Bis(2-ethylbutyl) phthalate

Details

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Internal ID 15c62e04-8643-43ef-acde-d0b6623bd910
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name bis(2-ethylbutyl) benzene-1,2-dicarboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H30O4/c1-5-15(6-2)13-23-19(21)17-11-9-10-12-18(17)20(22)24-14-16(7-3)8-4/h9-12,15-16H,5-8,13-14H2,1-4H3
InChI Key RXUXJHZMTDAMFZ-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O4
Molecular Weight 334.40 g/mol
Exact Mass 334.21440943 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.87
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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7299-89-0
bis(2-ethylbutyl) benzene-1,2-dicarboxylate
Bis(2-ethylbutyl)phthalate
Bis(2-ethyl-n-butyl) phthalate
Phthalic acid, bis(2-ethylbutyl) ester
1,2-Benzenedicarboxylic acid, bis(2-ethylbutyl) ester
UNII-Q298IR7BMM
Q298IR7BMM
EINECS 230-741-7
NSC 15317
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Bis(2-ethylbutyl) phthalate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.7927 79.27%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.8686 86.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9374 93.74%
OATP1B3 inhibitior + 0.9592 95.92%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5919 59.19%
P-glycoprotein inhibitior - 0.5392 53.92%
P-glycoprotein substrate - 0.9567 95.67%
CYP3A4 substrate - 0.6708 67.08%
CYP2C9 substrate - 0.7965 79.65%
CYP2D6 substrate - 0.8221 82.21%
CYP3A4 inhibition - 0.9058 90.58%
CYP2C9 inhibition - 0.7326 73.26%
CYP2C19 inhibition - 0.7239 72.39%
CYP2D6 inhibition - 0.9200 92.00%
CYP1A2 inhibition + 0.5394 53.94%
CYP2C8 inhibition - 0.8476 84.76%
CYP inhibitory promiscuity - 0.6259 62.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5036 50.36%
Carcinogenicity (trinary) Non-required 0.6139 61.39%
Eye corrosion - 0.8487 84.87%
Eye irritation + 0.7300 73.00%
Skin irritation - 0.7562 75.62%
Skin corrosion - 0.9712 97.12%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6817 68.17%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6052 60.52%
skin sensitisation + 0.6944 69.44%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity + 0.7125 71.25%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.4938 49.38%
Acute Oral Toxicity (c) IV 0.7049 70.49%
Estrogen receptor binding - 0.5223 52.23%
Androgen receptor binding + 0.6140 61.40%
Thyroid receptor binding - 0.6192 61.92%
Glucocorticoid receptor binding - 0.5729 57.29%
Aromatase binding + 0.6380 63.80%
PPAR gamma - 0.5839 58.39%
Honey bee toxicity - 0.9658 96.58%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5355 53.55%
Fish aquatic toxicity + 0.9944 99.44%

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 96.14% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.88% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 89.89% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.91% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 85.29% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.12% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.52% 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.
Oenanthe javanica

Cross-Links

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PubChem 81724
LOTUS LTS0229632
wikiData Q27286915