Pyrrole-2-carboxylic acid

Details

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Internal ID 2e70ff66-e866-4fa3-969c-eed1e6dd23c2
Taxonomy Organoheterocyclic compounds > Pyrroles > Pyrrole carboxylic acids and derivatives > Pyrrole carboxylic acids > Pyrrole 2-carboxylic acids
IUPAC Name 1H-pyrrole-2-carboxylic acid
SMILES (Canonical) C1=CNC(=C1)C(=O)O
SMILES (Isomeric) C1=CNC(=C1)C(=O)O
InChI InChI=1S/C5H5NO2/c7-5(8)4-2-1-3-6-4/h1-3,6H,(H,7,8)
InChI Key WRHZVMBBRYBTKZ-UHFFFAOYSA-N
Popularity 343 references in papers

Physical and Chemical Properties

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Molecular Formula C5H5NO2
Molecular Weight 111.10 g/mol
Exact Mass 111.032028402 g/mol
Topological Polar Surface Area (TPSA) 53.10 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.71
H-Bond Acceptor 1
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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634-97-9
1H-Pyrrole-2-carboxylic acid
Minaline
2-Pyrrolecarboxylic acid
Minalin
Pyrrole-2-carboxylicacid
Pyrrole-2-carboxylate
1H-Pyrrolecarboxylic acid
MFCD00005219
2NNB85QQT9
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Pyrrole-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.6769 67.69%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.5316 53.16%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9723 97.23%
OATP1B3 inhibitior + 0.9557 95.57%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9390 93.90%
P-glycoprotein inhibitior - 0.9896 98.96%
P-glycoprotein substrate - 0.9854 98.54%
CYP3A4 substrate - 0.8115 81.15%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.8924 89.24%
CYP3A4 inhibition - 0.9671 96.71%
CYP2C9 inhibition - 0.9052 90.52%
CYP2C19 inhibition - 0.9403 94.03%
CYP2D6 inhibition - 0.9621 96.21%
CYP1A2 inhibition - 0.8926 89.26%
CYP2C8 inhibition - 0.9513 95.13%
CYP inhibitory promiscuity - 0.9769 97.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.6496 64.96%
Eye corrosion - 0.9093 90.93%
Eye irritation + 0.9945 99.45%
Skin irritation + 0.6165 61.65%
Skin corrosion - 0.7941 79.41%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8948 89.48%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.9281 92.81%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.4605 46.05%
Acute Oral Toxicity (c) II 0.3866 38.66%
Estrogen receptor binding - 0.9383 93.83%
Androgen receptor binding - 0.9573 95.73%
Thyroid receptor binding - 0.8471 84.71%
Glucocorticoid receptor binding - 0.9044 90.44%
Aromatase binding - 0.9159 91.59%
PPAR gamma - 0.7812 78.12%
Honey bee toxicity - 0.9802 98.02%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.8365 83.65%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.09% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.56% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.99% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.94% 91.11%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.06% 81.11%

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.
Brachystemma calycinum
Capparis spinosa
Mimosa pudica
Pseudostellaria heterophylla

Cross-Links

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PubChem 12473
NPASS NPC33229
ChEMBL CHEMBL509027
LOTUS LTS0226371
wikiData Q27104383