N-Benzoylmescaline

Details

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Internal ID d910048f-8b8b-4e16-9ea3-25ae390458e1
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzamides
IUPAC Name N-[2-(3,4,5-trimethoxyphenyl)ethyl]benzamide
SMILES (Canonical) COC1=CC(=CC(=C1OC)OC)CCNC(=O)C2=CC=CC=C2
SMILES (Isomeric) COC1=CC(=CC(=C1OC)OC)CCNC(=O)C2=CC=CC=C2
InChI InChI=1S/C18H21NO4/c1-21-15-11-13(12-16(22-2)17(15)23-3)9-10-19-18(20)14-7-5-4-6-8-14/h4-8,11-12H,9-10H2,1-3H3,(H,19,20)
InChI Key LKEQQVSIASVWMD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H21NO4
Molecular Weight 315.40 g/mol
Exact Mass 315.14705815 g/mol
Topological Polar Surface Area (TPSA) 56.80 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.68
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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N-[2-(3,4,5-trimethoxyphenyl)ethyl]benzamide
AKOS000277025

2D Structure

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2D Structure of N-Benzoylmescaline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.8493 84.93%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7878 78.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9386 93.86%
OATP1B3 inhibitior + 0.9539 95.39%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6621 66.21%
P-glycoprotein inhibitior - 0.5161 51.61%
P-glycoprotein substrate + 0.5734 57.34%
CYP3A4 substrate + 0.5275 52.75%
CYP2C9 substrate - 0.8253 82.53%
CYP2D6 substrate - 0.7565 75.65%
CYP3A4 inhibition - 0.5189 51.89%
CYP2C9 inhibition - 0.7039 70.39%
CYP2C19 inhibition - 0.5354 53.54%
CYP2D6 inhibition - 0.8544 85.44%
CYP1A2 inhibition + 0.6875 68.75%
CYP2C8 inhibition + 0.8969 89.69%
CYP inhibitory promiscuity - 0.5471 54.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.6825 68.25%
Eye corrosion - 0.9799 97.99%
Eye irritation - 0.8705 87.05%
Skin irritation - 0.7459 74.59%
Skin corrosion - 0.9585 95.85%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7733 77.33%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.6214 62.14%
skin sensitisation - 0.9337 93.37%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.7991 79.91%
Acute Oral Toxicity (c) III 0.6706 67.06%
Estrogen receptor binding + 0.6602 66.02%
Androgen receptor binding - 0.4919 49.19%
Thyroid receptor binding + 0.6620 66.20%
Glucocorticoid receptor binding - 0.5834 58.34%
Aromatase binding - 0.7250 72.50%
PPAR gamma + 0.5358 53.58%
Honey bee toxicity - 0.9445 94.45%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5049 50.49%
Fish aquatic toxicity - 0.5095 50.95%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.45% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 94.91% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.69% 99.17%
CHEMBL2535 P11166 Glucose transporter 94.29% 98.75%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 92.85% 87.67%
CHEMBL2581 P07339 Cathepsin D 92.63% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.44% 86.33%
CHEMBL4208 P20618 Proteasome component C5 86.74% 90.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 86.04% 81.11%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 85.43% 96.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.88% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.39% 91.11%
CHEMBL5028 O14672 ADAM10 82.20% 97.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.01% 96.00%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 81.02% 89.33%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.10% 95.89%

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 umbellatum

Cross-Links

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PubChem 9972998
LOTUS LTS0055693
wikiData Q104398985