Agn-PC-036due

Details

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Internal ID b8e16407-555f-4920-a798-afc4afeb548c
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name deca-2,8-dien-4,6-diynyl 3-methylbutanoate
SMILES (Canonical) CC=CC#CC#CC=CCOC(=O)CC(C)C
SMILES (Isomeric) CC=CC#CC#CC=CCOC(=O)CC(C)C
InChI InChI=1S/C15H18O2/c1-4-5-6-7-8-9-10-11-12-17-15(16)13-14(2)3/h4-5,10-11,14H,12-13H2,1-3H3
InChI Key FPIBENZMUTVCEK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O2
Molecular Weight 230.30 g/mol
Exact Mass 230.130679813 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.71
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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DTXSID60336059
29444-87-9

2D Structure

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2D Structure of Agn-PC-036due

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.5227 52.27%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6480 64.80%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.8506 85.06%
OATP1B3 inhibitior + 0.9398 93.98%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5532 55.32%
P-glycoprotein inhibitior - 0.9242 92.42%
P-glycoprotein substrate - 0.9083 90.83%
CYP3A4 substrate - 0.5267 52.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8813 88.13%
CYP3A4 inhibition - 0.9016 90.16%
CYP2C9 inhibition - 0.9000 90.00%
CYP2C19 inhibition - 0.9062 90.62%
CYP2D6 inhibition - 0.9474 94.74%
CYP1A2 inhibition - 0.7165 71.65%
CYP2C8 inhibition - 0.9346 93.46%
CYP inhibitory promiscuity - 0.7549 75.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5483 54.83%
Carcinogenicity (trinary) Warning 0.4555 45.55%
Eye corrosion + 0.9521 95.21%
Eye irritation - 0.6567 65.67%
Skin irritation + 0.6598 65.98%
Skin corrosion - 0.8582 85.82%
Ames mutagenesis - 0.7037 70.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4230 42.30%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5428 54.28%
skin sensitisation + 0.8537 85.37%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.5762 57.62%
Acute Oral Toxicity (c) III 0.6470 64.70%
Estrogen receptor binding - 0.6812 68.12%
Androgen receptor binding - 0.7794 77.94%
Thyroid receptor binding - 0.5360 53.60%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.5881 58.81%
PPAR gamma - 0.7864 78.64%
Honey bee toxicity - 0.8258 82.58%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6855 68.55%
Fish aquatic toxicity + 0.9415 94.15%

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 94.49% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.32% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 86.14% 83.82%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.58% 96.47%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.64% 96.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.54% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.66% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.10% 96.95%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.74% 98.75%
CHEMBL2581 P07339 Cathepsin D 80.07% 98.95%

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.
Osmitopsis asteriscoides

Cross-Links

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PubChem 528757
LOTUS LTS0219919
wikiData Q82102880