Ursane (BioDeep_00000249655)

   

natural product


代谢物信息卡片


(1S,2R,4aR,6aR,6aR,6bR,8aS,12aS,14aR,14bS)-1,2,4a,6a,6b,9,9,12a-octamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydro-1H-picene

化学式: C30H52 (412.4068792)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1CCC2(C)CCC3(C)C(CCC4C5(C)CCCC(C)(C)C5CCC43C)C2C1C
InChI: InChI=1S/C30H52/c1-20-12-16-27(5)18-19-29(7)22(25(27)21(20)2)10-11-24-28(6)15-9-14-26(3,4)23(28)13-17-30(24,29)8/h20-25H,9-19H2,1-8H3/t20-,21+,22-,23+,24-,25+,27-,28+,29-,30-/m1/s1



数据库引用编号

5 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)

7 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

  • Siyuan Shao, Ruofei Li, Kexin Wang, Wenqi Xia, Baosong Cui, Shuai Li. Ilexchinene, a new seco-ursane triterpenoid from the leaves of Ilex chinensis with therapeutic effect on neuroinflammation by attenuating the MAPK/NF-κB signaling pathway. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2023 Dec; 121(?):155110. doi: 10.1016/j.phymed.2023.155110. [PMID: 37776618]
  • Longlong Wu, Jingwen Liu, Kaixian Chen, Liuqiang Zhang, Yiming Li. Triterpenoids from the roots of Sanguisorba officinalis and their Nrf2 stimulation activity. Phytochemistry. 2023 Oct; 214(?):113803. doi: 10.1016/j.phytochem.2023.113803. [PMID: 37516332]
  • Xiang Pu, Menghan Chen, Ming Lei, Xinyu Lin, Jiahua Zhang, Zhihui Ai, Jinwei He, Yuke Liu, Shengnan Yang, Hanguang Wang, Jinqiu Liao, Li Zhang, Qianming Huang. Discovery of unique CYP716C oxidase involved in pentacyclic triterpene biosynthesis from Camptotheca acuminata. Plant physiology and biochemistry : PPB. 2023 Aug; 202(?):107929. doi: 10.1016/j.plaphy.2023.107929. [PMID: 37542826]
  • Xiu-Qin Zheng, Lei-Xin Song, Zhu-Zhen Han, Ying-Bo Yang, Yi Zhang, Li-Hua Gu, Li Yang, Gui-Xin Chou, Zheng-Tao Wang. Pentacyclic triterpenoids from spikes of Prunella vulgaris L. with thyroid tumour cell cytostatic bioactivities. Natural product research. 2023 May; 37(9):1518-1526. doi: 10.1080/14786419.2021.2024532. [PMID: 35038938]
  • Fiammetta Alagna, James Reed, Ornella Calderini, Ramesha Thimmappa, Nicolò G M Cultrera, Alice Cattivelli, Davide Tagliazucchi, Soraya Mousavi, Roberto Mariotti, Anne Osbourn, Luciana Baldoni. OeBAS and CYP716C67 catalyze the biosynthesis of health-beneficial triterpenoids in olive (Olea europaea L.) fruits. The New phytologist. 2023 Mar; ?(?):. doi: 10.1111/nph.18863. [PMID: 36880371]
  • Jiao-Jiao Cui, Ying-Shan Han, Bin Zhou, Jian-Min Yue. Ursane and 24-Noroleanane-Type Triterpenoids with Anti-HIV Activity from the Twigs and Leaves of Antirhea chinensis. Chemistry & biodiversity. 2022 Oct; 19(10):e202200716. doi: 10.1002/cbdv.202200716. [PMID: 36008326]
  • Akifumi Nagatomo, Naoki Inoue, Takuya Konno, Yin Xu, Chinatsu Sakamoto, Mayuko Sone, Aya Shibasaka, Osamu Muraoka, Kiyofumi Ninomiya, Masayuki Yoshikawa, Yoshiaki Manse, Toshio Morikawa. Ursane-type triterpene oligoglycosides with anti-hepatosteatosis and anti-hyperlipidemic activity from the leaves of Ilex paraguariensis A. St.-Hil. Journal of natural medicines. 2022 Jun; 76(3):654-669. doi: 10.1007/s11418-022-01614-5. [PMID: 35292883]
