viminalol (BioDeep_00000859723)

Main id: BioDeep_00000001046

 

PANOMIX_OTCML-2023


代谢物信息卡片


(3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-Octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydro-picen-3-ol

化学式: C30H50O (426.386145)
中文名称: alpha-香树脂醇, α-香树脂醇
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C
InChI: InChI=1S/C30H50O/c1-19-11-14-27(5)17-18-29(7)21(25(27)20(19)2)9-10-23-28(6)15-13-24(31)26(3,4)22(28)12-16-30(23,29)8/h9,19-20,22-25,31H,10-18H2,1-8H3/t19-,20+,22+,23-,24+,25+,27-,28+,29-,30-/m1/s1

描述信息

Alpha-amyrin is a pentacyclic triterpenoid that is ursane which contains a double bond between positions 12 and 13 and in which the hydrogen at the 3beta position is substituted by a hydroxy group. It is a pentacyclic triterpenoid and a secondary alcohol. It derives from a hydride of an ursane.
alpha-Amyrin is a natural product found in Ficus septica, Ficus virens, and other organisms with data available.
See also: Calendula Officinalis Flower (part of); Viburnum opulus bark (part of); Eupatorium perfoliatum whole (part of) ... View More ...

同义名列表

38 个代谢物同义名

(3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-Octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydro-picen-3-ol; (3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-ol; (3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol; 4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-ol; alpha-Amyrin, analytical standard; 3.BETA.-HYDROXYURS-12-ENE; 5alpha-urs-12-en-3beta-ol; (3.beta.)-Urs-12-en-3-ol; Urs-12-en-3-ol, (3beta)-; amyrin, (3alpha)-isomer; 3beta-HYDROXYURS-12-ENE; (3beta)-urs-12-en-3-ol; Urs-12-en-3-ol, (3b)-; .ALPHA.-AMYRIN [MI]; urs-12-ene-3beta-ol; Urs-12-en-3beta-ol; .alpha.-Amyrenol; UNII-30ZAG40J8N; AMYRIN, ALPHA-; alpha-amyrenol; alpha-Amyrine; alpha -Amyrin; alpha-Amyrin; alfa-Amyrin; 30ZAG40J8N; viminalol; a-amyrin; α-Amyrin; Urs-12-en-3-ol, (3beta)- (9CI); EINECS 211-352-1; LMPR01060011; AIDS-070313; 53017_FLUKA; NSC 114787; AIDS070313; ST5411384; 638-95-9; C08615



数据库引用编号

14 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

PlantCyc(1)

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)

