Query results: A total of 2058 compounds were found (query results were for reference only) 1. 24-METHYL-5α-Cholest-24 (28) -ne-3β, 6α, 8,14α, 15β, 16β, 26-26- heptaol 相似度:66.6% Journal of Natural Products 1990 Vol 53 366 Starfish Saponins, Part 43. Structures of Two New Sulfated Steroidal Fucofuranosides (Imbricatosides A and B) and Six New Polyhydroxysteroids from the Starfish Dermasterias IMBricata Insto, Luigi Minale, Raffaele Riccio Structure 13C NMR carbon spectrum simulation graph 2. 24r-methylcholesta-3β, 5α, 6β-Triol Nature Product Research 1997 10 231-237 Two 11α-Acetoxysterols from the Palauan Soft Coral lobophytum cf. Pauciflorum Qing Lu; D. John Faulkner Structure 13C NMR 碳谱模拟图 3 . Compound 9a 相似度:64.2% Journal of Natural Products 1995 58 653-671 Chemical and Biological Investigation of the Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio PalagiaNO, Stefano Maurelli, Raffaele Riccio, Franco Zollo Structure 13C NMR carbon spectrum simulation map 4. 11α-ACETOXY-24R-METHYLCHOLESTA-3β, 5α, 6β-Triol c30H56NO5 similarity: 633.3%: 63.3% 123]Natural Product Research 1997 10 231-237 Two 11α-Acetoxysterols from the Palauan Soft Coral lobophytum cf. Pauciflorum Qing Lu; D. John Faulkner Structure 13C NMR 碳谱模拟图 5 . 24-O-Sulfate of (24s) -5α-Cholestane-3β, 5α, 6β, 15α, 24-petAol C27H47O8SNA similarity: 62.9% Journal of natural Products 2006 (2) 224-228 224-228 Polar Steroidal Compounds from the Far Eastern Starfish Henricia leviuscula Natalia V. Ivanchina, Alla A. Kicha, Anatoly I. Kalinovsky, Pavel S. Dmitrenok, Andrey S.Dmitrenok, Elena L. Chaikina, Valentin A. Stonik , Margherita Gavagnin, and Guido Cimino Structure 13C NMR 碳谱模拟图 6 . (22R,25S)-solanid-5-enine-3β,5α,6β-triol 相似度:62.9%[ 123] Chemical u0026 amp; PHARMACEUTICAL BULLETIN 1988 36 4700-4705 New Sterodial Alkaloids from the Chinese Herb Drug, u0026 QUOT; Bei-Mu u0026 Quot; KO KANEKO, TAKAO KATSUHARA, Yukie Kitamura, Makoto Nishizawa, YUH-PAN CHEN HON-YEN HSU Structure 13C NMR carbon spectrum 6. C29H41NO7 相似度:62.0% Tetrahedron 2004 60 2379-2385 Novel sesquiterpenoids as tyrosine kinase inhibitors produced by Stachybotrys chortarum Maru0026#305;u0026#769;a J Vázquez, Alfonso Vega, Alfonso Rivera-Sagredo , Mar u0026#305; u0026#769; A D Jiménez-ALFARO, Emilio D u0026#305; EZ, juan A Hueso-Rodr u0026#305; Guez Structure 13C NMR carbon spectrum [ 123]8 . compound 10 C28H50O4 相似度:60.7% Chemical u0026amp; Pharmaceutical Bulletin 1986 34 4590-4596 Marine Natural Products. XV. : Chemical Constituents of an Okinawan Soft Coral of Xenia sp. ( Xeniidae) Isao Kitagawa, Motomasa Kobayashi, CUI Zheng, Yutaka Kiyota and Mayumi Ohnishi Structure 13C NMR carbon spectrum simulation graph 9. 6β, 25ξ, 26-petol C28H50O5 similarity: 60.7% Chemical u0026 amp; Pharmaceutical Bulletin 1983 31 4127-4129 Marine Sterols. XIV. Isolation of (24S)-24-Methyl-5α-cholestane-3β, 5, 6β, 25ζ, 26-pentol from the Soft Coral Sarcophyton glaucum MASARU KOBAYASHI and HIROSHI MITSUHASHI Structure 13C NMR carbon spectrum simulation diagram 10. Compound 9 Similarity: 60.7% Chemical u0026 amp; PHARMACEUTICAL BULLETIN 1984 32 1244-1247 A New GlyCosyl Ester of A 3, 4-Seco-Triterpenene FROM KOREAN MEDICINAL PLANT, ACANTHOPANAX CHIISANENSIS (ARALIACEAE) DugRyong Hahn,Ryoji Kasai,JeungHee Kim,Shigenori Taniyasu and Osamu Tanaka Structure 13C NMR 碳谱模拟图 11 . compound 5 相似度: 60.7% Steroids 2008 73 562-567 New Anti-Inflammatic Steroids from the formosan soft Cral Clavularia viridis chin-hsiang Chang, zhi-hong wen, shng-kwihg, shng-kwihg, shang-kwihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kwihg, shang-kweihg, six ] Structure 13C NMR carbon spectrum simulation diagram 12. (24r) -24-METHYL-5α-cholesta-3β, 5,6β, 15α, 24,28-hexaol 28-Sulfate Similarity: 60.7%[60.7% 123] Journal of Nature Products 1995 VOL 58 653-671 Chemical and Biology Investigation of The Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio Palagiano, Stefano Maurelli, Raffaele Riccio, Franco Zollo