(3S)-3-aminopyrrolidin-1-ium-3-carboxylate

Details

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Internal ID e2a9400a-7b65-4e29-91a3-44e9f6ae4284
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > L-alpha-amino acids
IUPAC Name (3S)-3-aminopyrrolidin-1-ium-3-carboxylate
SMILES (Canonical) C1C[NH2+]CC1(C(=O)[O-])N
SMILES (Isomeric) C1C[NH2+]C[C@@]1(C(=O)[O-])N
InChI InChI=1S/C5H10N2O2/c6-5(4(8)9)1-2-7-3-5/h7H,1-3,6H2,(H,8,9)/t5-/m0/s1
InChI Key DWAKXSZUASEUHH-YFKPBYRVSA-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) 82.80 Ų
XlogP -3.20
Atomic LogP (AlogP) -3.60
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S)-3-aminopyrrolidin-1-ium-3-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7446 74.46%
Caco-2 - 0.7195 71.95%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.8708 87.08%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.9643 96.43%
OATP1B3 inhibitior + 0.9448 94.48%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9609 96.09%
P-glycoprotein inhibitior - 0.9905 99.05%
P-glycoprotein substrate - 0.9692 96.92%
CYP3A4 substrate - 0.6295 62.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7918 79.18%
CYP3A4 inhibition - 0.9680 96.80%
CYP2C9 inhibition - 0.9084 90.84%
CYP2C19 inhibition - 0.9032 90.32%
CYP2D6 inhibition - 0.9216 92.16%
CYP1A2 inhibition - 0.6722 67.22%
CYP2C8 inhibition - 0.9402 94.02%
CYP inhibitory promiscuity - 0.9880 98.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5860 58.60%
Eye corrosion - 0.9330 93.30%
Eye irritation + 0.6696 66.96%
Skin irritation - 0.6586 65.86%
Skin corrosion - 0.8241 82.41%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8564 85.64%
Micronuclear + 0.5800 58.00%
Hepatotoxicity + 0.6427 64.27%
skin sensitisation - 0.8585 85.85%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7040 70.40%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5956 59.56%
Acute Oral Toxicity (c) III 0.5421 54.21%
Estrogen receptor binding - 0.9476 94.76%
Androgen receptor binding - 0.8398 83.98%
Thyroid receptor binding - 0.8209 82.09%
Glucocorticoid receptor binding - 0.9098 90.98%
Aromatase binding - 0.8911 89.11%
PPAR gamma - 0.8478 84.78%
Honey bee toxicity - 0.9019 90.19%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.9399 93.99%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.90% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.43% 91.11%
CHEMBL233 P35372 Mu opioid receptor 91.04% 97.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.94% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.17% 95.56%

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.
Bryonia alba
Citrullus colocynthis
Cucurbita moschata
Ecballium elaterium

Cross-Links

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PubChem 28820550
NPASS NPC227738