Carpachromene (BioDeep_00000266451)
natural product PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C20H16O5 (336.0997686)
中文名称: 5-羟基-8-(4-羟基苯基)-2,2-二甲基-2H,6H-苯并[1,2-B:5,4-B']二吡喃-6-酮
谱图信息:
最多检出来源 Viridiplantae(plant) 5.31%
分子结构信息
SMILES: C(=O)(C=3)c(c2O)c(OC3c(c4)ccc(O)c4)cc(c12)OC(C=C1)(C)C
InChI: InChI=1S/C20H16O5/c1-20(2)8-7-13-16(25-20)10-17-18(19(13)23)14(22)9-15(24-17)11-3-5-12(21)6-4-11/h3-10,21,23H,1-2H3
描述信息
同义名列表
5 个代谢物同义名
Carpachromene; 5,4-Dihidroxy-6,6-dimethylpyrano[2,3:7,6]flavone; 5-Hydroxy-8- (4-hydroxyphenyl) -2,2-dimethyl-2H,6H-benzo [ 1,2-b:5,4-b ] dipyran-6-one; 5-Hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-2H,6H-benzo[1,2-b:5,4-b]dipyran-6-one; 5,4-Dihidroxy-6",6"-dimethylpyrano [ 2",3":7,6 ] flavone
数据库引用编号
26 个数据库交叉引用编号
- ChEBI: CHEBI:196359
- PubChem: 10449654
- Metlin: METLIN48857
- ChEMBL: CHEMBL4177103
- LipidMAPS: LMPK12110426
- KNApSAcK: C00013432
- CAS: 57498-96-1
- MoNA: VF-NPL-LTQ002504
- MoNA: VF-NPL-LTQ002503
- MoNA: VF-NPL-QEHF007980
- MoNA: VF-NPL-QEHF007979
- MoNA: VF-NPL-QEHF007978
- MoNA: VF-NPL-QEHF007977
- MoNA: VF-NPL-QEHF007976
- MoNA: VF-NPL-QEHF007975
- MoNA: VF-NPL-QEHF007974
- MoNA: VF-NPL-QEHF007973
- MoNA: VF-NPL-QEHF007972
- MoNA: VF-NPL-QEHF007971
- MoNA: VF-NPL-QEHF007970
- MoNA: VF-NPL-QEHF007969
- MoNA: VF-NPL-QEHF007968
- MoNA: VF-NPL-QEHF007967
- MoNA: VF-NPL-QEHF007966
- PMhub: MS000011689
- Flavonoid: FL3FAANP0007
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)
13 个相关的物种来源信息
- 1127366 Ficus formosana:
- 463862 Ficus nervosa: 10.1002/CBDV.200900227
- 194324 Maclura cochinchinensis:
- 984812 Dorstenia kameruniana: 10.1016/S0031-9422(98)00061-2
- 3496 Maclura pomifera: 10.1016/S0031-9422(98)00380-X
- 709069 Parartocarpus bracteatus:
- 1127059 Lonchocarpus guatemalensis:
- 2708828 Erythrina vogelii: 10.1016/J.PHYTOCHEM.2005.09.022
- 159025 Atalantia monophylla: 10.1016/0040-4020(76)87016-0
- 326052 Ficus subcuneata: 10.1055/S-2005-873163
- 67931 Flindersia laevicarpa: 10.1071/CH9762023
- 76951 Atalantia ceylanica: 10.1055/S-2006-962624
- 159062 Pamburus missionis: 10.1016/0031-9422(75)85361-1
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
- Luke P Robertson, Sandra Duffy, Yun Wang, Dongdong Wang, Vicky M Avery, Anthony R Carroll. Pimentelamines A-C, Indole Alkaloids Isolated from the Leaves of the Australian Tree Flindersia pimenteliana.
Journal of natural products.
2017 12; 80(12):3211-3217. doi:
10.1021/acs.jnatprod.7b00587
. [PMID: 29236492] - Li-Wen Chen, Ming-Jen Cheng, Chien-Fang Peng, Ih-Sheng Chen. Secondary metabolites and antimycobacterial activities from the roots of Ficus nervosa.
Chemistry & biodiversity.
2010 Jul; 7(7):1814-21. doi:
10.1002/cbdv.200900227
. [PMID: 20658670] - Muhammad Imran Ali, Zeeshan Ahmed, Alain Francois Kamdem Waffo, Muhammad Shaiq Ali. Flavonoids from Erythrina vogelii (Fabaceae) of Cameroon.
Natural product communications.
2010 Jun; 5(6):889-92. doi:
"
. [PMID: 20614816] - Zong-Ping Zheng, Ka-Wing Cheng, James Tsz-Kin To, Haitao Li, Mingfu Wang. Isolation of tyrosinase inhibitors from Artocarpus heterophyllus and use of its extract as antibrowning agent.
Molecular nutrition & food research.
2008 Dec; 52(12):1530-8. doi:
10.1002/mnfr.200700481
. [PMID: 18683821] - Ya-Wen Sheu, Lien-Chai Chiang, Ih-Sheng Chen, Yu-Chang Chen, Ian-Lih Tsai. Cytotoxic flavonoids and new chromenes from Ficus formosana f. formosana.
Planta medica.
2005 Dec; 71(12):1165-7. doi:
10.1055/s-2005-873163
. [PMID: 16395655] - Rocío Borges-Argáez, Luis M Peña-Rodríguez, Peter G Waterman. Flavonoids from two Lonchocarpus species of the Yucatan Peninsula.
Phytochemistry.
2002 Jul; 60(5):533-40. doi:
10.1016/s0031-9422(02)00131-0
. [PMID: 12052520]