905 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。



文献列表

  • Noha Mokhtar Abd-El-Aziz, Mohamed Saeed Hifnawy, Rehab Ahmed Lotfy, Inas Youssef Younis. LC/MS/MS and GC/MS/MS metabolic profiling of Leontodon hispidulus, in vitro and in silico anticancer activity evaluation targeting hexokinase 2 enzyme. Scientific reports. 2024 03; 14(1):6872. doi: 10.1038/s41598-024-57288-4. [PMID: 38519553]
  • Han-Bin Choi, Sangrea Shim, Myeong-Hyeon Wang, Yong-Eui Choi. De Novo Transcriptome Sequencing of Codonopsis lanceolata for Identification of Triterpene Synthase and Triterpene Acetyltransferase. International journal of molecular sciences. 2023 Mar; 24(6):. doi: 10.3390/ijms24065769. [PMID: 36982844]
  • Tran Duc Viet, Tran Dang Xuan, La Hoang Anh. α-Amyrin and β-Amyrin Isolated from Celastrus hindsii Leaves and Their Antioxidant, Anti-Xanthine Oxidase, and Anti-Tyrosinase Potentials. Molecules (Basel, Switzerland). 2021 Nov; 26(23):. doi: 10.3390/molecules26237248. [PMID: 34885832]
  • Bruna F Mazzeu, Tatiana M Souza-Moreira, Andrew A Oliveira, Melissa Remlinger, Lidiane G Felippe, Sandro R Valentini, Rafael V C Guido, Cleslei F Zanelli, Maysa Furlan. The Methionine 549 and Leucine 552 Residues of Friedelin Synthase from Maytenus ilicifolia Are Important for Substrate Binding Specificity. Molecules (Basel, Switzerland). 2021 Nov; 26(22):. doi: 10.3390/molecules26226806. [PMID: 34833897]
  • Jiawei Zhou, Tianyuan Hu, Yuan Liu, Lichan Tu, Yadi Song, Yun Lu, Yifeng Zhang, Yuru Tong, Yujun Zhao, Ping Su, Xiaoyi Wu, Luqi Huang, Wei Gao. Cytochrome P450 catalyses the 29-carboxyl group formation of celastrol. Phytochemistry. 2021 Oct; 190(?):112868. doi: 10.1016/j.phytochem.2021.112868. [PMID: 34273756]
  • María Antonela Zígolo, Matías Rivero Goytia, Hugo Ramiro Poma, Verónica Beatriz Rajal, Verónica Patricia Irazusta. Virtual screening of plant-derived compounds against SARS-CoV-2 viral proteins using computational tools. The Science of the total environment. 2021 Aug; 781(?):146400. doi: 10.1016/j.scitotenv.2021.146400. [PMID: 33794459]
  • Gabriele Vilkickyte, Lina Raudone. Optimization, Validation and Application of HPLC-PDA Methods for Quantification of Triterpenoids in Vaccinium vitis-idaea L. Molecules (Basel, Switzerland). 2021 Mar; 26(6):. doi: 10.3390/molecules26061645. [PMID: 33809511]
  • Alberto Asteggiano, Andrea Occhipinti, Andrea Capuzzo, Enrica Mecarelli, Riccardo Aigotti, Claudio Medana. Quali-Quantitative Characterization of Volatile and Non-Volatile Compounds in Protium heptaphyllum (Aubl.) Marchand Resin by GC-MS Validated Method, GC-FID and HPLC-HRMS2. Molecules (Basel, Switzerland). 2021 Mar; 26(5):. doi: 10.3390/molecules26051447. [PMID: 33800018]
  • Jiaming Wang, Mei Jin, Chunshi Jin, Chao Ye, Yi Zhou, Rongshen Wang, Huanhuan Cui, Wei Zhou, Gao Li. A new pentacyclic triterpenoid from the leaves of Rhododendron dauricum L. with inhibition of NO production in LPS-induced RAW 264.7 cells. Natural product research. 2020 Dec; 34(23):3313-3319. doi: 10.1080/14786419.2019.1566822. [PMID: 30810367]
  • Feilong Chen, Dong-Li Liu, Wei Wang, Xiao-Man Lv, Weixi Li, Li-Dong Shao, Wen-Jing Wang. Bioactive triterpenoids from Sambucus javanica Blume. Natural product research. 2020 Oct; 34(19):2816-2821. doi: 10.1080/14786419.2019.1596092. [PMID: 30968700]
