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13C-NMR£¨CDCl3£©£º199.6, 174.2, 173.6, 164.5, 156.2, 135.1, 134.1, 132.7, 124.6, 124.6, 123.1, 67.4, 66.8, 55.9, 44.5, 44.1, 43.0, 39.4, 38.9, 36.9, 35.7, 34.9, 34.6, 34.3, 34.3, 33.2, 32.1, 32.1, 30.6, 29.8, 29.8, 29.8, 29.7, 29.6, 29.6, 29.5, 29.5, 29.4, 29.4, 29.3, 29.3, 29.1, 27.9, 25.5, 25.2, 24, 23.1, 22.8, 22.0, 21.4, 20.1, 19.8, 19.1, 19.1, 17.8, 16.8, 14.3, 14.2, 11.1
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Angelina¡¢: ½ð±Ò+4, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл£¬ÒòΪÊÇÁ½¸öÈ˸øµÄ»Ø¸´£¬Ö»ÄÜÒ»ÈË4¸öÁË¡£ 2014-12-11 08:30:30
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1 .     ligustrin A
    ÏàËÆ¶È:61.0%
Phytochemistry          1997          46          977-979
Acylated triterpenoids from Ligustrum ovalifolium
Koichi Machida, Toshio Yamaguchi, Yoshiko Kamiya, Masao Kikuchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Kansuiphorin A
C54H90O9     ÏàËÆ¶È:61.0%
Journal of Natural Products          1991          Vol 54          823
Antitumor Agents, 119. Kansuiphorins A and B, Two Novel Antileukemic Diterpene Esters from Euphorbia kansui
Tian-Shung Wu, Yuh-Meei Lin, Mitsumasa Haruna, De-Ji Pan, Tetsuro Shingu, Yuh-pan Chen, Hong-Yen Hsu, Tatsuhiko Nakano, Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3-O-(2,3-dimethylbutanoyl)-5-O-acetyl-13-O-dodecanoyl-20-O-hexadecanoylingenol
C56H92O10     ÏàËÆ¶È:61.0%
Chinese Chemical Letters          2011          22          451-454
Isolation and characterization of ingenol esters from Euphorbia cornigera
Imam Bakhsh Baloch, Musa Kaleem Baloch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     4'-((5-cholesteryloxy-5-oxopentyl)oxy)biphenyl-4-yl 4-(nonyloxy)benzoate
C60H84O6     ÏàËÆ¶È:55.9%
Tetrahedron          2014          70          4745-4753
Synthesis and characterization of novel chiral dimers exhibiting highly frustrated liquid crystal phases
Uma S. Hiremath
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     4'-((6-cholesteryloxy-6-oxohexyl)oxy)bi-phenyl-4-yl 4-(hexadecyloxy)benzoate
C68H100O6     ÏàËÆ¶È:55.9%
Tetrahedron          2014          70          4745-4753
Synthesis and characterization of novel chiral dimers exhibiting highly frustrated liquid crystal phases
Uma S. Hiremath
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Benzyl (+/-)-3¦Á,7¦Á,12¦Á-tris(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oate
    ÏàËÆ¶È:55.7%
Steroids          2013          78          435-453
New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers
Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Benzyl (+/-)-7¦Á,12¦Á-dihydroxy-3¦Á-(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oate
    ÏàËÆ¶È:54.6%
Steroids          2013          78          435-453
New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers
Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     7,8-dihydroisoxuxuarine I¦Á
C58H74O9     ÏàËÆ¶È:54.2%
Helvetica Chimica Acta          2004          Vol. 87          1536
Nine Triterpene Dimers from Maytenus chuchuhuasca
Osamu Shirota, Setsuko Sekita, and Motoyoshi Satake
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     4-Ethylcholesta-4,24(28)-dien-3-one
C29H46O     ÏàËÆ¶È:54.2%
Chemistry of Natural Compounds          2011          Vol. 47, No. 3          465-466
POLYSACCHARIDES OF Fabaceae. VI. GALACTOMANNANS FROM SEEDS OF Astragalus alpinus AND A. tibetanus
