Glabranin (BioDeep_00000000936)
PANOMIX_OTCML-2023 natural product
代谢物信息卡片
化学式: C20H20O4 (324.1362)
中文名称: 裸禾蕨黄素, 欧亚甘草宁, 光甘草宁
谱图信息:
最多检出来源 Mus musculus(plant) 6.8%
Last reviewed on 2024-07-09.
Cite this Page
Glabranin. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/glabranin (retrieved
2024-12-22) (BioDeep RN: BioDeep_00000000936). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: C(c(c3)cccc3)(O2)([H])CC(=O)c(c21)c(cc(O)c1CC=C(C)C)O
InChI: InChI=1S/C20H20O4/c1-12(2)8-9-14-15(21)10-16(22)19-17(23)11-18(24-20(14)19)13-6-4-3-5-7-13/h3-8,10,18,21-22H,9,11H2,1-2H3
描述信息
Glabranin is a dihydroxyflavanone that is pinocembrin substituted by a prenyl group at position 8. It has a role as a plant metabolite. It is a dihydroxyflavanone and a (2S)-flavan-4-one. It is functionally related to a pinocembrin.
Glabranin is a natural product found in Sophora tomentosa, Annona squamosa, and other organisms with data available.
A dihydroxyflavanone that is pinocembrin substituted by a prenyl group at position 8.
Saponin from licorice (Glycyrrhiza glabra). Glabranin B is found in tea and herbs and spices.
Origin: Plant, Pyrans
Glabranin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=41983-91-9 (retrieved 2024-07-09) (CAS RN: 41983-91-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
同义名列表
26 个代谢物同义名
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-8-(3-methyl-2-butenyl)-2-phenyl-, (2S)-; (2S)-5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one; (2S)-5,7-dihydroxy-8-(3-methylbut-2-en-1-yl)-2-phenyl-2,3-dihydro-4H-1-benzopyran-4-one; 4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-8-(3-methyl-2-butenyl)-2-phenyl-, (S)-; (S)-2,3-Dihydro-5,7-dihydroxy-8-(3-methyl-2-butenyl)-2-phenyl-4H-1-benzopyran-4-one; (2S)-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one; (2S)-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2-phenyl-chroman-4-one; 8-dimethylallylpinocembrin; 8-Prenylpinocembrin; TimTec1_002029; Glabranine; Glabranin; Glabranin B; (2S)-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2-phenylchroman-4-one; (2S)-5,7-dihydroxy-8-(3-methylbut-2-enyl)-2-phenyl-4-chromanone; NCGC00017206-01; NCGC00142379-01; ZINC00113294; AIDS-095899; 41983-91-9; AIDS095899; ST024709; TNP00074; C09752; (S) -2,3-Dihydro-5,7-dihydroxy-2-phenyl-8-prenyl-4H-1-benzopyran-4-one; Glabranin
数据库引用编号
35 个数据库交叉引用编号
- ChEBI: CHEBI:5368
- KEGG: C09752
- PubChem: 124049
- PubChem: 3144815
- Metlin: METLIN52653
- ChEMBL: CHEMBL253998
- LipidMAPS: LMPK12140164
- ChemIDplus: 0041983919
- KNApSAcK: C00000965
- foodb: FDB017730
- CAS: 41983-91-9
- MoNA: NGA00468
- MoNA: NGA00467
- MoNA: NGA00466
- MoNA: NGA00465
- MoNA: CB000315
- MoNA: BML81303
- MoNA: BML81302
- MoNA: BML81301
- MoNA: BML81300
- MoNA: BML00154
- MoNA: BML00147
- MoNA: BML00140
- MoNA: BML00120
- MoNA: BML00108
- medchemexpress: HY-N3942
- PMhub: MS000010168
- Flavonoid: FL2FA9NI0001
- MetaboLights: MTBLC5368
- 3DMET: B03250
- NIKKAJI: J742.819G
- RefMet: Glabranin
- PubChem: 11940
- KNApSAcK: 5368
- LOTUS: LTS0250433
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)
52 个相关的物种来源信息
- 13336 - Annona: LTS0250433
- 301703 - Annona glabra: 10.1016/S0031-9422(97)00780-2
- 301703 - Annona glabra: 10.1021/NP0704957
- 301703 - Annona glabra: LTS0250433
- 301693 - Annona squamosa:
- 301693 - Annona squamosa: 10.1016/S0031-9422(97)00780-2