  • Derya Bakir, Mehmet Akdeniz, Abdulselam Ertas, Mustafa A Yilmaz, Ismail Yener, Mehmet Firat, Ufuk Kolak. A GC-MS method validation for quantitative investigation of some chemical markers in Salvia hypargeia Fisch. & C.A. Mey. of Turkey: Enzyme inhibitory potential of ferruginol. Journal of food biochemistry. 2020 09; 44(9):e13350. doi: 10.1111/jfbc.13350. [PMID: 32686189]
  • Jian Wang, Hui-Xin Lin, Huan Zhao, Juan Guo, Ping Su, Jian Yang, Xiao-Yi Wu, Lu-Qi Huang, Wei Gao. Molecular cloning and functional characterization of multiple ApOSCs from Andrographis paniculata. Chinese journal of natural medicines. 2020 Sep; 18(9):659-665. doi: 10.1016/s1875-5364(20)60004-8. [PMID: 32928509]
  • Bruna Karen Cardoso, Herika Line Marko de Oliveira, Ulisses Zonta Melo, Carla Maria Mariano Fernandez, Caio Franco de Araújo Almeida Campo, José Eduardo Gonçalves, Antônio Laverde, Mariza Barion Romagnolo, Giani Andrea Linde, Zilda Cristiani Gazim. Antioxidant activity of α and β-amyrin isolated from Myrcianthes pungens leaves. Natural product research. 2020 Jun; 34(12):1777-1781. doi: 10.1080/14786419.2018.1525715. [PMID: 30465617]
  • Emmanuel Mfotie Njoya, Hermine L D Maza, Pierre Mkounga, Ulrich Koert, Augustin E Nkengfack, Lyndy J McGaw. Selective cytotoxic activity of isolated compounds from Globimetula dinklagei and Phragmanthera capitata (Loranthaceae). Zeitschrift fur Naturforschung. C, Journal of biosciences. 2020 May; 75(5-6):135-144. doi: 10.1515/znc-2019-0171. [PMID: 32229684]
  • Pisanee Srisawat, Ery Odette Fukushima, Shuhei Yasumoto, Jekson Robertlee, Hideyuki Suzuki, Hikaru Seki, Toshiya Muranaka. Identification of oxidosqualene cyclases from the medicinal legume tree Bauhinia forficata: a step toward discovering preponderant α-amyrin-producing activity. The New phytologist. 2019 10; 224(1):352-366. doi: 10.1111/nph.16013. [PMID: 31230357]
  • Zhixue Wu, Hui Xu, Meiling Wang, Ruoting Zhan, Weiwen Chen, Ren Zhang, Zaoyuan Kuang, Fengxue Zhang, Kui Wang, Jiangyong Gu. Molecular Docking and Molecular Dynamics Studies on Selective Synthesis of α-Amyrin and β-Amyrin by Oxidosqualene Cyclases from Ilex Asprella. International journal of molecular sciences. 2019 Jul; 20(14):. doi: 10.3390/ijms20143469. [PMID: 31311103]
  • Juan Xiong, Jiang Wan, Jie Ding, Pei-Pei Wang, Guang-Lei Ma, Jia Li, Jin-Feng Hu. Camellianols A-G, Barrigenol-like Triterpenoids with PTP1B Inhibitory Effects from the Endangered Ornamental Plant Camellia crapnelliana. Journal of natural products. 2017 11; 80(11):2874-2882. doi: 10.1021/acs.jnatprod.7b00241. [PMID: 29064696]
  • Thanh Tra Nguyen, Bich Ngan Truong, Huong Doan Thi Mai, Marc Litaudon, Van Hung Nguyen, Thao Do Thi, Van Minh Chau, Van Cuong Pham. Cytotoxic dammarane-type triterpenoids from the leaves of Viburnum sambucinum. Bioorganic & medicinal chemistry letters. 2017 04; 27(8):1665-1669. doi: 10.1016/j.bmcl.2017.03.014. [PMID: 28318944]
  • Jaeyoung Kwon, Nguyen Tuan Hiep, Dong-Woo Kim, Sungeun Hong, Yuanqiang Guo, Bang Yeon Hwang, Hak Ju Lee, Woongchon Mar, Dongho Lee. Chemical Constituents Isolated from the Root Bark of Cudrania tricuspidata and Their Potential Neuroprotective Effects. Journal of natural products. 2016 08; 79(8):1938-51. doi: 10.1021/acs.jnatprod.6b00204. [PMID: 27420919]
