1,8-Dihydroxyheptadeca-9,16-dien-4,6-diyn-3-one

Details

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Internal ID 24238dc4-8bd0-4cf7-9f71-701c2c4aa80e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name 1,8-dihydroxyheptadeca-9,16-dien-4,6-diyn-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O3/c1-2-3-4-5-6-7-8-11-16(19)12-9-10-13-17(20)14-15-18/h2,8,11,16,18-19H,1,3-7,14-15H2
InChI Key VDJHTIHZCWUOHG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O3
Molecular Weight 274.35 g/mol
Exact Mass 274.15689456 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,8-Dihydroxyheptadeca-9,16-dien-4,6-diyn-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9451 94.51%
Caco-2 - 0.6265 62.65%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7693 76.93%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.8662 86.62%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7596 75.96%
P-glycoprotein inhibitior - 0.8808 88.08%
P-glycoprotein substrate - 0.7890 78.90%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8046 80.46%
CYP3A4 inhibition - 0.6516 65.16%
CYP2C9 inhibition - 0.8045 80.45%
CYP2C19 inhibition - 0.8002 80.02%
CYP2D6 inhibition - 0.9167 91.67%
CYP1A2 inhibition - 0.7461 74.61%
CYP2C8 inhibition - 0.7899 78.99%
CYP inhibitory promiscuity - 0.8293 82.93%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.7413 74.13%
Eye corrosion + 0.5244 52.44%
Eye irritation - 0.8154 81.54%
Skin irritation - 0.6957 69.57%
Skin corrosion - 0.7853 78.53%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4580 45.80%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation - 0.7303 73.03%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5568 55.68%
Estrogen receptor binding + 0.6384 63.84%
Androgen receptor binding - 0.7922 79.22%
Thyroid receptor binding + 0.5997 59.97%
Glucocorticoid receptor binding + 0.6860 68.60%
Aromatase binding + 0.6083 60.83%
PPAR gamma + 0.7567 75.67%
Honey bee toxicity - 0.7657 76.57%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6369 63.69%
Fish aquatic toxicity - 0.4831 48.31%

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 95.40% 99.17%
CHEMBL1829 O15379 Histone deacetylase 3 92.76% 95.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.74% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.55% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.67% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.13% 97.29%
CHEMBL325 Q13547 Histone deacetylase 1 86.71% 95.92%
CHEMBL1937 Q92769 Histone deacetylase 2 85.88% 94.75%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.53% 95.17%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 82.26% 82.05%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.31% 89.34%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 80.96% 91.24%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 80.12% 80.00%

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 scoparia

Cross-Links

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PubChem 162951144
LOTUS LTS0205513
wikiData Q105284201