methyl 4,5-dibromo-1H-pyrrole-2-carboxylate

Details

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Internal ID d73acf49-974f-4b7b-8a5c-2758cfc07d21
Taxonomy Organoheterocyclic compounds > Pyrroles > Pyrrole carboxylic acids and derivatives
IUPAC Name methyl 4,5-dibromo-1H-pyrrole-2-carboxylate
SMILES (Canonical) COC(=O)C1=CC(=C(N1)Br)Br
SMILES (Isomeric) COC(=O)C1=CC(=C(N1)Br)Br
InChI InChI=1S/C6H5Br2NO2/c1-11-6(10)4-2-3(7)5(8)9-4/h2,9H,1H3
InChI Key ISQWCRSAYRXYRS-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C6H5Br2NO2
Molecular Weight 282.92 g/mol
Exact Mass 282.86665 g/mol
Topological Polar Surface Area (TPSA) 42.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.33
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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937-16-6
NSC 288036
NSC288036
4,5-Dibromo-2-(methoxycarbonyl)-1H-pyrrole
CHEMBL391386
SCHEMBL17781270
DTXSID10314746
ISQWCRSAYRXYRS-UHFFFAOYSA-N
AMY25247
MFCD06200907
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of methyl 4,5-dibromo-1H-pyrrole-2-carboxylate

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 + 0.5096 50.96%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5497 54.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9308 93.08%
OATP1B3 inhibitior + 0.9595 95.95%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7644 76.44%
P-glycoprotein inhibitior - 0.9733 97.33%
P-glycoprotein substrate - 0.9422 94.22%
CYP3A4 substrate - 0.5961 59.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8394 83.94%
CYP3A4 inhibition - 0.8983 89.83%
CYP2C9 inhibition - 0.7737 77.37%
CYP2C19 inhibition - 0.6344 63.44%
CYP2D6 inhibition - 0.9667 96.67%
CYP1A2 inhibition + 0.8239 82.39%
CYP2C8 inhibition - 0.7370 73.70%
CYP inhibitory promiscuity - 0.5879 58.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7313 73.13%
Carcinogenicity (trinary) Non-required 0.5399 53.99%
Eye corrosion - 0.8724 87.24%
Eye irritation + 0.9794 97.94%
Skin irritation - 0.7367 73.67%
Skin corrosion - 0.9193 91.93%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5854 58.54%
Micronuclear + 0.6574 65.74%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.9045 90.45%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.6855 68.55%
Acute Oral Toxicity (c) II 0.4898 48.98%
Estrogen receptor binding - 0.6164 61.64%
Androgen receptor binding - 0.8103 81.03%
Thyroid receptor binding - 0.6857 68.57%
Glucocorticoid receptor binding - 0.6059 60.59%
Aromatase binding - 0.7603 76.03%
PPAR gamma - 0.6162 61.62%
Honey bee toxicity - 0.9619 96.19%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.3834 38.34%

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 96.26% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.33% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.09% 91.11%
CHEMBL4208 P20618 Proteasome component C5 86.00% 90.00%
CHEMBL2535 P11166 Glucose transporter 84.62% 98.75%
CHEMBL2581 P07339 Cathepsin D 83.93% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.17% 94.73%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.91% 91.07%
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.
Artemisia vestita
Monochaetum vulcanicum

Cross-Links

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PubChem 324097
NPASS NPC142688
LOTUS LTS0004038
wikiData Q82067053