(3S,9Z,11Z)-heptadeca-1,9,11,16-tetraen-4,6-diyn-3-ol

Details

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Internal ID f1f4c39d-6841-406f-b8bd-455fd8a68f2d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (3S,9Z,11Z)-heptadeca-1,9,11,16-tetraen-4,6-diyn-3-ol
SMILES (Canonical) C=CCCCC=CC=CCC#CC#CC(C=C)O
SMILES (Isomeric) C=CCCC/C=C\C=C/CC#CC#C[C@H](C=C)O
InChI InChI=1S/C17H20O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17(18)4-2/h3-4,8-11,17-18H,1-2,5-7,12H2/b9-8-,11-10-/t17-/m0/s1
InChI Key ADKVNLJOJPLERM-JBDKYTPXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H20O
Molecular Weight 240.34 g/mol
Exact Mass 240.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.40
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,9Z,11Z)-heptadeca-1,9,11,16-tetraen-4,6-diyn-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9761 97.61%
Caco-2 + 0.6436 64.36%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.3641 36.41%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8702 87.02%
OATP1B3 inhibitior + 0.9519 95.19%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8624 86.24%
P-glycoprotein inhibitior - 0.9200 92.00%
P-glycoprotein substrate - 0.8336 83.36%
CYP3A4 substrate - 0.5168 51.68%
CYP2C9 substrate - 0.6095 60.95%
CYP2D6 substrate - 0.7375 73.75%
CYP3A4 inhibition - 0.9088 90.88%
CYP2C9 inhibition - 0.8674 86.74%
CYP2C19 inhibition - 0.7840 78.40%
CYP2D6 inhibition - 0.9613 96.13%
CYP1A2 inhibition - 0.6081 60.81%
CYP2C8 inhibition - 0.7349 73.49%
CYP inhibitory promiscuity - 0.7174 71.74%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.5289 52.89%
Eye corrosion + 0.9661 96.61%
Eye irritation - 0.7228 72.28%
Skin irritation + 0.8233 82.33%
Skin corrosion + 0.8523 85.23%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4448 44.48%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.7310 73.10%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5974 59.74%
Acute Oral Toxicity (c) II 0.4404 44.04%
Estrogen receptor binding - 0.6314 63.14%
Androgen receptor binding - 0.7153 71.53%
Thyroid receptor binding + 0.5191 51.91%
Glucocorticoid receptor binding + 0.6745 67.45%
Aromatase binding + 0.5556 55.56%
PPAR gamma + 0.7848 78.48%
Honey bee toxicity - 0.6857 68.57%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.6154 61.54%

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
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 86.89% 97.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.16% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.16% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 83.37% 98.35%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.13% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 82.98% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.39% 96.09%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.69% 92.88%

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.
Hedera helix

Cross-Links

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PubChem 163044449
LOTUS LTS0171627
wikiData Q104909653