Gossypitrin (BioDeep_00000896043)

   

PANOMIX_OTCML-2023


代谢物信息卡片


Gossypetin 7-β-D-glucopyranoside

化学式: C21H20O13 (480.090387)
中文名称: 棉皮素
谱图信息: 最多检出来源 () 0%

Reviewed

Last reviewed on 2024-08-13.

Cite this Page

Gossypitrin. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/gossypitrin (retrieved 2024-09-21) (BioDeep RN: BioDeep_00000896043). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O
InChI: InChI=1S/C21H20O13/c22-5-11-13(26)16(29)18(31)21(33-11)32-10-4-9(25)12-15(28)17(30)19(34-20(12)14(10)27)6-1-2-7(23)8(24)3-6/h1-4,11,13,16,18,21-27,29-31H,5H2/t11-,13-,16+,18-,21-/m1/s1

描述信息

Gossypitrin is a naturally occurring compound classified under the flavonoid group. Flavonoids are a diverse class of secondary metabolites found in plants, known for their various biological activities and health benefits. Gossypitrin, specifically, is a flavonol, which is a subclass of flavonoids.
Chemically, gossypitrin has a basic structure of a 3-deoxyflavonol. Its molecular formula is C15H10O6. The structure of gossypitrin features two aromatic rings (A and B rings) connected by a linear three-carbon chain, which includes a keto group. This arrangement is characteristic of flavonoids. The "3-deoxy" part of its name indicates the absence of an oxygen atom at the C-3 position of the ring structure, which is a unique feature of gossypitrin.
Gossypitrin is primarily found in cotton plants, particularly in the roots, stems, leaves, and seeds. It is one of the many bioactive compounds in cotton that contribute to the plant's defense mechanisms against pests and diseases. In terms of biological activity, gossypitrin and other related flavonoids have been studied for their potential antioxidant, anti-inflammatory, and anticancer properties. The antioxidant activity is particularly noteworthy, as it can help in neutralizing harmful free radicals in the body, which are associated with aging and various diseases.
Research on gossypitrin and its derivatives is ongoing, exploring its potential uses in medicinal and pharmacological applications. The unique chemical structure of gossypitrin makes it an interesting subject for studying the structure-activity relationships of flavonoids and their impact on human health.

Gossypitrin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=489-34-9 (retrieved 2024-08-13) (CAS RN: 489-34-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

同义名列表

1 个代谢物同义名

Gossypitrin



数据库引用编号

2 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)

1 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。



文献列表

  • María Ángeles Bécquer-Viart, Adonis Armentero-López, Daniel Alvarez-Almiñaque, Roberto Fernández-Acosta, Yasser Matos-Peralta, Richard F D'Vries, Javier Marín-Prida, Gilberto L Pardo-Andreu. Gossypitrin, A Naturally Occurring Flavonoid, Attenuates Iron-Induced Neuronal and Mitochondrial Damage. Molecules (Basel, Switzerland). 2021 Jun; 26(11):. doi: 10.3390/molecules26113364. [PMID: 34199597]
  • Gilberto Pérez-Trueba, Cryslaine Ramos-Guanche, Belkis Martínez-Sánchez, Ingrid Márquez-Hernández, Attilia Giuliani, Gregorio Martínez-Sánchez. Protective effect of gossypitrin on carbon tetrachloride-induced in vivo hepatotoxicity. Redox report : communications in free radical research. 2003; 8(4):215-21. doi: 10.1179/135100003225002718. [PMID: 14599345]