Chevalone A

Details

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Internal ID f4d1ed70-a0fc-44b4-b5ca-b3f656b19845
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name (1R,2S,11S,14R,15R,18S,20R)-18-hydroxy-1,7,11,15,19,19-hexamethyl-6,10-dioxapentacyclo[12.8.0.02,11.04,9.015,20]docosa-4(9),7-dien-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H38O4/c1-15-13-17-16(22(28)29-15)14-20-25(5)10-7-18-23(2,3)21(27)9-11-24(18,4)19(25)8-12-26(20,6)30-17/h13,18-21,27H,7-12,14H2,1-6H3/t18-,19+,20-,21-,24-,25+,26-/m0/s1
InChI Key XVYAFRIRAFSVGL-KFCOXGNHSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C26H38O4
Molecular Weight 414.60 g/mol
Exact Mass 414.27700969 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 5.60

Synonyms

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CHEMBL5183521

2D Structure

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2D Structure of Chevalone A

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 97.27% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.81% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.01% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.04% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.23% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.69% 100.00%
CHEMBL1871 P10275 Androgen Receptor 86.54% 96.43%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.06% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.77% 94.45%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.89% 90.71%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.06% 90.24%

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 53475641
LOTUS LTS0024726
wikiData Q75065707