Structure 13C NMR 碳谱模拟图 13 . aervecdysteroid A C28H44O6 相似度:60.7% Steroids 2013 78 1098-1102 Ecdysteroids from the flowers of Aerva javanica Muhammad Saleem, Sara Musaddiq, Naheed Riaz, Momina Zubair , Muhammad Ashraf, Rumana Nasar, Abdul Jabbar Structure 13C NMR carbon spectrum simulation graph 14. ERGOST-3β, 5α, 6β-Triol Similarity: 60.7% Acta Scientiaarum Natures University United 46 (4) 116-118 The Secondary Metabolite of the Soft CORAL CESPITULALIA CECERULEA (Ⅱ) He xi-xin, yan su-jung-yu, zang long-mei structure 13c NMR carbon spectrum simulation diagram 15. (24s) -Eregostane-1α, 3β, 5α, 6β, 11α-petAol C28H50O5 similarity: 60.7% Marine Drugs 2013 11 775-787 bioactive Polyoxygenated Steroids from the South China SEA SOFT CORAL, SARCOPHYTON SP. ZENGLEI WANG, Hua Tang, Pan Wang, Wei Gong, Mei Xue, Hongwei ZHANG, TAOFANG LIU, BAOSHU LIU, yanghu yi and wen zhang structure 13c nmmmnmu 13c nmmmmuer 123] 16. 24e-METHYL-1α, 3β, 11α-Trihydrolest-5-E8-OIC Acid C28H44O4 Similarity: 60.7% The Journic CHEMISTRY 1985 50 2988-2992 STEROLS in marine invertebrates. 51. Isolation and structure elucidation of C-18 functionalized sterols from the soft coral Sinularia dissecta Barbara M. Jagodzinska, James S. Trimmer, William Fenical, Carl Djerassi Structure 13C NMR 碳谱模拟图 17. 5α-choosta-3β, 5,6β, 15α, 16β, 26-hexao C27H48O6 Similarity: 60% Russian Chemical Bulletin 1994 43 1726-1730 Polyhydroxysteroids FROM the FAR- Eastern starfishCtenodiscus crispatus A. A. Kicha, A. I. Kalinovskii, N. I. Ivanchina, Yu. N. El'kin and V. A. Stonik Structure 13C NMR 碳谱模拟图 18 . compound 41 C30H50O4 相似度:60 % heterocycles 2012 85 1117-1139 synthesis and Biological Evaluation of Oleanolic Acid Derivatives as Novel Inhibitors of Protein Tyrosine Phosphatase 1B Hui Li, Hui Zou, Lixin Gao, Ting Liu, Fan Yang, Jingya Li, Jia Li,* Wen-Wei Qiu,* and Jie Tang Structure 13C NMR carbon spectrum simulation diagram 19. 3β-activity-6α, 12β-dihydroxy-20r, 25-epoxydammarne C32H54O5 Similarity: 59.3% Chemistry of natural Compounds 2009 45 664-664-664-45 664- 672 Synthesis of Panaxatriol Glucosides L. N. Atopkkina and v. A. Denisenko Structure 13C NMR carbon spectrum simulation graph 20. 9,10-di-22-o-cerethl-beboutyll-injobout C32H46O6 相似度:59.3% Journal of Natural Products 2012 75 34-47 Proteasome Inhibitors from Neoboutonia melleri Christophe Long, Joséphine Beck, Frédéric Cantagrel, Laurence Marcourt, Laure Vendier, Bruno David, Fabien Plisson, Fadila Derguini, Isabelle Vandenberghe, Yannick Aussagues, Frédéric Ausseil, Catherine Lavaud, Franu0026#231;ois Sautel, and Georges Massiot Structure 13C NMR 碳谱模拟图 21 . 11α-acetoxy-gorgostane-3β,5α,6β,12α-tetraol C32H54O6 相似度:59.3% Marine Drugs 2013 11 775-787 Bioactive Polyoxygenated Steroids from the South China Sea Soft Coral, Sarcophyton sp. ZENGLEI WANG, HUA TANG, PAN WANG, Wei Gong, Mei Xue, HONGWEI ZHANG, TAOFANG LIU, BAOSHU LIU, Yanghu yi and wen zhang Structure 13C NMR carbon spectrum simulation picture 22. Compound 2333]相似度:59.2% Journal of Natural Products 2005 68 1116-1120 Polyhydroxylated Spirostanol Saponins from the Tubers of Dioscorea polygonoides Jaime Nio Osorio, Oscar M. Mosquera Martinez, Yaned M. Correa Navarro, Kazuki Watanabe , Hiroshi Sakagami, And Yoshihiro Mimaki Structure 13C NMR carbon spectrum simulation picture 23. , Spirostanol Sapogenins, and a Pregnane Genin from Tupistra Chinese and Their Cytotoxical wen-bin Pan, fang-Rong Chang, li-mei wei, and yang-chang wu 123] Chad C. STESSMAN, RAINER EBEL, Angelo J. Corvino, and Phillip Crews Structure 13C NMR carbon spectrum simulation diagram
