(S)-Pipermethystine

Details

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Internal ID 4cfdb62b-aaad-49b6-b7ee-15c308fb5e85
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Hydropyridines
IUPAC Name [(3S)-6-oxo-1-(3-phenylpropanoyl)-2,3-dihydropyridin-3-yl] acetate
SMILES (Canonical) CC(=O)OC1CN(C(=O)C=C1)C(=O)CCC2=CC=CC=C2
SMILES (Isomeric) CC(=O)O[C@@H]1CN(C(=O)C=C1)C(=O)CCC2=CC=CC=C2
InChI InChI=1S/C16H17NO4/c1-12(18)21-14-8-10-16(20)17(11-14)15(19)9-7-13-5-3-2-4-6-13/h2-6,8,10,14H,7,9,11H2,1H3/t14-/m0/s1
InChI Key JLNNQCUATONMIT-AWEZNQCLSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H17NO4
Molecular Weight 287.31 g/mol
Exact Mass 287.11575802 g/mol
Topological Polar Surface Area (TPSA) 63.70 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.48
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (S)-Pipermethystine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8985 89.85%
Caco-2 + 0.5994 59.94%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7791 77.91%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9093 90.93%
OATP1B3 inhibitior + 0.9398 93.98%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.8285 82.85%
P-glycoprotein inhibitior - 0.8089 80.89%
P-glycoprotein substrate - 0.6917 69.17%
CYP3A4 substrate + 0.5950 59.50%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.8872 88.72%
CYP3A4 inhibition - 0.6153 61.53%
CYP2C9 inhibition - 0.6512 65.12%
CYP2C19 inhibition + 0.5975 59.75%
CYP2D6 inhibition - 0.8782 87.82%
CYP1A2 inhibition - 0.7402 74.02%
CYP2C8 inhibition - 0.8362 83.62%
CYP inhibitory promiscuity + 0.7202 72.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5964 59.64%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9547 95.47%
Skin irritation - 0.8237 82.37%
Skin corrosion - 0.9641 96.41%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4195 41.95%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation - 0.9206 92.06%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.8305 83.05%
Nephrotoxicity - 0.6293 62.93%
Acute Oral Toxicity (c) III 0.7644 76.44%
Estrogen receptor binding + 0.6769 67.69%
Androgen receptor binding + 0.5341 53.41%
Thyroid receptor binding - 0.6994 69.94%
Glucocorticoid receptor binding + 0.5836 58.36%
Aromatase binding + 0.5741 57.41%
PPAR gamma - 0.6449 64.49%
Honey bee toxicity - 0.8737 87.37%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.8095 80.95%

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 99.02% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.69% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.26% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 93.82% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.66% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.48% 82.69%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 85.82% 94.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.32% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.90% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.61% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.12% 97.25%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.01% 95.50%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 81.32% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.75% 94.45%
CHEMBL5028 O14672 ADAM10 80.42% 97.50%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.07% 96.25%

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.
Piper methysticum

Cross-Links

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PubChem 11231515
NPASS NPC141371
LOTUS LTS0238323
wikiData Q105130937