NAV

N-[1-(2,6-dimethoxybenzyl)piperidin-4-yl]-4-sulfanylbutanamide

Identification

Generic Name
N-[1-(2,6-dimethoxybenzyl)piperidin-4-yl]-4-sulfanylbutanamide
DrugBank Accession Number
DB07735
Background

Not Available

Type
Small Molecule
Groups
Experimental
Structure
3D
Similar Structures
Weight
Average: 352.492
Monoisotopic: 352.182063462
Chemical Formula
C18H28N2O3S
Synonyms
Not Available

Pharmacology

Indication

Not Available

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Contraindications & Blackbox Warnings
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Pharmacodynamics

Not Available

Mechanism of action
TargetActionsOrganism
UBeta-secretase 1Not AvailableHumans
Absorption

Not Available

Volume of distribution

Not Available

Protein binding

Not Available

Metabolism
Not Available
Route of elimination

Not Available

Half-life

Not Available

Clearance

Not Available

Adverse Effects
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Toxicity

Not Available

Pathways
Not Available
Pharmacogenomic Effects/ADRs
Not Available

Interactions

Drug Interactions
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Not Available
Food Interactions
Not Available

Categories

Drug Categories
Not Available
Chemical TaxonomyProvided by Classyfire
Description
This compound belongs to the class of organic compounds known as n-benzylpiperidines. These are heterocyclic Compounds containing a piperidine ring conjugated to a benzyl group through one nitrogen ring atom.
Kingdom
Organic compounds
Super Class
Organoheterocyclic compounds
Class
Piperidines
Sub Class
Benzylpiperidines
Direct Parent
N-benzylpiperidines
Alternative Parents
Dimethoxybenzenes / Anisoles / Benzylamines / Phenylmethylamines / Phenoxy compounds / Alkyl aryl ethers / Aralkylamines / N-acyl amines / Secondary carboxylic acid amides / Trialkylamines
show 7 more
Substituents
Alkyl aryl ether / Alkylthiol / Amine / Amino acid or derivatives / Anisole / Aralkylamine / Aromatic heteromonocyclic compound / Azacycle / Benzenoid / Benzylamine
show 26 more
Molecular Framework
Aromatic heteromonocyclic compounds
External Descriptors
Not Available
Affected organisms
Not Available

Chemical Identifiers

UNII
Not Available
CAS number
Not Available
InChI Key
MUDVORCZGBAHNA-UHFFFAOYSA-N
InChI
InChI=1S/C18H28N2O3S/c1-22-16-5-3-6-17(23-2)15(16)13-20-10-8-14(9-11-20)19-18(21)7-4-12-24/h3,5-6,14,24H,4,7-13H2,1-2H3,(H,19,21)
IUPAC Name
N-{1-[(2,6-dimethoxyphenyl)methyl]piperidin-4-yl}-4-sulfanylbutanamide
SMILES
COC1=CC=CC(OC)=C1CN1CCC(CC1)NC(=O)CCCS

References

General References
Not Available
PubChem Compound
25134250
PubChem Substance
99444206
ChemSpider
25059120
ZINC
ZINC000039470956
PDBe Ligand
F1I
PDB Entries
2zji

Clinical Trials

Clinical Trials
PhaseStatusPurposeConditionsCount

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
Not Available
Prices
Not Available
Patents
Not Available

Properties

State
Solid
Experimental Properties
Not Available
Predicted Properties
PropertyValueSource
Water Solubility0.0137 mg/mLALOGPS
logP2.27ALOGPS
logP1.59Chemaxon
logS-4.4ALOGPS
pKa (Strongest Acidic)10.2Chemaxon
pKa (Strongest Basic)7.47Chemaxon
Physiological Charge1Chemaxon
Hydrogen Acceptor Count4Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area50.8 Å2Chemaxon
Rotatable Bond Count8Chemaxon
Refractivity99.54 m3·mol-1Chemaxon
Polarizability39.92 Å3Chemaxon
Number of Rings2Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon
Predicted ADMET Features
PropertyValueProbability
Human Intestinal Absorption+0.9822
Blood Brain Barrier+0.8769
Caco-2 permeable+0.5818
P-glycoprotein substrateSubstrate0.7355
P-glycoprotein inhibitor IInhibitor0.677
P-glycoprotein inhibitor IIInhibitor0.528
Renal organic cation transporterNon-inhibitor0.5532
CYP450 2C9 substrateNon-substrate0.8
CYP450 2D6 substrateNon-substrate0.5757
CYP450 3A4 substrateSubstrate0.6896
CYP450 1A2 substrateNon-inhibitor0.8316
CYP450 2C9 inhibitorNon-inhibitor0.8298
CYP450 2D6 inhibitorInhibitor0.5954
CYP450 2C19 inhibitorNon-inhibitor0.8211
CYP450 3A4 inhibitorNon-inhibitor0.6533
CYP450 inhibitory promiscuityLow CYP Inhibitory Promiscuity0.7592
Ames testNon AMES toxic0.7253
CarcinogenicityNon-carcinogens0.8938
BiodegradationNot ready biodegradable0.9522
Rat acute toxicity2.5459 LD50, mol/kg Not applicable
hERG inhibition (predictor I)Weak inhibitor0.8505
hERG inhibition (predictor II)Inhibitor0.9314
ADMET data is predicted using admetSAR, a free tool for evaluating chemical ADMET properties. (23092397)

Spectra

Mass Spec (NIST)
Not Available
Spectra
SpectrumSpectrum TypeSplash Key
Predicted MS/MS Spectrum - 10V, Positive (Annotated)Predicted LC-MS/MSNot Available
Predicted MS/MS Spectrum - 20V, Positive (Annotated)Predicted LC-MS/MSNot Available
Predicted MS/MS Spectrum - 40V, Positive (Annotated)Predicted LC-MS/MSNot Available
Predicted MS/MS Spectrum - 10V, Negative (Annotated)Predicted LC-MS/MSNot Available
Predicted MS/MS Spectrum - 20V, Negative (Annotated)Predicted LC-MS/MSNot Available
Predicted MS/MS Spectrum - 40V, Negative (Annotated)Predicted LC-MS/MSNot Available

Targets

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Details1. Beta-secretase 1
Kind
Protein
Organism
Humans
Pharmacological action
Unknown
General Function
Peptidase activity
Specific Function
Responsible for the proteolytic processing of the amyloid precursor protein (APP). Cleaves at the N-terminus of the A-beta peptide sequence, between residues 671 and 672 of APP, leads to the genera...
Gene Name
BACE1
Uniprot ID
P56817
Uniprot Name
Beta-secretase 1
Molecular Weight
55710.28 Da
References
  1. Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. [Article]

Drug created at September 15, 2010 21:25 / Updated at June 12, 2020 16:52