Compounds > pterulone
Page last updated: 2024-11-12

pterulone

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

pterulone: isolated from Pterula coral fungus; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID11424846
CHEMBL ID450490
SCHEMBL ID6107143
MeSH IDM0278032

Synonyms (11)

Synonym
CHEMBL450490
369376-61-4
SCHEMBL6107143
pterulone
1-[(3z)-3-(chloromethylidene)-1-benzoxepin-7-yl]ethanone
Q7256974
ethanone, 1-((3z)-3-(chloromethylene)-2,3-dihydro-1-benzoxepin-7-yl)-
a69767ww45 ,
1-((3z)-3-(chloromethylene)-2,3-dihydro-1-benzoxepin-7-yl)ethanone
(z)-1-(3-(chloromethylene)-2,3-dihydro-1-benzoxepin-7-yl)ethanone
unii-a69767ww45
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID334229Antimicrobial activity against Saccharomyces cerevisiae CBS 1394 assessed as relative growth at 50 ug/mL after 24 to 48 hrs relative to control2002Journal of natural products, Apr, Volume: 65, Issue:4
Total synthesis and bioactivity of some naturally occurring pterulones.
AID334228Antimicrobial activity against Rhodotorula glutinis ATCC 201718 assessed as relative growth at 50 ug/mL after 24 to 48 hrs relative to control2002Journal of natural products, Apr, Volume: 65, Issue:4
Total synthesis and bioactivity of some naturally occurring pterulones.
AID334231Antimicrobial activity against Saccharomyces cerevisiae CBS 1394 assessed as relative growth at 100 ug/mL after 24 to 48 hrs relative to control2002Journal of natural products, Apr, Volume: 65, Issue:4
Total synthesis and bioactivity of some naturally occurring pterulones.
AID334230Antimicrobial activity against Rhodotorula glutinis ATCC 201718 assessed as relative growth at 100 ug/mL after 24 to 48 hrs relative to control2002Journal of natural products, Apr, Volume: 65, Issue:4
Total synthesis and bioactivity of some naturally occurring pterulones.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (4)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's2 (50.00)29.6817
2010's0 (0.00)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
phenol
[no description available]		2.0110phenolsantiseptic drug;
disinfectant;
human xenobiotic metabolite;
mouse metabolite
phenyl acetate
phenyl acetate: The ester formed between phenol and acetic acid. Don't confuse with phenylacetic acid derivatives listed under PHENYLACETATES.. phenyl acetate : An acetate ester obtained by the formal condensation of phenol with acetic acid.		2.420benzenes;
phenyl acetates
benzofurans
Benzofurans: Compounds that contain a BENZENE ring fused to a furan ring.		2.6930
oxepins
Oxepins: Compounds based on a 7-membered heterocyclic ring including an oxygen. They can be considered a medium ring ether. A natural source is the MONTANOA plant genus. Some dibenzo-dioxepins, called depsidones, are found in GARCINIA plants.		2.6930
ConditionIndicatedRelationship StrengthStudiesTrials