3-Isopropyl-6-(4-methoxybenzyl)-4-methylmorpholine-2,5-dione

Details

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Internal ID 7370e2df-992c-433a-823f-595cd7515c22
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acid esters
IUPAC Name 6-[(4-methoxyphenyl)methyl]-4-methyl-3-propan-2-ylmorpholine-2,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H21NO4/c1-10(2)14-16(19)21-13(15(18)17(14)3)9-11-5-7-12(20-4)8-6-11/h5-8,10,13-14H,9H2,1-4H3
InChI Key UTROHFPONJQOAG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H21NO4
Molecular Weight 291.34 g/mol
Exact Mass 291.14705815 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 1.65
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 3-Isopropyl-6-(4-methoxybenzyl)-4-methylmorpholine-2,5-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5687 56.87%
Caco-2 + 0.8405 84.05%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5007 50.07%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.9332 93.32%
OATP1B3 inhibitior + 0.9284 92.84%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7268 72.68%
P-glycoprotein inhibitior - 0.6810 68.10%
P-glycoprotein substrate - 0.7093 70.93%
CYP3A4 substrate + 0.5332 53.32%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate - 0.8084 80.84%
CYP3A4 inhibition - 0.7110 71.10%
CYP2C9 inhibition - 0.6732 67.32%
CYP2C19 inhibition - 0.5955 59.55%
CYP2D6 inhibition - 0.9209 92.09%
CYP1A2 inhibition - 0.6793 67.93%
CYP2C8 inhibition - 0.9485 94.85%
CYP inhibitory promiscuity - 0.5330 53.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8507 85.07%
Carcinogenicity (trinary) Non-required 0.5351 53.51%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9547 95.47%
Skin irritation - 0.8412 84.12%
Skin corrosion - 0.9517 95.17%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4589 45.89%
Micronuclear + 0.6500 65.00%
Hepatotoxicity - 0.5627 56.27%
skin sensitisation - 0.9097 90.97%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.7337 73.37%
Nephrotoxicity - 0.8151 81.51%
Acute Oral Toxicity (c) III 0.7721 77.21%
Estrogen receptor binding + 0.6676 66.76%
Androgen receptor binding + 0.6208 62.08%
Thyroid receptor binding - 0.5372 53.72%
Glucocorticoid receptor binding + 0.6129 61.29%
Aromatase binding - 0.5282 52.82%
PPAR gamma - 0.7972 79.72%
Honey bee toxicity - 0.8553 85.53%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.5163 51.63%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.42% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.65% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.66% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.74% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.73% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.23% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.57% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.83% 85.14%
CHEMBL4208 P20618 Proteasome component C5 85.34% 90.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.31% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.17% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.23% 86.33%
CHEMBL3820 P35557 Hexokinase type IV 83.38% 91.96%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.17% 96.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.05% 96.77%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.73% 86.92%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.51% 93.99%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.21% 95.71%

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 72766294
LOTUS LTS0127782
wikiData Q105279043