DL-Pyroglutamic acid

Details

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Internal ID fe8eacc3-32a4-4030-89b6-7cedf6a4a8b7
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Proline and derivatives
IUPAC Name 5-oxopyrrolidine-2-carboxylic acid
SMILES (Canonical) C1CC(=O)NC1C(=O)O
SMILES (Isomeric) C1CC(=O)NC1C(=O)O
InChI InChI=1S/C5H7NO3/c7-4-2-1-3(6-4)5(8)9/h3H,1-2H2,(H,6,7)(H,8,9)
InChI Key ODHCTXKNWHHXJC-UHFFFAOYSA-N
Popularity 3,611 references in papers

Physical and Chemical Properties

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Molecular Formula C5H7NO3
Molecular Weight 129.11 g/mol
Exact Mass 129.042593085 g/mol
Topological Polar Surface Area (TPSA) 66.40 Ų
XlogP -0.80
Atomic LogP (AlogP) -0.65
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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149-87-1
5-Oxopyrrolidine-2-carboxylic acid
2-Pyrrolidone-5-carboxylic acid
5-Oxo-DL-proline
DL-Proline, 5-oxo-
DL-Pidolic acid
DL-2-Pyrrolidone-5-carboxylic acid
DL-Glutamic Acid Lactam
UNII-6VT1YZM21H
dl-pyrrolidonecarboxylic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of DL-Pyroglutamic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9150 91.50%
Caco-2 - 0.9028 90.28%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7605 76.05%
OATP2B1 inhibitior - 0.8423 84.23%
OATP1B1 inhibitior + 0.9568 95.68%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9846 98.46%
P-glycoprotein inhibitior - 0.9916 99.16%
P-glycoprotein substrate - 0.9777 97.77%
CYP3A4 substrate - 0.7102 71.02%
CYP2C9 substrate - 0.5955 59.55%
CYP2D6 substrate - 0.8648 86.48%
CYP3A4 inhibition - 0.9931 99.31%
CYP2C9 inhibition - 0.9782 97.82%
CYP2C19 inhibition - 0.9812 98.12%
CYP2D6 inhibition - 0.9678 96.78%
CYP1A2 inhibition - 0.9641 96.41%
CYP2C8 inhibition - 0.9864 98.64%
CYP inhibitory promiscuity - 0.9973 99.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7189 71.89%
Eye corrosion - 0.9647 96.47%
Eye irritation + 0.8914 89.14%
Skin irritation - 0.8518 85.18%
Skin corrosion - 0.9020 90.20%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8095 80.95%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.9000 90.00%
skin sensitisation - 0.9390 93.90%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6893 68.93%
Acute Oral Toxicity (c) III 0.8003 80.03%
Estrogen receptor binding - 0.9053 90.53%
Androgen receptor binding - 0.9280 92.80%
Thyroid receptor binding - 0.9153 91.53%
Glucocorticoid receptor binding - 0.8865 88.65%
Aromatase binding - 0.8514 85.14%
PPAR gamma - 0.7351 73.51%
Honey bee toxicity - 0.9770 97.70%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity - 0.9566 95.66%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293235 P02545 Prelamin-A/C 5.6 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4040 P28482 MAP kinase ERK2 97.54% 83.82%
CHEMBL2581 P07339 Cathepsin D 86.86% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.15% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.67% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.12% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.42% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.82% 94.45%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.27% 93.00%

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.
Agave americana
Aloe africana
Aloe ferox
Aloe spicata
Aloe vera
Arabidopsis thaliana
Isatis tinctoria
Lemna aequinoctialis
Lotus corniculatus subsp. corniculatus
Panax ginseng
Paris polyphylla
Pseudostellaria heterophylla

Cross-Links

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PubChem 499
NPASS NPC29950
ChEMBL CHEMBL284718
LOTUS LTS0198996
wikiData Q27887010