  • Huiqiang Wei, Jianghong Guo, Xiao Sun, Wenfeng Gou, Hongxin Ning, Haihua Shang, Qiang Liu, Wenbin Hou, Yiliang Li. Discovery of Natural Ursane-type SENP1 Inhibitors and the Platinum Resistance Reversal Activity Against Human Ovarian Cancer Cells: A Structure-Activity Relationship Study. Journal of natural products. 2022 05; 85(5):1248-1255. doi: 10.1021/acs.jnatprod.1c01166. [PMID: 35500202]
  • Luis Apaza Ticona, Karla Slowing, Andreea Madalina Serban, Marcos Humanes Bastante, María J Hernáiz. Wound healing, anti-inflammatory and anti-melanogenic activities of ursane-type triterpenes from Semialarium mexicanum (Miers) Mennega. Journal of ethnopharmacology. 2022 May; 289(?):115009. doi: 10.1016/j.jep.2022.115009. [PMID: 35077827]
  • Xiang-Jian Zhong, Na Zhou, Xin Wang, Jin-Jie Li, Hui Ma, Yue Jiao, Jia-Hui Xu, Peng-Cheng Lin, Xiao-Ya Shang. Three new ursane-type triterpenoids from Rosmarinus officinalis and their biological activities. Chinese journal of natural medicines. 2022 Feb; 20(2):155-160. doi: 10.1016/s1875-5364(21)60103-6. [PMID: 35279243]
  • Yutong Han, Ya Yang, Yan Li, Xin Yin, Zhiyu Chen, Danni Yang, Yongping Yang, Yunqiang Yang, Xuefei Yang. Genome-Wide Identification of OSC Gene Family and Potential Function in the Synthesis of Ursane- and Oleanane-Type Triterpene in Momordica charantia. International journal of molecular sciences. 2021 Dec; 23(1):. doi: 10.3390/ijms23010196. [PMID: 35008620]
  • Klaudia Michalska, Agnieszka Galanty, Thanh Nguyen Le, Janusz Malarz, Nguyen Quoc Vuong, Van Cuong Pham, Anna Stojakowska. New Polyesterified Ursane Derivatives from Leaves of Maesa membranacea and Their Cytotoxic Activity. Molecules (Basel, Switzerland). 2021 Nov; 26(22):. doi: 10.3390/molecules26227013. [PMID: 34834104]
  • Shima Hashemi, Amir Reza Jassbi, Nasrollah Erfani, Razieh Kiani, Hassan Seradj. Two new cytotoxic ursane triterpenoids from the aerial parts of Salvia urmiensis Bunge. Fitoterapia. 2021 Oct; 154(?):105030. doi: 10.1016/j.fitote.2021.105030. [PMID: 34506871]
  • Pham Hai Yen, Vu Van Doan, Giang Thi Kim Lien, Nguyen Thị Hong Chuong, Nguyen Thi Viet Thanh, Do Thi Trang, Duong Thi Dung, Nguyen Xuan Nhiem, Bui Huu Tai, Chau Van Minh, Phan Van Kiem. New lupane-type and ursane-type triterpene saponins from the leaves of Trevesia palmata. Natural product research. 2021 Oct; 35(19):3285-3292. doi: 10.1080/14786419.2019.1696797. [PMID: 31790291]
  • Zarina Bano, Sabira Begum, Syed Saqib Ali, Zareena Kiran, Bina S Siddiqui, Shariqa Khawaja, Ayaz Ahmed. Novel ursane-type triterpene from the fresh leaves of Carissa carandas and evaluation of cytotoxicity. Journal of Asian natural products research. 2021 Sep; 23(9):892-898. doi: 10.1080/10286020.2020.1791098. [PMID: 32646240]
