4,8a-Dimethyl-4a,5-epoxydecalin

Details

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Internal ID 74eb9217-ce72-4153-bdb2-7c2c3b99cbba
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name 4a,8-dimethyl-1a,2,3,4,5,6,7,8-octahydronaphtho[1,8a-b]oxirene
SMILES (Canonical) CC1CCCC2(C13C(O3)CCC2)C
SMILES (Isomeric) CC1CCCC2(C13C(O3)CCC2)C
InChI InChI=1S/C12H20O/c1-9-5-3-7-11(2)8-4-6-10-12(9,11)13-10/h9-10H,3-8H2,1-2H3
InChI Key KKXSVZHUGGQUGL-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H20O
Molecular Weight 180.29 g/mol
Exact Mass 180.151415257 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.13
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,8a-Dimethyl-4a,5-epoxydecalin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.9039 90.39%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.5598 55.98%
OATP2B1 inhibitior - 0.8465 84.65%
OATP1B1 inhibitior + 0.9439 94.39%
OATP1B3 inhibitior + 0.9682 96.82%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9380 93.80%
P-glycoprotein inhibitior - 0.9615 96.15%
P-glycoprotein substrate - 0.9452 94.52%
CYP3A4 substrate - 0.5269 52.69%
CYP2C9 substrate - 0.6298 62.98%
CYP2D6 substrate - 0.7280 72.80%
CYP3A4 inhibition - 0.8939 89.39%
CYP2C9 inhibition - 0.5887 58.87%
CYP2C19 inhibition - 0.5473 54.73%
CYP2D6 inhibition - 0.9403 94.03%
CYP1A2 inhibition + 0.5509 55.09%
CYP2C8 inhibition - 0.9141 91.41%
CYP inhibitory promiscuity - 0.8899 88.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.6185 61.85%
Eye corrosion - 0.8811 88.11%
Eye irritation + 0.7239 72.39%
Skin irritation - 0.5609 56.09%
Skin corrosion - 0.9207 92.07%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6842 68.42%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.5908 59.08%
skin sensitisation + 0.5144 51.44%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6880 68.80%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.5576 55.76%
Acute Oral Toxicity (c) III 0.7188 71.88%
Estrogen receptor binding - 0.7111 71.11%
Androgen receptor binding - 0.5561 55.61%
Thyroid receptor binding - 0.7699 76.99%
Glucocorticoid receptor binding - 0.8273 82.73%
Aromatase binding - 0.7551 75.51%
PPAR gamma - 0.8166 81.66%
Honey bee toxicity - 0.8956 89.56%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.8698 86.98%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.41% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.68% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.65% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.89% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 86.78% 96.61%
CHEMBL237 P41145 Kappa opioid receptor 86.17% 98.10%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.77% 86.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.07% 95.50%
CHEMBL3837 P07711 Cathepsin L 83.21% 96.61%
CHEMBL259 P32245 Melanocortin receptor 4 83.08% 95.38%
CHEMBL230 P35354 Cyclooxygenase-2 82.91% 89.63%
CHEMBL5203 P33316 dUTP pyrophosphatase 82.73% 99.18%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.03% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.95% 95.89%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.51% 96.21%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 80.36% 98.99%
CHEMBL4072 P07858 Cathepsin B 80.12% 93.67%

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.
Lophocolea bidentata

Cross-Links

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PubChem 15768061
LOTUS LTS0037438
wikiData Q105142424