  • Patrícia de Brum Vieira, Nícolas Luiz Feijó Silva, Gloria Narjara Santos da Silva, Denise Brentan Silva, Norberto Peporine Lopes, Simone Cristina Baggio Gnoatto, Márcia Vanusa da Silva, Alexandre José Macedo, Jaume Bastida, Tiana Tasca. Caatinga plants: Natural and semi-synthetic compounds potentially active against Trichomonas vaginalis. Bioorganic & medicinal chemistry letters. 2016 May; 26(9):2229-36. doi: 10.1016/j.bmcl.2016.03.061. [PMID: 27020521]
  • Lili Huang, Jia Li, Hechun Ye, Changfu Li, Hong Wang, Benye Liu, Yansheng Zhang. Molecular characterization of the pentacyclic triterpenoid biosynthetic pathway in Catharanthus roseus. Planta. 2012 Nov; 236(5):1571-81. doi: 10.1007/s00425-012-1712-0. [PMID: 22837051]
  • Xia Li, Junying Zhang, Wenyuan Gao, Haiyang Wang. Study on chemical composition, anti-inflammatory and anti-microbial activities of extracts from Chinese pear fruit (Pyrus bretschneideri Rehd.). Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2012 Oct; 50(10):3673-9. doi: 10.1016/j.fct.2012.07.019. [PMID: 22824088]
  • Cesar A Silva, Luiz A S Madureira. Source correlation of biomarkers in a mangrove ecosystem on Santa Catarina Island in southern Brazil. Anais da Academia Brasileira de Ciencias. 2012 Sep; 84(3):589-604. doi: 10.1590/s0001-37652012005000042. [PMID: 22782538]
  • A C Siani, M J Nakamura, M R R Tappin, S S Monteiro, A C Guimarães, M F S Ramos. Chemical composition of South American Burseraceae non-volatile oleoresins and preliminary solubility assessment of their commercial blend. Phytochemical analysis : PCA. 2012 Sep; 23(5):529-39. doi: 10.1002/pca.2351. [PMID: 22323110]
  • Anna Szakiel, Cezary Pączkowski, Heini Koivuniemi, Satu Huttunen. Comparison of the triterpenoid content of berries and leaves of lingonberry Vaccinium vitis-idaea from Finland and Poland. Journal of agricultural and food chemistry. 2012 May; 60(19):4994-5002. doi: 10.1021/jf300375b. [PMID: 22490120]
  • Baiquan Chen, Qian Zhang, Wei Wang, Huan Huang, Wenyi Kang. [Alpha-glucosidase inhibitory active constituents contained in nutshell of Trapa acornis]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2012 May; 37(10):1408-11. doi: . [PMID: 22860451]
  • Maha M Salama, Zeinab A Kandil, Wafaa T Islam. Cytotoxic compounds from the leaves of Gaillardia aristata Pursh. growing in Egypt. Natural product research. 2012; 26(22):2057-62. doi: 10.1080/14786419.2011.606219. [PMID: 21846263]
  • Shahira M Ezzat, Hossam M Abdallah, Ghada A Fawzy, Shohda A El-Maraghy. Hepatoprotective constituents of Torilis radiata Moench (Apiaceae). Natural product research. 2012; 26(3):282-5. doi: 10.1080/14786419.2011.587422. [PMID: 21867456]
  • Consolacion Y Ragasa, Dinah L Espineli, Chien-Chang Shen. A new triterpene from Barringtonia asiatica. Natural product research. 2012; 26(20):1869-75. doi: 10.1080/14786419.2011.619187. [PMID: 21929282]
  • Edyta Biskup, Marek Gołębiowski, Robert Gniadecki, Piotr Stepnowski, Ewa Łojkowska. Triterpenoid α-amyrin stimulates proliferation of human keratinocytes but does not protect them against UVB damage. Acta biochimica Polonica. 2012; 59(2):255-60. doi: . [PMID: 22577623]
