2-Methyl-2-(4-methylcyclohex-3-en-1-yl)-5-prop-1-en-2-yloxolane

Details

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Internal ID ef4d0054-688a-423f-b55b-579099228be6
Taxonomy Organoheterocyclic compounds > Tetrahydrofurans
IUPAC Name 2-methyl-2-(4-methylcyclohex-3-en-1-yl)-5-prop-1-en-2-yloxolane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-11(2)14-9-10-15(4,16-14)13-7-5-12(3)6-8-13/h5,13-14H,1,6-10H2,2-4H3
InChI Key AKAQULCXJUDSBA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.25
H-Bond Acceptor 1
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 2-Methyl-2-(4-methylcyclohex-3-en-1-yl)-5-prop-1-en-2-yloxolane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.8690 86.90%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.3673 36.73%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.9478 94.78%
OATP1B3 inhibitior + 0.8915 89.15%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8980 89.80%
P-glycoprotein inhibitior - 0.9174 91.74%
P-glycoprotein substrate - 0.8585 85.85%
CYP3A4 substrate + 0.5656 56.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7308 73.08%
CYP3A4 inhibition - 0.8368 83.68%
CYP2C9 inhibition - 0.7244 72.44%
CYP2C19 inhibition - 0.5377 53.77%
CYP2D6 inhibition - 0.9453 94.53%
CYP1A2 inhibition - 0.5360 53.60%
CYP2C8 inhibition - 0.7142 71.42%
CYP inhibitory promiscuity - 0.5446 54.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.4726 47.26%
Eye corrosion - 0.9014 90.14%
Eye irritation + 0.5419 54.19%
Skin irritation + 0.5089 50.89%
Skin corrosion - 0.9742 97.42%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4931 49.31%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6680 66.80%
skin sensitisation + 0.6151 61.51%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8130 81.30%
Estrogen receptor binding - 0.7215 72.15%
Androgen receptor binding - 0.6832 68.32%
Thyroid receptor binding - 0.5550 55.50%
Glucocorticoid receptor binding - 0.4744 47.44%
Aromatase binding - 0.7334 73.34%
PPAR gamma - 0.7803 78.03%
Honey bee toxicity - 0.8565 85.65%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9704 97.04%

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 96.84% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.46% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.08% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.57% 100.00%
CHEMBL1871 P10275 Androgen Receptor 84.85% 96.43%
CHEMBL218 P21554 Cannabinoid CB1 receptor 83.35% 96.61%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.34% 92.94%
CHEMBL259 P32245 Melanocortin receptor 4 81.56% 95.38%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.82% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.06% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.01% 97.09%

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.
Coreopsis grandiflora

Cross-Links

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PubChem 163046294
LOTUS LTS0259227
wikiData Q104913503