Epoxydine A

Details

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Internal ID 466fbcef-4ae5-4c3d-bb7e-c5ac6da6849b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name (4R,6S)-6-methyl-4-[(1R,5S)-5-methyl-4-oxocyclohex-2-en-1-yl]oxycyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H18O3/c1-9-7-11(3-5-13(9)15)17-12-4-6-14(16)10(2)8-12/h3-6,9-12H,7-8H2,1-2H3/t9-,10-,11-,12-/m0/s1
InChI Key AJRXCMFONRLPJH-BJDJZHNGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O3
Molecular Weight 234.29 g/mol
Exact Mass 234.125594432 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.07
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Epoxydine A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8089 80.89%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8905 89.05%
OATP2B1 inhibitior - 0.8634 86.34%
OATP1B1 inhibitior + 0.9388 93.88%
OATP1B3 inhibitior + 0.9762 97.62%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6871 68.71%
P-glycoprotein inhibitior - 0.8881 88.81%
P-glycoprotein substrate - 0.9100 91.00%
CYP3A4 substrate - 0.5914 59.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8722 87.22%
CYP3A4 inhibition - 0.8258 82.58%
CYP2C9 inhibition - 0.7559 75.59%
CYP2C19 inhibition - 0.5511 55.11%
CYP2D6 inhibition - 0.8973 89.73%
CYP1A2 inhibition - 0.7255 72.55%
CYP2C8 inhibition - 0.9800 98.00%
CYP inhibitory promiscuity - 0.6964 69.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7281 72.81%
Carcinogenicity (trinary) Non-required 0.5758 57.58%
Eye corrosion - 0.8388 83.88%
Eye irritation - 0.8532 85.32%
Skin irritation - 0.7106 71.06%
Skin corrosion - 0.9602 96.02%
Ames mutagenesis - 0.7991 79.91%
Human Ether-a-go-go-Related Gene inhibition + 0.7123 71.23%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.6824 68.24%
skin sensitisation + 0.5533 55.33%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6064 60.64%
Estrogen receptor binding - 0.5393 53.93%
Androgen receptor binding - 0.5961 59.61%
Thyroid receptor binding - 0.6182 61.82%
Glucocorticoid receptor binding - 0.6388 63.88%
Aromatase binding - 0.5095 50.95%
PPAR gamma - 0.7955 79.55%
Honey bee toxicity - 0.8743 87.43%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.9773 97.73%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.03% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.75% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.48% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.95% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.71% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.86% 97.25%

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 139583546
LOTUS LTS0051319
wikiData Q75063793