Pyrrolidine-1-carboxamide

Details

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Internal ID 6aaa884c-d8ec-42d7-b482-dc5e90dec22d
Taxonomy Organoheterocyclic compounds > Pyrrolidines > Pyrrolidine carboxylic acids and derivatives > Pyrrolidinecarboxamides
IUPAC Name pyrrolidine-1-carboxamide
SMILES (Canonical) C1CCN(C1)C(=O)N
SMILES (Isomeric) C1CCN(C1)C(=O)N
InChI InChI=1S/C5H10N2O/c6-5(8)7-3-1-2-4-7/h1-4H2,(H2,6,8)
InChI Key LCDCPQHFCOBUEF-UHFFFAOYSA-N
Popularity 54 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10N2O
Molecular Weight 114.15 g/mol
Exact Mass 114.079312947 g/mol
Topological Polar Surface Area (TPSA) 46.30 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.16
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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4736-71-4
1-Pyrrolidinecarboxamide
Pyrrolidine-1-carboxylic acid amide
pyrrolidine carboxamide
pyrroldineamide
pyrrolidineamide
pyrrolidine amide
NSC117254
pyrrolidine carboxarnide
SCHEMBL302276
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Pyrrolidine-1-carboxamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9867 98.67%
Caco-2 + 0.8553 85.53%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Lysosomes 0.7376 73.76%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.9900 99.00%
OATP1B3 inhibitior + 0.9487 94.87%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6348 63.48%
BSEP inhibitior - 0.9249 92.49%
P-glycoprotein inhibitior - 0.9913 99.13%
P-glycoprotein substrate - 0.9725 97.25%
CYP3A4 substrate - 0.7899 78.99%
CYP2C9 substrate - 0.5650 56.50%
CYP2D6 substrate - 0.7372 73.72%
CYP3A4 inhibition - 0.9848 98.48%
CYP2C9 inhibition - 0.8492 84.92%
CYP2C19 inhibition - 0.8362 83.62%
CYP2D6 inhibition - 0.9389 93.89%
CYP1A2 inhibition - 0.7911 79.11%
CYP2C8 inhibition - 0.9987 99.87%
CYP inhibitory promiscuity - 0.9345 93.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5090 50.90%
Eye corrosion - 0.7657 76.57%
Eye irritation + 0.8967 89.67%
Skin irritation - 0.5938 59.38%
Skin corrosion - 0.7950 79.50%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7865 78.65%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.8500 85.00%
skin sensitisation - 0.9306 93.06%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6987 69.87%
Acute Oral Toxicity (c) III 0.6850 68.50%
Estrogen receptor binding - 0.9458 94.58%
Androgen receptor binding - 0.8326 83.26%
Thyroid receptor binding - 0.8345 83.45%
Glucocorticoid receptor binding - 0.7836 78.36%
Aromatase binding - 0.7679 76.79%
PPAR gamma - 0.8149 81.49%
Honey bee toxicity - 0.9709 97.09%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity - 0.9380 93.80%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.00% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 88.14% 83.82%
CHEMBL3474 P14555 Phospholipase A2 group IIA 87.99% 94.05%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.30% 93.04%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 81.16% 93.90%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.06% 92.94%

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.
Brassica rapa
Lepidium draba

Cross-Links

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PubChem 138335
NPASS NPC176455