PARIS V (BioDeep_00000230579)

Main id: BioDeep_00000007053

 

PANOMIX_OTCML-2023


代谢物信息卡片


(2S,3R,4R,5R,6S)-2-(((2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(((4S,5R,6aR,6bS,8aS,8bR,9S,10R,11aS,12aS,12bS)-5,6a,8a,9-tetramethyl-1,3,3,4,4,5,5,6,6a,6b,6,7,8,8a,8b,9,11a,12,12a,12b-icosahydrospiro[naphtho[2,1:4,5]indeno[2,1-b]furan-10,2-pyran]-4-yl)oxy)tetrahydro-2H-pyran-3-yl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triol

化学式: C39H62O12 (722.4241)
中文名称: 次皂甙元 A, 薯蓣次皂苷A, 次皂甙元A, 薯蓣皂苷A
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1
InChI: InChI=1S/C39H62O12/c1-18-8-13-39(46-17-18)19(2)28-26(51-39)15-25-23-7-6-21-14-22(9-11-37(21,4)24(23)10-12-38(25,28)5)48-36-34(32(44)30(42)27(16-40)49-36)50-35-33(45)31(43)29(41)20(3)47-35/h6,18-20,22-36,40-45H,7-17H2,1-5H3/t18-,19+,20+,22+,23-,24+,25+,26+,27-,28+,29+,30-,31-,32+,33-,34-,35+,36-,37+,38+,39-/m1/s1

描述信息

Prosapogenin A is a natural product found in Ophiopogon planiscapus, Dracaena draco, and other organisms with data available.
Prosapogenin A, a natural product from Veratrum, induces apoptosis in human cancer cells in vitro via inhibition of the STAT3 signaling pathway and glycolysis[1].
Prosapogenin A, a natural product from Veratrum, induces apoptosis in human cancer cells in vitro via inhibition of the STAT3 signaling pathway and glycolysis[1].

同义名列表

19 个代谢物同义名

(2S,3R,4R,5R,6S)-2-(((2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(((4S,5R,6aR,6bS,8aS,8bR,9S,10R,11aS,12aS,12bS)-5,6a,8a,9-tetramethyl-1,3,3,4,4,5,5,6,6a,6b,6,7,8,8a,8b,9,11a,12,12a,12b-icosahydrospiro[naphtho[2,1:4,5]indeno[2,1-b]furan-10,2-pyran]-4-yl)oxy)tetrahydro-2H-pyran-3-yl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triol; (2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,5R,6R,7S,8R,9S,12S,13R,16S)-5,7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2-oxane]-16-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol; .BETA.-D-GLUCOPYRANOSIDE, (3.BETA.,25R)-SPIROST-5-EN-3-YL 2-O-(6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL)-; beta-Glucopyranoside, (3beta,25R)-spirost-5-en-3-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-; (25R)-spirost-5en-3beta-ol 3-O-alpha-L-rhamnopyranosyl-(1-2)-beta-D-glucopyranoside; (25R)-3beta-(2-O-alpha-L-Rhamnopyranosyl-beta-D-glucopyranosyloxy)spirosta-5-ene; DIOSGENIN 3-O-.ALPHA.-L-RHAMNOPYRANOSYL-(1->2)-.BETA.-D-GLUCOPYRANOSIDE; 3-O-(Rhaa1-2Glcb)-(25R)-spirost-5en-3beta-ol; HDXIQHTUNGFJIC-FOAHKCLGSA-N; Lilioglycoside D; 17-DEOXYPARIS VI; Paris saponin V; prosapogenin D1; Prosapogenin A; Ophiopogonin C; Progenin III; prosapogenin; Saponin Ta; PARIS V



