Oxalic acid, allyl nonyl ester

Details

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Internal ID 04fda7ac-9d68-43ad-83db-cb114ed3a543
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 1-O-nonyl 2-O-prop-2-enyl oxalate
SMILES (Canonical) CCCCCCCCCOC(=O)C(=O)OCC=C
SMILES (Isomeric) CCCCCCCCCOC(=O)C(=O)OCC=C
InChI InChI=1S/C14H24O4/c1-3-5-6-7-8-9-10-12-18-14(16)13(15)17-11-4-2/h4H,2-3,5-12H2,1H3
InChI Key OBTRGHJXSNHSHW-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H24O4
Molecular Weight 256.34 g/mol
Exact Mass 256.16745924 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 5.00
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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oxalic acid allyl nonyl ester
QSPL 020
OBTRGHJXSNHSHW-UHFFFAOYSA-N
nonyl prop-2-en-1-yl ethanedioate

2D Structure

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2D Structure of Oxalic acid, allyl nonyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9654 96.54%
Caco-2 + 0.6509 65.09%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.6862 68.62%
OATP2B1 inhibitior - 0.8497 84.97%
OATP1B1 inhibitior + 0.9210 92.10%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6195 61.95%
P-glycoprotein inhibitior - 0.8866 88.66%
P-glycoprotein substrate - 0.9439 94.39%
CYP3A4 substrate - 0.5608 56.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8384 83.84%
CYP3A4 inhibition - 0.8583 85.83%
CYP2C9 inhibition - 0.8757 87.57%
CYP2C19 inhibition - 0.8322 83.22%
CYP2D6 inhibition - 0.9200 92.00%
CYP1A2 inhibition - 0.7451 74.51%
CYP2C8 inhibition - 0.7405 74.05%
CYP inhibitory promiscuity - 0.8763 87.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7023 70.23%
Carcinogenicity (trinary) Non-required 0.6251 62.51%
Eye corrosion + 0.7432 74.32%
Eye irritation + 0.9339 93.39%
Skin irritation + 0.7853 78.53%
Skin corrosion - 0.9687 96.87%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3956 39.56%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7054 70.54%
skin sensitisation - 0.6324 63.24%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.7864 78.64%
Acute Oral Toxicity (c) IV 0.7512 75.12%
Estrogen receptor binding - 0.8818 88.18%
Androgen receptor binding - 0.5324 53.24%
Thyroid receptor binding + 0.5723 57.23%
Glucocorticoid receptor binding - 0.7590 75.90%
Aromatase binding - 0.8062 80.62%
PPAR gamma - 0.7133 71.33%
Honey bee toxicity - 0.9687 96.87%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.6865 68.65%
Fish aquatic toxicity + 0.9940 99.40%

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
CHEMBL240 Q12809 HERG 94.76% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.04% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.96% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 92.30% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.64% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.34% 85.94%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 87.48% 90.24%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.02% 89.34%
CHEMBL2581 P07339 Cathepsin D 86.09% 98.95%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 84.96% 96.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.04% 92.08%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.73% 91.81%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.64% 94.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.52% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 81.40% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.65% 97.25%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.46% 100.00%

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.
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

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PubChem 6420231
NPASS NPC124294