Cyclohexadecane, 1,2-diethyl-

Details

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Internal ID 698ffff5-b63c-4ceb-b99e-d1f747fc8d74
Taxonomy Hydrocarbons > Saturated hydrocarbons > Cycloalkanes
IUPAC Name 1,2-diethylcyclohexadecane
SMILES (Canonical) CCC1CCCCCCCCCCCCCCC1CC
SMILES (Isomeric) CCC1CCCCCCCCCCCCCCC1CC
InChI InChI=1S/C20H40/c1-3-19-17-15-13-11-9-7-5-6-8-10-12-14-16-18-20(19)4-2/h19-20H,3-18H2,1-2H3
InChI Key WTKPOZCPQVMNOI-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H40
Molecular Weight 280.50 g/mol
Exact Mass 280.313001276 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 10.30
Atomic LogP (AlogP) 7.51
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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1,2-Diethylcyclohexadecane
1,2-Diethylcyclohexadecane #
WTKPOZCPQVMNOI-UHFFFAOYSA-N

2D Structure

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2D Structure of Cyclohexadecane, 1,2-diethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.8803 88.03%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.6443 64.43%
OATP2B1 inhibitior - 0.8474 84.74%
OATP1B1 inhibitior + 0.9720 97.20%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5677 56.77%
P-glycoprotein inhibitior - 0.9185 91.85%
P-glycoprotein substrate - 0.9610 96.10%
CYP3A4 substrate - 0.7566 75.66%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9843 98.43%
CYP2C9 inhibition - 0.9140 91.40%
CYP2C19 inhibition - 0.9286 92.86%
CYP2D6 inhibition - 0.9302 93.02%
CYP1A2 inhibition - 0.7095 70.95%
CYP2C8 inhibition - 0.9642 96.42%
CYP inhibitory promiscuity - 0.7782 77.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.5790 57.90%
Eye corrosion + 0.9837 98.37%
Eye irritation + 0.9139 91.39%
Skin irritation + 0.6843 68.43%
Skin corrosion - 0.9845 98.45%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5394 53.94%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6657 66.57%
skin sensitisation + 0.9250 92.50%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.7327 73.27%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.6264 62.64%
Acute Oral Toxicity (c) IV 0.5051 50.51%
Estrogen receptor binding + 0.7185 71.85%
Androgen receptor binding - 0.7250 72.50%
Thyroid receptor binding - 0.5494 54.94%
Glucocorticoid receptor binding - 0.7631 76.31%
Aromatase binding - 0.7044 70.44%
PPAR gamma - 0.7289 72.89%
Honey bee toxicity - 0.9854 98.54%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9781 97.81%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.26% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.01% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.92% 97.09%
CHEMBL3012 Q13946 Phosphodiesterase 7A 86.77% 99.29%
CHEMBL226 P30542 Adenosine A1 receptor 86.04% 95.93%
CHEMBL2581 P07339 Cathepsin D 85.85% 98.95%
CHEMBL1968 P07099 Epoxide hydrolase 1 85.68% 98.57%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.73% 95.50%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 82.19% 90.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.99% 92.62%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 81.93% 95.27%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.08% 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.
Astilbe rubra

Cross-Links

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PubChem 536940
NPASS NPC133593