数据库引用编号

8 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

23 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表


文献列表

  • Chengyu Yang, Bo Li, Jinwei Zhou, Yufei Chen, Guohua Xia, Yuping Shen, Jixuan Chen, Jiali Shao, Yaya Yang, Huan Yang. Conversion of Dioscorea zingiberensis saponins to prosapogenin A by enzymatic hydrolysis. Natural product research. 2023 May; 37(9):1421-1428. doi: 10.1080/14786419.2021.2011273. [PMID: 34866518]
  • Ryota Akiyama, Masaru Nakayasu, Naoyuki Umemoto, Junpei Kato, Midori Kobayashi, Hyoung Jae Lee, Yukihiro Sugimoto, Yoko Iijima, Kazuki Saito, Toshiya Muranaka, Masaharu Mizutani. Tomato E8 Encodes a C-27 Hydroxylase in Metabolic Detoxification of α-Tomatine during Fruit Ripening. Plant & cell physiology. 2021 Oct; 62(5):775-783. doi: 10.1093/pcp/pcab080. [PMID: 34100555]
  • Zhi Dai, Hui Liu, Bei Wang, Dong Yang, Yan-Yan Zhu, Huan Yan, Pei-Feng Zhu, Ya-Ping Liu, Hui-Cheng Chen, Yun-Li Zhao, Li-Xing Zhao, Xu-Dong Zhao, Hai-Yang Liu, Xiao-Dong Luo. Structures/cytotoxicity/selectivity relationship of natural steroidal saponins against GSCs and primary mechanism of tribulosaponin A. European journal of medicinal chemistry. 2021 Jan; 210(?):113068. doi: 10.1016/j.ejmech.2020.113068. [PMID: 33310292]
  • Michela Maestrini, Aldo Tava, Simone Mancini, Doriana Tedesco, Stefania Perrucci. In Vitro Anthelmintic Activity of Saponins from Medicago spp. Against Sheep Gastrointestinal Nematodes. Molecules (Basel, Switzerland). 2020 Jan; 25(2):. doi: 10.3390/molecules25020242. [PMID: 31936073]
  • Qinghua Han, Yi Qian, Xuda Wang, Qingying Zhang, Jingrong Cui, Pengfei Tu, Hong Liang. Cytotoxic oleanane triterpenoid saponins from Albizia julibrissin. Fitoterapia. 2017 Sep; 121(?):183-193. doi: 10.1016/j.fitote.2017.07.015. [PMID: 28764915]
  • Xuejiao Li, Chengcheng Zhao, Songsong Jing, Jiachen Sun, Xia Li, Shuli Man, Ying Wang, Wenyuan Gao. Novel phenanthrene and isocoumarin from the rhizomes of Dioscorea nipponica Makino subsp. rosthornii (Prain et Burkill) C. T. Ting (Dioscoreaceae). Bioorganic & medicinal chemistry letters. 2017 08; 27(15):3595-3601. doi: 10.1016/j.bmcl.2017.03.095. [PMID: 28606759]
  • Yu-Cai Liu, He Zhu, Shailendra Shakya, Jun-Wen Wu. Metabolic profile and pharmacokinetics of polyphyllin I, an anticancer candidate, in rats by UPLC-QTOF-MS/MS and LC-TQ-MS/MS. Biomedical chromatography : BMC. 2017 Mar; 31(3):. doi: 10.1002/bmc.3817. [PMID: 27552088]
  • Nuanjan Jaiaree, Arunporn Itharat, Srisapa Ruangnoo. Cytotoxic and Anti-inflammatory Activities of Medicinal Plants and Women’s Health Remedy Found in “Mahachotarat Scripture” of Thai Traditional Medicine. Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 2016 Jul; 99 Suppl 4(?):S211-21. doi: . [PMID: 29926715]
  • Yunkyung Han, Hyo Won Jung, Dong Hwa Lee, Sang Yong Kwon, Kun Ho Son, Yong-Ki Park. Anti-inflammatory effects of prosapogenin III from the dried roots of Liriope platyphylla in LPS-stimulated RAW264.7 cells. Journal of Asian natural products research. 2013 Sep; 15(9):1038-49. doi: 10.1080/10286020.2013.825253. [PMID: 23944983]
  • Kee Dong Yoon, Young-Won Chin, Min Hye Yang, Janggyoo Choi, Jinwoong Kim. Application of high-speed countercurrent chromatography-evaporative light scattering detection for the separation of seven steroidal saponins from Dioscorea villosa. Phytochemical analysis : PCA. 2012 Sep; 23(5):462-8. doi: 10.1002/pca.2342. [PMID: 22407490]
  • Lu Zheng, Jian Zheng, Qingying Zhang, Bin Wang, Yuying Zhao, Lijun Wu. Three new oleanane triterpenoid saponins acetylated with monoterpenoid acid from Albizia julibrissin. Fitoterapia. 2010 Oct; 81(7):859-63. doi: 10.1016/j.fitote.2010.05.014. [PMID: 20562005]
  • Jian-Ming Jin, Ying-Jun Zhang, Hai-Zhou Li, Chong-Ren Yang. Cytotoxic steroidal saponins from Polygonatum zanlanscianense. Journal of natural products. 2004 Dec; 67(12):1992-5. doi: 10.1021/np049897u. [PMID: 15620239]
  • Lu Zheng, Gang Wu, Bin Wang, Li-jun Wu, Yu-ying Zhao. [Isolation and identification of chemical constituents from Albizia julibrissin Durazz]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences. 2004 Aug; 36(4):421-5. doi: ". [PMID: 15303140]
  • San-Long Wang, Bing Cai, Cheng-Bin Cui, Hong-Wei Liu, Chun-Fu Wu, Xin-Sheng Yao. [Apoptosis of human chronic myeloid leukemia k562 cell induced by prosapogenin B of dioscin (P.B) in vitro]. Ai zheng = Aizheng = Chinese journal of cancer. 2003 Aug; 22(8):795-800. doi: NULL. [PMID: 12917022]
  • Kyung-Tae Lee, Jongwon Choi, Won-Tae Jung, Jung-Hwan Nam, Hyun-Ju Jung, Hee-Juhn Park. Structure of a new echinocystic acid bisdesmoside isolated from Codonopsis lanceolata roots and the cytotoxic activity of prosapogenins. Journal of agricultural and food chemistry. 2002 Jul; 50(15):4190-3. doi: 10.1021/jf011647l. [PMID: 12105944]
  • Laurence Voutquenne, Cécile Kokougan, Catherine Lavaud, Isabelle Pouny, Marc Litaudon. Triterpenoid saponins and acylated prosapogenins from Harpullia austro-caledonica. Phytochemistry. 2002 Apr; 59(8):825-32. doi: 10.1016/s0031-9422(01)00482-4. [PMID: 11937161]
  • H C Chiang, T H Tseng, C J Wang, C F Chen, W S Kan. Experimental antitumor agents from Solanum indicum L. Anticancer research. 1991 Sep; 11(5):1911-7. doi: . [PMID: 1768063]
  • H Yokoyama, S Hiai, H Oura. [Rat plasma corticosterone secretion-inducing activities of total saponin and prosapogenin methyl esters from the roots of Platycodon grandiflorum A.DC]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan. 1982 Dec; 102(12):1191-4. doi: 10.1248/yakushi1947.102.12_1191. [PMID: 7182453]
  • R C Sengers. Urinary red blood-cells in rhabdomyolysis. Lancet (London, England). 1977 Jan; 1(8004):192. doi: 10.1016/s0140-6736(77)91785-8. [PMID: 64718]