2-Methyl-6-(3-methyl-7-oxoocta-2,5-dienyl)cyclohexa-2,5-diene-1,4-dione

Details

Top
Internal ID a1037967-dd1c-4e65-885e-bd84b156847e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylquinones
IUPAC Name 2-methyl-6-(3-methyl-7-oxoocta-2,5-dienyl)cyclohexa-2,5-diene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H18O3/c1-11(5-4-6-13(3)17)7-8-14-10-15(18)9-12(2)16(14)19/h4,6-7,9-10H,5,8H2,1-3H3
InChI Key TWUGTWWCFXHNCH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H18O3
Molecular Weight 258.31 g/mol
Exact Mass 258.125594432 g/mol
Topological Polar Surface Area (TPSA) 51.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.88
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-Methyl-6-(3-methyl-7-oxoocta-2,5-dienyl)cyclohexa-2,5-diene-1,4-dione

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.9215 92.15%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7539 75.39%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.8959 89.59%
OATP1B3 inhibitior + 0.9505 95.05%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6213 62.13%
P-glycoprotein inhibitior - 0.9387 93.87%
P-glycoprotein substrate - 0.8742 87.42%
CYP3A4 substrate - 0.5406 54.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8620 86.20%
CYP3A4 inhibition - 0.7909 79.09%
CYP2C9 inhibition - 0.7771 77.71%
CYP2C19 inhibition - 0.7659 76.59%
CYP2D6 inhibition - 0.8149 81.49%
CYP1A2 inhibition - 0.6925 69.25%
CYP2C8 inhibition - 0.9277 92.77%
CYP inhibitory promiscuity - 0.6858 68.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6552 65.52%
Carcinogenicity (trinary) Non-required 0.5560 55.60%
Eye corrosion - 0.9095 90.95%
Eye irritation - 0.7278 72.78%
Skin irritation + 0.5987 59.87%
Skin corrosion - 0.9383 93.83%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4553 45.53%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.6302 63.02%
skin sensitisation + 0.7997 79.97%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5060 50.60%
Acute Oral Toxicity (c) III 0.4331 43.31%
Estrogen receptor binding + 0.6463 64.63%
Androgen receptor binding - 0.5487 54.87%
Thyroid receptor binding - 0.7600 76.00%
Glucocorticoid receptor binding + 0.6816 68.16%
Aromatase binding - 0.6265 62.65%
PPAR gamma - 0.5910 59.10%
Honey bee toxicity - 0.9107 91.07%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9922 99.22%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.65% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 90.20% 94.73%
CHEMBL2581 P07339 Cathepsin D 82.57% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 81.46% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.54% 96.09%

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 123611826
LOTUS LTS0195333
wikiData Q105266114