Page last updated: 2024-11-11

estin

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

Description

geodin: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

(+)-geodin : An oxaspiro compound that is 3H,4'H-spiro[[1]benzofuran-2,1'-cyclohexa[2,5]diene]-3,4'-dione substituted by methoxycarbonyl, hydroxy, chloro, methyl, methoxy and chloro groups at positions 2', 4, 5, 6, 6' and 7, respectively. It is a fungal metabolite isolated from Aspergillus terreus and Penicillium glabrum. [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]

Cross-References

ID SourceID
PubMed CID9887146
CHEMBL ID1956530
CHEBI ID150867
MeSH IDM0147912

Synonyms (20)

Synonym
geodin
(+)-erdin methyl ester
CHEBI:150867
(+)-geodin
erdin (+)-form methyl ester
methyl (1'r)-5,7-dichloro-4-hydroxy-6'-methoxy-6-methyl-3,4'-dioxo-3h-spiro[[1]benzofuran-2,1'-cyclohexa[2,5]diene]-2'-carboxylate
(2r)-methyl-5,7-dichloro-4-hydroxy-6'-methoxy-6-methyl-3,4'-dioxospiro-[benzofuran-2,1'-cyclohexa-2',5'-diene]-2'-carboxylate
estin
d-geodin
unii-4293r7b06x
spiro(benzofuran-2(3h),1'-(2,5)cyclohexadiene)-2'-carboxylic acid, 5,7-dichloro-4-hydroxy-6'-methoxy-6-methyl-3,4'-dioxo-, methyl ester, (+)-
4293r7b06x ,
CHEMBL1956530
spiro(benzofuran-2(3h),1'-(2,5)cyclohexadiene)-2'-carboxylic acid, 5,7-dichloro-4-hydroxy-6'-methoxy-6-methyl-3,4'-dioxo-, methyl ester, (1'r)-
erdin (+)-form methyl ester [mi]
Q27258516
methyl (2r)-5,7-dichloro-4-hydroxy-5'-methoxy-6-methyl-3,3'-dioxospiro[1-benzofuran-2,6'-cyclohexa-1,4-diene]-1'-carboxylate
HY-N10227
CS-0084104
AKOS040755696
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
Penicillium metaboliteAny fungal metabolite produced during a metabolic reaction in Penicillium.
Aspergillus metaboliteAny fungal metabolite produced during a metabolic reaction in the mould, Aspergillus.
[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 (6)

ClassDescription
methyl esterAny carboxylic ester resulting from the formal condensation of a carboxy group with methanol.
oxaspiro compoundA spiro compound in which at least one of the cyclic components is an oxygen heterocyle.
organochlorine compoundAn organochlorine compound is a compound containing at least one carbon-chlorine bond.
1-benzofuransA member of the class of benzofurans consisting of a 1-benzofuran skeleton and its substituted derivatives thereof.
phenolsOrganic aromatic compounds having one or more hydroxy groups attached to a benzene or other arene ring.
etherAn organooxygen compound with formula ROR, where R is not hydrogen.
[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]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID649243Cytotoxicity against human MDA-MB-231 cells assessed as cell viability after 48 hrs by MTT assay2012Journal of medicinal chemistry, Jan-26, Volume: 55, Issue:2
Disparate SAR data of griseofulvin analogues for the dermatophytes Trichophyton mentagrophytes, T. rubrum, and MDA-MB-231 cancer cells.
AID649245Antifungal activity against Trichophyton rubrum IBT 29284 at 50 uM after 7 days by micro broth dilution method2012Journal of medicinal chemistry, Jan-26, Volume: 55, Issue:2
Disparate SAR data of griseofulvin analogues for the dermatophytes Trichophyton mentagrophytes, T. rubrum, and MDA-MB-231 cancer cells.
AID649246Ratio of griseofulvin IC50 to compound IC50 for human MDA-MB-231 cells2012Journal of medicinal chemistry, Jan-26, Volume: 55, Issue:2
Disparate SAR data of griseofulvin analogues for the dermatophytes Trichophyton mentagrophytes, T. rubrum, and MDA-MB-231 cancer cells.
AID649244Antifungal activity against Trichophyton mentagrophytes IBT 2724 at 50 uM after 7 days by micro broth dilution method2012Journal of medicinal chemistry, Jan-26, Volume: 55, Issue:2
Disparate SAR data of griseofulvin analogues for the dermatophytes Trichophyton mentagrophytes, T. rubrum, and MDA-MB-231 cancer cells.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (24)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (8.33)18.7374
1990's0 (0.00)18.2507
2000's9 (37.50)29.6817
2010's10 (41.67)24.3611
2020's3 (12.50)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 63.63

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index63.63 (24.57)
Research Supply Index3.22 (2.92)
Research Growth Index5.33 (4.65)
Search Engine Demand Index103.05 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (63.63)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews4 (16.67%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other20 (83.33%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]