Isomenthone, (+/-)-

Details

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Internal ID ed2ac23d-afb0-4a2d-83c6-51b1a75e2ddb
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (2S,5S)-5-methyl-2-propan-2-ylcyclohexan-1-one
SMILES (Canonical) CC1CCC(C(=O)C1)C(C)C
SMILES (Isomeric) C[C@H]1CC[C@H](C(=O)C1)C(C)C
InChI InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-9H,4-6H2,1-3H3/t8-,9-/m0/s1
InChI Key NFLGAXVYCFJBMK-IUCAKERBSA-N
Popularity 16 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 2.70
Atomic LogP (AlogP) 2.65
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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(-)-isomenthone
18309-28-9
L-isomenthone
dl-Isomenthone
cis-Menthone
(+/-)-isomenthone
cis-p-menthone
p-Menthan-3-one, cis-
Isomenthone, (+/-)-
36977-92-1
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isomenthone, (+/-)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.6871 68.71%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.7285 72.85%
OATP2B1 inhibitior - 0.8425 84.25%
OATP1B1 inhibitior + 0.9674 96.74%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9392 93.92%
P-glycoprotein inhibitior - 0.9784 97.84%
P-glycoprotein substrate - 0.8022 80.22%
CYP3A4 substrate - 0.6522 65.22%
CYP2C9 substrate - 0.6168 61.68%
CYP2D6 substrate - 0.7682 76.82%
CYP3A4 inhibition - 0.9700 97.00%
CYP2C9 inhibition - 0.9000 90.00%
CYP2C19 inhibition - 0.9399 93.99%
CYP2D6 inhibition - 0.9535 95.35%
CYP1A2 inhibition - 0.7503 75.03%
CYP2C8 inhibition - 0.9963 99.63%
CYP inhibitory promiscuity - 0.9679 96.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.7053 70.53%
Eye corrosion + 0.7224 72.24%
Eye irritation + 0.9884 98.84%
Skin irritation + 0.8622 86.22%
Skin corrosion - 0.8439 84.39%
Ames mutagenesis + 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7475 74.75%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.9500 95.00%
skin sensitisation + 0.9334 93.34%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.6807 68.07%
Acute Oral Toxicity (c) III 0.7891 78.91%
Estrogen receptor binding - 0.9559 95.59%
Androgen receptor binding - 0.7272 72.72%
Thyroid receptor binding - 0.8887 88.87%
Glucocorticoid receptor binding - 0.8706 87.06%
Aromatase binding - 0.8411 84.11%
PPAR gamma - 0.9284 92.84%
Honey bee toxicity - 0.9063 90.63%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9304 93.04%

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
CHEMBL2581 P07339 Cathepsin D 95.47% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.25% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.24% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.07% 90.71%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.27% 86.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.94% 97.25%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.77% 94.80%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.07% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.75% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.04% 93.56%

Cross-Links

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PubChem 6432469
NPASS NPC71092
LOTUS LTS0265025
wikiData Q27116856