Pentadeca-1,7,14-trien-3,5-diyn-2-ol

Details

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Internal ID e9052b76-a76c-44f2-aa85-552cad743b99
Taxonomy Organic oxygen compounds > Organooxygen compounds > Enols
IUPAC Name pentadeca-1,7,14-trien-3,5-diyn-2-ol
SMILES (Canonical) C=CCCCCCC=CC#CC#CC(=C)O
SMILES (Isomeric) C=CCCCCCC=CC#CC#CC(=C)O
InChI InChI=1S/C15H18O/c1-3-4-5-6-7-8-9-10-11-12-13-14-15(2)16/h3,9-10,16H,1-2,4-8H2
InChI Key JBTDJZUDBLPALT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O
Molecular Weight 214.30 g/mol
Exact Mass 214.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.90
Atomic LogP (AlogP) 3.76
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pentadeca-1,7,14-trien-3,5-diyn-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9794 97.94%
Caco-2 + 0.5946 59.46%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.3806 38.06%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.8914 89.14%
OATP1B3 inhibitior + 0.9477 94.77%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9187 91.87%
P-glycoprotein inhibitior - 0.9671 96.71%
P-glycoprotein substrate - 0.8728 87.28%
CYP3A4 substrate - 0.5514 55.14%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.7892 78.92%
CYP3A4 inhibition - 0.8890 88.90%
CYP2C9 inhibition - 0.8225 82.25%
CYP2C19 inhibition - 0.8221 82.21%
CYP2D6 inhibition - 0.9553 95.53%
CYP1A2 inhibition - 0.6165 61.65%
CYP2C8 inhibition - 0.7317 73.17%
CYP inhibitory promiscuity - 0.6106 61.06%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) + 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.5686 56.86%
Eye corrosion + 0.9161 91.61%
Eye irritation - 0.6061 60.61%
Skin irritation + 0.6622 66.22%
Skin corrosion - 0.7228 72.28%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4827 48.27%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5572 55.72%
skin sensitisation + 0.8027 80.27%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.6662 66.62%
Acute Oral Toxicity (c) III 0.3494 34.94%
Estrogen receptor binding - 0.5966 59.66%
Androgen receptor binding - 0.7464 74.64%
Thyroid receptor binding - 0.5352 53.52%
Glucocorticoid receptor binding + 0.6687 66.87%
Aromatase binding + 0.5981 59.81%
PPAR gamma + 0.7578 75.78%
Honey bee toxicity - 0.7842 78.42%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5224 52.24%
Fish aquatic toxicity + 0.8362 83.62%

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 90.04% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 88.65% 90.17%
CHEMBL1951 P21397 Monoamine oxidase A 86.65% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.05% 91.11%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 84.98% 91.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.67% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.35% 95.17%
CHEMBL1829 O15379 Histone deacetylase 3 80.36% 95.00%

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.
Artemisia xanthochroa

Cross-Links

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PubChem 162872148
LOTUS LTS0136687
wikiData Q105124571