(-)-Montanine (BioDeep_00000840639)
代谢物信息卡片
化学式: C17H19NO4 (301.1314014)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: COC1C=C2C(CC1O)N3CC2C4=CC5=C(C=C4C3)OCO5
InChI: InChI=1S/C17H19NO4/c1-20-15-4-11-12-7-18(13(11)5-14(15)19)6-9-2-16-17(3-10(9)12)22-8-21-16/h2-4,12-15,19H,5-8H2,1H3/t12-,13-,14-,15-/m0/s1
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)
6 个相关的物种来源信息
- 68527 - Aegle marmelos: 10.1080/14786410310001608037
- 527307 - Haemanthus montanus: 10.1021/JA01610A045
- 4695 - Hippeastrum: 10.1016/S0305-1978(03)00129-7
- 231486 - Hippeastrum vittatum: 10.1016/J.PHYMED.2007.12.001
- 112568 - Lycoris squamigera: 10.3987/COM-08-S(F)92
- 82246 - Scadoxus multiflorus: 10.1021/JO01064A076
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
- Darja Koutová, Negar Maafi, Radim Havelek, Lubomír Opletal, Gerald Blunden, Martina Řezáčová, Lucie Cahlíková. Chemical and Biological Aspects of Montanine-Type Alkaloids Isolated from Plants of the Amaryllidaceae Family.
Molecules (Basel, Switzerland).
2020 May; 25(10):. doi:
10.3390/molecules25102337
. [PMID: 32429491] - Jerald J Nair, Johannes van Staden. Antiprotozoal alkaloid principles of the plant family Amaryllidaceae.
Bioorganic & medicinal chemistry letters.
2019 10; 29(20):126642. doi:
10.1016/j.bmcl.2019.126642
. [PMID: 31515186] - Andressa Reis, Kevin Magne, Sophie Massot, Luciana R Tallini, Marina Scopel, Jaume Bastida, Pascal Ratet, José A S Zuanazzi. Amaryllidaceae alkaloids: identification and partial characterization of montanine production in Rhodophiala bifida plant.
Scientific reports.
2019 06; 9(1):8471. doi:
10.1038/s41598-019-44746-7
. [PMID: 31186470] - Jerald J Nair, Anke Wilhelm, Susanna L Bonnet, Johannes van Staden. Antibacterial constituents of the plant family Amaryllidaceae.
Bioorganic & medicinal chemistry letters.
2017 11; 27(22):4943-4951. doi:
10.1016/j.bmcl.2017.09.052
. [PMID: 29033234] - Mirian Farinon, Vanessa S Clarimundo, Graziele P R Pedrazza, Pércio S Gulko, José A S Zuanazzi, Ricardo M Xavier, Patricia G de Oliveira. Disease modifying anti-rheumatic activity of the alkaloid montanine on experimental arthritis and fibroblast-like synoviocytes.
European journal of pharmacology.
2017 Mar; 799(?):180-187. doi:
10.1016/j.ejphar.2017.02.013
. [PMID: 28192100] - Javier E Ortiz, Natalia B Pigni, Sebastián A Andujar, German Roitman, Fernando D Suvire, Ricardo D Enriz, Alejandro Tapia, Jaume Bastida, Gabriela E Feresin. Alkaloids from Hippeastrum argentinum and Their Cholinesterase-Inhibitory Activities: An in Vitro and in Silico Study.
Journal of natural products.
2016 05; 79(5):1241-8. doi:
10.1021/acs.jnatprod.5b00785
. [PMID: 27096334] - L B Pagliosa, S C Monteiro, K B Silva, J P de Andrade, J Dutilh, J Bastida, M Cammarota, J A S Zuanazzi. Effect of isoquinoline alkaloids from two Hippeastrum species on in vitro acetylcholinesterase activity.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
2010 Jul; 17(8-9):698-701. doi:
10.1016/j.phymed.2009.10.003
. [PMID: 19969445] - Ana Flávia Schürmann da Silva, Jean Paulo de Andrade, Lia R M Bevilaqua, Márcia Maria de Souza, Ivan Izquierdo, Amélia Teresinha Henriques, José Angelo Silveira Zuanazzi. Anxiolytic-, antidepressant- and anticonvulsant-like effects of the alkaloid montanine isolated from Hippeastrum vittatum.
Pharmacology, biochemistry, and behavior.
2006 Sep; 85(1):148-54. doi:
10.1016/j.pbb.2006.07.027
. [PMID: 16950504] - Muhammad Shaiq Ali, Muhammad Kashif Pervez. Marmenol: a 7-geranyloxycoumarin from the leaves of Aegle marmelos Corr.
Natural product research.
2004 Apr; 18(2):141-6. doi:
10.1080/14786410310001608037
. [PMID: 14984087]