4,6,6-Trimethyl-5-oxocyclohexa-1,3-diene-1-carbaldehyde

Details

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Internal ID 1130bff4-bcab-4515-b5b4-3b7afc3801ea
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 4,6,6-trimethyl-5-oxocyclohexa-1,3-diene-1-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H12O2/c1-7-4-5-8(6-11)10(2,3)9(7)12/h4-6H,1-3H3
InChI Key NJBPXWCZSHLTGL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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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

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There are no found synonyms.

2D Structure

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2D Structure of 4,6,6-Trimethyl-5-oxocyclohexa-1,3-diene-1-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.9117 91.17%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8139 81.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8615 86.15%
OATP1B3 inhibitior + 0.9594 95.94%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9148 91.48%
P-glycoprotein inhibitior - 0.9742 97.42%
P-glycoprotein substrate - 0.9867 98.67%
CYP3A4 substrate - 0.6290 62.90%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8665 86.65%
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 - 0.9431 94.31%
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 + 0.9521 95.21%
Skin irritation + 0.6117 61.17%
Skin corrosion - 0.8918 89.18%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7329 73.29%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.9510 95.10%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.8823 88.23%
Nephrotoxicity + 0.6483 64.83%
Acute Oral Toxicity (c) II 0.5471 54.71%
Estrogen receptor binding - 0.9303 93.03%
Androgen receptor binding - 0.8716 87.16%
Thyroid receptor binding - 0.8026 80.26%
Glucocorticoid receptor binding - 0.8732 87.32%
Aromatase binding - 0.8785 87.85%
PPAR gamma - 0.9154 91.54%
Honey bee toxicity - 0.9374 93.74%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8997 89.97%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.38% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.75% 98.95%

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.
Carum carvi

Cross-Links

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PubChem 130025349
LOTUS LTS0048332
wikiData Q105180075