(2R,3S,6S)-3-methyl-6-propan-2-yl-2-propylcyclohexan-1-one

Details

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Internal ID 660a4db1-09b6-4f8d-abc9-d55b06c2ae72
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (2R,3S,6S)-3-methyl-6-propan-2-yl-2-propylcyclohexan-1-one
SMILES (Canonical) CCCC1C(CCC(C1=O)C(C)C)C
SMILES (Isomeric) CCC[C@@H]1[C@H](CC[C@H](C1=O)C(C)C)C
InChI InChI=1S/C13H24O/c1-5-6-12-10(4)7-8-11(9(2)3)13(12)14/h9-12H,5-8H2,1-4H3/t10-,11-,12+/m0/s1
InChI Key WITOAKKBBDHCCW-SDDRHHMPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C13H24O
Molecular Weight 196.33 g/mol
Exact Mass 196.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3S,6S)-3-methyl-6-propan-2-yl-2-propylcyclohexan-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 + 0.9973 99.73%
Caco-2 + 0.9302 93.02%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.6624 66.24%
OATP2B1 inhibitior - 0.8299 82.99%
OATP1B1 inhibitior + 0.9397 93.97%
OATP1B3 inhibitior + 0.9571 95.71%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8670 86.70%
P-glycoprotein inhibitior - 0.9249 92.49%
P-glycoprotein substrate - 0.7069 70.69%
CYP3A4 substrate - 0.6154 61.54%
CYP2C9 substrate - 0.6168 61.68%
CYP2D6 substrate - 0.7682 76.82%
CYP3A4 inhibition - 0.9708 97.08%
CYP2C9 inhibition - 0.8050 80.50%
CYP2C19 inhibition - 0.9109 91.09%
CYP2D6 inhibition - 0.9063 90.63%
CYP1A2 inhibition - 0.5900 59.00%
CYP2C8 inhibition - 0.9838 98.38%
CYP inhibitory promiscuity - 0.8511 85.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.6971 69.71%
Eye corrosion + 0.7156 71.56%
Eye irritation + 0.8599 85.99%
Skin irritation + 0.5888 58.88%
Skin corrosion - 0.8359 83.59%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5636 56.36%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.9422 94.22%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.6398 63.98%
Acute Oral Toxicity (c) III 0.8146 81.46%
Estrogen receptor binding - 0.9172 91.72%
Androgen receptor binding - 0.6109 61.09%
Thyroid receptor binding - 0.7606 76.06%
Glucocorticoid receptor binding - 0.8721 87.21%
Aromatase binding - 0.9037 90.37%
PPAR gamma - 0.9165 91.65%
Honey bee toxicity - 0.9454 94.54%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9824 98.24%

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 97.18% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.98% 97.25%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 95.29% 96.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.16% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.85% 93.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.29% 97.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.38% 96.47%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.27% 94.80%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.72% 95.56%
CHEMBL2842 P42345 Serine/threonine-protein kinase mTOR 80.70% 92.78%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.36% 99.18%

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.
Cupressus bakeri

Cross-Links

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PubChem 15241198
LOTUS LTS0005149
wikiData Q105306495