1-(3-Methyloxiran-2-yl)tetradeca-6,13-dien-1,3-diyn-5-ol

Details

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Internal ID b82c424e-c629-4b40-9adc-0ae4abbd8ed9
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 1-(3-methyloxiran-2-yl)tetradeca-6,13-dien-1,3-diyn-5-ol
SMILES (Canonical) CC1C(O1)C#CC#CC(C=CCCCCCC=C)O
SMILES (Isomeric) CC1C(O1)C#CC#CC(C=CCCCCCC=C)O
InChI InChI=1S/C17H22O2/c1-3-4-5-6-7-8-9-12-16(18)13-10-11-14-17-15(2)19-17/h3,9,12,15-18H,1,4-8H2,2H3
InChI Key HEYJULODWUSFKN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O2
Molecular Weight 258.35 g/mol
Exact Mass 258.161979940 g/mol
Topological Polar Surface Area (TPSA) 32.80 Ų
XlogP 3.80
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 2
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 1-(3-Methyloxiran-2-yl)tetradeca-6,13-dien-1,3-diyn-5-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9631 96.31%
Caco-2 + 0.5985 59.85%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.4585 45.85%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.8637 86.37%
OATP1B3 inhibitior + 0.9499 94.99%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9326 93.26%
P-glycoprotein inhibitior - 0.9225 92.25%
P-glycoprotein substrate - 0.8339 83.39%
CYP3A4 substrate + 0.5287 52.87%
CYP2C9 substrate - 0.8002 80.02%
CYP2D6 substrate - 0.7681 76.81%
CYP3A4 inhibition - 0.7537 75.37%
CYP2C9 inhibition - 0.7016 70.16%
CYP2C19 inhibition - 0.6224 62.24%
CYP2D6 inhibition - 0.9266 92.66%
CYP1A2 inhibition - 0.5830 58.30%
CYP2C8 inhibition - 0.7886 78.86%
CYP inhibitory promiscuity - 0.6743 67.43%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7228 72.28%
Carcinogenicity (trinary) Non-required 0.5366 53.66%
Eye corrosion + 0.5408 54.08%
Eye irritation - 0.9206 92.06%
Skin irritation + 0.6115 61.15%
Skin corrosion - 0.6322 63.22%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3659 36.59%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.5466 54.66%
skin sensitisation + 0.6853 68.53%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.5994 59.94%
Acute Oral Toxicity (c) III 0.6851 68.51%
Estrogen receptor binding + 0.5355 53.55%
Androgen receptor binding - 0.6954 69.54%
Thyroid receptor binding + 0.6115 61.15%
Glucocorticoid receptor binding + 0.7138 71.38%
Aromatase binding - 0.4879 48.79%
PPAR gamma + 0.6448 64.48%
Honey bee toxicity - 0.7813 78.13%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5563 55.63%
Fish aquatic toxicity + 0.8129 81.29%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.32% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.94% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.93% 96.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 89.90% 95.58%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.87% 96.47%
CHEMBL3401 O75469 Pregnane X receptor 87.52% 94.73%
CHEMBL2581 P07339 Cathepsin D 87.03% 98.95%
CHEMBL1829 O15379 Histone deacetylase 3 85.75% 95.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.12% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.41% 86.33%
CHEMBL325 Q13547 Histone deacetylase 1 80.06% 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

Cross-Links

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PubChem 73805560
LOTUS LTS0016340
wikiData Q105027141