3-Aminopyrrolidine-2-carboxylic acid

Details

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Internal ID 6e192a63-5178-4b60-8405-50e6456700d8
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Proline and derivatives
IUPAC Name 3-aminopyrrolidine-2-carboxylic acid
SMILES (Canonical) C1CNC(C1N)C(=O)O
SMILES (Isomeric) C1CNC(C1N)C(=O)O
InChI InChI=1S/C5H10N2O2/c6-3-1-2-7-4(3)5(8)9/h3-4,7H,1-2,6H2,(H,8,9)
InChI Key VJLXSTXGGXYQCT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10N2O2
Molecular Weight 130.15 g/mol
Exact Mass 130.074227566 g/mol
Topological Polar Surface Area (TPSA) 75.40 Ų
XlogP -3.40
Atomic LogP (AlogP) -1.24
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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L-cis-3-Amino-2-pyrrolidinecarboxylic acid
L-cis-3-Aminoproline
SCHEMBL203721
CHEBI:191454

2D Structure

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2D Structure of 3-Aminopyrrolidine-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 + 0.9219 92.19%
Caco-2 - 0.9003 90.03%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.6203 62.03%
OATP2B1 inhibitior - 0.8422 84.22%
OATP1B1 inhibitior + 0.9777 97.77%
OATP1B3 inhibitior + 0.9469 94.69%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9731 97.31%
P-glycoprotein inhibitior - 0.9888 98.88%
P-glycoprotein substrate - 0.9498 94.98%
CYP3A4 substrate - 0.7275 72.75%
CYP2C9 substrate - 0.6124 61.24%
CYP2D6 substrate - 0.7391 73.91%
CYP3A4 inhibition - 0.9722 97.22%
CYP2C9 inhibition - 0.9471 94.71%
CYP2C19 inhibition - 0.9591 95.91%
CYP2D6 inhibition - 0.9617 96.17%
CYP1A2 inhibition - 0.8235 82.35%
CYP2C8 inhibition - 0.9460 94.60%
CYP inhibitory promiscuity - 0.9890 98.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.7078 70.78%
Eye corrosion - 0.9566 95.66%
Eye irritation - 0.5230 52.30%
Skin irritation - 0.7243 72.43%
Skin corrosion - 0.8006 80.06%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8073 80.73%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.8995 89.95%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6512 65.12%
Acute Oral Toxicity (c) III 0.5343 53.43%
Estrogen receptor binding - 0.9397 93.97%
Androgen receptor binding - 0.8032 80.32%
Thyroid receptor binding - 0.8462 84.62%
Glucocorticoid receptor binding - 0.8159 81.59%
Aromatase binding - 0.8929 89.29%
PPAR gamma - 0.7959 79.59%
Honey bee toxicity - 0.9475 94.75%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.9605 96.05%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 96.89% 97.09%
CHEMBL4040 P28482 MAP kinase ERK2 88.40% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.99% 96.09%
CHEMBL284 P27487 Dipeptidyl peptidase IV 82.49% 95.69%
CHEMBL4979 P13866 Sodium/glucose cotransporter 1 81.44% 98.24%
CHEMBL340 P08684 Cytochrome P450 3A4 81.14% 91.19%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.93% 96.95%

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 21998160
LOTUS LTS0141707
wikiData Q105287346