(2S)-2-hydroxy-1-(3-phenylpropanoyl)-2H-pyrrol-5-one

Details

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Internal ID 6b241a84-6e59-4d65-85a6-d30073e0925a
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name (2S)-2-hydroxy-1-(3-phenylpropanoyl)-2H-pyrrol-5-one
SMILES (Canonical) C1=CC=C(C=C1)CCC(=O)N2C(C=CC2=O)O
SMILES (Isomeric) C1=CC=C(C=C1)CCC(=O)N2[C@H](C=CC2=O)O
InChI InChI=1S/C13H13NO3/c15-11(14-12(16)8-9-13(14)17)7-6-10-4-2-1-3-5-10/h1-5,8-9,12,16H,6-7H2/t12-/m0/s1
InChI Key PXEVZSYBBRKIJW-LBPRGKRZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H13NO3
Molecular Weight 231.25 g/mol
Exact Mass 231.08954328 g/mol
Topological Polar Surface Area (TPSA) 57.60 Ų
XlogP 1.50
Atomic LogP (AlogP) 0.86
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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CHEMBL4103076

2D Structure

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2D Structure of (2S)-2-hydroxy-1-(3-phenylpropanoyl)-2H-pyrrol-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 + 0.9762 97.62%
Caco-2 + 0.7516 75.16%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7589 75.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9237 92.37%
OATP1B3 inhibitior + 0.9461 94.61%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7860 78.60%
BSEP inhibitior - 0.6780 67.80%
P-glycoprotein inhibitior - 0.9755 97.55%
P-glycoprotein substrate - 0.8726 87.26%
CYP3A4 substrate - 0.5304 53.04%
CYP2C9 substrate - 0.8028 80.28%
CYP2D6 substrate - 0.8566 85.66%
CYP3A4 inhibition - 0.8894 88.94%
CYP2C9 inhibition - 0.8478 84.78%
CYP2C19 inhibition - 0.8300 83.00%
CYP2D6 inhibition - 0.9075 90.75%
CYP1A2 inhibition - 0.8853 88.53%
CYP2C8 inhibition - 0.8484 84.84%
CYP inhibitory promiscuity - 0.9443 94.43%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5464 54.64%
Eye corrosion - 0.9398 93.98%
Eye irritation + 0.8209 82.09%
Skin irritation - 0.6781 67.81%
Skin corrosion - 0.8405 84.05%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7596 75.96%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.6160 61.60%
skin sensitisation - 0.9098 90.98%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.6576 65.76%
Nephrotoxicity - 0.6558 65.58%
Acute Oral Toxicity (c) III 0.6353 63.53%
Estrogen receptor binding - 0.7395 73.95%
Androgen receptor binding - 0.4873 48.73%
Thyroid receptor binding - 0.7593 75.93%
Glucocorticoid receptor binding - 0.6558 65.58%
Aromatase binding + 0.6308 63.08%
PPAR gamma - 0.6500 65.00%
Honey bee toxicity - 0.9188 91.88%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.5552 55.52%

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 97.62% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.64% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.54% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.83% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.38% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 83.82% 90.17%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.14% 96.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.16% 85.14%

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.
Acanthosyris paulo-alvinii
Aglaia perviridis
Ardisia japonica
Betula alnoides
Phoebe grandis
Piper sarmentosum
Rubus pileatus

Cross-Links

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PubChem 102442767
NPASS NPC193699