D. N. Olennikov and A. V. Rokhin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     4'-((6-cholesteryloxy-6-oxohexyl)oxy)biphenyl-4-yl 4-(decyloxy)benzoate
C62H88O6     ÏàËÆ¶È:54.2%
Tetrahedron          2014          70          4745-4753
Synthesis and characterization of novel chiral dimers exhibiting highly frustrated liquid crystal phases
Uma S. Hiremath
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     4'-((6-cholesteryloxy-6-oxohexyl)oxy)biphenyl-4-yl 4-(dodecyloxy)benzoate
C64H92O6     ÏàËÆ¶È:54.2%
Tetrahedron          2014          70          4745-4753
Synthesis and characterization of novel chiral dimers exhibiting highly frustrated liquid crystal phases
Uma S. Hiremath
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound 14
C69H103N9O12     ÏàËÆ¶È:53.9%
Tetrahedron          2014          70          3297-3305
The CuI-catalyzed alkyne¨Cazide cycloaddition as direct conjugation/cyclization method of peptides to steroids
Radell Echemend¨ªa, Odette Concepci¨®n, Fidel E. Morales, M¨¢rcio W. Paixão, Daniel G. Rivera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (+/-)-3¦Á,7¦Á,12¦Á-Tris(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oic aci
C123H196O17     ÏàËÆ¶È:53.3%
Steroids          2013          78          435-453
New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers
Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     4-{[(3¦Á,5¦Â,7¦Á,12¦Á)-7,12-bis(formyloxy)-24-oxo-24-[(3¦Â,22E)-stigmasta-5,22-dien-3-yloxy]cholan-3-yl]oxy}-4-oxobutanoic acid
C59H90O10     ÏàËÆ¶È:52.5%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     4'-((6-cholesteryloxy-6-oxohexyl)oxy)biphenyl-4-yl 4-(nonyloxy)benzoate
C61H86O6     ÏàËÆ¶È:52.5%
Tetrahedron          2014          70          4745-4753
Synthesis and characterization of novel chiral dimers exhibiting highly frustrated liquid crystal phases
Uma S. Hiremath
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (+/-)-7¦Á,12¦Á-Dihydroxy-3¦Á-(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oic acid
C57H92O9     ÏàËÆ¶È:52.5%
Steroids          2013          78          435-453
New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers
Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound 9
C62H92N10O10     ÏàËÆ¶È:52.5%
Tetrahedron          2014          70          3297-3305
The CuI-catalyzed alkyne¨Cazide cycloaddition as direct conjugation/cyclization method of peptides to steroids
Radell Echemend¨ªa, Odette Concepci¨®n, Fidel E. Morales, M¨¢rcio W. Paixão, Daniel G. Rivera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     7,8-dihydro-scutionin ¦Á A
C60H82O8     ÏàËÆ¶È:51.6%
Tetrahedron          1996          52          9597-9608
Structure and absolute configuration of triterpene dimers from Maytenus scutioides
Antonio G. Gonz¨¢lez, Nelson L. Alvarenga, Ana Est¨¦vez-Braun, Angel G. Ravelo, Isabel L. Bazzocchi, Laila Moujir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     (5S)-5-(4-(2-trimethylsilylethoxycarbonyl)oxybenzyl)-3-(phenylselanyl)-3-((1S,2R,4aR,6R,8aS)-3,4a,6-trimethyl-2-((2E,4E)-4-methylhexa-2,4-dien-2-yl)-1,2,4a,5,6,7,8,8a-octahydronaphthalene-1-carbonyl)pyrrolidin-2-one
    ÏàËÆ¶È:51.6%
Chemistry ¨C An Asian Journal          2013          8          1243-1252
Total Synthesis of Diaporthichalasin by Using the IntramolecularDiels¨CAlder Reaction of an ¦Á,¦Â-Unsaturated ¦Ã-Hydroxylactam in Aqueous Media
