CID 559558

Details

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Internal ID 42d91e49-6605-471a-a9b1-ef60338fd0c0
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name hexadeca-7,11-dien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h5-6,9-10,17H,2-4,7-8,11-16H2,1H3
InChI Key ZWMPSFHVSWYKPO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H30O
Molecular Weight 238.41 g/mol
Exact Mass 238.229665576 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 559558

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.9308 93.08%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Lysosomes 0.5404 54.04%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.8061 80.61%
OATP1B3 inhibitior + 0.8796 87.96%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5691 56.91%
P-glycoprotein inhibitior - 0.9087 90.87%
P-glycoprotein substrate - 0.9432 94.32%
CYP3A4 substrate - 0.6824 68.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9065 90.65%
CYP2C9 inhibition - 0.8810 88.10%
CYP2C19 inhibition - 0.9136 91.36%
CYP2D6 inhibition - 0.9196 91.96%
CYP1A2 inhibition + 0.5542 55.42%
CYP2C8 inhibition - 0.9170 91.70%
CYP inhibitory promiscuity - 0.8235 82.35%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.7272 72.72%
Eye corrosion + 0.7375 73.75%
Eye irritation + 0.9729 97.29%
Skin irritation + 0.8261 82.61%
Skin corrosion - 0.9507 95.07%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6463 64.63%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5801 58.01%
skin sensitisation + 0.8671 86.71%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5261 52.61%
Acute Oral Toxicity (c) IV 0.6293 62.93%
Estrogen receptor binding - 0.5844 58.44%
Androgen receptor binding - 0.8335 83.35%
Thyroid receptor binding + 0.6669 66.69%
Glucocorticoid receptor binding - 0.6159 61.59%
Aromatase binding - 0.7134 71.34%
PPAR gamma + 0.7951 79.51%
Honey bee toxicity - 0.9931 99.31%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5446 54.46%
Fish aquatic toxicity + 0.8334 83.34%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 93.71% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 92.65% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.98% 97.29%
CHEMBL2581 P07339 Cathepsin D 91.13% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.97% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.70% 92.86%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.19% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 87.66% 89.63%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.43% 96.95%
CHEMBL1781 P11387 DNA topoisomerase I 86.40% 97.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.52% 91.81%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 559558
LOTUS LTS0117635
wikiData Q105385041