Query results: A total of 2058 compounds were found (query results were for reference only) 1. 24-METHYL-5α-Cholest-24 (28) -ne-3β, 6α, 8,14α, 15β, 16β, 26-26- heptaol 相似度:66.6% Journal of Natural Products 1990 Vol 53 366 Starfish Saponins, Part 43. Structures of Two New Sulfated Steroidal Fucofuranosides (Imbricatosides A and B) and Six New Polyhydroxysteroids from the Starfish Dermasterias IMBricata Insto, Luigi Minale, Raffaele Riccio Structure 13C NMR carbon spectrum simulation graph 2. 24r-methylcholesta-3β, 5α, 6β-Triol Nature Product Research 1997 10 231-237 Two 11α-Acetoxysterols from the Palauan Soft Coral lobophytum cf. Pauciflorum Qing Lu; D. John Faulkner Structure 13C NMR 碳谱模拟图 3 . Compound 9a 相似度:64.2% Journal of Natural Products 1995 58 653-671 Chemical and Biological Investigation of the Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio PalagiaNO, Stefano Maurelli, Raffaele Riccio, Franco Zollo Structure 13C NMR carbon spectrum simulation map 4. 11α-ACETOXY-24R-METHYLCHOLESTA-3β, 5α, 6β-Triol c30H56NO5 similarity: 633.3%: 63.3% 123]Natural Product Research 1997 10 231-237 Two 11α-Acetoxysterols from the Palauan Soft Coral lobophytum cf. Pauciflorum Qing Lu; D. John Faulkner Structure 13C NMR 碳谱模拟图 5 . 24-O-Sulfate of (24s) -5α-Cholestane-3β, 5α, 6β, 15α, 24-petAol C27H47O8SNA similarity: 62.9% Journal of natural Products 2006 (2) 224-228 224-228 Polar Steroidal Compounds from the Far Eastern Starfish Henricia leviuscula Natalia V. Ivanchina, Alla A. Kicha, Anatoly I. Kalinovsky, Pavel S. Dmitrenok, Andrey S.Dmitrenok, Elena L. Chaikina, Valentin A. Stonik , Margherita Gavagnin, and Guido Cimino Structure 13C NMR 碳谱模拟图 6 . (22R,25S)-solanid-5-enine-3β,5α,6β-triol 相似度:62.9%[ 123] Chemical u0026 amp; PHARMACEUTICAL BULLETIN 1988 36 4700-4705 New Sterodial Alkaloids from the Chinese Herb Drug, u0026 QUOT; Bei-Mu u0026 Quot; KO KANEKO, TAKAO KATSUHARA, Yukie Kitamura, Makoto Nishizawa, YUH-PAN CHEN HON-YEN HSU Structure 13C NMR carbon spectrum 6. C29H41NO7 相似度:62.0% Tetrahedron 2004 60 2379-2385 Novel sesquiterpenoids as tyrosine kinase inhibitors produced by Stachybotrys chortarum Maru0026#305;u0026#769;a J Vázquez, Alfonso Vega, Alfonso Rivera-Sagredo , Mar u0026#305; u0026#769; A D Jiménez-ALFARO, Emilio D u0026#305; EZ, juan A Hueso-Rodr u0026#305; Guez Structure 13C NMR carbon spectrum [ 123]8 . compound 10 C28H50O4 相似度:60.7% Chemical u0026amp; Pharmaceutical Bulletin 1986 34 4590-4596 Marine Natural Products. XV. : Chemical Constituents of an Okinawan Soft Coral of Xenia sp. ( Xeniidae) Isao Kitagawa, Motomasa Kobayashi, CUI Zheng, Yutaka Kiyota and Mayumi Ohnishi Structure 13C NMR carbon spectrum simulation graph 9. 6β, 25ξ, 26-petol C28H50O5 similarity: 60.7% Chemical u0026 amp; Pharmaceutical Bulletin 1983 31 4127-4129 Marine Sterols. XIV. Isolation of (24S)-24-Methyl-5α-cholestane-3β, 5, 6β, 25ζ, 26-pentol from the Soft Coral Sarcophyton glaucum MASARU KOBAYASHI and HIROSHI MITSUHASHI Structure 13C NMR carbon spectrum simulation diagram 10. Compound 9 Similarity: 60.7% Chemical u0026 amp; PHARMACEUTICAL BULLETIN 1984 32 1244-1247 A New GlyCosyl Ester of A 3, 4-Seco-Triterpenene FROM KOREAN MEDICINAL PLANT, ACANTHOPANAX CHIISANENSIS (ARALIACEAE) DugRyong Hahn,Ryoji Kasai,JeungHee Kim,Shigenori Taniyasu and Osamu Tanaka Structure 13C NMR 碳谱模拟图 11 . compound 5 相似度: 60.7% Steroids 2008 73 562-567 New Anti-Inflammatic Steroids from the formosan soft Cral Clavularia viridis chin-hsiang Chang, zhi-hong wen, shng-kwihg, shng-kwihg, shang-kwihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kwihg, shang-kweihg, six ] Structure 13C NMR carbon spectrum simulation diagram 12. (24r) -24-METHYL-5α-cholesta-3β, 5,6β, 15α, 24,28-hexaol 28-Sulfate Similarity: 60.7%[60.7% 123] Journal of Nature Products 1995 VOL 58 653-671 Chemical and Biology Investigation of The Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio Palagiano, Stefano Maurelli, Raffaele Riccio, Franco Zollo Structure 13C NMR 碳谱模拟图 13 . aervecdysteroid A C28H44O6 相似度:60.7% Steroids 2013 78 1098-1102 Ecdysteroids from the flowers of Aerva javanica Muhammad Saleem, Sara Musaddiq, Naheed Riaz, Momina Zubair , Muhammad Ashraf, Rumana Nasar, Abdul Jabbar Structure 13C NMR carbon spectrum simulation graph 14. ERGOST-3β, 5α, 6β-Triol Similarity: 60.7% Acta Scientiaarum Natures University United 46 (4) 116-118 The Secondary Metabolite of the Soft CORAL CESPITULALIA CECERULEA (Ⅱ) He xi-xin, yan su-jung-yu, zang long-mei structure 13c NMR carbon spectrum simulation diagram 15. (24s) -Eregostane-1α, 3β, 5α, 6β, 11α-petAol C28H50O5 similarity: 60.7% Marine Drugs 2013 11 775-787 bioactive Polyoxygenated Steroids from the South China SEA SOFT CORAL, SARCOPHYTON SP. ZENGLEI WANG, Hua Tang, Pan Wang, Wei Gong, Mei Xue, Hongwei ZHANG, TAOFANG LIU, BAOSHU LIU, yanghu yi and wen zhang structure 13c nmmmnmu 13c nmmmmuer 123] 16. 