(1-Methylpyrrolidin-2-yl)acetic acid

Details

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Internal ID db31670c-6941-491b-8549-5826e56c7f94
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-alkylpyrrolidines
IUPAC Name 2-(1-methylpyrrolidin-2-yl)acetic acid
SMILES (Canonical) CN1CCCC1CC(=O)O
SMILES (Isomeric) CN1CCCC1CC(=O)O
InChI InChI=1S/C7H13NO2/c1-8-4-2-3-6(8)5-7(9)10/h6H,2-5H2,1H3,(H,9,10)
InChI Key WQGHBXNTZFIOSX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H13NO2
Molecular Weight 143.18 g/mol
Exact Mass 143.094628657 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP -2.00
Atomic LogP (AlogP) 0.56
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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(1-Methylpyrrolidin-2-yl)acetic acid
2-(1-Methylpyrrolidin-2-yl)acetic acid
(1-methyl-2-pyrrolidinyl)acetic acid
SCHEMBL8198672
1-methyl-2-pyrrolidineacetic acid
MFCD14642575
AKOS005264615
LS-10734
CS-0300999
EN300-815141
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (1-Methylpyrrolidin-2-yl)acetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9508 95.08%
Caco-2 + 0.8355 83.55%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.4718 47.18%
OATP2B1 inhibitior - 0.8418 84.18%
OATP1B1 inhibitior + 0.9549 95.49%
OATP1B3 inhibitior + 0.9384 93.84%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.6250 62.50%
BSEP inhibitior - 0.9509 95.09%
P-glycoprotein inhibitior - 0.9852 98.52%
P-glycoprotein substrate - 0.8744 87.44%
CYP3A4 substrate - 0.6662 66.62%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate + 0.3722 37.22%
CYP3A4 inhibition - 0.9799 97.99%
CYP2C9 inhibition - 0.9526 95.26%
CYP2C19 inhibition - 0.9417 94.17%
CYP2D6 inhibition - 0.9282 92.82%
CYP1A2 inhibition - 0.7802 78.02%
CYP2C8 inhibition - 0.9963 99.63%
CYP inhibitory promiscuity - 0.9952 99.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6405 64.05%
Eye corrosion - 0.8934 89.34%
Eye irritation + 0.9015 90.15%
Skin irritation - 0.5873 58.73%
Skin corrosion - 0.6178 61.78%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7919 79.19%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5212 52.12%
skin sensitisation - 0.8767 87.67%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.6808 68.08%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8867 88.67%
Acute Oral Toxicity (c) III 0.6435 64.35%
Estrogen receptor binding - 0.9000 90.00%
Androgen receptor binding - 0.9004 90.04%
Thyroid receptor binding - 0.9133 91.33%
Glucocorticoid receptor binding - 0.8857 88.57%
Aromatase binding - 0.8619 86.19%
PPAR gamma - 0.8828 88.28%
Honey bee toxicity - 0.9884 98.84%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.6162 61.62%

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 97.55% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.22% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.57% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.90% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.08% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.68% 93.00%
CHEMBL5203 P33316 dUTP pyrophosphatase 80.68% 99.18%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 80.06% 96.03%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.05% 93.04%

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.
Erythroxylum coca

Cross-Links

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PubChem 14021870
LOTUS LTS0227380
wikiData Q105310706