CID 172416

Details

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Internal ID 08daa83c-5737-4ab0-9dc7-9ff424279df6
Taxonomy Hydrocarbons > Saturated hydrocarbons
IUPAC Name
SMILES (Canonical) CCCCCCCCCCCCCCC[CH2]
SMILES (Isomeric) CCCCCCCCCCCCCCC[CH2]
InChI InChI=1S/C16H33/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h1,3-16H2,2H3
InChI Key VHOGADCBMMJONL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H33
Molecular Weight 225.43 g/mol
Exact Mass 225.258226053 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 8.30
Atomic LogP (AlogP) 6.30
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 172416

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.9629 96.29%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.5667 56.67%
OATP2B1 inhibitior - 0.8462 84.62%
OATP1B1 inhibitior + 0.9382 93.82%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6493 64.93%
P-glycoprotein inhibitior - 0.9287 92.87%
P-glycoprotein substrate - 0.9206 92.06%
CYP3A4 substrate - 0.7229 72.29%
CYP2C9 substrate - 0.8415 84.15%
CYP2D6 substrate - 0.7215 72.15%
CYP3A4 inhibition - 0.9898 98.98%
CYP2C9 inhibition - 0.9317 93.17%
CYP2C19 inhibition - 0.9498 94.98%
CYP2D6 inhibition - 0.9457 94.57%
CYP1A2 inhibition - 0.5392 53.92%
CYP2C8 inhibition - 0.9483 94.83%
CYP inhibitory promiscuity - 0.7857 78.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6082 60.82%
Eye corrosion + 0.9966 99.66%
Eye irritation + 0.9945 99.45%
Skin irritation + 0.9227 92.27%
Skin corrosion - 0.9707 97.07%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5926 59.26%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.8476 84.76%
skin sensitisation + 0.9418 94.18%
Respiratory toxicity - 1.0000 100.00%
Reproductive toxicity - 0.8472 84.72%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.6892 68.92%
Acute Oral Toxicity (c) III 0.6772 67.72%
Estrogen receptor binding - 0.8167 81.67%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.7568 75.68%
Glucocorticoid receptor binding - 0.9110 91.10%
Aromatase binding - 0.8696 86.96%
PPAR gamma - 0.6555 65.55%
Honey bee toxicity - 0.9802 98.02%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity + 0.8769 87.69%
Fish aquatic toxicity + 0.9745 97.45%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.47% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.15% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 90.91% 89.63%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.90% 85.94%
CHEMBL2581 P07339 Cathepsin D 89.81% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.38% 91.81%
CHEMBL2885 P07451 Carbonic anhydrase III 88.08% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.84% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.63% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 85.65% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.38% 99.17%
CHEMBL240 Q12809 HERG 83.78% 89.76%
CHEMBL1907 P15144 Aminopeptidase N 81.50% 93.31%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.31% 95.17%

Cross-Links

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PubChem 172416
NPASS NPC21180