24e-METHYL-1α, 3β, 11α-Trihydrolest-5-E8-OIC Acid C28H44O4 Similarity: 60.7% The Journic CHEMISTRY 1985 50 2988-2992 STEROLS in marine invertebrates. 51. Isolation and structure elucidation of C-18 functionalized sterols from the soft coral Sinularia dissecta Barbara M. Jagodzinska, James S. Trimmer, William Fenical, Carl Djerassi Structure 13C NMR 碳谱模拟图 17. 5α-choosta-3β, 5,6β, 15α, 16β, 26-hexao C27H48O6 Similarity: 60% Russian Chemical Bulletin 1994 43 1726-1730 Polyhydroxysteroids FROM the FAR- Eastern starfishCtenodiscus crispatus A. A. Kicha, A. I. Kalinovskii, N. I. Ivanchina, Yu. N. El'kin and V. A. Stonik Structure 13C NMR 碳谱模拟图 18 . compound 41 C30H50O4 相似度:60 % heterocycles 2012 85 1117-1139 synthesis and Biological Evaluation of Oleanolic Acid Derivatives as Novel Inhibitors of Protein Tyrosine Phosphatase 1B Hui Li, Hui Zou, Lixin Gao, Ting Liu, Fan Yang, Jingya Li, Jia Li,* Wen-Wei Qiu,* and Jie Tang Structure 13C NMR carbon spectrum simulation diagram 19. 3β-activity-6α, 12β-dihydroxy-20r, 25-epoxydammarne C32H54O5 Similarity: 59.3% Chemistry of natural Compounds 2009 45 664-664-664-45 664- 672 Synthesis of Panaxatriol Glucosides L. N. Atopkkina and v. A. Denisenko Structure 13C NMR carbon spectrum simulation graph 20. 9,10-di-22-o-cerethl-beboutyll-injobout C32H46O6 相似度:59.3% Journal of Natural Products 2012 75 34-47 Proteasome Inhibitors from Neoboutonia melleri Christophe Long, Joséphine Beck, Frédéric Cantagrel, Laurence Marcourt, Laure Vendier, Bruno David, Fabien Plisson, Fadila Derguini, Isabelle Vandenberghe, Yannick Aussagues, Frédéric Ausseil, Catherine Lavaud, Franu0026#231;ois Sautel, and Georges Massiot Structure 13C NMR 碳谱模拟图 21 . 11α-acetoxy-gorgostane-3β,5α,6β,12α-tetraol C32H54O6 相似度:59.3% Marine Drugs 2013 11 775-787 Bioactive Polyoxygenated Steroids from the South China Sea Soft Coral, Sarcophyton sp. ZENGLEI WANG, HUA TANG, PAN WANG, Wei Gong, Mei Xue, HONGWEI ZHANG, TAOFANG LIU, BAOSHU LIU, Yanghu yi and wen zhang Structure 13C NMR carbon spectrum simulation picture 22. Compound 2333]相似度:59.2% Journal of Natural Products 2005 68 1116-1120 Polyhydroxylated Spirostanol Saponins from the Tubers of Dioscorea polygonoides Jaime Nio Osorio, Oscar M. Mosquera Martinez, Yaned M. Correa Navarro, Kazuki Watanabe , Hiroshi Sakagami, And Yoshihiro Mimaki Structure 13C NMR carbon spectrum simulation picture 23. , Spirostanol Sapogenins, and a Pregnane Genin from Tupistra Chinese and Their Cytotoxical wen-bin Pan, fang-Rong Chang, li-mei wei, and yang-chang wu 123] Chad C. STESSMAN, RAINER EBEL, Angelo J. Corvino, and Phillip Crews Structure 13C NMR carbon spectrum simulation diagram
1. 24-METHYL-5α-Cholest-24 (28) -ne-3β, 6α, 8,14α, 15β, 16β, 26-26- heptaol
相似度:66.6%
Journal of Natural Products 1990 Vol 53 366
Starfish Saponins, Part 43. Structures of Two New Sulfated Steroidal Fucofuranosides (Imbricatosides A and B) and Six New Polyhydroxysteroids from the Starfish Dermasterias IMBricata
Insto, Luigi Minale, Raffaele Riccio
Structure 13C NMR carbon spectrum simulation graph
2. 24r-methylcholesta-3β, 5α, 6β-Triol
Nature Product Research 1997 10 231-237
Two 11α-Acetoxysterols from the Palauan Soft Coral lobophytum cf. Pauciflorum
Qing Lu; D. John Faulkner
Structure 13C NMR 碳谱模拟图
3 . Compound 9a
相似度:64.2%
Journal of Natural Products 1995 58 653-671
Chemical and Biological Investigation of the Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico
Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio PalagiaNO, Stefano Maurelli, Raffaele Riccio, Franco Zollo
Structure 13C NMR carbon spectrum simulation map
4. 11α-ACETOXY-24R-METHYLCHOLESTA-3β, 5α, 6β-Triol
c30H56NO5 similarity: 633.3%: 63.3% 123]Natural Product Research 1997 10 231-237
Two 11α-Acetoxysterols from the Palauan Soft Coral lobophytum cf. Pauciflorum
Qing Lu; D. John Faulkner
Structure 13C NMR 碳谱模拟图
5 . 24-O-Sulfate of (24s) -5α-Cholestane-3β, 5α, 6β, 15α, 24-petAol
C27H47O8SNA similarity: 62.9%
Journal of natural Products 2006 (2) 224-228 224-228
Polar Steroidal Compounds from the Far Eastern Starfish Henricia leviuscula
Natalia V. Ivanchina, Alla A. Kicha, Anatoly I. Kalinovsky, Pavel S. Dmitrenok, Andrey S.Dmitrenok, Elena L. Chaikina, Valentin A. Stonik , Margherita Gavagnin, and Guido Cimino
Structure 13C NMR 碳谱模拟图
6 . (22R,25S)-solanid-5-enine-3β,5α,6β-triol
相似度:62.9%[ 123] Chemical u0026 amp; PHARMACEUTICAL BULLETIN 1988 36 4700-4705
New Sterodial Alkaloids from the Chinese Herb Drug, u0026 QUOT; Bei-Mu u0026 Quot;
KO KANEKO, TAKAO KATSUHARA, Yukie Kitamura, Makoto Nishizawa, YUH-PAN CHEN HON-YEN HSU
Structure 13C NMR carbon spectrum
6. C29H41NO7 相似度:62.0%
Tetrahedron 2004 60 2379-2385
Novel sesquiterpenoids as tyrosine kinase inhibitors produced by Stachybotrys chortarum
Maru0026#305;u0026#769;a J Vázquez, Alfonso Vega, Alfonso Rivera-Sagredo , Mar u0026#305; u0026#769; A D Jiménez-ALFARO, Emilio D u0026#305; EZ, juan A Hueso-Rodr u0026#305; Guez
Structure 13C NMR carbon spectrum [ 123]8 . compound 10
C28H50O4 相似度:60.7%
Chemical u0026amp; Pharmaceutical Bulletin 1986 34 4590-4596
Marine Natural Products. XV. : Chemical Constituents of an Okinawan Soft Coral of Xenia sp. ( Xeniidae)
Isao Kitagawa, Motomasa Kobayashi, CUI Zheng, Yutaka Kiyota and Mayumi Ohnishi
Structure 13C NMR carbon spectrum simulation graph
9. 6β, 25ξ, 26-petol
C28H50O5 similarity: 60.7%
Chemical u0026 amp; Pharmaceutical Bulletin 1983 31 4127-4129
Marine Sterols. XIV. Isolation of (24S)-24-Methyl-5α-cholestane-3β, 5, 6β, 25ζ, 26-pentol from the Soft Coral Sarcophyton glaucum
MASARU KOBAYASHI and HIROSHI MITSUHASHI
Structure 13C NMR carbon spectrum simulation diagram
10. Compound 9
Similarity: 60.7%
Chemical u0026 amp; PHARMACEUTICAL BULLETIN 1984 32 1244-1247
A New GlyCosyl Ester of A 3, 4-Seco-Triterpenene FROM KOREAN MEDICINAL PLANT, ACANTHOPANAX CHIISANENSIS (ARALIACEAE)
DugRyong Hahn,Ryoji Kasai,JeungHee Kim,Shigenori Taniyasu and Osamu Tanaka
Structure 13C NMR 碳谱模拟图
11 . compound 5
相似度: 60.7%
Steroids 2008 73 562-567
New Anti-Inflammatic Steroids from the formosan soft Cral Clavularia viridis
chin-hsiang Chang, zhi-hong wen, shng-kwihg, shng-kwihg, shang-kwihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kwihg, shang-kweihg, six ] Structure 13C NMR carbon spectrum simulation diagram
12. (24r) -24-METHYL-5α-cholesta-3β, 5,6β, 15α, 24,28-hexaol 28-Sulfate
Similarity: 60.7%[60.7% 123] Journal of Nature Products 1995 VOL 58 653-671
Chemical and Biology Investigation of The Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico
Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio Palagiano, Stefano Maurelli, Raffaele Riccio, Franco Zollo
Structure 13C NMR 碳谱模拟图
13 . aervecdysteroid A
C28H44O6 相似度:60.7%
Steroids 2013 78 1098-1102
Ecdysteroids from the flowers of Aerva javanica
Muhammad Saleem, Sara Musaddiq, Naheed Riaz, Momina Zubair , Muhammad Ashraf, Rumana Nasar, Abdul Jabbar
Structure 13C NMR carbon spectrum simulation graph
14. ERGOST-3β, 5α, 6β-Triol
Similarity: 60.7%
Acta Scientiaarum Natures University United 46 (4) 116-118
The Secondary Metabolite of the Soft CORAL CESPITULALIA CECERULEA (Ⅱ)
He xi-xin, yan su-jung-yu, zang long-mei
structure 13c NMR carbon spectrum simulation diagram
15. (24s) -Eregostane-1α, 3β, 5α, 6β, 11α-petAol
C28H50O5 similarity: 60.7%
Marine Drugs 2013 11 775-787
bioactive Polyoxygenated Steroids from the South China SEA SOFT CORAL, SARCOPHYTON SP.
