Indane (BioDeep_00000023230)

   

human metabolite


代谢物信息卡片


2,3-dihydro-1H-indene

化学式: C9H10 (118.0782)
中文名称: 茚满
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1CC2=CC=CC=C2C1
InChI: InChI=1S/C9H10/c1-2-5-9-7-3-6-8(9)4-1/h1-2,4-5H,3,6-7H2

描述信息

Indane belongs to the family of Indanes. These are compounds containing an indane moiety, which consists of a cyclopentane fused to a benzene ring.

同义名列表

5 个代谢物同义名

2,3-dihydro-1H-indene; Benzocyclopentane; Indane; INDAN; Indan



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)

1 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

  • Valeriy P Shendrikov, Anna S Alekseeva, Erik F Kot, Konstantin S Mineev, Daria S Tretiakova, Abdulilah Ece, Ivan A Boldyrev. Indane Based Molecular Motors: UV-Switching Increases Number of Isomers. Molecules (Basel, Switzerland). 2022 Oct; 27(19):. doi: 10.3390/molecules27196716. [PMID: 36235252]
  • Alicia Jiménez-Almarza, Daniel Diez-Iriepa, Mourad Chioua, Beatriz Chamorro, Isabel Iriepa, Ricardo Martínez-Murillo, Dimitra Hadjipavlou-Litina, María Jesús Oset-Gasque, José Marco-Contelles. Synthesis, neuroprotective and antioxidant capacity of PBN-related indanonitrones. Bioorganic chemistry. 2019 05; 86(?):445-451. doi: 10.1016/j.bioorg.2019.01.071. [PMID: 30771691]
  • Neil Frankish, Helen Sheridan. 6-(methylamino)hexane-1,2,3,4,5-pentanol 4-(((1S,2S)-1-hydroxy-2,3-dihydro-1H,1'H-[2,2-biinden]-2-yl)methyl)benzoate (PH46A): a novel small molecule with efficacy in murine models of colitis. Journal of medicinal chemistry. 2012 Jun; 55(11):5497-505. doi: 10.1021/jm300390f. [PMID: 22663546]
  • Hiroaki Shiohara, Tetsuya Nakamura, Norihiko Kikuchi, Tomonaga Ozawa, Ryuichi Nagano, Akane Matsuzawa, Hideki Ohnota, Takahide Miyamoto, Kazuo Ichikawa, Kiyoshi Hashizume. Discovery of novel indane derivatives as liver-selective thyroid hormone receptor β (TRβ) agonists for the treatment of dyslipidemia. Bioorganic & medicinal chemistry. 2012 Jun; 20(11):3622-34. doi: 10.1016/j.bmc.2012.03.056. [PMID: 22542282]
  • Branislav R Ranković, Marijana M Kosanić, Tatjana P Stanojković. Antioxidant, antimicrobial and anticancer activity of the lichens Cladonia furcata, Lecanora atra and Lecanora muralis. BMC complementary and alternative medicine. 2011 Oct; 11(?):97. doi: 10.1186/1472-6882-11-97. [PMID: 22013953]
  • Hedi Ben Mansour, Sonia Yatouji, Sihem Mbarek, Ikram Houas, Afef Delai, Dorra Dridi. Correlation between antibutyrylcholinesterasic and antioxidant activities of three aqueous extracts from Tunisian Rhus pentaphyllum. Annals of clinical microbiology and antimicrobials. 2011 Aug; 10(?):32. doi: 10.1186/1476-0711-10-32. [PMID: 21880140]
  • V Ani, Kamatham A Naidu. Antioxidant potential of bitter cumin (Centratherum anthelminticum (L.) Kuntze) seeds in in vitro models. BMC complementary and alternative medicine. 2011 May; 11(?):40. doi: 10.1186/1472-6882-11-40. [PMID: 21599890]
  • J Lowe, S Drozda, W Qian, M-C Peakman, J Liu, J Gibbs, J Harms, C Schmidt, K Fisher, C Strick, A Schmidt, M Vanase, L Lebel. A novel, non-substrate-based series of glycine type 1 transporter inhibitors derived from high-throughput screening. Bioorganic & medicinal chemistry letters. 2007 Mar; 17(6):1675-8. doi: 10.1016/j.bmcl.2006.12.109. [PMID: 17257843]
  • Bahar Ahmed, Adnan J Al-Rehaily, Jaber S Mossa. Barbeyol: a new phenolic indane type component from Barbeya oleoides. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2002 Jan; 57(1-2):17-20. doi: ". [PMID: 11926530]
  • 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]
  • C J BROOKS, L YOUNG. Biochemical studies of toxic agents. 9. The metabolic conversion of indene into cis- and trans- indane-1: 2-diol. The Biochemical journal. 1956 Jun; 63(2):264-9. doi: 10.1042/bj0630264. [PMID: 13328820]