2-(2,5,6,6-Tetramethylcyclohex-2-en-1-yl)acetaldehyde

Details

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Internal ID 769a072f-679a-428e-9477-a00dc417ce32
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Alpha-hydrogen aldehydes
IUPAC Name 2-(2,5,6,6-tetramethylcyclohex-2-en-1-yl)acetaldehyde
SMILES (Canonical) CC1CC=C(C(C1(C)C)CC=O)C
SMILES (Isomeric) CC1CC=C(C(C1(C)C)CC=O)C
InChI InChI=1S/C12H20O/c1-9-5-6-10(2)12(3,4)11(9)7-8-13/h5,8,10-11H,6-7H2,1-4H3
InChI Key IUPRIYPYBZEDHE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O
Molecular Weight 180.29 g/mol
Exact Mass 180.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.20
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(2,5,6,6-Tetramethylcyclohex-2-en-1-yl)acetaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.6590 65.90%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.4279 42.79%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.9227 92.27%
OATP1B3 inhibitior - 0.2215 22.15%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8747 87.47%
P-glycoprotein inhibitior - 0.9567 95.67%
P-glycoprotein substrate - 0.8548 85.48%
CYP3A4 substrate - 0.5465 54.65%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8100 81.00%
CYP3A4 inhibition - 0.8844 88.44%
CYP2C9 inhibition - 0.8770 87.70%
CYP2C19 inhibition - 0.8490 84.90%
CYP2D6 inhibition - 0.9447 94.47%
CYP1A2 inhibition - 0.8318 83.18%
CYP2C8 inhibition - 0.9344 93.44%
CYP inhibitory promiscuity - 0.6827 68.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5117 51.17%
Carcinogenicity (trinary) Non-required 0.5503 55.03%
Eye corrosion - 0.7722 77.22%
Eye irritation - 0.5356 53.56%
Skin irritation + 0.7953 79.53%
Skin corrosion - 0.9211 92.11%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4706 47.06%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5321 53.21%
skin sensitisation + 0.9610 96.10%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5538 55.38%
Acute Oral Toxicity (c) III 0.7894 78.94%
Estrogen receptor binding - 0.8403 84.03%
Androgen receptor binding - 0.8058 80.58%
Thyroid receptor binding - 0.8537 85.37%
Glucocorticoid receptor binding - 0.9189 91.89%
Aromatase binding - 0.9035 90.35%
PPAR gamma - 0.7737 77.37%
Honey bee toxicity - 0.8386 83.86%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9862 98.62%

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 92.18% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.40% 96.09%
CHEMBL2581 P07339 Cathepsin D 84.48% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.66% 97.25%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.07% 90.24%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.26% 86.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.51% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.94% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.63% 100.00%

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 13922605
LOTUS LTS0021469
wikiData Q105120758