ZENGLEI WANG, Hua Tang, Pan Wang, Wei Gong, Mei Xue, Hongwei ZHANG, TAOFANG LIU, BAOSHU LIU, yanghu yi and wen zhang
structure 13c nmmmnmu 13c nmmmmuer 123] 16. 24e-METHYL-1α, 3β, 11α-Trihydrolest-5-E8-OIC Acid
C28H44O4 Similarity: 60.7%
The Journic CHEMISTRY 1985 50 2988-2992
STEROLS in marine invertebrates. 51. Isolation and structure elucidation of C-18 functionalized sterols from the soft coral Sinularia dissecta
Barbara M. Jagodzinska, James S. Trimmer, William Fenical, Carl Djerassi
Structure 13C NMR 碳谱模拟图
17. 5α-choosta-3β, 5,6β, 15α, 16β, 26-hexao
C27H48O6 Similarity: 60%
Russian Chemical Bulletin 1994 43 1726-1730
Polyhydroxysteroids FROM the FAR- Eastern starfishCtenodiscus crispatus
A. A. Kicha, A. I. Kalinovskii, N. I. Ivanchina, Yu. N. El'kin and V. A. Stonik
Structure 13C NMR 碳谱模拟图
18 . compound 41
C30H50O4 相似度:60 %
heterocycles 2012 85 1117-1139
synthesis and Biological Evaluation of Oleanolic Acid Derivatives as Novel Inhibitors of Protein Tyrosine Phosphatase 1B
Hui Li, Hui Zou, Lixin Gao, Ting Liu, Fan Yang, Jingya Li, Jia Li,* Wen-Wei Qiu,* and Jie Tang
Structure 13C NMR carbon spectrum simulation diagram
19. 3β-activity-6α, 12β-dihydroxy-20r, 25-epoxydammarne
C32H54O5 Similarity: 59.3%
Chemistry of natural Compounds 2009 45 664-664-664-45 664- 672
Synthesis of Panaxatriol Glucosides
L. N. Atopkkina and v. A. Denisenko
Structure 13C NMR carbon spectrum simulation graph
20. 9,10-di-22-o-cerethl-beboutyll-injobout
C32H46O6 相似度:59.3%
Journal of Natural Products 2012 75 34-47
Proteasome Inhibitors from Neoboutonia melleri
Christophe Long, Joséphine Beck, Frédéric Cantagrel, Laurence Marcourt, Laure Vendier, Bruno David, Fabien Plisson, Fadila Derguini, Isabelle Vandenberghe, Yannick Aussagues, Frédéric Ausseil, Catherine Lavaud, Franu0026#231;ois Sautel, and Georges Massiot
Structure 13C NMR 碳谱模拟图
21 . 11α-acetoxy-gorgostane-3β,5α,6β,12α-tetraol
C32H54O6 相似度:59.3%
Marine Drugs 2013 11 775-787
Bioactive Polyoxygenated Steroids from the South China Sea Soft Coral, Sarcophyton sp.
