3-Cyclohexyldodecane

Details

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Internal ID 461621b2-28ef-45dc-a717-d708bf2210f9
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name dodecan-3-ylcyclohexane
SMILES (Canonical) CCCCCCCCCC(CC)C1CCCCC1
SMILES (Isomeric) CCCCCCCCCC(CC)C1CCCCC1
InChI InChI=1S/C18H36/c1-3-5-6-7-8-9-11-14-17(4-2)18-15-12-10-13-16-18/h17-18H,3-16H2,1-2H3
InChI Key ZDMYCNLANBQLOI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H36
Molecular Weight 252.50 g/mol
Exact Mass 252.281701148 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 9.20
Atomic LogP (AlogP) 6.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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DTXSID601312361
13151-83-2
RefChem:1049248
DTXCID301742159
3-Cyclohexyldodecane
Dodecane, 3-cyclohexyl-
Cyclohexane, 1-ethyldecyl
dodecan-3-ylcyclohexane
9-Cyclohexyl-Eicosane
(1-Ethyldecyl)cyclohexane #
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Cyclohexyldodecane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.9116 91.16%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.6135 61.35%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.9372 93.72%
OATP1B3 inhibitior + 0.9416 94.16%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5826 58.26%
P-glycoprotein inhibitior - 0.9169 91.69%
P-glycoprotein substrate - 0.8024 80.24%
CYP3A4 substrate - 0.5821 58.21%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9727 97.27%
CYP2C9 inhibition - 0.9255 92.55%
CYP2C19 inhibition - 0.9417 94.17%
CYP2D6 inhibition - 0.9190 91.90%
CYP1A2 inhibition - 0.6585 65.85%
CYP2C8 inhibition - 0.8762 87.62%
CYP inhibitory promiscuity - 0.7492 74.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5656 56.56%
Eye corrosion + 0.9869 98.69%
Eye irritation + 0.9477 94.77%
Skin irritation + 0.6381 63.81%
Skin corrosion - 0.9778 97.78%
Ames mutagenesis - 0.9437 94.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5334 53.34%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5275 52.75%
skin sensitisation + 0.9521 95.21%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.8139 81.39%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.4546 45.46%
Acute Oral Toxicity (c) III 0.7427 74.27%
Estrogen receptor binding - 0.4845 48.45%
Androgen receptor binding - 0.6112 61.12%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.7177 71.77%
Aromatase binding - 0.7446 74.46%
PPAR gamma - 0.6908 69.08%
Honey bee toxicity - 0.9859 98.59%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.7169 71.69%
Fish aquatic toxicity + 0.9910 99.10%

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
CHEMBL240 Q12809 HERG 99.34% 89.76%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 95.79% 90.24%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 95.01% 91.81%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.08% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.96% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.91% 85.94%
CHEMBL2581 P07339 Cathepsin D 92.97% 98.95%
CHEMBL1968 P07099 Epoxide hydrolase 1 92.69% 98.57%
CHEMBL3359 P21462 Formyl peptide receptor 1 92.16% 93.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 91.88% 100.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 91.67% 96.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.32% 97.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.33% 92.86%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 89.24% 97.23%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 88.56% 95.50%
CHEMBL5203 P33316 dUTP pyrophosphatase 88.05% 99.18%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 86.66% 95.27%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 86.34% 96.00%
CHEMBL4777 P25929 Neuropeptide Y receptor type 1 84.67% 96.67%
CHEMBL5255 O00206 Toll-like receptor 4 84.67% 92.50%
CHEMBL3012 Q13946 Phosphodiesterase 7A 84.66% 99.29%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.53% 92.88%
CHEMBL5331 Q12866 Proto-oncogene tyrosine-protein kinase MER 84.00% 91.67%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 83.62% 98.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.44% 92.08%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.43% 95.17%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 82.78% 95.58%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 82.76% 94.55%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.59% 82.69%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 82.57% 97.47%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.29% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.05% 100.00%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 81.97% 95.00%
CHEMBL1907 P15144 Aminopeptidase N 81.78% 93.31%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.13% 90.71%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.68% 97.50%
CHEMBL2996 Q05655 Protein kinase C delta 80.28% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.18% 99.17%

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.
Angelica pubescens
Panax quinquefolius

Cross-Links

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PubChem 524423
NPASS NPC265929