5-hydroxy-4-methoxy-1-methyl-3H-pyridine-2,6-dione

Details

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Internal ID f48d555b-0122-49f6-838a-09906cbe105d
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Hydropyridines
IUPAC Name 5-hydroxy-4-methoxy-1-methyl-3H-pyridine-2,6-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H9NO4/c1-8-5(9)3-4(12-2)6(10)7(8)11/h10H,3H2,1-2H3
InChI Key JFMQRHZXDOZVMO-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C7H9NO4
Molecular Weight 171.15 g/mol
Exact Mass 171.05315777 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.21
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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Hermidin
Hermadine
NSC363737
5-hydroxy-4-methoxy-1-methyl-3H-pyridine-2,6-dione
5-Hydroxy-4-methoxy-1-methylpyridine-2,6(1H,3H)-dione
DTXSID50320700
NSC-363737
NS00094729

2D Structure

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2D Structure of 5-hydroxy-4-methoxy-1-methyl-3H-pyridine-2,6-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9119 91.19%
Caco-2 - 0.5237 52.37%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6453 64.53%
OATP2B1 inhibitior - 0.8562 85.62%
OATP1B1 inhibitior + 0.9630 96.30%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9469 94.69%
P-glycoprotein inhibitior - 0.9799 97.99%
P-glycoprotein substrate - 0.9391 93.91%
CYP3A4 substrate - 0.5959 59.59%
CYP2C9 substrate - 0.8063 80.63%
CYP2D6 substrate - 0.8702 87.02%
CYP3A4 inhibition - 0.9778 97.78%
CYP2C9 inhibition - 0.9576 95.76%
CYP2C19 inhibition - 0.9292 92.92%
CYP2D6 inhibition - 0.9405 94.05%
CYP1A2 inhibition - 0.8823 88.23%
CYP2C8 inhibition - 0.9892 98.92%
CYP inhibitory promiscuity - 0.9775 97.75%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6315 63.15%
Eye corrosion - 0.9814 98.14%
Eye irritation + 0.6521 65.21%
Skin irritation - 0.7523 75.23%
Skin corrosion - 0.9506 95.06%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8190 81.90%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.5959 59.59%
skin sensitisation - 0.9014 90.14%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.5655 56.55%
Acute Oral Toxicity (c) III 0.5987 59.87%
Estrogen receptor binding - 0.8153 81.53%
Androgen receptor binding - 0.8254 82.54%
Thyroid receptor binding - 0.8010 80.10%
Glucocorticoid receptor binding - 0.7587 75.87%
Aromatase binding - 0.7905 79.05%
PPAR gamma - 0.7365 73.65%
Honey bee toxicity - 0.9362 93.62%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.8760 87.60%

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 93.30% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.53% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.42% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.82% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.54% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.24% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.83% 99.23%
CHEMBL4208 P20618 Proteasome component C5 81.38% 90.00%

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.
Mercurialis perennis

Cross-Links

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PubChem 338913
LOTUS LTS0199058
wikiData Q82078109