ZENGLEI WANG, HUA TANG, PAN WANG, Wei Gong, Mei Xue, HONGWEI ZHANG, TAOFANG LIU, BAOSHU LIU, Yanghu yi and wen zhang
Structure 13C NMR carbon spectrum simulation picture
22. Compound 2333]相似度:59.2%
Journal of Natural Products 2005 68 1116-1120
Polyhydroxylated Spirostanol Saponins from the Tubers of Dioscorea polygonoides
Jaime Nio Osorio, Oscar M. Mosquera Martinez, Yaned M. Correa Navarro, Kazuki Watanabe , Hiroshi Sakagami, And Yoshihiro Mimaki
Structure 13C NMR carbon spectrum simulation picture
23. , Spirostanol Sapogenins, and a Pregnane Genin from Tupistra Chinese and Their Cytotoxical
wen-bin Pan, fang-Rong Chang, li-mei wei, and yang-chang wu
123] Chad C. STESSMAN, RAINER EBEL, Angelo J. Corvino, and Phillip Crews
Structure 13C NMR carbon spectrum simulation diagram
1. 24-METHYL-5α-Cholest-24 (28) -ne-3β, 6α, 8,14α, 15β, 16β, 26-26- heptaol
相似度:66.6%
Journal of Natural Products 1990 Vol 53 366
Starfish Saponins, Part 43. Structures of Two New Sulfated Steroidal Fucofuranosides (Imbricatosides A and B) and Six New Polyhydroxysteroids from the Starfish Dermasterias IMBricata
Insto, Luigi Minale, Raffaele Riccio
Structure 13C NMR carbon spectrum simulation graph
2. 24r-methylcholesta-3β, 5α, 6β-Triol
Nature Product Research 1997 10 231-237
Two 11α-Acetoxysterols from the Palauan Soft Coral lobophytum cf. Pauciflorum
Qing Lu; D. John Faulkner
Structure 13C NMR 碳谱模拟图
3 . Compound 9a
相似度:64.2%
Journal of Natural Products 1995 58 653-671
Chemical and Biological Investigation of the Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico
Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio PalagiaNO, Stefano Maurelli, Raffaele Riccio, Franco Zollo
Structure 13C NMR carbon spectrum simulation map
4. 11α-ACETOXY-24R-METHYLCHOLESTA-3β, 5α, 6β-Triol
c30H56NO5 similarity: 633.3%: 63.3% 123]Natural Product Research 1997 10 231-237
Two 11α-Acetoxysterols from the Palauan Soft Coral lobophytum cf. Pauciflorum
Qing Lu; D. John Faulkner
Structure 13C NMR 碳谱模拟图
5 . 24-O-Sulfate of (24s) -5α-Cholestane-3β, 5α, 6β, 15α, 24-petAol
C27H47O8SNA similarity: 62.9%
Journal of natural Products 2006 (2) 224-228 224-228
Polar Steroidal Compounds from the Far Eastern Starfish Henricia leviuscula
Natalia V. Ivanchina, Alla A. Kicha, Anatoly I. Kalinovsky, Pavel S. Dmitrenok, Andrey S.Dmitrenok, Elena L. Chaikina, Valentin A. Stonik , Margherita Gavagnin, and Guido Cimino
Structure 13C NMR 碳谱模拟图
6 . (22R,25S)-solanid-5-enine-3β,5α,6β-triol
相似度:62.9%[ 123] Chemical u0026 amp; PHARMACEUTICAL BULLETIN 1988 36 4700-4705
New Sterodial Alkaloids from the Chinese Herb Drug, u0026 QUOT; Bei-Mu u0026 Quot;
KO KANEKO, TAKAO KATSUHARA, Yukie Kitamura, Makoto Nishizawa, YUH-PAN CHEN HON-YEN HSU
Structure 13C NMR carbon spectrum
6. C29H41NO7 相似度:62.0%
Tetrahedron 2004 60 2379-2385
Novel sesquiterpenoids as tyrosine kinase inhibitors produced by Stachybotrys chortarum
Maru0026#305;u0026#769;a J Vázquez, Alfonso Vega, Alfonso Rivera-Sagredo , Mar u0026#305; u0026#769; A D Jiménez-ALFARO, Emilio D u0026#305; EZ, juan A Hueso-Rodr u0026#305; Guez
Structure 13C NMR carbon spectrum [ 123]8 . compound 10
C28H50O4 相似度:60.7%
Chemical u0026amp; Pharmaceutical Bulletin 1986 34 4590-4596
Marine Natural Products. XV. : Chemical Constituents of an Okinawan Soft Coral of Xenia sp. ( Xeniidae)
Isao Kitagawa, Motomasa Kobayashi, CUI Zheng, Yutaka Kiyota and Mayumi Ohnishi
Structure 13C NMR carbon spectrum simulation graph
9. 6β, 25ξ, 26-petol
C28H50O5 similarity: 60.7%
Chemical u0026 amp; Pharmaceutical Bulletin 1983 31 4127-4129
Marine Sterols. XIV. Isolation of (24S)-24-Methyl-5α-cholestane-3β, 5, 6β, 25ζ, 26-pentol from the Soft Coral Sarcophyton glaucum
MASARU KOBAYASHI and HIROSHI MITSUHASHI
Structure 13C NMR carbon spectrum simulation diagram
10. Compound 9
Similarity: 60.7%
Chemical u0026 amp; PHARMACEUTICAL BULLETIN 1984 32 1244-1247
A New GlyCosyl Ester of A 3, 4-Seco-Triterpenene FROM KOREAN MEDICINAL PLANT, ACANTHOPANAX CHIISANENSIS (ARALIACEAE)
DugRyong Hahn,Ryoji Kasai,JeungHee Kim,Shigenori Taniyasu and Osamu Tanaka
Structure 13C NMR 碳谱模拟图
11 . compound 5
相似度: 60.7%
Steroids 2008 73 562-567
New Anti-Inflammatic Steroids from the formosan soft Cral Clavularia viridis
chin-hsiang Chang, zhi-hong wen, shng-kwihg, shng-kwihg, shang-kwihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kweihg, shang-kwihg, shang-kweihg, six ] Structure 13C NMR carbon spectrum simulation diagram
12. (24r) -24-METHYL-5α-cholesta-3β, 5,6β, 15α, 24,28-hexaol 28-Sulfate
Similarity: 60.7%[60.7% 123] Journal of Nature Products 1995 VOL 58 653-671
Chemical and Biology Investigation of The Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico
Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio Palagiano, Stefano Maurelli, Raffaele Riccio, Franco Zollo
Structure 13C NMR 碳谱模拟图
13 . aervecdysteroid A
C28H44O6 相似度:60.7%
Steroids 2013 78 1098-1102
Ecdysteroids from the flowers of Aerva javanica
Muhammad Saleem, Sara Musaddiq, Naheed Riaz, Momina Zubair , Muhammad Ashraf, Rumana Nasar, Abdul Jabbar
Structure 13C NMR carbon spectrum simulation graph
14. ERGOST-3β, 5α, 6β-Triol
Similarity: 60.7%
Acta Scientiaarum Natures University United 46 (4) 116-118
The Secondary Metabolite of the Soft CORAL CESPITULALIA CECERULEA (Ⅱ)
He xi-xin, yan su-jung-yu, zang long-mei
structure 13c NMR carbon spectrum simulation diagram
15. (24s) -Eregostane-1α, 3β, 5α, 6β, 11α-petAol
C28H50O5 similarity: 60.7%
Marine Drugs 2013 11 775-787
bioactive Polyoxygenated Steroids from the South China SEA SOFT CORAL, SARCOPHYTON SP.
