1-Butyl 2-methyl 1,2-benzenedicarboxylate

Details

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Internal ID e7dab336-95cf-452f-be9e-1a198f6625b4
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name 2-O-butyl 1-O-methyl benzene-1,2-dicarboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H16O4/c1-3-4-9-17-13(15)11-8-6-5-7-10(11)12(14)16-2/h5-8H,3-4,9H2,1-2H3
InChI Key XXFSYINDUHLBIL-UHFFFAOYSA-N
Popularity 16 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O4
Molecular Weight 236.26 g/mol
Exact Mass 236.10485899 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.43
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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34006-76-3
DTXSID7074325
RefChem:1055158
DTXCID3038777
1-Butyl 2-methyl 1,2-benzenedicarboxylate
Methyl butyl phthalate
2-O-butyl 1-O-methyl benzene-1,2-dicarboxylate
Phthalic acid, butyl methyl ester
1,2-Benzenedicarboxylic acid, butyl methyl ester
AI3-03342
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Butyl 2-methyl 1,2-benzenedicarboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 + 0.8623 86.23%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8989 89.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9284 92.84%
OATP1B3 inhibitior + 0.9582 95.82%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6668 66.68%
P-glycoprotein inhibitior - 0.9234 92.34%
P-glycoprotein substrate - 0.8734 87.34%
CYP3A4 substrate - 0.5616 56.16%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8123 81.23%
CYP3A4 inhibition - 0.9053 90.53%
CYP2C9 inhibition - 0.7934 79.34%
CYP2C19 inhibition - 0.6160 61.60%
CYP2D6 inhibition - 0.9305 93.05%
CYP1A2 inhibition + 0.5896 58.96%
CYP2C8 inhibition + 0.5431 54.31%
CYP inhibitory promiscuity - 0.7443 74.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6543 65.43%
Carcinogenicity (trinary) Non-required 0.5544 55.44%
Eye corrosion - 0.9106 91.06%
Eye irritation + 0.9489 94.89%
Skin irritation - 0.8577 85.77%
Skin corrosion - 0.9812 98.12%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4469 44.69%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5961 59.61%
skin sensitisation - 0.6266 62.66%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.7560 75.60%
Acute Oral Toxicity (c) III 0.6655 66.55%
Estrogen receptor binding + 0.5313 53.13%
Androgen receptor binding + 0.7268 72.68%
Thyroid receptor binding - 0.5937 59.37%
Glucocorticoid receptor binding - 0.6843 68.43%
Aromatase binding - 0.7383 73.83%
PPAR gamma - 0.5934 59.34%
Honey bee toxicity - 0.9909 99.09%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9860 98.60%

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 95.99% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.57% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.90% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 90.78% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.72% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.24% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 84.42% 94.73%
CHEMBL3891 P07384 Calpain 1 81.62% 93.04%

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.
Panax ginseng

Cross-Links

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PubChem 36655
NPASS NPC20754