2,5,6,6-Tetramethylcyclohexa-1,3-diene-1-carbaldehyde

Details

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Internal ID 2787d8bb-207e-42cf-9f2d-ff86fc674a8b
Taxonomy Organic oxygen compounds > Organic oxides
IUPAC Name 2,5,6,6-tetramethylcyclohexa-1,3-diene-1-carbaldehyde
SMILES (Canonical) CC1C=CC(=C(C1(C)C)C=O)C
SMILES (Isomeric) CC1C=CC(=C(C1(C)C)C=O)C
InChI InChI=1S/C11H16O/c1-8-5-6-9(2)11(3,4)10(8)7-12/h5-7,9H,1-4H3
InChI Key UQVUDZCZDLISBR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O
Molecular Weight 164.24 g/mol
Exact Mass 164.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.73
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 2,5,6,6-Tetramethylcyclohexa-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 + 0.9947 99.47%
Caco-2 + 0.9055 90.55%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.5256 52.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8681 86.81%
OATP1B3 inhibitior + 0.9142 91.42%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8530 85.30%
P-glycoprotein inhibitior - 0.9573 95.73%
P-glycoprotein substrate - 0.9401 94.01%
CYP3A4 substrate - 0.5625 56.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8667 86.67%
CYP3A4 inhibition - 0.8088 80.88%
CYP2C9 inhibition - 0.8214 82.14%
CYP2C19 inhibition - 0.7919 79.19%
CYP2D6 inhibition - 0.9450 94.50%
CYP1A2 inhibition - 0.8329 83.29%
CYP2C8 inhibition - 0.9787 97.87%
CYP inhibitory promiscuity - 0.5111 51.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5217 52.17%
Carcinogenicity (trinary) Non-required 0.5723 57.23%
Eye corrosion + 0.8117 81.17%
Eye irritation + 0.7106 71.06%
Skin irritation + 0.8170 81.70%
Skin corrosion - 0.6374 63.74%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6543 65.43%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.7824 78.24%
skin sensitisation + 0.9623 96.23%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.9169 91.69%
Nephrotoxicity + 0.5706 57.06%
Acute Oral Toxicity (c) III 0.8346 83.46%
Estrogen receptor binding - 0.9379 93.79%
Androgen receptor binding - 0.8839 88.39%
Thyroid receptor binding - 0.8012 80.12%
Glucocorticoid receptor binding - 0.9500 95.00%
Aromatase binding - 0.7797 77.97%
PPAR gamma - 0.9193 91.93%
Honey bee toxicity - 0.9004 90.04%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9463 94.63%

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 95.41% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.46% 86.33%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.19% 86.00%
CHEMBL1937 Q92769 Histone deacetylase 2 81.67% 94.75%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.30% 93.40%
CHEMBL3401 O75469 Pregnane X receptor 80.02% 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 14489312
LOTUS LTS0107515
wikiData Q105277525