  • Garland More, Namrita Lall, Ahmed Hussein, Thilivhali Emmanuel Tshikalange. Antimicrobial Constituents of Artemisia afra Jacq. ex Willd. against Periodontal Pathogens. Evidence-based complementary and alternative medicine : eCAM. 2012; 2012(?):252758. doi: 10.1155/2012/252758. [PMID: 22693528]
  • Laís Goyos Pieroni, Fernanda Mendes de Rezende, Valdecir Farias Ximenes, Anne Lígia Dokkedal. Antioxidant activity and total phenols from the methanolic extract of Miconia albicans (Sw.) Triana leaves. Molecules (Basel, Switzerland). 2011 Nov; 16(11):9439-50. doi: 10.3390/molecules16119439. [PMID: 22075573]
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  • Cyril Brendolise, Yar-Khing Yauk, Ellen D Eberhard, Mindy Wang, David Chagne, Christelle Andre, David R Greenwood, Lesley L Beuning. An unusual plant triterpene synthase with predominant α-amyrin-producing activity identified by characterizing oxidosqualene cyclases from Malus × domestica. The FEBS journal. 2011 Jul; 278(14):2485-99. doi: 10.1111/j.1742-4658.2011.08175.x. [PMID: 21575133]
  • Chun-ying Xie, Le-wei Lin. [Study on the chemical constituents of Pithecellobium clypearia]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2011 Jul; 34(7):1060-2. doi: . [PMID: 22066399]
  • Jianhong Ching, Hai-Shu Lin, Chay-Hoon Tan, Hwee-Ling Koh. Quantification of α- and β-amyrin in rat plasma by gas chromatography-mass spectrometry: application to preclinical pharmacokinetic study. Journal of mass spectrometry : JMS. 2011 May; 46(5):457-64. doi: 10.1002/jms.1912. [PMID: 21500304]
  • Taha S El-Alfy, Shahira M Ezzat, Ahmed K Hegazy, Aziza M M Amer, Gehan M Kamel. Isolation of biologically active constituents from Moringa peregrina (Forssk.) Fiori. (family: Moringaceae) growing in Egypt. Pharmacognosy magazine. 2011 Apr; 7(26):109-15. doi: 10.4103/0973-1296.80667. [PMID: 21716619]
  • D D Duan, C Y Bu, J Cheng, Y N Wang, G L Shi. Isolation and identification of acaricidal compounds in Inula japonica (Asteraceae). Journal of economic entomology. 2011 Apr; 104(2):375-8. doi: 10.1603/ec10129. [PMID: 21510182]
  • Rajnish Gupta, Jai B S Kachhawa, R S Gupta, Anil Kumar Sharma, M C Sharma, M P Dobhal. Phytochemical evaluation and antispermatogenic activity of Thevetia peruviana methanol extract in male albino rats. Human fertility (Cambridge, England). 2011 Mar; 14(1):53-9. doi: 10.3109/14647273.2010.542230. [PMID: 21466267]
  • Feng Wang, Zhan-Lin Li, Hong-Hua Cui, Hui-Ming Hua, Yong-Kui Jing, Sheng-Wang Liang. Two new triterpenoids from the resin of Boswellia carterii. Journal of Asian natural products research. 2011 Mar; 13(3):193-7. doi: 10.1080/10286020.2010.548808. [PMID: 21409679]
  • Ali M El-Hagrassi, Mamdouh M Ali, Abeer F Osman, Mohamed Shaaban. Phytochemical investigation and biological studies of Bombax malabaricum flowers. Natural product research. 2011 Jan; 25(2):141-51. doi: 10.1080/14786419.2010.518146. [PMID: 21246441]
  • Bertin Vouffo, Etienne Dongo, Petrea Facey, Andrea Thorn, George Sheldrick, Armin Maier, Heinz Herbert Fiebig, Hartmut Laatsch. Antiarol cinnamate and africanoside, a cinnamoyl triterpene and a hydroperoxy-cardenolide from the stem bark of Antiaris africana. Planta medica. 2010 Oct; 76(15):1717-23. doi: 10.1055/s-0030-1249958. [PMID: 20533166]
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