Phthalic acid, octyl propyl ester

Details

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Internal ID dffa998d-0b5b-457b-863a-6ec0a66e6eac
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name 2-O-octyl 1-O-propyl benzene-1,2-dicarboxylate
SMILES (Canonical) CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCC
SMILES (Isomeric) CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCC
InChI InChI=1S/C19H28O4/c1-3-5-6-7-8-11-15-23-19(21)17-13-10-9-12-16(17)18(20)22-14-4-2/h9-10,12-13H,3-8,11,14-15H2,1-2H3
InChI Key KPZOYFNNKQODDX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H28O4
Molecular Weight 320.40 g/mol
Exact Mass 320.19875937 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 6.50
Atomic LogP (AlogP) 4.77
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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SCHEMBL6400040
KPZOYFNNKQODDX-UHFFFAOYSA-N

2D Structure

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2D Structure of Phthalic acid, octyl propyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.7974 79.74%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8914 89.14%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.9403 94.03%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6576 65.76%
P-glycoprotein inhibitior - 0.4532 45.32%
P-glycoprotein substrate - 0.9230 92.30%
CYP3A4 substrate - 0.5988 59.88%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8123 81.23%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.8318 83.18%
CYP2C19 inhibition - 0.6765 67.65%
CYP2D6 inhibition - 0.8275 82.75%
CYP1A2 inhibition - 0.6448 64.48%
CYP2C8 inhibition + 0.5133 51.33%
CYP inhibitory promiscuity - 0.6788 67.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6923 69.23%
Carcinogenicity (trinary) Warning 0.5091 50.91%
Eye corrosion - 0.9274 92.74%
Eye irritation + 0.8488 84.88%
Skin irritation - 0.9337 93.37%
Skin corrosion - 0.9948 99.48%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8281 82.81%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7927 79.27%
skin sensitisation - 0.8333 83.33%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 0.8325 83.25%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.6873 68.73%
Acute Oral Toxicity (c) IV 0.6802 68.02%
Estrogen receptor binding - 0.5853 58.53%
Androgen receptor binding + 0.8330 83.30%
Thyroid receptor binding + 0.5938 59.38%
Glucocorticoid receptor binding - 0.5454 54.54%
Aromatase binding - 0.6939 69.39%
PPAR gamma - 0.6446 64.46%
Honey bee toxicity - 0.9933 99.33%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.7553 75.53%
Fish aquatic toxicity + 1.0000 100.00%

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 96.44% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.19% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.12% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.56% 92.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.54% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 88.30% 90.17%
CHEMBL2885 P07451 Carbonic anhydrase III 87.86% 87.45%
CHEMBL3401 O75469 Pregnane X receptor 87.19% 94.73%
CHEMBL3891 P07384 Calpain 1 82.91% 93.04%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.12% 91.11%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.31% 85.94%

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.
Polyscias bracteata subsp. subincisa

Cross-Links

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PubChem 6423858
LOTUS LTS0174060
wikiData Q105144428