ZENGLEI WANG, Hua Tang, Pan Wang, Wei Gong, Mei Xue, Hongwei ZHANG, TAOFANG LIU, BAOSHU LIU, yanghu yi and wen zhang
structure 13c nmmmnmu 13c nmmmmuer 123] 16. 24e-METHYL-1α, 3β, 11α-Trihydrolest-5-E8-OIC Acid
C28H44O4 Similarity: 60.7%
The Journic CHEMISTRY 1985 50 2988-2992
STEROLS in marine invertebrates. 51. Isolation and structure elucidation of C-18 functionalized sterols from the soft coral Sinularia dissecta
Barbara M. Jagodzinska, James S. Trimmer, William Fenical, Carl Djerassi
Structure 13C NMR 碳谱模拟图
17. 5α-choosta-3β, 5,6β, 15α, 16β, 26-hexao
C27H48O6 Similarity: 60%
Russian Chemical Bulletin 1994 43 1726-1730
Polyhydroxysteroids FROM the FAR- Eastern starfishCtenodiscus crispatus
A. A. Kicha, A. I. Kalinovskii, N. I. Ivanchina, Yu. N. El'kin and V. A. Stonik
Structure 13C NMR 碳谱模拟图
18 . compound 41
C30H50O4 相似度:60 %
heterocycles 2012 85 1117-1139
synthesis and Biological Evaluation of Oleanolic Acid Derivatives as Novel Inhibitors of Protein Tyrosine Phosphatase 1B
Hui Li, Hui Zou, Lixin Gao, Ting Liu, Fan Yang, Jingya Li, Jia Li,* Wen-Wei Qiu,* and Jie Tang
Structure 13C NMR carbon spectrum simulation diagram
19. 3β-activity-6α, 12β-dihydroxy-20r, 25-epoxydammarne
C32H54O5 Similarity: 59.3%
Chemistry of natural Compounds 2009 45 664-664-664-45 664- 672
Synthesis of Panaxatriol Glucosides
L. N. Atopkkina and v. A. Denisenko
Structure 13C NMR carbon spectrum simulation graph
20. 9,10-di-22-o-cerethl-beboutyll-injobout
C32H46O6 相似度:59.3%
Journal of Natural Products 2012 75 34-47
Proteasome Inhibitors from Neoboutonia melleri
Christophe Long, Joséphine Beck, Frédéric Cantagrel, Laurence Marcourt, Laure Vendier, Bruno David, Fabien Plisson, Fadila Derguini, Isabelle Vandenberghe, Yannick Aussagues, Frédéric Ausseil, Catherine Lavaud, Franu0026#231;ois Sautel, and Georges Massiot
Structure 13C NMR 碳谱模拟图
21 . 11α-acetoxy-gorgostane-3β,5α,6β,12α-tetraol
C32H54O6 相似度:59.3%
Marine Drugs 2013 11 775-787
Bioactive Polyoxygenated Steroids from the South China Sea Soft Coral, Sarcophyton sp.
ZENGLEI WANG, HUA TANG, PAN WANG, Wei Gong, Mei Xue, HONGWEI ZHANG, TAOFANG LIU, BAOSHU LIU, Yanghu yi and wen zhang
Structure 13C NMR carbon spectrum simulation picture
22. Compound 2333]相似度:59.2%
Journal of Natural Products 2005 68 1116-1120
Polyhydroxylated Spirostanol Saponins from the Tubers of Dioscorea polygonoides
Jaime Nio Osorio, Oscar M. Mosquera Martinez, Yaned M. Correa Navarro, Kazuki Watanabe , Hiroshi Sakagami, And Yoshihiro Mimaki
Structure 13C NMR carbon spectrum simulation picture
23. , Spirostanol Sapogenins, and a Pregnane Genin from Tupistra Chinese and Their Cytotoxical
wen-bin Pan, fang-Rong Chang, li-mei wei, and yang-chang wu
123] Chad C. STESSMAN, RAINER EBEL, Angelo J. Corvino, and Phillip Crews
Structure 13C NMR carbon spectrum simulation diagram
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