Nobuhiro Shionozaki, Naoki Iwamura, Ryo Tanaka, Prof. Kimiko Makino and Prof. Hiromi Uchiro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     7,8-dihydroisoxuxuarine H¦Á
C58H74O9     ÏàËÆ¶È:50.8%
Helvetica Chimica Acta          2004          Vol. 87          1536
Nine Triterpene Dimers from Maytenus chuchuhuasca
Osamu Shirota, Setsuko Sekita, and Motoyoshi Satake
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     milicifoline D
C58H76O7     ÏàËÆ¶È:50.8%
Journal of Natural Products          2007          70          1049-1052
3-(3'-methoxy-4'-hydroxybenzoyloxy)- 6-oxotingenol
F¨¢tima Guti¨¦rrez,Ana Est¨¦vez-Braun,¨¢ngel G. Ravelo,Luis Astudillo,and Rafael Z¨¢rate
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     7¦Â-tert-Butyldimethylsilyloxysitosteryl-9,10-ditert-butyldimethylsilyloxystearate
C65H126O5Si3     ÏàËÆ¶È:50.8%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     trichoderins B
C59H108N10O12     ÏàËÆ¶È:50.8%
Bioorganic & Medicinal Chemistry Letters          2010          20          3658-3663
Trichoderins, novel aminolipopeptides from a marine sponge-derived Trichoderma sp., are active against dormant mycobacteria
Patamaporn Pruksakorn, Masayoshi Arai, Naoyuki Kotoku, Catherine Vilch¨¨ze, Anthony D. Baughn, Prashini Moodley, William R. Jacobs Jr., Motomasa Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     4'-((6-cholesteryloxy-6-oxohexyl)oxy)biphenyl-4-yl 4-(octyloxy)benzoate
C60H84O6     ÏàËÆ¶È:50.8%
Tetrahedron          2014          70          4745-4753
Synthesis and characterization of novel chiral dimers exhibiting highly frustrated liquid crystal phases
Uma S. Hiremath
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     6'¦Â-Methoxy-6',7'-dihydro-scutionin ¦Á B
C61H84O9     ÏàËÆ¶È:50.8%
Tetrahedron          2001          57          1283-1287
Absolute configuration of triterpene dimers from Maytenus species (Celastraceae)
Antonio G Gonz¨¢lez, Marı́a L Kennedy, F¨¦lix M Rodrı́guez, Isabel L Bazzocchi, Ignacio A Jim¨¦nez, Angel G Ravelo, Laila Moujir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     7,8-dihydroisoxuxuarine E¦Á
C60H80O9     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1998          46          102-106
New Geometric and Stereoisomeric Triterpene Dimers from Maytenus chuchuhuasca
Osamu SHIROTA,Hiroshi MORITA,Koichi TAKEYA and Hideji ITOKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     6',7'-Dihydro-scutionin ¦Á B
C60H82O8     ÏàËÆ¶È:50%
Tetrahedron          2001          57          1283-1287
Absolute configuration of triterpene dimers from Maytenus species (Celastraceae)
Antonio G Gonz¨¢lez, Marı́a L Kennedy, F¨¦lix M Rodrı́guez, Isabel L Bazzocchi, Ignacio A Jim¨¦nez, Angel G Ravelo, Laila Moujir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     scutionin ¦Á A
C60H48O8     ÏàËÆ¶È:50%
Tetrahedron          1996          52          9597-9608
Structure and absolute configuration of triterpene dimers from Maytenus scutioides
Antonio G. Gonz¨¢lez, Nelson L. Alvarenga, Ana Est¨¦vez-Braun, Angel G. Ravelo, Isabel L. Bazzocchi, Laila Moujir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     7,8-dihydro-scutionin ¦Á B
C60H82O8     ÏàËÆ¶È:50%
Tetrahedron          1996          52          9597-9608
Structure and absolute configuration of triterpene dimers from Maytenus scutioides
