Coumaran (BioDeep_00000862598)

Main id: BioDeep_00000017466

 

PANOMIX_OTCML-2023


代谢物信息卡片


InChI=1\C8H8O\c1-2-4-8-7(3-1)5-6-9-8\h1-4H,5-6H

化学式: C8H8O (120.0575118)
中文名称: 2,3-二氢苯并呋喃
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C12=CC=CC=C1CCO2
InChI: InChI=1S/C8H8O/c1-2-4-8-7(3-1)5-6-9-8/h1-4H,5-6H2

描述信息

Coumaran (2,3-Dihydrobenzofuran) is an acetylcholinesterase (AChE) inhibitor isolated from leaves of L. camara. Coumaran can be used as a biopesticide[1].
Coumaran (2,3-Dihydrobenzofuran) is an acetylcholinesterase (AChE) inhibitor isolated from leaves of L. camara. Coumaran can be used as a biopesticide[1].

同义名列表

10 个代谢物同义名

InChI=1\C8H8O\c1-2-4-8-7(3-1)5-6-9-8\h1-4H,5-6H; Benzofuran, 2,3-dihydro-; 2,3-Dihydro-1-benzofuran; 2,3-Dihydrobenzofuran; EINECS 207-817-3; 183962_ALDRICH; 37281_FLUKA; SB 01482; Coumaran; 496-16-2



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)

