7-[4-[[(3E)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid (BioDeep_00001005852)

   


代谢物信息卡片


7-[4-[[(3E)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid

化学式: C40H38F2N8O7 (780.2831)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=CC(=CC(=C1OC)OC)CC2=CN=C(N=C2N)N=C3C4=C(C=CC(=C4)F)N(C3=O)CN5CCN(CC5)C6=C(C=C7C(=C6)N(C=C(C7=O)C(=O)O)C8CC8)F
InChI: InChI=1S/C40H38F2N8O7/c1-55-32-13-21(14-33(56-2)36(32)57-3)12-22-18-44-40(46-37(22)43)45-34-25-15-23(41)4-7-29(25)50(38(34)52)20-47-8-10-48(11-9-47)31-17-30-26(16-28(31)42)35(51)27(39(53)54)19-49(30)24-5-6-24/h4,7,13-19,24H,5-6,8-12,20H2,1-3H3,(H,53,54)(H2,43,44,46)/b45-34+



数据库引用编号

1 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)

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。

亚细胞结构定位 关联基因列表


文献列表

  • Rosa Purgatorio, Modesto de Candia, Marco Catto, Mariagrazia Rullo, Leonardo Pisani, Nunzio Denora, Antonio Carrieri, Alisa A Nevskaya, Leonid G Voskressensky, Cosimo D Altomare. Evaluation of Water-Soluble Mannich Base Prodrugs of 2,3,4,5-Tetrahydroazepino[4,3-b]indol-1(6H)-one as Multitarget-Directed Agents for Alzheimer's Disease. ChemMedChem. 2021 02; 16(3):589-598. doi: 10.1002/cmdc.202000583. [PMID: 33156950]
  • Songül Boy, Fikret Türkan, Murat Beytur, Abdülmelik Aras, Onur Akyıldırım, Halide Sedef Karaman, Haydar Yüksek. Synthesis, design, and assessment of novel morpholine-derived Mannich bases as multifunctional agents for the potential enzyme inhibitory properties including docking study. Bioorganic chemistry. 2021 02; 107(?):104524. doi: 10.1016/j.bioorg.2020.104524. [PMID: 33317836]
  • Łukasz Szczukowski, Edward Krzyżak, Adrianna Zborowska, Patrycja Zając, Katarzyna Potyrak, Krzysztof Peregrym, Benita Wiatrak, Aleksandra Marciniak, Piotr Świątek. Design, Synthesis and Comprehensive Investigations of Pyrrolo[3,4-d]pyridazinone-Based 1,3,4-Oxadiazole as New Class of Selective COX-2 Inhibitors. International journal of molecular sciences. 2020 Dec; 21(24):. doi: 10.3390/ijms21249623. [PMID: 33348757]
  • Sha Ding, Katherine R Fike, Michael Klemba, Paul R Carlier. In vitro and in vivo evaluation of the antimalarial MMV665831 and structural analogs. Bioorganic & medicinal chemistry letters. 2020 09; 30(17):127348. doi: 10.1016/j.bmcl.2020.127348. [PMID: 32738996]
  • Swetha K Maddili, Leela Prasad Yandrati, Shakuntala Siddam, Vijaya Kumar Kannekanti, Himabindu Gandham. Green synthesis, biological and spectroscopic study on the interaction of multi-component Mannich bases of imidazo[2,1-b]benzothiazoles with human serum albumin. Journal of photochemistry and photobiology. B, Biology. 2017 Nov; 176(?):9-16. doi: 10.1016/j.jphotobiol.2017.08.026. [PMID: 28938203]
  • Bhupendra M Mistry, Han-Seung Shin, Young-Soo Keum, Muthuraman Pandurangan, Doo Hwan Kim, So Hyun Moon, Avinash A Kadam, Surendra K Shinde, Rahul V Patel. Synthesis and Evaluation of Antioxidant and Cytotoxicity of the N-Mannich Base of Berberine Bearing Benzothiazole Moieties. Anti-cancer agents in medicinal chemistry. 2017; 17(12):1652-1660. doi: 10.2174/1871520617666170710180549. [PMID: 28699489]
  • A E Parlak, S Celik, M Karatepe, S Turkoglu, N O Alayunt, S D Dastan, M Ulas, S Sandal, S Tekin, M Koparir. Investigation of biological effects of some Mannich Bases containing Bis-1,2,4- Triazole. Cellular and molecular biology (Noisy-le-Grand, France). 2016 Jun; 62(7):46-54. doi: NULL. [PMID: 27453272]
  • Ebtehal S Al-Abdullah, Hanaa M Al-Tuwaijri, Hanan M Hassan, Mogedda E Haiba, Elsayed E Habib, Ali A El-Emam. Antimicrobial and hypoglycemic activities of novel N-Mannich bases derived from 5-(1-adamantyl)-4-substituted-1,2,4-triazoline-3-thiones. International journal of molecular sciences. 2014 Dec; 15(12):22995-3010. doi: 10.3390/ijms151222995. [PMID: 25514407]
  • Anna Czopek, Marcin Kołaczkowski, Adam Bucki, Hanna Byrtus, Maciej Pawłowski, Agata Siwek, Andrzej J Bojarski, Marek Bednarski, Dagmara Wróbel, Anna Wesołowska. Novel mannich bases, 5-arylimidazolidine-2,4-dione derivatives with dual 5-HT(1A) receptor and serotonin transporter affinity. Archiv der Pharmazie. 2013 Feb; 346(2):98-109. doi: 10.1002/ardp.201200378. [PMID: 23288448]
  • Stanislaw M Stepkowski, Judy Kao, Mou-Er Wang, Neelam Tejpal, Hemangshu Podder, Lucrezia Furian, Jonathan Dimmock, Amitabh Jha, Umashankar Das, Barry D Kahan, Robert A Kirken. The Mannich base NC1153 promotes long-term allograft survival and spares the recipient from multiple toxicities. Journal of immunology (Baltimore, Md. : 1950). 2005 Oct; 175(7):4236-46. doi: 10.4049/jimmunol.175.7.4236. [PMID: 16177063]
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  • N W Hamon, D L Bassendowski, D E Wright, J R Dimmock, L M Noble. Effect of antineoplastic and cytotoxic Mannich Bases derived from conjugated styryl ketones on mitochondrial respiration in rat liver cells. Journal of pharmaceutical sciences. 1978 Nov; 67(11):1539-42. doi: 10.1002/jps.2600671112. [PMID: 712588]
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