1,5,8-Trimethyl-1,3a,4,9a-tetrahydroazuleno[6,5-b]furan-2,6-dione

Details

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Internal ID 633e4f31-d91a-4e95-9ea5-4528a3cdea7a
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 1,5,8-trimethyl-1,3a,4,9a-tetrahydroazuleno[6,5-b]furan-2,6-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O3/c1-7-4-12(16)14-8(2)5-13-11(6-10(7)14)9(3)15(17)18-13/h4,6,9,11,13H,5H2,1-3H3
InChI Key FRBORWNVTCITAQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O3
Molecular Weight 244.28 g/mol
Exact Mass 244.109944368 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 1.30

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,5,8-Trimethyl-1,3a,4,9a-tetrahydroazuleno[6,5-b]furan-2,6-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.78% 94.80%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.75% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.26% 93.40%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.89% 86.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.98% 91.11%
CHEMBL2581 P07339 Cathepsin D 83.63% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.08% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.11% 85.14%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.17% 90.71%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 4663224
LOTUS LTS0098478
wikiData Q105000080