  • Larissa Kom Ma'mag, Auguste Abouem A Zintchem, Kopa Kowa Théodora, Alex de Théodore Atchadé, Tchokouaha Yamthe Lauve, Michel Frédérich, Dominique Serge Ngono Bikobo, Dieudonné Emmanuel Pegnyemb. Antiplasmodial and antileishmanial inhibitory activity of triterpenes and steroidal alkaloid from the leaves of Funtumia elastica (Preuss) Stapf (Apocynaceae). Fitoterapia. 2021 Jun; 151(?):104869. doi: 10.1016/j.fitote.2021.104869. [PMID: 33657429]
  • Yu-Nong Tian, Bai-Lin Li, Juan-Juan Hu, Jin-Dan Xie, Wen-Jing Xiao, Ling-Hui Nie, Jie-Wei Wu. Rosanortriterpenes A-B, two new nortriterpenes from the fruits of Rosa laevigata var. leiocapus. Natural product research. 2021 Apr; 35(7):1172-1179. doi: 10.1080/14786419.2019.1644512. [PMID: 31328555]
  • Giuseppina Chianese, Francesca Masi, Donatella Cicia, Daniele Ciceri, Sabrina Arpini, Mario Falzoni, Ester Pagano, Orazio Taglialatela-Scafati. Isomadecassoside, a New Ursane-Type Triterpene Glycoside from Centella asiatica Leaves, Reduces Nitrite Levels in LPS-Stimulated Macrophages. Biomolecules. 2021 03; 11(4):. doi: 10.3390/biom11040494. [PMID: 33806006]
  • Natalia A Luchnikova, Victoria V Grishko, Irina B Ivshina. Biotransformation of Oleanane and Ursane Triterpenic Acids. Molecules (Basel, Switzerland). 2020 Nov; 25(23):. doi: 10.3390/molecules25235526. [PMID: 33255782]
  • Zhou-Wei Wu, Wei-Bo Li, Jing Zhou, Xin Liu, Lun Wang, Bin Chen, Ming-Kui Wang, Lilian Ji, Wei-Cheng Hu, Fu Li. Oleanane- and Ursane-Type Triterpene Saponins from Centella asiatica Exhibit Neuroprotective Effects. Journal of agricultural and food chemistry. 2020 Jul; 68(26):6977-6986. doi: 10.1021/acs.jafc.0c01476. [PMID: 32502339]
  • Haiyan Feng, Jihe Tang, Peiliang Zhang, Yu Miao, Tao Wu, Zhihong Cheng. Anti-adipogenic 18,19-seco-ursane stereoisomers and oleane-type saponins from Ilex cornuta leaves. Phytochemistry. 2020 Jul; 175(?):112363. doi: 10.1016/j.phytochem.2020.112363. [PMID: 32278135]
  • 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]
  • Ahmed Galal Osman, Zulfiqar Ali, Omer Fantoukh, Vijayasankar Raman, Ramsay S T Kamdem, Ikhlas Khan. Glycosides of ursane-type triterpenoid, benzophenone, and iridoid from Vangueria agrestis (Fadogia agrestis) and their anti-infective activities. Natural product research. 2020 Mar; 34(5):683-691. doi: 10.1080/14786419.2018.1497031. [PMID: 30325205]
  • Yunzhi Li, Mingli Liang, Lu Ma, Qi Chen, Xian Huang. A novel Ursane-type triterpene saponin from Ajuga multiflora. Natural product research. 2020 Jan; 34(2):300-304. doi: 10.1080/14786419.2018.1527837. [PMID: 30375259]
  • Xue-Li Tong, Hai-Tao Wang, Jiang-Ping Xu, Li-Wen Tian. A new polyhydroxylated oleanane triterpenoid from the roots of Rhodomyrtus tomentosa. Natural product research. 2020 Jan; 34(2):204-209. doi: 10.1080/14786419.2018.1525376. [PMID: 30580617]
