Ethyl-(Z)-2,3-dibromopropenoate

Details

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Internal ID c309243e-153e-4986-abf5-aab0c3453a92
Taxonomy Organohalogen compounds > Vinyl halides > Vinylogous halides
IUPAC Name ethyl (Z)-2,3-dibromoprop-2-enoate
SMILES (Canonical) CCOC(=O)C(=CBr)Br
SMILES (Isomeric) CCOC(=O)/C(=C/Br)/Br
InChI InChI=1S/C5H6Br2O2/c1-2-9-5(8)4(7)3-6/h3H,2H2,1H3/b4-3-
InChI Key RCZNRJVVXOOAHG-ARJAWSKDSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C5H6Br2O2
Molecular Weight 257.91 g/mol
Exact Mass 257.87141 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2-Propenoic acid, 2,3-dibromo-, ethyl ester, (2Z)-
2,3-Dibromoacrylic acid ethyl ester
ethyl (2Z)-2,3-dibromo-2-propenoate
ETHYL-(Z)-2,3-DIBROMOPROPENOATE
(Z)-2,3-Dibromoacrylic acid ethyl ester
(Z)-2,3-dibromo-acrylic acid ethyl ester

2D Structure

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2D Structure of Ethyl-(Z)-2,3-dibromopropenoate

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 + 0.6657 66.57%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6582 65.82%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9435 94.35%
OATP1B3 inhibitior + 0.9532 95.32%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8806 88.06%
P-glycoprotein inhibitior - 0.9852 98.52%
P-glycoprotein substrate - 0.9902 99.02%
CYP3A4 substrate - 0.6051 60.51%
CYP2C9 substrate - 0.7929 79.29%
CYP2D6 substrate - 0.8666 86.66%
CYP3A4 inhibition - 0.9608 96.08%
CYP2C9 inhibition - 0.7805 78.05%
CYP2C19 inhibition - 0.7807 78.07%
CYP2D6 inhibition - 0.9339 93.39%
CYP1A2 inhibition - 0.5063 50.63%
CYP2C8 inhibition - 0.9362 93.62%
CYP inhibitory promiscuity - 0.7326 73.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5644 56.44%
Carcinogenicity (trinary) Non-required 0.4149 41.49%
Eye corrosion + 0.9843 98.43%
Eye irritation + 0.9931 99.31%
Skin irritation + 0.8150 81.50%
Skin corrosion - 0.6006 60.06%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7973 79.73%
Micronuclear - 0.8526 85.26%
Hepatotoxicity + 0.5449 54.49%
skin sensitisation + 0.5799 57.99%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.6461 64.61%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6376 63.76%
Acute Oral Toxicity (c) II 0.5230 52.30%
Estrogen receptor binding - 0.8479 84.79%
Androgen receptor binding - 0.9299 92.99%
Thyroid receptor binding - 0.8771 87.71%
Glucocorticoid receptor binding - 0.9327 93.27%
Aromatase binding - 0.8309 83.09%
PPAR gamma - 0.9062 90.62%
Honey bee toxicity - 0.8673 86.73%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5755 57.55%
Fish aquatic toxicity + 0.9286 92.86%

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 91.17% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.78% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.93% 97.21%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.26% 89.34%
CHEMBL221 P23219 Cyclooxygenase-1 84.07% 90.17%
CHEMBL230 P35354 Cyclooxygenase-2 81.95% 89.63%
CHEMBL3401 O75469 Pregnane X receptor 81.78% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.72% 99.17%

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.
Ainsliaea dissecta
Platycarphella carlinoides
Pulicaria dysenterica
Uncaria homomalla

Cross-Links

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PubChem 6380781
NPASS NPC9008
LOTUS LTS0144626
wikiData Q105234085