N-carbamimidoyl-4-hydroxy-N-(4-hydroxybutyl)-3,5-dimethoxybenzamide

Details

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Internal ID 8e0eb4fc-99a3-4814-82dd-bdece76820cc
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name N-carbamimidoyl-4-hydroxy-N-(4-hydroxybutyl)-3,5-dimethoxybenzamide
SMILES (Canonical) COC1=CC(=CC(=C1O)OC)C(=O)N(CCCCO)C(=N)N
SMILES (Isomeric) COC1=CC(=CC(=C1O)OC)C(=O)N(CCCCO)C(=N)N
InChI InChI=1S/C14H21N3O5/c1-21-10-7-9(8-11(22-2)12(10)19)13(20)17(14(15)16)5-3-4-6-18/h7-8,18-19H,3-6H2,1-2H3,(H3,15,16)
InChI Key DEQFJPVWHOMNOG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H21N3O5
Molecular Weight 311.33 g/mol
Exact Mass 311.14812078 g/mol
Topological Polar Surface Area (TPSA) 129.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.52
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of N-carbamimidoyl-4-hydroxy-N-(4-hydroxybutyl)-3,5-dimethoxybenzamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8992 89.92%
Caco-2 - 0.5932 59.32%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8291 82.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8793 87.93%
OATP1B3 inhibitior + 0.9437 94.37%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.6855 68.55%
P-glycoprotein inhibitior - 0.8719 87.19%
P-glycoprotein substrate - 0.5512 55.12%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.7636 76.36%
CYP3A4 inhibition - 0.8663 86.63%
CYP2C9 inhibition - 0.8526 85.26%
CYP2C19 inhibition - 0.8002 80.02%
CYP2D6 inhibition - 0.8088 80.88%
CYP1A2 inhibition - 0.6843 68.43%
CYP2C8 inhibition - 0.6446 64.46%
CYP inhibitory promiscuity - 0.9381 93.81%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6603 66.03%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.8325 83.25%
Skin irritation - 0.7571 75.71%
Skin corrosion - 0.9301 93.01%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6297 62.97%
Micronuclear + 0.7800 78.00%
Hepatotoxicity - 0.6258 62.58%
skin sensitisation - 0.8533 85.33%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.9124 91.24%
Acute Oral Toxicity (c) III 0.6703 67.03%
Estrogen receptor binding + 0.8045 80.45%
Androgen receptor binding - 0.5848 58.48%
Thyroid receptor binding + 0.6826 68.26%
Glucocorticoid receptor binding + 0.7850 78.50%
Aromatase binding + 0.6196 61.96%
PPAR gamma + 0.5639 56.39%
Honey bee toxicity - 0.9510 95.10%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7482 74.82%
Fish aquatic toxicity - 0.8387 83.87%

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 97.83% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.99% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.86% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 95.70% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.93% 86.33%
CHEMBL204 P00734 Thrombin 89.05% 96.01%
CHEMBL3286 P00749 Urokinase-type plasminogen activator 88.86% 97.88%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.10% 96.95%
CHEMBL2535 P11166 Glucose transporter 86.31% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.31% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.26% 96.00%
CHEMBL4581 P52732 Kinesin-like protein 1 83.64% 93.18%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.00% 92.94%

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.
Leonurus sibiricus

Cross-Links

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PubChem 162939509
LOTUS LTS0011007
wikiData Q104977427