4-Methyl-2-(2,5,6,6-tetramethylcyclohex-2-en-1-yl)furan

Details

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Internal ID b26f001b-81c8-4fa5-b16a-5911b87d21ec
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 4-methyl-2-(2,5,6,6-tetramethylcyclohex-2-en-1-yl)furan
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O/c1-10-8-13(16-9-10)14-11(2)6-7-12(3)15(14,4)5/h6,8-9,12,14H,7H2,1-5H3
InChI Key FWQWDKFOBXECQW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.68
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Methyl-2-(2,5,6,6-tetramethylcyclohex-2-en-1-yl)furan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.7889 78.89%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.4365 43.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9468 94.68%
OATP1B3 inhibitior + 0.9223 92.23%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7868 78.68%
P-glycoprotein inhibitior - 0.9123 91.23%
P-glycoprotein substrate - 0.8584 85.84%
CYP3A4 substrate - 0.5473 54.73%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7172 71.72%
CYP3A4 inhibition - 0.8535 85.35%
CYP2C9 inhibition - 0.7019 70.19%
CYP2C19 inhibition + 0.5329 53.29%
CYP2D6 inhibition - 0.9234 92.34%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.8725 87.25%
CYP inhibitory promiscuity + 0.8892 88.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7417 74.17%
Carcinogenicity (trinary) Warning 0.3792 37.92%
Eye corrosion - 0.9096 90.96%
Eye irritation - 0.8577 85.77%
Skin irritation + 0.5567 55.67%
Skin corrosion - 0.9204 92.04%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6457 64.57%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.7964 79.64%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.7800 78.00%
Nephrotoxicity - 0.5917 59.17%
Acute Oral Toxicity (c) III 0.7742 77.42%
Estrogen receptor binding - 0.7306 73.06%
Androgen receptor binding - 0.5232 52.32%
Thyroid receptor binding - 0.6858 68.58%
Glucocorticoid receptor binding - 0.9083 90.83%
Aromatase binding - 0.7345 73.45%
PPAR gamma - 0.4878 48.78%
Honey bee toxicity - 0.8237 82.37%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9807 98.07%

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 92.74% 91.11%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 92.20% 86.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.98% 94.80%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.73% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.98% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.92% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.05% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 80.62% 94.73%

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 14489332
LOTUS LTS0114363
wikiData Q105003523