Muscimol

Details

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Internal ID 7a63c405-1c29-4685-ae08-94c3485d5ca5
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Amines > Aralkylamines
IUPAC Name 5-(aminomethyl)-1,2-oxazol-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H6N2O2/c5-2-3-1-4(7)6-8-3/h1H,2,5H2,(H,6,7)
InChI Key ZJQHPWUVQPJPQT-UHFFFAOYSA-N
Popularity 8,349 references in papers

Physical and Chemical Properties

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Molecular Formula C4H6N2O2
Molecular Weight 114.10 g/mol
Exact Mass 114.042927438 g/mol
Topological Polar Surface Area (TPSA) 64.40 Ų
XlogP -1.40
Atomic LogP (AlogP) -0.57
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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2763-96-4
Agarin
Pantherine
Agarine
3(2H)-Isoxazolone, 5-(aminomethyl)-
5-Aminomethyl-3-hydroxyisoxazole
3-Hydroxy-5-aminomethylisoxazole
Pantherin
5-(Aminomethyl)-3(2H)-isoxazolone
5-(Aminomethyl)-3-isoxazolol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Muscimol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9636 96.36%
Caco-2 - 0.5374 53.74%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.5144 51.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9479 94.79%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9308 93.08%
P-glycoprotein inhibitior - 0.9861 98.61%
P-glycoprotein substrate - 0.9673 96.73%
CYP3A4 substrate - 0.7745 77.45%
CYP2C9 substrate - 0.7929 79.29%
CYP2D6 substrate - 0.8378 83.78%
CYP3A4 inhibition - 0.9241 92.41%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9025 90.25%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition - 0.9510 95.10%
CYP inhibitory promiscuity - 0.7097 70.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.4317 43.17%
Eye corrosion - 0.9834 98.34%
Eye irritation + 0.7048 70.48%
Skin irritation - 0.7678 76.78%
Skin corrosion - 0.9186 91.86%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7173 71.73%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.5593 55.93%
skin sensitisation - 0.8355 83.55%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.5583 55.83%
Acute Oral Toxicity (c) I 0.7921 79.21%
Estrogen receptor binding - 0.9221 92.21%
Androgen receptor binding - 0.6850 68.50%
Thyroid receptor binding - 0.8293 82.93%
Glucocorticoid receptor binding - 0.7656 76.56%
Aromatase binding - 0.7221 72.21%
PPAR gamma - 0.6414 64.14%
Honey bee toxicity - 0.9372 93.72%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.9900 99.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.86% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.14% 94.45%
CHEMBL2581 P07339 Cathepsin D 87.50% 98.95%
CHEMBL4581 P52732 Kinesin-like protein 1 86.77% 93.18%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.74% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.97% 94.80%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.52% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 83.41% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.34% 89.34%
CHEMBL3384 Q16512 Protein kinase N1 80.88% 80.71%

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.
There are no matching plants.

Cross-Links

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PubChem 4266
LOTUS LTS0006526
wikiData Q412504