Dicyclohexyl ketone

Details

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Internal ID 937202f4-3dd0-414c-b958-970c9ef9ade0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name dicyclohexylmethanone
SMILES (Canonical) C1CCC(CC1)C(=O)C2CCCCC2
SMILES (Isomeric) C1CCC(CC1)C(=O)C2CCCCC2
InChI InChI=1S/C13H22O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h11-12H,1-10H2
InChI Key TWXWPPKDQOWNSX-UHFFFAOYSA-N
Popularity 28 references in papers

Physical and Chemical Properties

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Molecular Formula C13H22O
Molecular Weight 194.31 g/mol
Exact Mass 194.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.72
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Dicyclohexylmethanone
119-60-8
Methanone, dicyclohexyl-
Cyclohexane ketone
KETONE, DICYCLOHEXYL
NSC 49725
EINECS 204-336-0
BRN 1909406
UNII-4JW244G15F
AI3-05564
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Dicyclohexyl ketone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.5766 57.66%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5456 54.56%
OATP2B1 inhibitior - 0.8424 84.24%
OATP1B1 inhibitior + 0.9767 97.67%
OATP1B3 inhibitior + 0.9600 96.00%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6806 68.06%
P-glycoprotein inhibitior - 0.9404 94.04%
P-glycoprotein substrate - 0.9930 99.30%
CYP3A4 substrate - 0.7338 73.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7190 71.90%
CYP3A4 inhibition - 0.9601 96.01%
CYP2C9 inhibition - 0.8208 82.08%
CYP2C19 inhibition - 0.8395 83.95%
CYP2D6 inhibition - 0.9728 97.28%
CYP1A2 inhibition - 0.5908 59.08%
CYP2C8 inhibition - 0.9891 98.91%
CYP inhibitory promiscuity - 0.5879 58.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6651 66.51%
Eye corrosion + 0.9781 97.81%
Eye irritation + 0.9850 98.50%
Skin irritation + 0.6986 69.86%
Skin corrosion - 0.6494 64.94%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6154 61.54%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.6715 67.15%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.9275 92.75%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.6015 60.15%
Acute Oral Toxicity (c) IV 0.4749 47.49%
Estrogen receptor binding - 0.7606 76.06%
Androgen receptor binding - 0.7440 74.40%
Thyroid receptor binding - 0.7642 76.42%
Glucocorticoid receptor binding - 0.8209 82.09%
Aromatase binding - 0.8145 81.45%
PPAR gamma - 0.8001 80.01%
Honey bee toxicity - 0.9747 97.47%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.7699 76.99%

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
CHEMBL4040 P28482 MAP kinase ERK2 88.26% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.02% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 82.83% 91.19%
CHEMBL3012 Q13946 Phosphodiesterase 7A 82.05% 99.29%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.42% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.38% 96.61%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.19% 93.04%
CHEMBL5255 O00206 Toll-like receptor 4 80.54% 92.50%

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.
Scutellaria barbata

Cross-Links

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PubChem 8403
NPASS NPC121549
LOTUS LTS0069653
wikiData Q27259791