Antonio G. Gonz¨¢lez, Nelson L. Alvarenga, Ana Est¨¦vez-Braun, Angel G. Ravelo, Isabel L. Bazzocchi, Laila Moujir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     netzascutionin ¦Á A
    ÏàËÆ¶È:50%
Tetrahedron          1996          52          9597-9608
Structure and absolute configuration of triterpene dimers from Maytenus scutioides
Antonio G. Gonz¨¢lez, Nelson L. Alvarenga, Ana Est¨¦vez-Braun, Angel G. Ravelo, Isabel L. Bazzocchi, Laila Moujir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     compound 11
C71H110N10O9     ÏàËÆ¶È:50%
Tetrahedron          2014          70          3297-3305
The CuI-catalyzed alkyne¨Cazide cycloaddition as direct conjugation/cyclization method of peptides to steroids
Radell Echemend¨ªa, Odette Concepci¨®n, Fidel E. Morales, M¨¢rcio W. Paixão, Daniel G. Rivera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     magellanin
    ÏàËÆ¶È:50%
Drugs & Clinic          2013          28          274-277
Chemical constituents in ethyl acetate extracting fraction from Salacia amplifolia
LI Jun-li, HUANG Dou-dou, YUAN Yuan, WANG Yan, CHEN Cheng, HUANG Guang-hui, SUN Lian-na
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)

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¡ï ¡ï ¡ï ¡ï
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Angelina¡¢: ½ð±Ò+4, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл£¬ÒòΪÊÇÁ½¸öÈ˸øµÄ»Ø¸´£¬Ö»ÄÜÒ»ÈË4¸öÁË¡£ 2014-12-11 08:30:53
1 .     ligustrin A
    ÏàËÆ¶È:61.0%
Phytochemistry          1997          46          977-979
Acylated triterpenoids from Ligustrum ovalifolium
Koichi Machida, Toshio Yamaguchi, Yoshiko Kamiya, Masao Kikuchi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     Kansuiphorin A
C54H90O9     ÏàËÆ¶È:61.0%
Journal of Natural Products          1991          Vol 54          823
Antitumor Agents, 119. Kansuiphorins A and B, Two Novel Antileukemic Diterpene Esters from Euphorbia kansui
Tian-Shung Wu, Yuh-Meei Lin, Mitsumasa Haruna, De-Ji Pan, Tetsuro Shingu, Yuh-pan Chen, Hong-Yen Hsu, Tatsuhiko Nakano, Kuo-Hsiung Lee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     3-O-(2,3-dimethylbutanoyl)-5-O-acetyl-13-O-dodecanoyl-20-O-hexadecanoylingenol
C56H92O10     ÏàËÆ¶È:61.0%
Chinese Chemical Letters          2011          22          451-454
Isolation and characterization of ingenol esters from Euphorbia cornigera
Imam Bakhsh Baloch, Musa Kaleem Baloch
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     Citrusteryl arachidate
C55H98O7     ÏàËÆ¶È:55.9%
Natural Product Research          2010          24          610-620
Phytochemical investigation of the fruit peels of Citrus reticulata Blanco
M. Aasim Khan; M. Ali; Prawez Alam
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     4'-((5-cholesteryloxy-5-oxopentyl)oxy)biphenyl-4-yl 4-(nonyloxy)benzoate
C60H84O6     ÏàËÆ¶È:55.9%
Tetrahedron          2014          70          4745-4753
Synthesis and characterization of novel chiral dimers exhibiting highly frustrated liquid crystal phases
Uma S. Hiremath
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     4'-((6-cholesteryloxy-6-oxohexyl)oxy)bi-phenyl-4-yl 4-(hexadecyloxy)benzoate
C68H100O6     ÏàËÆ¶È:55.9%
Tetrahedron          2014          70          4745-4753
Synthesis and characterization of novel chiral dimers exhibiting highly frustrated liquid crystal phases
Uma S. Hiremath
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     Benzyl (+/-)-3¦Á,7¦Á,12¦Á-tris(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oate
