(2R)-pyrrolidinium-2-carboxylate

Details

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Internal ID 93d921db-8ecf-40e7-9048-e030e2ec8e33
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Proline and derivatives
IUPAC Name (2R)-pyrrolidin-1-ium-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m1/s1
InChI Key ONIBWKKTOPOVIA-SCSAIBSYSA-N
Popularity 54 references in papers

Physical and Chemical Properties

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Molecular Formula C5H9NO2
Molecular Weight 115.13 g/mol
Exact Mass 115.063328530 g/mol
Topological Polar Surface Area (TPSA) 56.70 Ų
XlogP -1.90
Atomic LogP (AlogP) -2.54
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEBI:57726
(2R)-pyrrolidinium-2-carboxylate

2D Structure

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2D Structure of (2R)-pyrrolidinium-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 + 0.9899 98.99%
Caco-2 - 0.7908 79.08%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.7815 78.15%
OATP2B1 inhibitior - 0.8172 81.72%
OATP1B1 inhibitior + 0.9513 95.13%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9748 97.48%
P-glycoprotein inhibitior - 0.9912 99.12%
P-glycoprotein substrate - 0.9870 98.70%
CYP3A4 substrate - 0.6647 66.47%
CYP2C9 substrate - 0.6077 60.77%
CYP2D6 substrate - 0.8174 81.74%
CYP3A4 inhibition - 0.9937 99.37%
CYP2C9 inhibition - 0.9466 94.66%
CYP2C19 inhibition - 0.9447 94.47%
CYP2D6 inhibition - 0.9317 93.17%
CYP1A2 inhibition - 0.7848 78.48%
CYP2C8 inhibition - 0.9799 97.99%
CYP inhibitory promiscuity - 0.9787 97.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6422 64.22%
Eye corrosion - 0.8332 83.32%
Eye irritation + 0.9756 97.56%
Skin irritation - 0.6203 62.03%
Skin corrosion - 0.5448 54.48%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8042 80.42%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation - 0.9383 93.83%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.5657 56.57%
Acute Oral Toxicity (c) II 0.4860 48.60%
Estrogen receptor binding - 0.9362 93.62%
Androgen receptor binding - 0.7660 76.60%
Thyroid receptor binding - 0.9138 91.38%
Glucocorticoid receptor binding - 0.8966 89.66%
Aromatase binding - 0.8609 86.09%
PPAR gamma - 0.8323 83.23%
Honey bee toxicity - 0.9266 92.66%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.9496 94.96%

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
CHEMBL241 Q14432 Phosphodiesterase 3A 83.76% 92.94%
CHEMBL340 P08684 Cytochrome P450 3A4 81.33% 91.19%

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 6971012
NPASS NPC302003
ChEMBL CHEMBL80257