(S)-1-Oxo-2,3-dihydro-1H-pyrrolizine-3-carboxylic acid

Details

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Internal ID a205db49-47c7-4566-80fa-7cf8144f452b
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives
IUPAC Name (3S)-1-oxo-2,3-dihydropyrrolizine-3-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H7NO3/c10-7-4-6(8(11)12)9-3-1-2-5(7)9/h1-3,6H,4H2,(H,11,12)/t6-/m0/s1
InChI Key IMIZZCOVJKIYFE-LURJTMIESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H7NO3
Molecular Weight 165.15 g/mol
Exact Mass 165.042593085 g/mol
Topological Polar Surface Area (TPSA) 59.30 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.70
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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(S)-1-Oxo-2,3-dihydro-1H-pyrrolizine-3-carboxylic acid
(2S)-4-oxo-1-azabicyclo<3.3.0>octa-5,7-diene-2-carboxylic acid
CHEBI:215783
(3S)-1-OXO-2,3-DIHYDROPYRROLIZINE-3-CARBOXYLIC ACID

2D Structure

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2D Structure of (S)-1-Oxo-2,3-dihydro-1H-pyrrolizine-3-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 + 0.9944 99.44%
Caco-2 - 0.7814 78.14%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7068 70.68%
OATP2B1 inhibitior - 0.8646 86.46%
OATP1B1 inhibitior + 0.9703 97.03%
OATP1B3 inhibitior + 0.9466 94.66%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8567 85.67%
BSEP inhibitior - 0.9385 93.85%
P-glycoprotein inhibitior - 0.9880 98.80%
P-glycoprotein substrate - 0.9589 95.89%
CYP3A4 substrate - 0.6956 69.56%
CYP2C9 substrate + 0.5552 55.52%
CYP2D6 substrate - 0.8728 87.28%
CYP3A4 inhibition - 0.9749 97.49%
CYP2C9 inhibition - 0.8999 89.99%
CYP2C19 inhibition - 0.9284 92.84%
CYP2D6 inhibition - 0.9443 94.43%
CYP1A2 inhibition - 0.8114 81.14%
CYP2C8 inhibition - 0.9865 98.65%
CYP inhibitory promiscuity - 0.9878 98.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5706 57.06%
Eye corrosion - 0.9655 96.55%
Eye irritation + 0.8423 84.23%
Skin irritation - 0.7095 70.95%
Skin corrosion - 0.9230 92.30%
Ames mutagenesis - 0.8054 80.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8769 87.69%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.7584 75.84%
skin sensitisation - 0.8850 88.50%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.5680 56.80%
Acute Oral Toxicity (c) III 0.4686 46.86%
Estrogen receptor binding - 0.9200 92.00%
Androgen receptor binding - 0.6150 61.50%
Thyroid receptor binding - 0.8766 87.66%
Glucocorticoid receptor binding - 0.8645 86.45%
Aromatase binding - 0.8338 83.38%
PPAR gamma - 0.6533 65.33%
Honey bee toxicity - 0.9459 94.59%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.8671 86.71%

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 90.91% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.41% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.59% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 86.50% 83.82%
CHEMBL4208 P20618 Proteasome component C5 83.18% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.27% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.23% 99.23%

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 45115953
LOTUS LTS0239435
wikiData Q77563347