Page last updated: 2024-10-15
chrysogine
Description
chrysogine: metabolite of Penicillium chrysogenum; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
Synonyms (22)
| Synonym |
|---|
| 42599-89-3 |
| 2-(1-hydroxyethyl)-3h-quinazolin-4-one |
| CHEBI:166873 |
| nsc-708217 |
| nsc708217 |
| chrysogine |
| 2-(1-hydroxyethyl)-4(3h)-quinazolinone |
| 4(3h)-quinazolinone, 2-(1-hydroxyethyl)- |
| 14422-59-4 |
| F2185-0769 |
| 2-(1-hydroxyethyl)quinazolin-4(3h)-one |
| AKOS026719423 |
| 4(3h)-quinazolinone, 2-(1-hydroxyethyl)-, (+/-)- |
| (+/-)-crysogine |
| unii-07lc03nl3i |
| crysogine, (+/-)- |
| 07lc03nl3i , |
| 4(1h)-quinazolinone, 2-(1-hydroxyethyl)-, (+/-)- |
| 2-(1-hydroxyethyl)quinazolin-4-ol |
| DTXSID60962594 |
| 2-(1-hydroxyethyl)-4(3h)quinazoline |
| 2-(1-hydroxyethyl)-3,4-dihydroquinazolin-4-one |
Research Excerpts
Overview
Chrysogine is a yellow pigment produced by Chrysogine. It is a type of yellow pigment used in the manufacture of pigments.
Roles (3)
| Role | Description |
|---|
| biological pigment | An endogenous molecular entity that results in a colour of an organism as the consequence of the selective absorption of light. |
| Aspergillus metabolite | Any fungal metabolite produced during a metabolic reaction in the mould, Aspergillus. |
| marine metabolite | Any metabolite produced during a metabolic reaction in marine macro- and microorganisms. |
| [role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Drug Classes (5)
| Class | Description |
|---|
| quinazoline alkaloid | Any alkaloid based on a quinazoline skeleton and its substituted derivatives. |
| secondary alcohol | A secondary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has two other carbon atoms attached to it. |
| quinazolines | Any organic heterobicyclic compound based on a quinazoline skeleton and its substituted derivatives. |
| cyclic amide | |
| secondary amide | A derivative of two oxoacids RkE(=O)l(OH)m (l =/= 0) in which two acyl groups are attached to the amino or substituted amino group. |
| [compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Research
Studies (4)
| Timeframe | Studies, This Drug (%) | All Drugs % |
|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Study Types
| Publication Type | This drug (%) | All Drugs (%) |
|---|
| Trials | 0 (0.00%) | 5.53% |
| Reviews | 0 (0.00%) | 6.00% |
| Case Studies | 0 (0.00%) | 4.05% |
| Observational | 0 (0.00%) | 0.25% |
| Other | 5 (100.00%) | 84.16% |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |