Pentadeca-5,7-dien-9,11,13-triyn-1-ol

Details

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Internal ID 5fe87567-e63d-44ea-800c-a614773fe870
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name pentadeca-5,7-dien-9,11,13-triyn-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h8-11,16H,12-15H2,1H3
InChI Key PJFQPJRXYFAJFZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O
Molecular Weight 212.29 g/mol
Exact Mass 212.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.29
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pentadeca-5,7-dien-9,11,13-triyn-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9749 97.49%
Caco-2 + 0.7820 78.20%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.4866 48.66%
OATP2B1 inhibitior - 0.8619 86.19%
OATP1B1 inhibitior + 0.8188 81.88%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9277 92.77%
P-glycoprotein inhibitior - 0.9582 95.82%
P-glycoprotein substrate - 0.8932 89.32%
CYP3A4 substrate - 0.5272 52.72%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7877 78.77%
CYP3A4 inhibition - 0.8321 83.21%
CYP2C9 inhibition - 0.8169 81.69%
CYP2C19 inhibition - 0.8998 89.98%
CYP2D6 inhibition - 0.9465 94.65%
CYP1A2 inhibition - 0.5518 55.18%
CYP2C8 inhibition - 0.8812 88.12%
CYP inhibitory promiscuity - 0.7812 78.12%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.5892 58.92%
Eye corrosion + 0.8433 84.33%
Eye irritation + 0.5682 56.82%
Skin irritation + 0.8211 82.11%
Skin corrosion - 0.5518 55.18%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4851 48.51%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5402 54.02%
skin sensitisation + 0.7295 72.95%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6649 66.49%
Acute Oral Toxicity (c) II 0.4689 46.89%
Estrogen receptor binding - 0.7702 77.02%
Androgen receptor binding + 0.5653 56.53%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.7021 70.21%
Aromatase binding + 0.5240 52.40%
PPAR gamma - 0.6329 63.29%
Honey bee toxicity - 0.9270 92.70%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6837 68.37%
Fish aquatic toxicity - 0.7572 75.72%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.97% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.46% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 86.05% 87.45%
CHEMBL2581 P07339 Cathepsin D 83.68% 98.95%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 80.69% 96.42%
CHEMBL226 P30542 Adenosine A1 receptor 80.20% 95.93%

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 85626703
LOTUS LTS0097214
wikiData Q105209924