Streptokordin

Details

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Internal ID 85eae745-0e86-40a1-b7c3-87ae94f223d6
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aryl ketones > Aryl alkyl ketones
IUPAC Name 4-acetyl-6-methyl-1H-pyridin-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H9NO2/c1-5-3-7(6(2)10)4-8(11)9-5/h3-4H,1-2H3,(H,9,11)
InChI Key JCPDZXJDYRLFMC-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C8H9NO2
Molecular Weight 151.16 g/mol
Exact Mass 151.063328530 g/mol
Topological Polar Surface Area (TPSA) 46.20 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.89
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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4-acetyl-6-methyl-1H-pyridin-2-one
4-acetyl-6-methylpyridin-2(1H)-one
CHEBI:66524
RefChem:185934
905828-76-4
1-(2-HYDROXY-6-METHYLPYRIDIN-4-YL)ETHANONE
4-acetyl-6-methyl-1H-pyridine-2-one
SCHEMBL2714624
SCHEMBL17866899
MFCD22545510
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Streptokordin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.5344 53.44%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7955 79.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9614 96.14%
OATP1B3 inhibitior + 0.9659 96.59%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8419 84.19%
P-glycoprotein inhibitior - 0.9754 97.54%
P-glycoprotein substrate - 0.9628 96.28%
CYP3A4 substrate - 0.6869 68.69%
CYP2C9 substrate + 0.6054 60.54%
CYP2D6 substrate - 0.8873 88.73%
CYP3A4 inhibition - 0.9780 97.80%
CYP2C9 inhibition - 0.9648 96.48%
CYP2C19 inhibition - 0.9800 98.00%
CYP2D6 inhibition - 0.9669 96.69%
CYP1A2 inhibition - 0.8475 84.75%
CYP2C8 inhibition - 0.9766 97.66%
CYP inhibitory promiscuity - 0.9713 97.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8236 82.36%
Carcinogenicity (trinary) Non-required 0.5708 57.08%
Eye corrosion - 0.9267 92.67%
Eye irritation + 0.9588 95.88%
Skin irritation - 0.5495 54.95%
Skin corrosion - 0.9505 95.05%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7216 72.16%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.8507 85.07%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7879 78.79%
Estrogen receptor binding - 0.9660 96.60%
Androgen receptor binding - 0.7251 72.51%
Thyroid receptor binding - 0.7853 78.53%
Glucocorticoid receptor binding - 0.8576 85.76%
Aromatase binding - 0.8151 81.51%
PPAR gamma - 0.9284 92.84%
Honey bee toxicity - 0.9782 97.82%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.9379 93.79%

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 88.92% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.01% 85.14%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.49% 97.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.29% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.05% 94.80%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.02% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.63% 96.09%
CHEMBL2535 P11166 Glucose transporter 82.33% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 81.98% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.29% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 11579160
LOTUS LTS0103662
wikiData Q27135131