Decyl pentyl phthalate

Details

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Internal ID b2659e2f-0455-4b2c-bff2-6368621ae0e1
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name 2-O-octyl 1-O-pentyl benzene-1,2-dicarboxylate
SMILES (Canonical) CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCC
SMILES (Isomeric) CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCC
InChI InChI=1S/C21H32O4/c1-3-5-7-8-9-13-17-25-21(23)19-15-11-10-14-18(19)20(22)24-16-12-6-4-2/h10-11,14-15H,3-9,12-13,16-17H2,1-2H3
InChI Key HWWDJUQKDQKXQH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O4
Molecular Weight 348.50 g/mol
Exact Mass 348.23005950 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 7.40
Atomic LogP (AlogP) 5.55
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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SCHEMBL7185161
HWWDJUQKDQKXQH-UHFFFAOYSA-N
Dimethyl(2,3,4,5,6-pentafluorophenyl)[(1-propylundecyl)oxy]silane

2D Structure

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2D Structure of Decyl pentyl phthalate

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 + 0.7523 75.23%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8914 89.14%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.9433 94.33%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6154 61.54%
P-glycoprotein inhibitior - 0.4435 44.35%
P-glycoprotein substrate - 0.9390 93.90%
CYP3A4 substrate - 0.6165 61.65%
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 + 0.4476 44.76%
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 + 0.8897 88.97%
Skin irritation - 0.9337 93.37%
Skin corrosion - 0.9948 99.48%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6996 69.96%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.8052 80.52%
skin sensitisation - 0.8333 83.33%
Respiratory toxicity - 1.0000 100.00%
Reproductive toxicity - 0.8325 83.25%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.6411 64.11%
Acute Oral Toxicity (c) IV 0.6802 68.02%
Estrogen receptor binding - 0.7640 76.40%
Androgen receptor binding + 0.8503 85.03%
Thyroid receptor binding + 0.6215 62.15%
Glucocorticoid receptor binding - 0.6694 66.94%
Aromatase binding - 0.7243 72.43%
PPAR gamma - 0.6852 68.52%
Honey bee toxicity - 0.9940 99.40%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity + 0.7653 76.53%
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
CHEMBL2581 P07339 Cathepsin D 96.21% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.94% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.12% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.56% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 89.09% 90.17%
CHEMBL2885 P07451 Carbonic anhydrase III 88.78% 87.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.54% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.82% 94.73%
CHEMBL3891 P07384 Calpain 1 82.60% 93.04%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.89% 85.94%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.01% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.00% 95.56%

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 525140
LOTUS LTS0134434
wikiData Q105034851