Z-11-Pentadecenol

Details

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Internal ID c77749e6-46f4-4d33-8a63-8fe8840638f8
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (Z)-pentadec-11-en-1-ol
SMILES (Canonical) CCCC=CCCCCCCCCCCO
SMILES (Isomeric) CCC/C=C\CCCCCCCCCCO
InChI InChI=1S/C15H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h4-5,16H,2-3,6-15H2,1H3/b5-4-
InChI Key ANWGEPOASAJNOG-PLNGDYQASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H30O
Molecular Weight 226.40 g/mol
Exact Mass 226.229665576 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.85
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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ANWGEPOASAJNOG-PLNGDYQASA-N
(11Z)-11-Pentadecen-1-ol #

2D Structure

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2D Structure of Z-11-Pentadecenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.9190 91.90%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.4653 46.53%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.8317 83.17%
OATP1B3 inhibitior + 0.8979 89.79%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5320 53.20%
P-glycoprotein inhibitior - 0.9419 94.19%
P-glycoprotein substrate - 0.9541 95.41%
CYP3A4 substrate - 0.6844 68.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7528 75.28%
CYP3A4 inhibition - 0.9091 90.91%
CYP2C9 inhibition - 0.8840 88.40%
CYP2C19 inhibition - 0.9176 91.76%
CYP2D6 inhibition - 0.9261 92.61%
CYP1A2 inhibition - 0.5341 53.41%
CYP2C8 inhibition - 0.9297 92.97%
CYP inhibitory promiscuity - 0.8292 82.92%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6579 65.79%
Eye corrosion + 0.7373 73.73%
Eye irritation + 0.9623 96.23%
Skin irritation + 0.7491 74.91%
Skin corrosion - 0.9782 97.82%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7299 72.99%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6093 60.93%
skin sensitisation + 0.8343 83.43%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.4563 45.63%
Acute Oral Toxicity (c) III 0.6431 64.31%
Estrogen receptor binding - 0.6501 65.01%
Androgen receptor binding - 0.8016 80.16%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6717 67.17%
Aromatase binding - 0.7034 70.34%
PPAR gamma + 0.6665 66.65%
Honey bee toxicity - 0.9874 98.74%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.6242 62.42%
Fish aquatic toxicity + 0.6674 66.74%

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 92.01% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 91.14% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.23% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.12% 97.29%
CHEMBL2581 P07339 Cathepsin D 85.96% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.08% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.62% 96.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.09% 92.86%
CHEMBL1781 P11387 DNA topoisomerase I 82.81% 97.00%

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.
Platycladus orientalis

Cross-Links

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PubChem 5364635
NPASS NPC246315