(2R)-2-hydroxy-3-methyl-1,2-dihydropyrrol-5-one

Details

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Internal ID 6bc028b5-e4c0-4a3e-bb9e-f986e6af968d
Taxonomy Organic acids and derivatives > Carboximidic acids and derivatives > Carboximidic acids > Cyclic carboximidic acids
IUPAC Name (2R)-2-hydroxy-3-methyl-1,2-dihydropyrrol-5-one
SMILES (Canonical) CC1=CC(=O)NC1O
SMILES (Isomeric) CC1=CC(=O)N[C@@H]1O
InChI InChI=1S/C5H7NO2/c1-3-2-4(7)6-5(3)8/h2,5,8H,1H3,(H,6,7)/t5-/m1/s1
InChI Key CYAOUMDYSMFSPI-RXMQYKEDSA-N
Popularity 0 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) 49.30 Ų
XlogP -1.00
Atomic LogP (AlogP) -0.62
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-2-hydroxy-3-methyl-1,2-dihydropyrrol-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.7203 72.03%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.4904 49.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9408 94.08%
OATP1B3 inhibitior + 0.9541 95.41%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9561 95.61%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.9522 95.22%
CYP3A4 substrate - 0.6647 66.47%
CYP2C9 substrate + 0.5991 59.91%
CYP2D6 substrate - 0.9053 90.53%
CYP3A4 inhibition - 0.9652 96.52%
CYP2C9 inhibition - 0.8454 84.54%
CYP2C19 inhibition - 0.9149 91.49%
CYP2D6 inhibition - 0.9007 90.07%
CYP1A2 inhibition - 0.8239 82.39%
CYP2C8 inhibition - 0.9931 99.31%
CYP inhibitory promiscuity - 0.9311 93.11%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7528 75.28%
Carcinogenicity (trinary) Non-required 0.5033 50.33%
Eye corrosion - 0.8069 80.69%
Eye irritation + 0.9420 94.20%
Skin irritation - 0.7471 74.71%
Skin corrosion - 0.9155 91.55%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8484 84.84%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.6552 65.52%
skin sensitisation - 0.8714 87.14%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.6200 62.00%
Acute Oral Toxicity (c) III 0.5197 51.97%
Estrogen receptor binding - 0.9425 94.25%
Androgen receptor binding - 0.8888 88.88%
Thyroid receptor binding - 0.7293 72.93%
Glucocorticoid receptor binding - 0.7727 77.27%
Aromatase binding - 0.8924 89.24%
PPAR gamma - 0.8688 86.88%
Honey bee toxicity - 0.9383 93.83%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.7712 77.12%

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 92.01% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.98% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.59% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.29% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.53% 99.23%

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.
Jatropha macrorhiza

Cross-Links

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PubChem 162893056
LOTUS LTS0262971
wikiData Q104972214