  • Sara Bechkri, Abdulmagid Alabdul Magid, Laurence Voutquenne-Nazabadioko, Djemaa Berrehal, Ahmed Kabouche, Meryem Lehbili, Hichem Lakhal, Amin Abedini, Sophie C Gangloff, Hamid Morjani, Zahia Kabouche. Triterpenes from Salvia argentea var. aurasiaca and their antibacterial and cytotoxic activities. Fitoterapia. 2019 Nov; 139(?):104296. doi: 10.1016/j.fitote.2019.104296. [PMID: 31401222]
  • Dan Lu, Weiyang Zhang, Yingnan Jiang, Yu Zhang, Dabo Pan, Dan Zhang, Xinsheng Yao, Yang Yu. Two new triterpenoids from Gardenia jasminoides fruits. Natural product research. 2019 Oct; 33(19):2789-2794. doi: 10.1080/14786419.2018.1502764. [PMID: 30518256]
  • Fu-Cai Ren, Guan-Yan Li, Nuosu Nama, Zhen-Hua Liu, Liu Yang, Jun Zhou, Jiang-Miao Hu. 13,27-Cycloursane, ursane and oleanane triterpenoids from the leaves of Lucuma nervosa. Fitoterapia. 2019 Jul; 136(?):104178. doi: 10.1016/j.fitote.2019.104178. [PMID: 31121254]
  • Giancarlo Verardo, Andrea Gorassini, Daniele Fraternale. New triterpenic acids produced in callus culture from fruit pulp of Acca sellowiana (O. Berg) Burret. Food research international (Ottawa, Ont.). 2019 05; 119(?):596-604. doi: 10.1016/j.foodres.2018.10.037. [PMID: 30884693]
  • Hui-Juan Zhai, Jin-Hai Yu, Qianqian Zhang, Hai-Shan Liu, Jun-Sheng Zhang, Xiu-Qing Song, Yuying Zhang, Hua Zhang. Cytotoxic and antibacterial triterpenoids from the roots of Morinda officinalis var. officinalis. Fitoterapia. 2019 Mar; 133(?):56-61. doi: 10.1016/j.fitote.2018.12.011. [PMID: 30579769]
  • Yu-Dan Mei, Nan Zhang, Wei-Yang Zhang, Jin-Shan Tang, Hua Zhou, Yang Yu, Xin-Sheng Yao. Two new ursane-type nortriterpenes from Lonicera macranthoides and their iNOS-inhibitory activities. Chinese journal of natural medicines. 2019 Jan; 17(1):27-32. doi: 10.1016/s1875-5364(19)30006-8. [PMID: 30704620]
  • Xiang-Yu Zhang, Wei Li, Jian Wang, Ning Li, Mao-Sheng Cheng, Kazuo Koike. Protein tyrosine phosphatase 1B inhibitory activities of ursane-type triterpenes from Chinese raspberry, fruits of Rubus chingii. Chinese journal of natural medicines. 2019 Jan; 17(1):15-21. doi: 10.1016/s1875-5364(19)30004-4. [PMID: 30704618]
  • Yunong Tian, Lu Feng, Bailin Li, Juanjuan Hu, Jindan Xie, Wenjing Xiao, Linghui Nie, Jiewei Wu. Rosanortriterpene C, a 3,24-Dinor-2,4-seco-ursane Triterpene from the Fruits of Rosa laevigata var. leiocapus. Chemical & pharmaceutical bulletin. 2019; 67(11):1255-1258. doi: 10.1248/cpb.c19-00648. [PMID: 31685754]
  • Hai-Xia Zhan, Juan Li, Han-Li Ruan, Peng Zhang, Hui-Fang Pi. Two New Ursane-type Triterpenoid Glycosides from Ilex Cornuta. Current medical science. 2018 Dec; 38(6):976-981. doi: 10.1007/s11596-018-1972-4. [PMID: 30536058]
  • Pérez-Gutiérrez Rosa Martha, Enriquez-Alvirde Susana Gabriela. Ursane derivatives isolated from leaves of Hylocereus undatus inhibit glycation at multiple stages. Chinese journal of natural medicines. 2018 Nov; 16(11):856-865. doi: 10.1016/s1875-5364(18)30127-4. [PMID: 30502767]
