(8S,9Z)-heptadeca-1,9,16-trien-4,6-diyn-8-ol

Details

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Internal ID 2ed88ad8-2475-489c-b41b-67c6f5f7ff49
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (8S,9Z)-heptadeca-1,9,16-trien-4,6-diyn-8-ol
SMILES (Canonical) C=CCCCCCC=CC(C#CC#CCC=C)O
SMILES (Isomeric) C=CCCCCC/C=C\[C@@H](C#CC#CCC=C)O
InChI InChI=1S/C17H22O/c1-3-5-7-9-10-12-14-16-17(18)15-13-11-8-6-4-2/h3-4,14,16-18H,1-2,5-7,9-10,12H2/b16-14-/t17-/m1/s1
InChI Key AOVBGZVPTYLNNI-YHKKIHSWSA-N
Popularity 1 reference 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 5.00
Atomic LogP (AlogP) 3.62
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 (8S,9Z)-heptadeca-1,9,16-trien-4,6-diyn-8-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9635 96.35%
Caco-2 - 0.5165 51.65%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.4097 40.97%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.8848 88.48%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8809 88.09%
P-glycoprotein inhibitior - 0.9207 92.07%
P-glycoprotein substrate - 0.8727 87.27%
CYP3A4 substrate - 0.5381 53.81%
CYP2C9 substrate - 0.8004 80.04%
CYP2D6 substrate - 0.7210 72.10%
CYP3A4 inhibition - 0.9043 90.43%
CYP2C9 inhibition - 0.7760 77.60%
CYP2C19 inhibition - 0.8201 82.01%
CYP2D6 inhibition - 0.9498 94.98%
CYP1A2 inhibition - 0.5629 56.29%
CYP2C8 inhibition - 0.7598 75.98%
CYP inhibitory promiscuity - 0.6447 64.47%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.5646 56.46%
Eye corrosion + 0.9432 94.32%
Eye irritation - 0.8053 80.53%
Skin irritation + 0.7086 70.86%
Skin corrosion - 0.5653 56.53%
Ames mutagenesis - 0.6483 64.83%
Human Ether-a-go-go-Related Gene inhibition - 0.4134 41.34%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6466 64.66%
skin sensitisation + 0.8141 81.41%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.5534 55.34%
Acute Oral Toxicity (c) III 0.3365 33.65%
Estrogen receptor binding + 0.5521 55.21%
Androgen receptor binding - 0.7112 71.12%
Thyroid receptor binding - 0.5248 52.48%
Glucocorticoid receptor binding + 0.6529 65.29%
Aromatase binding + 0.5288 52.88%
PPAR gamma + 0.7060 70.60%
Honey bee toxicity - 0.6887 68.87%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5663 56.63%
Fish aquatic toxicity + 0.8127 81.27%

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 90.00% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.08% 94.45%
CHEMBL1829 O15379 Histone deacetylase 3 88.52% 95.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.91% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 86.53% 94.75%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 83.51% 85.40%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.25% 91.11%
CHEMBL2581 P07339 Cathepsin D 82.39% 98.95%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 82.18% 92.95%
CHEMBL2885 P07451 Carbonic anhydrase III 82.01% 87.45%

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.
Baccharis thesioides
Bonnetia paniculata
Glycosmis ovoidea
Raukaua simplex
Veronica chamaedrys
Vitex agnus-castus

Cross-Links

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PubChem 10399497
NPASS NPC297931
LOTUS LTS0052278
wikiData Q104915967