3,4-Dihydro-2H-pyrrole-5-carboxylic acid

Details

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Internal ID 80c05a82-2c81-4d41-b571-23942866cde1
Taxonomy Organoheterocyclic compounds > Pyrrolines
IUPAC Name 3,4-dihydro-2H-pyrrole-5-carboxylic acid
SMILES (Canonical) C1CC(=NC1)C(=O)O
SMILES (Isomeric) C1CC(=NC1)C(=O)O
InChI InChI=1S/C5H7NO2/c7-5(8)4-2-1-3-6-4/h1-3H2,(H,7,8)
InChI Key RHTAIKJZSXNELN-UHFFFAOYSA-N
Popularity 93 references in papers

Physical and Chemical Properties

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Molecular Formula C5H7NO2
Molecular Weight 113.11 g/mol
Exact Mass 113.047678466 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP -0.40
Atomic LogP (AlogP) 0.31
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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1-Pyrroline-2-carboxylic acid
2139-03-9
Pyrroline-5-carboxylate
1-Pyrroline-2-carboxylate
delta1-Pyrroline 2-carboxylate
3,4-DIHYDRO-2H-PYRROLIUM-5-CARBOXYLATE
CHEBI:36761
2H-Pyrrole-5-carboxylic acid, 3,4-dihydro-
1,2-Didehydroproline
3,4-dihydro-2H-pyrrole-5-carboxylicacid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,4-Dihydro-2H-pyrrole-5-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 + 0.9840 98.40%
Caco-2 + 0.5775 57.75%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6994 69.94%
OATP2B1 inhibitior - 0.8392 83.92%
OATP1B1 inhibitior + 0.9854 98.54%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9546 95.46%
P-glycoprotein inhibitior - 0.9902 99.02%
P-glycoprotein substrate - 0.9905 99.05%
CYP3A4 substrate - 0.7694 76.94%
CYP2C9 substrate + 0.6012 60.12%
CYP2D6 substrate - 0.8858 88.58%
CYP3A4 inhibition - 0.9738 97.38%
CYP2C9 inhibition - 0.9380 93.80%
CYP2C19 inhibition - 0.9521 95.21%
CYP2D6 inhibition - 0.9210 92.10%
CYP1A2 inhibition - 0.6706 67.06%
CYP2C8 inhibition - 0.9926 99.26%
CYP inhibitory promiscuity - 0.9887 98.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6683 66.83%
Eye corrosion - 0.7341 73.41%
Eye irritation + 0.9894 98.94%
Skin irritation - 0.5273 52.73%
Skin corrosion + 0.6405 64.05%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7236 72.36%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8812 88.12%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.5845 58.45%
Acute Oral Toxicity (c) III 0.4912 49.12%
Estrogen receptor binding - 0.9509 95.09%
Androgen receptor binding - 0.9131 91.31%
Thyroid receptor binding - 0.8789 87.89%
Glucocorticoid receptor binding - 0.8661 86.61%
Aromatase binding - 0.8417 84.17%
PPAR gamma - 0.8222 82.22%
Honey bee toxicity - 0.9813 98.13%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity - 0.8918 89.18%

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
CHEMBL2581 P07339 Cathepsin D 88.11% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.61% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.54% 96.09%

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.
Populus tremula

Cross-Links

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PubChem 440046
LOTUS LTS0021214
wikiData Q27093798