(2S)-4-Hydroxy-5-oxopyrrolidine-2-carboxylic acid

Details

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Internal ID 6bb43059-c615-427f-ab89-3391c0f36f98
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Proline and derivatives
IUPAC Name (2S)-4-hydroxy-5-oxopyrrolidine-2-carboxylic acid
SMILES (Canonical) C1C(C(=O)NC1C(=O)O)O
SMILES (Isomeric) C1[C@H](NC(=O)C1O)C(=O)O
InChI InChI=1S/C5H7NO4/c7-3-1-2(5(9)10)6-4(3)8/h2-3,7H,1H2,(H,6,8)(H,9,10)/t2-,3?/m0/s1
InChI Key FMMYTMPRUGLGBL-SCQFTWEKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C5H7NO4
Molecular Weight 145.11 g/mol
Exact Mass 145.03750770 g/mol
Topological Polar Surface Area (TPSA) 86.60 Ų
XlogP -1.30
Atomic LogP (AlogP) -1.68
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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(2S)-4-Hydroxy-5-oxopyrrolidine-2-carboxylic acid
4-oxy-5-oxo-l-proline
SCHEMBL2354388

2D Structure

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2D Structure of (2S)-4-Hydroxy-5-oxopyrrolidine-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 + 0.6529 65.29%
Caco-2 - 0.9483 94.83%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6450 64.50%
OATP2B1 inhibitior - 0.8497 84.97%
OATP1B1 inhibitior + 0.9582 95.82%
OATP1B3 inhibitior + 0.9409 94.09%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9808 98.08%
P-glycoprotein inhibitior - 0.9892 98.92%
P-glycoprotein substrate - 0.9264 92.64%
CYP3A4 substrate - 0.6645 66.45%
CYP2C9 substrate - 0.6031 60.31%
CYP2D6 substrate - 0.8367 83.67%
CYP3A4 inhibition - 0.9964 99.64%
CYP2C9 inhibition - 0.9774 97.74%
CYP2C19 inhibition - 0.9777 97.77%
CYP2D6 inhibition - 0.9631 96.31%
CYP1A2 inhibition - 0.9667 96.67%
CYP2C8 inhibition - 0.9766 97.66%
CYP inhibitory promiscuity - 0.9946 99.46%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.7292 72.92%
Eye corrosion - 0.9844 98.44%
Eye irritation + 0.6353 63.53%
Skin irritation - 0.7903 79.03%
Skin corrosion - 0.9441 94.41%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8247 82.47%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.6634 66.34%
skin sensitisation - 0.9061 90.61%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5922 59.22%
Acute Oral Toxicity (c) III 0.5918 59.18%
Estrogen receptor binding - 0.7569 75.69%
Androgen receptor binding - 0.7870 78.70%
Thyroid receptor binding - 0.8142 81.42%
Glucocorticoid receptor binding - 0.7471 74.71%
Aromatase binding - 0.8821 88.21%
PPAR gamma - 0.7940 79.40%
Honey bee toxicity - 0.9424 94.24%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity - 0.9558 95.58%

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
CHEMBL221 P23219 Cyclooxygenase-1 86.31% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.28% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.04% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.30% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.72% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.57% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 80.45% 91.19%

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.
Cota triumfetti
Pseudostellaria heterophylla

Cross-Links

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PubChem 45082769
LOTUS LTS0139487
wikiData Q105291321