4-(2,5,6,6-Tetramethylcyclohex-2-en-1-yl)butan-2-one

Details

Top
Internal ID 0c08a51b-b9af-4e16-b4f6-115521d8a603
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4-(2,5,6,6-tetramethylcyclohex-2-en-1-yl)butan-2-one
SMILES (Canonical) CC1CC=C(C(C1(C)C)CCC(=O)C)C
SMILES (Isomeric) CC1CC=C(C(C1(C)C)CCC(=O)C)C
InChI InChI=1S/C14H24O/c1-10-6-7-11(2)14(4,5)13(10)9-8-12(3)15/h6,11,13H,7-9H2,1-5H3
InChI Key GOWGYNUJGXNVOU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H24O
Molecular Weight 208.34 g/mol
Exact Mass 208.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.98
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4-(2,5,6,6-Tetramethylcyclohex-2-en-1-yl)butan-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.8900 89.00%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4758 47.58%
OATP2B1 inhibitior - 0.8499 84.99%
OATP1B1 inhibitior + 0.9445 94.45%
OATP1B3 inhibitior - 0.2516 25.16%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7456 74.56%
P-glycoprotein inhibitior - 0.9451 94.51%
P-glycoprotein substrate - 0.8327 83.27%
CYP3A4 substrate - 0.5529 55.29%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.8038 80.38%
CYP3A4 inhibition - 0.9084 90.84%
CYP2C9 inhibition - 0.8944 89.44%
CYP2C19 inhibition - 0.8854 88.54%
CYP2D6 inhibition - 0.9526 95.26%
CYP1A2 inhibition - 0.7189 71.89%
CYP2C8 inhibition - 0.9429 94.29%
CYP inhibitory promiscuity - 0.6620 66.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.5369 53.69%
Eye corrosion - 0.9056 90.56%
Eye irritation + 0.5309 53.09%
Skin irritation + 0.8274 82.74%
Skin corrosion - 0.9803 98.03%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4937 49.37%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6622 66.22%
skin sensitisation + 0.9594 95.94%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.6187 61.87%
Acute Oral Toxicity (c) III 0.7979 79.79%
Estrogen receptor binding - 0.7499 74.99%
Androgen receptor binding - 0.8204 82.04%
Thyroid receptor binding - 0.7843 78.43%
Glucocorticoid receptor binding - 0.8345 83.45%
Aromatase binding - 0.8006 80.06%
PPAR gamma - 0.7328 73.28%
Honey bee toxicity - 0.8910 89.10%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9505 95.05%

Targets

Top

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 94.60% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.84% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.27% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.87% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.16% 97.25%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.33% 96.95%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 14489318
LOTUS LTS0031411
wikiData Q105014631