Phthalic acid, butyl 2-ethylbutyl ester

Details

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Internal ID 341c09ee-2569-4a70-bcfe-472307f3fc94
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name 1-O-butyl 2-O-(2-ethylbutyl) benzene-1,2-dicarboxylate
SMILES (Canonical) CCCCOC(=O)C1=CC=CC=C1C(=O)OCC(CC)CC
SMILES (Isomeric) CCCCOC(=O)C1=CC=CC=C1C(=O)OCC(CC)CC
InChI InChI=1S/C18H26O4/c1-4-7-12-21-17(19)15-10-8-9-11-16(15)18(20)22-13-14(5-2)6-3/h8-11,14H,4-7,12-13H2,1-3H3
InChI Key CAVFYDHVOPETLG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H26O4
Molecular Weight 306.40 g/mol
Exact Mass 306.18310931 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.24
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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Phthalic acid, butyl 2-ethylbutyl ester

2D Structure

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2D Structure of Phthalic acid, butyl 2-ethylbutyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 + 0.9008 90.08%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8721 87.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9159 91.59%
OATP1B3 inhibitior + 0.9507 95.07%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6887 68.87%
P-glycoprotein inhibitior - 0.6116 61.16%
P-glycoprotein substrate - 0.8707 87.07%
CYP3A4 substrate - 0.5537 55.37%
CYP2C9 substrate - 0.7965 79.65%
CYP2D6 substrate - 0.8221 82.21%
CYP3A4 inhibition - 0.8753 87.53%
CYP2C9 inhibition - 0.6787 67.87%
CYP2C19 inhibition - 0.5671 56.71%
CYP2D6 inhibition - 0.9001 90.01%
CYP1A2 inhibition + 0.5938 59.38%
CYP2C8 inhibition - 0.6834 68.34%
CYP inhibitory promiscuity - 0.6915 69.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5923 59.23%
Carcinogenicity (trinary) Warning 0.5591 55.91%
Eye corrosion - 0.9100 91.00%
Eye irritation + 0.7651 76.51%
Skin irritation - 0.8910 89.10%
Skin corrosion - 0.9739 97.39%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6672 66.72%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.6318 63.18%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity + 0.8484 84.84%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.6626 66.26%
Acute Oral Toxicity (c) IV 0.6615 66.15%
Estrogen receptor binding - 0.7229 72.29%
Androgen receptor binding + 0.8200 82.00%
Thyroid receptor binding - 0.6586 65.86%
Glucocorticoid receptor binding - 0.6041 60.41%
Aromatase binding + 0.5439 54.39%
PPAR gamma - 0.5724 57.24%
Honey bee toxicity - 0.9848 98.48%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.9911 99.11%

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 97.44% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.42% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 92.45% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.44% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.69% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.60% 97.25%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.16% 85.94%
CHEMBL3401 O75469 Pregnane X receptor 84.89% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.47% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.23% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.00% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 81.23% 93.31%
CHEMBL2885 P07451 Carbonic anhydrase III 80.67% 87.45%

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.
Conioselinum anthriscoides
Oenanthe javanica

Cross-Links

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PubChem 5315567
NPASS NPC152749
LOTUS LTS0150672
wikiData Q104951974