Methyl 5-bromo-1H-pyrrole-2-carboxylate

Details

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Internal ID 0fa7e160-390e-466f-86f5-a85568a8c179
Taxonomy Organoheterocyclic compounds > Pyrroles > Pyrrole carboxylic acids and derivatives
IUPAC Name methyl 5-bromo-1H-pyrrole-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H6BrNO2/c1-10-6(9)4-2-3-5(7)8-4/h2-3,8H,1H3
InChI Key ZYBOXSDTMZRWBC-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C6H6BrNO2
Molecular Weight 204.02 g/mol
Exact Mass 202.95819 g/mol
Topological Polar Surface Area (TPSA) 42.10 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.56
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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934-07-6
METHYL 5-BROMOPYRROLE-2-CARBOXYLATE
1H-Pyrrole-2-carboxylic acid, 5-bromo-, methyl ester
5-BROMO-1H-PYRROLE-2-CARBOXYLIC ACID METHYL ESTER
MFCD09801030
SCHEMBL1422544
DTXSID30469242
ZYBOXSDTMZRWBC-UHFFFAOYSA-N
AKOS015920458
CS-W006646
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 5-bromo-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 + 0.5278 52.78%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4856 48.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9510 95.10%
OATP1B3 inhibitior + 0.9575 95.75%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8922 89.22%
P-glycoprotein inhibitior - 0.9851 98.51%
P-glycoprotein substrate - 0.9639 96.39%
CYP3A4 substrate - 0.6112 61.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8394 83.94%
CYP3A4 inhibition - 0.9407 94.07%
CYP2C9 inhibition - 0.8416 84.16%
CYP2C19 inhibition - 0.6862 68.62%
CYP2D6 inhibition - 0.9618 96.18%
CYP1A2 inhibition + 0.6609 66.09%
CYP2C8 inhibition - 0.8299 82.99%
CYP inhibitory promiscuity - 0.7823 78.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7231 72.31%
Carcinogenicity (trinary) Non-required 0.5199 51.99%
Eye corrosion - 0.7549 75.49%
Eye irritation + 0.9906 99.06%
Skin irritation - 0.6368 63.68%
Skin corrosion - 0.8763 87.63%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6575 65.75%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.5909 59.09%
skin sensitisation - 0.8872 88.72%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5140 51.40%
Acute Oral Toxicity (c) II 0.4808 48.08%
Estrogen receptor binding - 0.8986 89.86%
Androgen receptor binding - 0.9355 93.55%
Thyroid receptor binding - 0.7881 78.81%
Glucocorticoid receptor binding - 0.8858 88.58%
Aromatase binding - 0.8562 85.62%
PPAR gamma - 0.8061 80.61%
Honey bee toxicity - 0.9738 97.38%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.6049 60.49%

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 94.52% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.26% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.95% 91.11%
CHEMBL2581 P07339 Cathepsin D 84.72% 98.95%
CHEMBL4208 P20618 Proteasome component C5 84.25% 90.00%
CHEMBL2535 P11166 Glucose transporter 84.01% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 81.55% 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 11600885
LOTUS LTS0058203
wikiData Q82296869