4-Hydroxy-2,7,17-trioxapentacyclo[10.7.0.01,16.03,11.04,8]nonadecane-10,14-dione

Details

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Internal ID a56243c7-b77f-422f-94aa-0e30df5eb0cf
Taxonomy Organoheterocyclic compounds > Tetrahydrofurans
IUPAC Name 4-hydroxy-2,7,17-trioxapentacyclo[10.7.0.01,16.03,11.04,8]nonadecane-10,14-dione
SMILES (Canonical) C1COC2C13C(CC(=O)C2)C4C(O3)C5(CCOC5CC4=O)O
SMILES (Isomeric) C1COC2C13C(CC(=O)C2)C4C(O3)C5(CCOC5CC4=O)O
InChI InChI=1S/C16H20O6/c17-8-5-9-13-10(18)7-11-15(19,1-3-20-11)14(13)22-16(9)2-4-21-12(16)6-8/h9,11-14,19H,1-7H2
InChI Key OLMMLZKKSGZLQH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O6
Molecular Weight 308.33 g/mol
Exact Mass 308.12598835 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP -1.70

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-2,7,17-trioxapentacyclo[10.7.0.01,16.03,11.04,8]nonadecane-10,14-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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.98% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.43% 97.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 89.26% 96.61%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.34% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.84% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.45% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.35% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.23% 89.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Incarvillea delavayi

Cross-Links

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PubChem 74954680
LOTUS LTS0126519
wikiData Q105194031