Ethyl dibromoacetate

Details

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Internal ID 3a2aefbf-3a96-4945-9936-21b8a10d16ce
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Alpha-halocarboxylic acids and derivatives > Alpha-halocarboxylic acid derivatives
IUPAC Name ethyl 2,2-dibromoacetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H6Br2O2/c1-2-8-4(7)3(5)6/h3H,2H2,1H3
InChI Key NIJGVVHCUXNSLL-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C4H6Br2O2
Molecular Weight 245.90 g/mol
Exact Mass 245.87141 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.67
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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617-33-4
ethyl 2,2-dibromoacetate
Acetic acid, dibromo-, ethyl ester
ethyldibromoacetate
Dibromoacetic acid, ethyl ester
Acetic acid, 2,2-dibromo-, ethyl ester
dibromo-acetic acid ethyl ester
U57B34JKE5
NSC-8830
MFCD00041718
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl dibromoacetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.6022 60.22%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7155 71.55%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.9540 95.40%
OATP1B3 inhibitior + 0.9570 95.70%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9396 93.96%
P-glycoprotein inhibitior - 0.9819 98.19%
P-glycoprotein substrate - 0.9950 99.50%
CYP3A4 substrate - 0.6593 65.93%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.8800 88.00%
CYP3A4 inhibition - 0.9745 97.45%
CYP2C9 inhibition - 0.8403 84.03%
CYP2C19 inhibition - 0.8385 83.85%
CYP2D6 inhibition - 0.9455 94.55%
CYP1A2 inhibition + 0.5689 56.89%
CYP2C8 inhibition - 0.9901 99.01%
CYP inhibitory promiscuity - 0.8851 88.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5657 56.57%
Carcinogenicity (trinary) Non-required 0.4634 46.34%
Eye corrosion + 1.0000 100.00%
Eye irritation + 0.9918 99.18%
Skin irritation + 0.8969 89.69%
Skin corrosion + 0.5195 51.95%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8262 82.62%
Micronuclear - 0.8526 85.26%
Hepatotoxicity + 0.7134 71.34%
skin sensitisation - 0.6805 68.05%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity + 0.6094 60.94%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5603 56.03%
Acute Oral Toxicity (c) III 0.5438 54.38%
Estrogen receptor binding - 0.8216 82.16%
Androgen receptor binding - 0.9182 91.82%
Thyroid receptor binding - 0.9019 90.19%
Glucocorticoid receptor binding - 0.9236 92.36%
Aromatase binding - 0.8430 84.30%
PPAR gamma - 0.8907 89.07%
Honey bee toxicity - 0.9169 91.69%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.7855 78.55%
Fish aquatic toxicity + 0.7757 77.57%

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 93.78% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.79% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.02% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.50% 99.17%
CHEMBL2581 P07339 Cathepsin D 81.39% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 80.74% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 69237
LOTUS LTS0157667
wikiData Q81989154