Compounds > chrysogine
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

ID SourceID
PubMed CID135505243
CHEBI ID166873
MeSH IDM0047138

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.

ExcerptReference
"Chrysogine is a yellow pigment produced by "( Pathway for the Biosynthesis of the Pigment Chrysogine by Penicillium chrysogenum.
Ali, H; Bovenberg, RAL; Driessen, AJM; Lankhorst, PP; Nygård, Y; Salo, O; Szymanski, W; Viggiano, A, 2018)
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
biological pigmentAn endogenous molecular entity that results in a colour of an organism as the consequence of the selective absorption of light.
Aspergillus metaboliteAny fungal metabolite produced during a metabolic reaction in the mould, Aspergillus.
marine metaboliteAny 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)

ClassDescription
quinazoline alkaloidAny alkaloid based on a quinazoline skeleton and its substituted derivatives.
secondary alcoholA 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.
quinazolinesAny organic heterobicyclic compound based on a quinazoline skeleton and its substituted derivatives.
cyclic amide
secondary amideA 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)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
anthranilic acid
anthranilic acid: RN given refers to parent cpd; structure in Negwer, 5th ed, #565. anthranilic acid : An aminobenzoic acid that is benzoic acid having a single amino substituent located at position 2. It is a metabolite produced in L-tryptophan-kynurenine pathway in the central nervous system.		2.1510aminobenzoic acidhuman metabolite;
mouse metabolite
pyruvic acid
Pyruvic Acid: An intermediate compound in the metabolism of carbohydrates, proteins, and fats. In thiamine deficiency, its oxidation is retarded and it accumulates in the tissues, especially in nervous structures. (From Stedman, 26th ed). pyruvic acid : A 2-oxo monocarboxylic acid that is the 2-keto derivative of propionic acid. It is a metabolite obtained during glycolysis.		2.15102-oxo monocarboxylic acidcofactor;
fundamental metabolite
1-anilino-8-naphthalenesulfonate
1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd. 8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.		1.9810aminonaphthalene;
naphthalenesulfonic acid		fluorescent probe
quinazolines
Quinazolines: A group of aromatic heterocyclic compounds that contain a bicyclic structure with two fused six-membered aromatic rings, a benzene ring and a pyrimidine ring.. quinazoline : A mancude organic heterobicyclic parent that is naphthalene in which the carbon atoms at positions 1 and 3 have been replaced by nitrogen atoms.. quinazolines : Any organic heterobicyclic compound based on a quinazoline skeleton and its substituted derivatives.		2.420azaarene;
mancude organic heterobicyclic parent;
ortho-fused heteroarene;
quinazolines
griseofulvin
Griseofulvin: An antifungal agent used in the treatment of TINEA infections.. griseofulvin : An oxaspiro compound produced by Penicillium griseofulvum. It is used by mouth as an antifungal drug for infections involving the scalp, hair, nails and skin that do not respond to topical treatment.		7.02101-benzofurans;
antibiotic antifungal drug;
benzofuran antifungal drug;
organochlorine compound;
oxaspiro compound		antibacterial agent;
Penicillium metabolite
roquefortine
roquefortine: metabolite of Penicillium roqueforti; structure		7.0210pyrroloindole
ConditionIndicatedRelationship StrengthStudiesTrials