(2E,8S,9Z)-2,9,16-Heptadecatriene-4,6-diyne-8-ol

Details

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Internal ID f0230e78-3db9-4caf-8906-cd5d9a2a28a3
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (2E,8S,9Z)-heptadeca-2,9,16-trien-4,6-diyn-8-ol
SMILES (Canonical) CC=CC#CC#CC(C=CCCCCCC=C)O
SMILES (Isomeric) C/C=C/C#CC#C[C@H](/C=C\CCCCCC=C)O
InChI InChI=1S/C17H22O/c1-3-5-7-9-10-12-14-16-17(18)15-13-11-8-6-4-2/h3-4,6,14,16-18H,1,5,7,9-10,12H2,2H3/b6-4+,16-14-/t17-/m1/s1
InChI Key BVVCAUWTOOENBU-AGTQTVRUSA-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 4.90
Atomic LogP (AlogP) 3.62
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 (2E,8S,9Z)-2,9,16-Heptadecatriene-4,6-diyne-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 + 0.9708 97.08%
Caco-2 + 0.5569 55.69%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.4284 42.84%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.8470 84.70%
OATP1B3 inhibitior + 0.9485 94.85%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7570 75.70%
P-glycoprotein inhibitior - 0.9241 92.41%
P-glycoprotein substrate - 0.8321 83.21%
CYP3A4 substrate - 0.5119 51.19%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.7649 76.49%
CYP3A4 inhibition - 0.8892 88.92%
CYP2C9 inhibition - 0.8134 81.34%
CYP2C19 inhibition - 0.8244 82.44%
CYP2D6 inhibition - 0.9511 95.11%
CYP1A2 inhibition - 0.5729 57.29%
CYP2C8 inhibition - 0.8312 83.12%
CYP inhibitory promiscuity - 0.6645 66.45%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.5810 58.10%
Eye corrosion + 0.9258 92.58%
Eye irritation - 0.7942 79.42%
Skin irritation + 0.6561 65.61%
Skin corrosion - 0.6195 61.95%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4241 42.41%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5966 59.66%
skin sensitisation + 0.8400 84.00%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.4862 48.62%
Estrogen receptor binding + 0.6072 60.72%
Androgen receptor binding - 0.7710 77.10%
Thyroid receptor binding + 0.5178 51.78%
Glucocorticoid receptor binding + 0.6801 68.01%
Aromatase binding + 0.5293 52.93%
PPAR gamma + 0.6183 61.83%
Honey bee toxicity - 0.7946 79.46%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5563 55.63%
Fish aquatic toxicity + 0.8291 82.91%

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 91.42% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.22% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.72% 99.17%
CHEMBL1829 O15379 Histone deacetylase 3 88.32% 95.00%
CHEMBL1937 Q92769 Histone deacetylase 2 87.64% 94.75%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.29% 95.17%
CHEMBL2885 P07451 Carbonic anhydrase III 87.06% 87.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.11% 91.11%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.77% 97.29%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.61% 93.99%
CHEMBL325 Q13547 Histone deacetylase 1 81.33% 95.92%

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

Cross-Links

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PubChem 101745966
NPASS NPC120150
LOTUS LTS0057236
wikiData Q104946884