Roquefortine F (BioDeep_00000016012)
natural product Antibiotics Antitumor activity
代谢物信息卡片
化学式: C23H25N5O3 (419.1957)
中文名称: 罗克福青霉素F
谱图信息:
最多检出来源 Homo sapiens(otcml) 1.85%
Last reviewed on 2024-10-11.
Cite this Page
Roquefortine F. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/roquefortine_f (retrieved
2024-12-22) (BioDeep RN: BioDeep_00000016012). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: CC(C)(C=C)C12CC3C(=O)NC(=CC4=CN=CN4)C(=O)N3C1N(C5=CC=CC=C25)OC
InChI: InChI=1S/C23H25N5O3/c1-5-22(2,3)23-11-18-19(29)26-16(10-14-12-24-13-25-14)20(30)27(18)21(23)28(31-4)17-9-7-6-8-15(17)23/h5-10,12-13,18,21H,1,11H2,2-4H3,(H,24,25)(H,26,29)/b16-10+
描述信息
Roquefortine F is a fungal secondary metabolite classified as an indole diterpene. It is produced by certain species of Penicillium fungi, notably those used in the production of Roquefort cheese. This compound belongs to a family of organic compounds characterized by the presence of an indole ring and a diterpene backbone.
Indole diterpenes are known for their diverse biological activities, which can include antibiotic, antitumor, and anti-inflammatory effects. Roquefortine F, in particular, has been of interest in the fields of food science and pharmaceutical research. In the context of food, it can contribute to the flavor profile and safety of certain fermented products. In drug development, it may serve as a template molecule for the synthesis of new pharmaceuticals due to its unique chemical structure and potential therapeutic properties.
The exact chemical structure of Roquefortine F can be complex, featuring a bicyclic core with various functional groups attached to the indole ring and diterpene scaffold. This complexity contributes to its diverse biological activities and potential applications in different fields.
同义名列表
相关代谢途径
Reactome(0)
PlantCyc(0)
代谢反应
2 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(2)
- neoxaline biosynthesis:
N1-hydroxy-roquefortine C + SAM ⟶ H+ + SAH + roquefortine F
- superpathway of roquefortine, meleagrin and neoxaline biosynthesis:
O2 + a reduced [NADPH-hemoprotein reductase] + roquefortine D ⟶ H2O + an oxidized [NADPH-hemoprotein reductase] + roquefortine C
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
0 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。
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