- 301693 - Annona squamosa: 10.1021/NP0704957
- 301693 - Annona squamosa: 10.1055/S-0028-1084499
- 301693 - Annona squamosa: LTS0250433
- 22140 - Annonaceae: LTS0250433
- 4037 - Apiaceae: LTS0250433
- 4210 - Asteraceae: LTS0250433
- 2759 - Eukaryota: LTS0250433
- 3803 - Fabaceae: LTS0250433
- 46347 - Glycyrrhiza: LTS0250433
- 49827 - Glycyrrhiza glabra:
- 49827 - Glycyrrhiza glabra: 10.1007/BF00564618
- 49827 - Glycyrrhiza glabra: 10.1007/BF00574601
- 49827 - Glycyrrhiza glabra: 10.1007/BF02759632
- 49827 - Glycyrrhiza glabra: 10.1021/NP020365S
- 49827 - Glycyrrhiza glabra: 10.1248/CPB.51.1338
- 49827 - Glycyrrhiza glabra: LTS0250433
- 49827 - Glycyrrhiza glabra: NA
- 47080 - Glycyrrhiza lepidota: 10.1016/0031-9422(83)83049-0
- 47080 - Glycyrrhiza lepidota: LTS0250433
- 47080 - Glycyrrhiza lepidota: NA
- 74613 - Glycyrrhiza uralensis: 10.1007/BF02329609
- 74613 - Glycyrrhiza uralensis: LTS0250433
- 59430 - Helichrysum: LTS0250433
- 630302 - Helichrysum forskahlii:
- 630302 - Helichrysum forskahlii: 10.1016/0031-9422(79)83068-X
- 630302 - Helichrysum forskahlii: 10.1016/J.PHYTOCHEM.2008.03.025
- 630302 - Helichrysum forskahlii: 10.3390/MOLECULES20047143
- 630302 - Helichrysum forskahlii: LTS0250433
- 3398 - Magnoliopsida: LTS0250433
- 62113 - Piscidia: LTS0250433
- 62123 - Piscidia piscipula: 10.1016/S0031-9422(00)81326-6
- 62123 - Piscidia piscipula: LTS0250433
- 241806 - Polypodiopsida: LTS0250433
- 13819 - Pteridaceae: LTS0250433
- 325733 - Semenovia: 10.1007/BF00563632
- 3896 - Sophora: LTS0250433
- 256637 - Sophora tomentosa: 10.1016/S0031-9422(97)00474-3
- 256637 - Sophora tomentosa: LTS0250433
- 35493 - Streptophyta: LTS0250433
- 32176 - Taenitis: 10.1007/BF00563632
- 32176 - Taenitis: LTS0250433
- 47097 - Tephrosia: LTS0250433
- 3092001 - Tephrosia major: LTS0250433
- 58023 - Tracheophyta: LTS0250433
- 33090 - Viridiplantae: LTS0250433
- 33090 - 甘草: -
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
- Namrita Lall, Elizabeth Mogapi, Marco Nuno de Canha, Bridget Crampton, Mabatho Nqephe, Ahmed A Hussein, Vivek Kumar. Insights into tyrosinase inhibition by compounds isolated from Greyia radlkoferi Szyszyl using biological activity, molecular docking and gene expression analysis.
Bioorganic & medicinal chemistry.
2016 11; 24(22):5953-5959. doi:
10.1016/j.bmc.2016.09.054
. [PMID: 27720556] - Van Trinh Thi Thanh, Huong Doan Thi Mai, Van Cuong Pham, Marc Litaudon, Vincent Dumontet, Françoise Guéritte, Van Hung Nguyen, Van Minh Chau. Acetylcholinesterase inhibitors from the leaves of Macaranga kurzii.
Journal of natural products.
2012 Nov; 75(11):2012-5. doi:
10.1021/np300660y
. [PMID: 23134335] - José M Narvaez-Mastache, María Luisa Garduño-Ramírez, Laura Alvarez, Guillermo Delgado. Antihyperglycemic activity and chemical constituents of Eysenhardtia platycarpa.
Journal of natural products.
2006 Dec; 69(12):1687-91. doi:
10.1021/np060166z
. [PMID: 17190443] - Daniela M Biondi, Concetta Rocco, Giuseppe Ruberto. Dihydrostilbene derivatives from Glycyrrhiza glabra leaves.
Journal of natural products.
2005 Jul; 68(7):1099-102. doi:
10.1021/np050034q
. [PMID: 16038558] - Daniela M Biondi, Concetta Rocco, Giuseppe Ruberto. New dihydrostilbene derivatives from the leaves of Glycyrrhiza glabra and evaluation of their antioxidant activity.
Journal of natural products.
2003 Apr; 66(4):477-80. doi:
10.1021/np020365s
. [PMID: 12713396]