Heptadeca-2,4,8,10,16-pentaen-6-yn-1-ol

Details

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Internal ID 09c3f6be-b2ef-4205-8c2a-f60cf55ce687
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name heptadeca-2,4,8,10,16-pentaen-6-yn-1-ol
SMILES (Canonical) C=CCCCCC=CC=CC#CC=CC=CCO
SMILES (Isomeric) C=CCCCCC=CC=CC#CC=CC=CCO
InChI InChI=1S/C17H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h2,7-10,13-16,18H,1,3-6,17H2
InChI Key IWDABMVYFCSCSS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O
Molecular Weight 242.36 g/mol
Exact Mass 242.167065321 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.95
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Heptadeca-2,4,8,10,16-pentaen-6-yn-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 + 0.9729 97.29%
Caco-2 + 0.5598 55.98%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4024 40.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8885 88.85%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6162 61.62%
P-glycoprotein inhibitior - 0.8780 87.80%
P-glycoprotein substrate - 0.9356 93.56%
CYP3A4 substrate - 0.5663 56.63%
CYP2C9 substrate - 0.8075 80.75%
CYP2D6 substrate - 0.7593 75.93%
CYP3A4 inhibition - 0.8828 88.28%
CYP2C9 inhibition - 0.8312 83.12%
CYP2C19 inhibition - 0.8411 84.11%
CYP2D6 inhibition - 0.9539 95.39%
CYP1A2 inhibition - 0.6468 64.68%
CYP2C8 inhibition - 0.8323 83.23%
CYP inhibitory promiscuity - 0.7382 73.82%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5000 50.00%
Carcinogenicity (trinary) Non-required 0.5565 55.65%
Eye corrosion + 0.9747 97.47%
Eye irritation + 0.5941 59.41%
Skin irritation + 0.7886 78.86%
Skin corrosion + 0.6432 64.32%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.6932 69.32%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6129 61.29%
Acute Oral Toxicity (c) II 0.4798 47.98%
Estrogen receptor binding + 0.8635 86.35%
Androgen receptor binding - 0.6694 66.94%
Thyroid receptor binding + 0.6371 63.71%
Glucocorticoid receptor binding + 0.6749 67.49%
Aromatase binding + 0.8115 81.15%
PPAR gamma + 0.8211 82.11%
Honey bee toxicity - 0.7940 79.40%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6855 68.55%
Fish aquatic toxicity - 0.4049 40.49%

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 86.94% 99.17%
CHEMBL242 Q92731 Estrogen receptor beta 86.91% 98.35%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.21% 91.11%
CHEMBL1977 P11473 Vitamin D receptor 82.91% 99.43%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.56% 89.34%
CHEMBL279 P35968 Vascular endothelial growth factor receptor 2 80.56% 95.52%

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.
Tridax trilobata

Cross-Links

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PubChem 162938647
LOTUS LTS0025497
wikiData Q105121506