INDENE (BioDeep_00000307870)
代谢物信息卡片
INDENE
化学式: C9H8 (116.0625968)
中文名称: 茚
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1=Cc2ccccc2C1
InChI: InChI=1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2
数据库引用编号
7 个数据库交叉引用编号
- ChEBI: CHEBI:41921
- PubChem: 7219
- ChEMBL: CHEMBL192812
- CAS: 71551-80-9
- CAS: 9003-64-9
- CAS: 95-13-6
- PMhub: MS000076478
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)
0 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
- Ru-Feng Xia, Jun-Cheng Su, Jun Yu, Hong-Jing Zha, Jia-Le Wu, Xiao-Na Fu, Qin Cai, Luo-Sheng Wan. Anti-inflammatory lanostane triterpenoids with rearranged spirobi[indene] scaffold and their biogenetically related analogues from Euphorbia maculata.
Phytochemistry.
2023 Jul; 211(?):113682. doi:
10.1016/j.phytochem.2023.113682. [PMID: 37084863] - Najeeb Akhter, Chengqian Pan, Yanqin Liu, Yutong Shi, Bin Wu. Isolation and structure determination of a new indene derivative from endophytic fungus Aspergillus flavipes Y-62.
Natural product research.
2019 Oct; 33(20):2939-2944. doi:
10.1080/14786419.2018.1510399. [PMID: 30470134] - Kiyofumi Wanibuchi, Kouichi Hosoda, Masato Ihara, Kentaro Tajiri, Yuki Sakai, Hisashi Masui, Takashi Takahashi, Yoshikazu Hirai, Hirofumi Shimomura. Indene Compounds Synthetically Derived from Vitamin D Have Selective Antibacterial Action on Helicobacter pylori.
Lipids.
2018 04; 53(4):393-401. doi:
10.1002/lipd.12043. [PMID: 29766504] - Jone Corrales, Lauren A Kristofco, W Baylor Steele, Gavin N Saari, Jakub Kostal, E Spencer Williams, Margaret Mills, Evan P Gallagher, Terrance J Kavanagh, Nancy Simcox, Longzhu Q Shen, Fjodor Melnikov, Julie B Zimmerman, Adelina M Voutchkova-Kostal, Paul T Anastas, Bryan W Brooks. Toward the Design of Less Hazardous Chemicals: Exploring Comparative Oxidative Stress in Two Common Animal Models.
Chemical research in toxicology.
2017 04; 30(4):893-904. doi:
10.1021/acs.chemrestox.6b00246. [PMID: 27750016] - Andy J Liedtke, Brenda C Crews, Cristina M Daniel, Anna L Blobaum, Philip J Kingsley, Kebreab Ghebreselasie, Lawrence J Marnett. Cyclooxygenase-1-selective inhibitors based on the (E)-2'-des-methyl-sulindac sulfide scaffold.
Journal of medicinal chemistry.
2012 Mar; 55(5):2287-300. doi:
10.1021/jm201528b. [PMID: 22263894] - Zhi-Qiang Wang, Yong Lei, Ming-Bo Zhou, Guo-Xiang Chen, Ren-Jie Song, Ye-Xiang Xie, Jin-Heng Li. Iron-mediated [3 + 2] or [3 + 3] annulation of 2-(2-(ethynyl)phenoxy)-1-arylethanones: selective synthesis of indeno[1,2-c]chromenes and 5H-naphtho[1,2-c]chromenes.
Organic letters.
2011 Jan; 13(1):14-7. doi:
10.1021/ol102761m. [PMID: 21121634] - Ermitas Alcalde, Neus Mesquida, Sara López-Pérez, Jordi Frigola, Ramon Mercè. Indene-based scaffolds. 2. An indole-indene switch: discovery of novel indenylsulfonamides as 5-HT6 serotonin receptor agonists.
Journal of medicinal chemistry.
2009 Feb; 52(3):675-87. doi:
10.1021/jm8009469. [PMID: 19159187] - Hoon Kim, John Ralph, Fachuang Lu, Gilles Pilate, Jean-Charles Leplé, Brigitte Pollet, Catherine Lapierre. Identification of the structure and origin of thioacidolysis marker compounds for cinnamyl alcohol dehydrogenase deficiency in angiosperms.
The Journal of biological chemistry.
2002 Dec; 277(49):47412-9. doi:
10.1074/jbc.m208860200. [PMID: 12351655] - David A Nugiel, Anup Vidwans, Anna-Marie Etzkorn, Karen A Rossi, Pamela A Benfield, Catherine R Burton, Sarah Cox, Deborah Doleniak, Steven P Seitz. Synthesis and evaluation of indenopyrazoles as cyclin-dependent kinase inhibitors. 2. Probing the indeno ring substituent pattern.
Journal of medicinal chemistry.
2002 Nov; 45(24):5224-32. doi:
10.1021/jm020171+. [PMID: 12431050] - C Bakermans, A M Hohnstock-Ashe, S Padmanabhan, P Padmanabhan, E L Madsen. Geochemical and physiological evidence for mixed aerobic and anaerobic field biodegradation of coal tar waste by subsurface microbial communities.
Microbial ecology.
2002 Aug; 44(2):107-17. doi:
10.1007/s00248-002-3011-y. [PMID: 12087424] - A Fürstner, J Grabowski, C W Lehmann, T Kataoka, K Nagai. Synthesis and biological evaluation of nonylprodigiosin and macrocyclic prodigiosin analogues.
Chembiochem : a European journal of chemical biology.
2001 Jan; 2(1):60-8. doi:
10.1002/1439-7633(20010105)2:1<60::aid-cbic60>3.0.co;2-p. [PMID: 11828428] - 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] - M ALESSANDRINI, G F LANFORTI. [Determination of residues of hepatchlor (1,4,5,6,7,8,8-hepatachlor-3a,4,7,7a-tetranydro-4,7-methano indene) in olive oil].
Rendiconti - Istituto superiore di sanita.
1957; 20(7-8):816-22. doi:
". [PMID: 13485497] - 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]