3,3,4,5-Tetramethylcyclohexan-1-one

Details

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Internal ID 18fd8439-c90b-4fbc-bbfe-171697d84efb
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 3,3,4,5-tetramethylcyclohexan-1-one
SMILES (Canonical) CC1CC(=O)CC(C1C)(C)C
SMILES (Isomeric) CC1CC(=O)CC(C1C)(C)C
InChI InChI=1S/C10H18O/c1-7-5-9(11)6-10(3,4)8(7)2/h7-8H,5-6H2,1-4H3
InChI Key RIAQBNSPOHNARJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O
Molecular Weight 154.25 g/mol
Exact Mass 154.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.65
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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RIAQBNSPOHNARJ-UHFFFAOYSA-N
3,3,4,5-tetramethylcyclohexan-1-one

2D Structure

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2D Structure of 3,3,4,5-Tetramethylcyclohexan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9957 99.57%
Caco-2 + 0.8668 86.68%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.6624 66.24%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.9551 95.51%
OATP1B3 inhibitior + 0.9554 95.54%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8599 85.99%
P-glycoprotein inhibitior - 0.9539 95.39%
P-glycoprotein substrate - 0.9546 95.46%
CYP3A4 substrate - 0.5470 54.70%
CYP2C9 substrate - 0.7747 77.47%
CYP2D6 substrate - 0.8013 80.13%
CYP3A4 inhibition - 0.9468 94.68%
CYP2C9 inhibition - 0.8856 88.56%
CYP2C19 inhibition - 0.9281 92.81%
CYP2D6 inhibition - 0.9479 94.79%
CYP1A2 inhibition - 0.8326 83.26%
CYP2C8 inhibition - 0.9849 98.49%
CYP inhibitory promiscuity - 0.9691 96.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6917 69.17%
Carcinogenicity (trinary) Non-required 0.6176 61.76%
Eye corrosion + 0.5604 56.04%
Eye irritation + 0.8980 89.80%
Skin irritation + 0.8038 80.38%
Skin corrosion - 0.8840 88.40%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7882 78.82%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.9527 95.27%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.7412 74.12%
Acute Oral Toxicity (c) III 0.5844 58.44%
Estrogen receptor binding - 0.9162 91.62%
Androgen receptor binding - 0.8933 89.33%
Thyroid receptor binding - 0.8622 86.22%
Glucocorticoid receptor binding - 0.9156 91.56%
Aromatase binding - 0.8762 87.62%
PPAR gamma - 0.8375 83.75%
Honey bee toxicity - 0.8684 86.84%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.8831 88.31%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.53% 97.25%
CHEMBL2581 P07339 Cathepsin D 88.96% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.85% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.76% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.82% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.20% 85.14%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.45% 86.00%
CHEMBL1902 P62942 FK506-binding protein 1A 82.69% 97.05%

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.
Crocus sativus

Cross-Links

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PubChem 89211994
NPASS NPC244062