(S)-3-methylcyclohexanone

Details

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Internal ID 0b15498f-10f0-491b-b171-088a296fbfde
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name (3S)-3-methylcyclohexan-1-one
SMILES (Canonical) CC1CCCC(=O)C1
SMILES (Isomeric) C[C@H]1CCCC(=O)C1
InChI InChI=1S/C7H12O/c1-6-3-2-4-7(8)5-6/h6H,2-5H2,1H3/t6-/m0/s1
InChI Key UJBOOUHRTQVGRU-LURJTMIESA-N
Popularity 13 references in papers

Physical and Chemical Properties

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Molecular Formula C7H12O
Molecular Weight 112.17 g/mol
Exact Mass 112.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.77
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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24965-87-5
(3S)-3-methylcyclohexan-1-one
3-Methylcyclohexanone, (-)-
UNII-CJE8VS4G3R
CJE8VS4G3R
(-)-3-methylcyclohexanone
Cyclohexanone, 3-methyl-, (S)-
3beta-Methylcyclohexanone
(3s)-3-methylcyclohexanone
SCHEMBL857124
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (S)-3-methylcyclohexanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.8802 88.02%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.6271 62.71%
OATP2B1 inhibitior - 0.8471 84.71%
OATP1B1 inhibitior + 0.9539 95.39%
OATP1B3 inhibitior + 0.9683 96.83%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9522 95.22%
P-glycoprotein inhibitior - 0.9886 98.86%
P-glycoprotein substrate - 0.9680 96.80%
CYP3A4 substrate - 0.6646 66.46%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.9800 98.00%
CYP2C9 inhibition - 0.9269 92.69%
CYP2C19 inhibition - 0.9628 96.28%
CYP2D6 inhibition - 0.9658 96.58%
CYP1A2 inhibition - 0.7487 74.87%
CYP2C8 inhibition - 0.9816 98.16%
CYP inhibitory promiscuity - 0.9690 96.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.7020 70.20%
Eye corrosion + 0.9616 96.16%
Eye irritation + 0.9941 99.41%
Skin irritation + 0.9337 93.37%
Skin corrosion - 0.5405 54.05%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7621 76.21%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.9553 95.53%
skin sensitisation + 0.7520 75.20%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.7251 72.51%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6211 62.11%
Acute Oral Toxicity (c) III 0.8666 86.66%
Estrogen receptor binding - 0.9717 97.17%
Androgen receptor binding - 0.9301 93.01%
Thyroid receptor binding - 0.9242 92.42%
Glucocorticoid receptor binding - 0.8992 89.92%
Aromatase binding - 0.8451 84.51%
PPAR gamma - 0.9056 90.56%
Honey bee toxicity - 0.9608 96.08%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.8115 81.15%

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 91.58% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.76% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.25% 97.09%
CHEMBL1902 P62942 FK506-binding protein 1A 84.85% 97.05%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.64% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.87% 97.25%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.67% 93.04%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 7057964
NPASS NPC63963