  • Bora Kim, Jae Woo Han, Men Thi Ngo, Quang Le Dang, Jin-Cheol Kim, Hun Kim, Gyung Ja Choi. Identification of novel compounds, oleanane- and ursane-type triterpene glycosides, from Trevesia palmata: their biocontrol activity against phytopathogenic fungi. Scientific reports. 2018 09; 8(1):14522. doi: 10.1038/s41598-018-32956-4. [PMID: 30266953]
  • Changcai Bai, Xiuping Zhou, Lu Han, Yongjie Yu, Nan Li, Ming Zhang, Zhuo Qu, Pengfei Tu. Two new 18, 19-seco Triterpenoids from Ilex asprella (Hook. et Arn.) Champ. ex Benth. Fitoterapia. 2018 Jun; 127(?):42-46. doi: 10.1016/j.fitote.2018.04.014. [PMID: 29698682]
  • Ok Tae Kim, Yurry Um, Mei Lan Jin, Jang Uk Kim, Daniela Hegebarth, Lucas Busta, Radu C Racovita, Reinhard Jetter. A Novel Multifunctional C-23 Oxidase, CYP714E19, is Involved in Asiaticoside Biosynthesis. Plant & cell physiology. 2018 Jun; 59(6):1200-1213. doi: 10.1093/pcp/pcy055. [PMID: 29579306]
  • Nabila Zergainoh, Maria Letizia Ciavatta, Marianna Carbone, Fatma Bitam, Mohamed Cherif Aberkane, Margherita Gavagnin. Exploring the Chemical Diversity of Algerian Plants: Three New Pentacyclic Triterpenoids from Launaea acanthoclada Roots. Molecules (Basel, Switzerland). 2017 Dec; 23(1):. doi: 10.3390/molecules23010080. [PMID: 29301201]
  • Yanyan Deng, Juan Hua, Wenjia Wang, Zhonglang Zhan, Anqi Wang, Shihong Luo. Cytotoxic Terpenoids from the Roots of Dracocephalum taliense. Molecules (Basel, Switzerland). 2017 Dec; 23(1):. doi: 10.3390/molecules23010057. [PMID: 29280951]
  • Yong Luo, Li-Zhi Cheng, Qi Luo, Yong-Ming Yan, Shu-Mei Wang, Qin Sun, Yong-Xian Cheng. New ursane-type triterpenoids from Clerodendranthus spicatus. Fitoterapia. 2017 Jun; 119(?):69-74. doi: 10.1016/j.fitote.2017.04.001. [PMID: 28392270]
  • Rajesh Chandra Misra, Shubha Sharma, Sandeep, Anchal Garg, Chandan Singh Chanotiya, Sumit Ghosh. Two CYP716A subfamily cytochrome P450 monooxygenases of sweet basil play similar but nonredundant roles in ursane- and oleanane-type pentacyclic triterpene biosynthesis. The New phytologist. 2017 Apr; 214(2):706-720. doi: 10.1111/nph.14412. [PMID: 28967669]
  • Quan Wen, Yan Lu, Zhi Chao, Dao-Feng Chen. Anticomplement triterpenoids from the roots of Ilex asprella. Bioorganic & medicinal chemistry letters. 2017 02; 27(4):880-886. doi: 10.1016/j.bmcl.2017.01.007. [PMID: 28094185]
  • Sachiko Sugimoto. The Chemical Constituents of Uninvestigated Plants in Hiroshima Prefecture. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan. 2017; 137(2):215-220. doi: 10.1248/yakushi.16-00205. [PMID: 28154334]
  • Saori Terazawa, Yuka Uemura, Yuka Koyama, Susumu Kawakami, Sachiko Sugimoto, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Masatoshi Kawahata, Kentaro Yamaguchi. Microtropins Q-W, ent-Labdane Glucosides: Microtropiosides G-I, Ursane-Type Triterpene Diglucoside and Flavonol Glycoside from the Leaves of Microtropis japonica. Chemical & pharmaceutical bulletin. 2017; 65(10):930-939. doi: 10.1248/cpb.c17-00459. [PMID: 28966277]
