epoxy-5¦Á-cholest-7-enr-3¦Â,5,6¦Â-triol
C27H44O4     ÏàËÆ¶È:62.9%
Steroids          1991          56          154-158
Synthesis of the marine epoxy sterol 9¦Á,11¦Á-epoxy-5¦Á-cholest-7-ene-3¦Â,5,6¦Â-triol
Anna Migliuolo, Giacomo Notaro, Vincenzo Piccialli, Donato Sica
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     compound 3
C27H46O3     ÏàËÆ¶È:62.9%
Tetrahedron          1998          54          179-186
New cytotoxic sterols from the soft coral Gersemia fruticosa
Reet Koljak, Annika Lopp, Tõnis Pehk, K¨¹lliki Varvas, Aleksander-Mati M¨¹¨¹risepp, Ivar Järving, Nigulas Samel
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-05-13 12:26:17
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