Cyclotetradecane

Details

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Internal ID 48d06912-4feb-4212-85d7-a46ea83a749a
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name cyclotetradecane
SMILES (Canonical) C1CCCCCCCCCCCCC1
SMILES (Isomeric) C1CCCCCCCCCCCCC1
InChI InChI=1S/C14H28/c1-2-4-6-8-10-12-14-13-11-9-7-5-3-1/h1-14H2
InChI Key KATXJJSCAPBIOB-UHFFFAOYSA-N
Popularity 56 references in papers

Physical and Chemical Properties

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Molecular Formula C14H28
Molecular Weight 196.37 g/mol
Exact Mass 196.219100893 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 7.80
Atomic LogP (AlogP) 5.46
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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295-17-0
EINECS 206-038-6
O1MV54BB89
UNII-O1MV54BB89
CHEBI:89715
DTXSID70183697
KATXJJSCAPBIOB-UHFFFAOYSA-N
AKOS006272110
FT-0693190
Q7485816
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyclotetradecane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 + 0.7998 79.98%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.6143 61.43%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.9859 98.59%
OATP1B3 inhibitior + 0.9676 96.76%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8723 87.23%
P-glycoprotein inhibitior - 0.9716 97.16%
P-glycoprotein substrate - 0.9977 99.77%
CYP3A4 substrate - 0.8678 86.78%
CYP2C9 substrate - 0.7696 76.96%
CYP2D6 substrate - 0.7147 71.47%
CYP3A4 inhibition - 0.9829 98.29%
CYP2C9 inhibition - 0.9276 92.76%
CYP2C19 inhibition - 0.9481 94.81%
CYP2D6 inhibition - 0.9679 96.79%
CYP1A2 inhibition - 0.8094 80.94%
CYP2C8 inhibition - 0.9974 99.74%
CYP inhibitory promiscuity - 0.8187 81.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Warning 0.4801 48.01%
Eye corrosion + 0.9951 99.51%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8569 85.69%
Skin corrosion + 0.5757 57.57%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5404 54.04%
Micronuclear - 0.9958 99.58%
Hepatotoxicity + 0.8750 87.50%
skin sensitisation + 0.6508 65.08%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity - 0.9762 97.62%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5386 53.86%
Acute Oral Toxicity (c) III 0.4947 49.47%
Estrogen receptor binding - 0.9450 94.50%
Androgen receptor binding - 0.9149 91.49%
Thyroid receptor binding - 0.8306 83.06%
Glucocorticoid receptor binding - 0.9238 92.38%
Aromatase binding - 0.8769 87.69%
PPAR gamma - 0.9013 90.13%
Honey bee toxicity - 0.8911 89.11%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.7881 78.81%

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
No predicted targets yet!

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.
Conioselinum anthriscoides
Hypericum perforatum
Ligusticum officinale
Vitis vinifera

Cross-Links

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PubChem 67524
NPASS NPC27584
LOTUS LTS0065862
wikiData Q7485816