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

  • Zili Ren, Min Lv, Huqi Liu, Houpeng Wen, Yuling Zhang, Hui Xu. Optimization of Osthole as a Pesticide Candidate: Synthesis, Crystal Structures, and Agrochemical Properties of Acrylate Derivatives of Isopropenyl 2,3-Dihydrobenzofurans. Journal of agricultural and food chemistry. 2023 Nov; ?(?):. doi: 10.1021/acs.jafc.3c02213. [PMID: 37966481]
  • Mariana Sánchez-Ramos, Silvia Marquina-Bahena, Laura Alvarez, Antonio Bernabé-Antonio, Emmanuel Cabañas-García, Angélica Román-Guerrero, Francisco Cruz-Sosa. Obtaining 2,3-Dihydrobenzofuran and 3-Epilupeol from Ageratina pichinchensis (Kunth) R.King & Ho.Rob. Cell Cultures Grown in Shake Flasks under Photoperiod and Darkness, and Its Scale-Up to an Airlift Bioreactor for Enhanced Production. Molecules (Basel, Switzerland). 2023 Jan; 28(2):. doi: 10.3390/molecules28020578. [PMID: 36677637]
  • Yallappa Rajashekar, Anjanappa Raghavendra, Nandagopal Bakthavatsalam. Acetylcholinesterase inhibition by biofumigant (Coumaran) from leaves of Lantana camara in stored grain and household insect pests. BioMed research international. 2014; 2014(?):187019. doi: 10.1155/2014/187019. [PMID: 25025036]
  • V D Kancheva, L Saso, S E Angelova, M C Foti, A Slavova-Kasakova, C Daquino, V Enchev, O Firuzi, J Nechev. Antiradical and antioxidant activities of new bio-antioxidants. Biochimie. 2012 Feb; 94(2):403-15. doi: 10.1016/j.biochi.2011.08.008. [PMID: 21884748]
  • Hiroaki Aoshima, Toshio Miyase, Tsutomu Warashina. Caffeic acid oligomers with hyaluronidase inhibitory activity from Clinopodium gracile. Chemical & pharmaceutical bulletin. 2012; 60(4):499-507. doi: 10.1248/cpb.60.499. [PMID: 22466733]
  • Young-Won Chin, Hee-Byung Chai, William J Keller, A Douglas Kinghorn. Lignans and other constituents of the fruits of Euterpe oleracea (Acai) with antioxidant and cytoprotective activities. Journal of agricultural and food chemistry. 2008 Sep; 56(17):7759-64. doi: 10.1021/jf801792n. [PMID: 18656934]
  • Jin-ao Duan, Liuying Wang, Shihui Qian, Shulan Su, Yuping Tang. A new cytotoxic prenylated dihydrobenzofuran derivative and other chemical constituents from the rhizomes of Atractylodes lancea DC. Archives of pharmacal research. 2008 Aug; 31(8):965-9. doi: 10.1007/s12272-001-1252-z. [PMID: 18787781]
  • Surat Boonphong, Pakawan Puangsombat, Apiwat Baramee, Chulabhorn Mahidol, Somsak Ruchirawat, Prasat Kittakoop. Bioactive compounds from Bauhinia purpurea possessing antimalarial, antimycobacterial, antifungal, anti-inflammatory, and cytotoxic activities. Journal of natural products. 2007 May; 70(5):795-801. doi: 10.1021/np070010e. [PMID: 17480099]
  • Hirotsugu Ogura, Takako Nakanishi-Ueda, Toshihiko Ueda, Shinichi Iwai, Seiichi Uchida, Yuta Saito, Yoko Taguchi, Hajime Yasuhara, Donald Armstrong, Katsuji Oguchi, Ryohei Koide. Effect of a dihydrobenzofuran derivative on lipid hydroperoxide-induced rabbit corneal neovascularization. Journal of pharmacological sciences. 2007 Feb; 103(2):234-40. doi: 10.1254/jphs.fp0061301. [PMID: 17287586]
  • Andrej Skerjanec. The clinical pharmacokinetics of darifenacin. Clinical pharmacokinetics. 2006; 45(4):325-50. doi: 10.2165/00003088-200645040-00001. [PMID: 16584282]
  • Luisa Ugolini, Isabella Della Noce, Paolo Trincia, Valerio Borzatta, Sandro Palmieri. Benzodioxole derivatives as negative effectors of plant proteases. Journal of agricultural and food chemistry. 2005 Sep; 53(19):7494-501. doi: 10.1021/jf0580418. [PMID: 16159178]
  • Xiao-Mei Li, Mao Lin, Ying-Hong Wang. Stilbenoids from the lianas of Gnetum pendulum. Journal of Asian natural products research. 2003 Jun; 5(2):113-9. doi: 10.1080/1028602021000054964. [PMID: 12765195]
  • J Malmström, M Jonsson, I A Cotgreave, L Hammarström, M Sjödin, L Engman. The antioxidant profile of 2,3-dihydrobenzo[b]furan-5-ol and its 1-thio, 1-seleno, and 1-telluro analogues. Journal of the American Chemical Society. 2001 Apr; 123(15):3434-40. doi: 10.1021/ja0035811. [PMID: 11472114]
  • F N Melo, V R Navarro, M S Silva, E V Da-Cunha, J M Barbosa-Filho, R Braz-Filho. Bowdenol, a new 2,3-dihydrobenzofuran constituent from Bowdichia virgilioides. Natural product letters. 2001; 15(4):261-6. doi: 10.1080/10575630108041290. [PMID: 11833621]
  • S Ohkawa, K Fukatsu, S Miki, T Hashimoto, J Sakamoto, T Doi, Y Nagai, T Aono. 5-aminocoumarans: dual inhibitors of lipid peroxidation and dopamine release with protective effects against central nervous system trauma and ischemia. Journal of medicinal chemistry. 1997 Feb; 40(4):559-73. doi: 10.1021/jm960411j. [PMID: 9046347]
  • D T Gibson, S M Resnick, K Lee, J M Brand, D S Torok, L P Wackett, M J Schocken, B E Haigler. Desaturation, dioxygenation, and monooxygenation reactions catalyzed by naphthalene dioxygenase from Pseudomonas sp. strain 9816-4. Journal of bacteriology. 1995 May; 177(10):2615-21. doi: 10.1128/jb.177.10.2615-2621.1995. [PMID: 7751268]