Magnoline (BioDeep_00000005740)
natural product
代谢物信息卡片
化学式: C36H40N2O6 (596.2886)
中文名称: 木兰脂素
谱图信息:
最多检出来源 Homo sapiens(plant) 13.73%
分子结构信息
SMILES: CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)O)O)OC
InChI: InChI=1S/C36H40N2O6/c1-37-13-11-24-18-34(42-3)32(40)20-27(24)29(37)15-22-5-8-26(9-6-22)44-36-17-23(7-10-31(36)39)16-30-28-21-33(41)35(43-4)19-25(28)12-14-38(30)2/h5-10,17-21,29-30,39-41H,11-16H2,1-4H3
数据库引用编号
27 个数据库交叉引用编号
- ChEBI: CHEBI:16777
- ChEBI: CHEBI:6642
- KEGG: C05177
- KEGG: C06515
- PubChem: 440585
- PubChem: 362563
- Metlin: METLIN64382
- ChEMBL: CHEMBL1187468
- ChEMBL: CHEMBL503882
- MetaCyc: CPD-8925
- KNApSAcK: C00025880
- CAS: 6859-66-1
- CAS: 485-18-7
- PMhub: MS000018599
- MetaboLights: MTBLC16777
- MetaboLights: MTBLC6642
- PubChem: 7588
- KNApSAcK: C00025262
- 3DMET: B01820
- NIKKAJI: J2.403.084I
- PubChem: 8746
- NIKKAJI: J8.848J
- KNApSAcK: 6642
- KNApSAcK: 16777
- LOTUS: LTS0229024
- LOTUS: LTS0151399
- wikidata: Q27102072
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)
36 个相关的物种来源信息
- 341012 - Abuta: LTS0229024
- 341013 - Abuta grandifolia: 10.1055/S-1999-14017
- 341013 - Abuta grandifolia: LTS0229024
- 41773 - Berberidaceae: LTS0229024
- 22774 - Berberis: LTS0229024
- 258140 - Berberis amurensis: 10.1007/BF00630534
- 752791 - Berberis angulosa: 10.1016/S0031-9422(00)82337-7
- 258147 - Berberis canadensis: 10.1016/S0031-9422(00)82337-7
- 1433307 - Berberis cretica: 10.1021/NP50043A025
- 38786 - Berberis dictyophylla: 10.1016/S0031-9422(00)82337-7
- 186724 - Berberis empetrifolia: 10.1016/S0031-9422(00)82337-7
- 1433312 - Berberis heteropoda:
- 2761039 - Berberis iliensis: 10.1007/BF00631020
- 258178 - Berberis julianae: 10.1016/S0031-9422(00)82337-7
- 659594 - Berberis lycium:
- 1439896 - Berberis nummularia:
- 2294045 - Berberis papillifera: 10.1016/S0031-9422(00)82337-7
- 2602266 - Berberis salicaria: 10.1016/S0031-9422(00)82337-7
- 33814 - Berberis stolonifera:
- 33814 - Berberis stolonifera: 10.1016/0031-9422(88)87027-4
- 33814 - Berberis stolonifera: LTS0229024
- 2602268 - Berberis taliensis: 10.1016/S0031-9422(00)82337-7
- 258209 - Berberis vulgaris:
- 258211 - Berberis wilsoniae: 10.1016/S0031-9422(00)82337-7
- 2759 - Eukaryota: LTS0229024
- 3402 - Magnolia: LTS0229024
- 54732 - Magnolia kobus: 10.1016/J.JCHROMB.2011.10.023
- 54732 - Magnolia kobus: LTS0229024
- 3401 - Magnoliaceae: LTS0229024
- 3398 - Magnoliopsida: LTS0229024
- 3455 - Menispermaceae: LTS0229024
- 1924984 - Stephania pierrei: 10.1021/NP50064A031
- 35493 - Streptophyta: LTS0229024
- 58023 - Tracheophyta: LTS0229024
- 295132 - Trepobates: 10.1021/NP50064A031
- 33090 - Viridiplantae: LTS0229024
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
- James T Payne, Timothy R Valentic, Christina D Smolke. Complete biosynthesis of the bisbenzylisoquinoline alkaloids guattegaumerine and berbamunine in yeast.
Proceedings of the National Academy of Sciences of the United States of America.
2021 12; 118(51):. doi:
10.1073/pnas.2112520118
. [PMID: 34903659] - Hui Sun, Ai-Hua Zhang, Shao-Bo Liu, Shi Qiu, Xian-Na Li, Tian-Lei Zhang, Liang Liu, Xi-Jun Wang. Cell metabolomics identify regulatory pathways and targets of magnoline against prostate cancer.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
2018 Dec; 1102-1103(?):143-151. doi:
10.1016/j.jchromb.2018.10.017
. [PMID: 30391728] - Yang Zhou, Feng Wang, Lirong Hao, Niansong Wang. Effects of magnoline on P-selectin's expression in diabetic rats and its reno-protection.
Kidney & blood pressure research.
2013; 37(2-3):211-20. doi:
10.1159/000350146
. [PMID: 23736780] - Maria Francesca Cometa, Stefano Fortuna, Giovanna Palazzino, Maria Teresa Volpe, Elsa Rengifo Salgado, Marcello Nicoletti, Lamberto Tomassini. New cholinesterase inhibiting bisbenzylisoquinoline alkaloids from Abuta grandifolia.
Fitoterapia.
2012 Apr; 83(3):476-80. doi:
10.1016/j.fitote.2011.12.015
. [PMID: 22230193] - Nobuhiro Ikezawa, Kinuko Iwasa, Fumihiko Sato. Molecular cloning and characterization of CYP80G2, a cytochrome P450 that catalyzes an intramolecular C-C phenol coupling of (S)-reticuline in magnoflorine biosynthesis, from cultured Coptis japonica cells.
The Journal of biological chemistry.
2008 Apr; 283(14):8810-21. doi:
10.1074/jbc.m705082200
. [PMID: 18230623] - T M Kutchan. Heterologous expression of alkaloid biosynthetic genes--a review.
Gene.
1996 Nov; 179(1):73-81. doi:
10.1016/s0378-1119(96)00426-x
. [PMID: 8955631]