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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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²éѯ½á¹û£º¹²²éµ½32¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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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 Structure & 13C NMR ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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