4,6,6-Trimethyl-3-oxocyclohexa-1,4-diene-1-carbaldehyde

Details

Top
Internal ID 994e53cf-023d-41dc-b6c6-7ae22db43fb0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 4,6,6-trimethyl-3-oxocyclohexa-1,4-diene-1-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H12O2/c1-7-5-10(2,3)8(6-11)4-9(7)12/h4-6H,1-3H3
InChI Key CNXDUKOIOUAQPE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H12O2
Molecular Weight 164.20 g/mol
Exact Mass 164.083729621 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.67
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4,6,6-Trimethyl-3-oxocyclohexa-1,4-diene-1-carbaldehyde

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.9177 91.77%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.8139 81.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8733 87.33%
OATP1B3 inhibitior + 0.9594 95.94%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8471 84.71%
P-glycoprotein inhibitior - 0.9572 95.72%
P-glycoprotein substrate - 0.9649 96.49%
CYP3A4 substrate - 0.5803 58.03%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.8859 88.59%
CYP3A4 inhibition - 0.8440 84.40%
CYP2C9 inhibition - 0.8439 84.39%
CYP2C19 inhibition - 0.7059 70.59%
CYP2D6 inhibition - 0.8905 89.05%
CYP1A2 inhibition - 0.8403 84.03%
CYP2C8 inhibition - 0.9557 95.57%
CYP inhibitory promiscuity - 0.6940 69.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6683 66.83%
Carcinogenicity (trinary) Non-required 0.5622 56.22%
Eye corrosion - 0.5863 58.63%
Eye irritation + 0.9692 96.92%
Skin irritation + 0.6117 61.17%
Skin corrosion - 0.8918 89.18%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7772 77.72%
Micronuclear - 0.6000 60.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.9510 95.10%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.8823 88.23%
Nephrotoxicity + 0.7895 78.95%
Acute Oral Toxicity (c) II 0.5471 54.71%
Estrogen receptor binding - 0.8699 86.99%
Androgen receptor binding - 0.7256 72.56%
Thyroid receptor binding - 0.7928 79.28%
Glucocorticoid receptor binding - 0.8771 87.71%
Aromatase binding - 0.7724 77.24%
PPAR gamma - 0.8460 84.60%
Honey bee toxicity - 0.9389 93.89%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.8997 89.97%

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 95.54% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 89.21% 93.40%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.56% 94.80%
CHEMBL2581 P07339 Cathepsin D 85.70% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 83.42% 94.75%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 82.31% 85.30%

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.
Carum carvi

Cross-Links

Top
PubChem 129716150
LOTUS LTS0038588
wikiData Q104966404