    ÏàËÆ¶È:55.7%
Steroids          2013          78          435-453
New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers
Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     Benzyl (+/-)-7¦Á,12¦Á-dihydroxy-3¦Á-(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oate
    ÏàËÆ¶È:54.6%
Steroids          2013          78          435-453
New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers
Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     7,8-dihydroisoxuxuarine I¦Á
C58H74O9     ÏàËÆ¶È:54.2%
Helvetica Chimica Acta          2004          Vol. 87          1536
Nine Triterpene Dimers from Maytenus chuchuhuasca
Osamu Shirota, Setsuko Sekita, and Motoyoshi Satake
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     4-Ethylcholesta-4,24(28)-dien-3-one
C29H46O     ÏàËÆ¶È:54.2%
Chemistry of Natural Compounds          2011          Vol. 47, No. 3          465-466
POLYSACCHARIDES OF Fabaceae. VI. GALACTOMANNANS FROM SEEDS OF Astragalus alpinus AND A. tibetanus
D. N. Olennikov and A. V. Rokhin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     4'-((6-cholesteryloxy-6-oxohexyl)oxy)biphenyl-4-yl 4-(decyloxy)benzoate
C62H88O6     ÏàËÆ¶È:54.2%
Tetrahedron          2014          70          4745-4753
Synthesis and characterization of novel chiral dimers exhibiting highly frustrated liquid crystal phases
Uma S. Hiremath
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     4'-((6-cholesteryloxy-6-oxohexyl)oxy)biphenyl-4-yl 4-(dodecyloxy)benzoate
C64H92O6     ÏàËÆ¶È:54.2%
Tetrahedron          2014          70          4745-4753
Synthesis and characterization of novel chiral dimers exhibiting highly frustrated liquid crystal phases
Uma S. Hiremath
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     minutissamide H
C60H102N12O16     ÏàËÆ¶È:54.2%
Bioorganic & Medicinal Chemistry          2012          20          6134-6143
Minutissamides E¨CL, antiproliferative cyclic lipodecapeptides from the cultured freshwater cyanobacterium cf. Anabaena sp.
Hahk-Soo Kang, Megan Sturdy, Aleksej Krunic, Hyunjung Kim, Qi Shen, Steven M. Swanson, Jimmy Orjala
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     compound 14
C69H103N9O12     ÏàËÆ¶È:53.9%
Tetrahedron          2014          70          3297-3305
The CuI-catalyzed alkyne¨Cazide cycloaddition as direct conjugation/cyclization method of peptides to steroids
Radell Echemend¨ªa, Odette Concepci¨®n, Fidel E. Morales, M¨¢rcio W. Paixão, Daniel G. Rivera
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     (+/-)-3¦Á,7¦Á,12¦Á-Tris(3-{[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yl]oxycarbonyl}propanoyloxy)-5¦Â-cholan-24-oic aci
C123H196O17     ÏàËÆ¶È:53.3%
Steroids          2013          78          435-453
New propanoyloxy derivatives of 5¦Â-cholan-24-oic acid as drug absorption modifiers
Lenka Coufalov¨¢, Lech Mr¨®zek, Lucie R¨¢rov¨¢, Luk¨¢š Plaček, Radka Opatřilov¨¢, Jiř¨ª Dohnal, Katar¨ªna Kr¨¢l¡¯ov¨¢, Oldřich Paleta, Vladim¨ªr Kr¨¢l, Pavel Drašar, Josef Jamp¨ªlek
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     4-{[(3¦Á,5¦Â,7¦Á,12¦Á)-7,12-bis(formyloxy)-24-oxo-24-[(3¦Â,22E)-stigmasta-5,22-dien-3-yloxy]cholan-3-yl]oxy}-4-oxobutanoic acid
C59H90O10     ÏàËÆ¶È:52.5%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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