  • Wirongrong Kaweetripob, Chulabhorn Mahidol, Sanit Thongnest, Hunsa Prawat, Somsak Ruchirawat. Polyoxygenated ursane and oleanane triterpenes from Siphonodon celastrineus. Phytochemistry. 2016 Sep; 129(?):58-67. doi: 10.1016/j.phytochem.2016.07.006. [PMID: 27469098]
  • Lawrence Onyango Arot Manguro, Samuel Otieno Wagai. Ursane and tirucallane-type triterpenes of Boswellia rivae oleo-gum resin. Journal of Asian natural products research. 2016 Sep; 18(9):854-64. doi: 10.1080/10286020.2016.1165674. [PMID: 27049028]
  • Amgad I M Khedr, Sabrin R M Ibrahim, Gamal A Mohamed, Hany E A Ahmed, Amany S Ahmad, Mahmoud A Ramadan, Atef E Abd El-Baky, Koji Yamada, Samir A Ross. New ursane triterpenoids from Ficus pandurata and their binding affinity for human cannabinoid and opioid receptors. Archives of pharmacal research. 2016 Jul; 39(7):897-911. doi: 10.1007/s12272-016-0784-y. [PMID: 27350550]
  • Jin-Dong Zhong, Xue-Wei Zhao, Xuan-Qin Chen, Hong-Mei Li, Chin-Ho Chen, Xue-Shan Xia, Rong-Tao Li. Two new ursane-type triterpenoid saponins from Elsholtzia bodinieri. Archives of pharmacal research. 2016 Jun; 39(6):771-7. doi: 10.1007/s12272-016-0750-8. [PMID: 27138284]
  • I-Hsiao Chen, Ying-Chi Du, Tsong-Long Hwang, I-Fen Chen, Yu-Hsuan Lan, Hsin-Fu Yen, Fang-Rong Chang, Yang-Chang Wu. Anti-inflammatory triterpenoids from the stems of Microtropis fokienensis. Molecules (Basel, Switzerland). 2014 Apr; 19(4):4608-23. doi: 10.3390/molecules19044608. [PMID: 24736870]
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  • André L Rüdiger, Valdir F Veiga-Junior. Chemodiversity of ursane- and oleanane-type triterpenes in Amazonian Burseraceae oleoresins. Chemistry & biodiversity. 2013 Jun; 10(6):1142-53. doi: 10.1002/cbdv.201200315. [PMID: 23776030]
  • Chuangjun Li, Li Li, Chao Wang, Jingzhi Yang, Fei Ye, Jinying Tian, Yikang Si, Dongming Zhang. A new ursane-type nor-triterpenoid from the leaves of Eucommia ulmoides Oliv. Molecules (Basel, Switzerland). 2012 Nov; 17(12):13960-8. doi: 10.3390/molecules171213960. [PMID: 23183887]
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  • Jie Gao, Jianmei Shi, Xiaomeng Lu, Cuirong Sun, Yuanjiang Pan. Differentiation of common diastereoisomeric ursane-type triterpenoids by high-performance liquid chromatography/tandem mass spectrometry. Rapid communications in mass spectrometry : RCM. 2011 May; 25(10):1349-55. doi: 10.1002/rcm.4978. [PMID: 21503999]
  • Gedson Rodrigues de Morais Lima, Camila de Albuquerque Montenegro, Cynthia Layse Ferreira de Almeida, Petrônio Filgueiras de Athayde-Filho, José Maria Barbosa-Filho, Leônia Maria Batista. Database survey of anti-inflammatory plants in South America: a review. International journal of molecular sciences. 2011; 12(4):2692-749. doi: 10.3390/ijms12042692. [PMID: 21731467]
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