Ilaprazole

This drug entry is a stub and has not been fully annotated. It is scheduled to be annotated soon.

Identification

Generic Name
Ilaprazole
DrugBank Accession Number
DB11964
Background

Ilaprazole has been investigated in Helicobacter Infections.

Type
Small Molecule
Groups
Investigational
Structure
Weight
Average: 366.44
Monoisotopic: 366.11504701
Chemical Formula
C19H18N4O2S
Synonyms
  • Ilaprazole
  • Ilaprazolum
External IDs
  • IY 81149
  • IY-81149
  • IY81149

Pharmacology

Indication

Not Available

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Contraindications & Blackbox Warnings
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Pharmacodynamics

Not Available

Mechanism of action
Not Available
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.
DrugInteraction
Alendronic acidThe therapeutic efficacy of Alendronic acid can be decreased when used in combination with Ilaprazole.
AmphetamineIlaprazole can cause an increase in the absorption of Amphetamine resulting in an increased serum concentration and potentially a worsening of adverse effects.
BelumosudilThe serum concentration of Belumosudil can be decreased when it is combined with Ilaprazole.
BosutinibThe serum concentration of Ilaprazole can be decreased when it is combined with Bosutinib.
BudesonideIlaprazole can cause a decrease in the absorption of Budesonide resulting in a reduced serum concentration and potentially a decrease in efficacy.
Food Interactions
Not Available

Products

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International/Other Brands
Noltec

Categories

Drug Categories
Chemical TaxonomyProvided by Classyfire
Description
This compound belongs to the class of organic compounds known as sulfinylbenzimidazoles. These are polycyclic aromatic compounds containing a sulfinyl group attached at the position 2 of a benzimidazole moiety.
Kingdom
Organic compounds
Super Class
Organoheterocyclic compounds
Class
Benzimidazoles
Sub Class
Sulfinylbenzimidazoles
Direct Parent
Sulfinylbenzimidazoles
Alternative Parents
Methylpyridines / Alkyl aryl ethers / Substituted pyrroles / Benzenoids / Imidazoles / Heteroaromatic compounds / Sulfoxides / Sulfinyl compounds / Azacyclic compounds / Organopnictogen compounds
show 3 more
Substituents
Alkyl aryl ether / Aromatic heteropolycyclic compound / Azacycle / Azole / Benzenoid / Ether / Heteroaromatic compound / Hydrocarbon derivative / Imidazole / Methylpyridine
show 13 more
Molecular Framework
Aromatic heteropolycyclic compounds
External Descriptors
Not Available
Affected organisms
Not Available

Chemical Identifiers

UNII
776Q6XX45J
CAS number
172152-36-2
InChI Key
HRRXCXABAPSOCP-UHFFFAOYSA-N
InChI
InChI=1S/C19H18N4O2S/c1-13-17(20-8-7-18(13)25-2)12-26(24)19-21-15-6-5-14(11-16(15)22-19)23-9-3-4-10-23/h3-11H,12H2,1-2H3,(H,21,22)
IUPAC Name
2-[(4-methoxy-3-methylpyridin-2-yl)methanesulfinyl]-5-(1H-pyrrol-1-yl)-1H-1,3-benzodiazole
SMILES
COC1=C(C)C(CS(=O)C2=NC3=C(N2)C=CC(=C3)N2C=CC=C2)=NC=C1

References

General References
Not Available
PubChem Compound
214351
PubChem Substance
347828288
ChemSpider
185839
ChEBI
135544
ChEMBL
CHEMBL2106370
PharmGKB
PA165947499
Wikipedia
Ilaprazole

Clinical Trials

Clinical Trials
Clinical Trial & Rare Diseases Add-on Data Package
Explore 4,000+ rare diseases, orphan drugs & condition pairs, clinical trial why stopped data, & more. Preview package
PhaseStatusPurposeConditionsCountStart DateWhy Stopped100+ additional columns
4CompletedTreatmentDuodenal Ulcer Due to Helicobacter Pylori1somestatusstop reasonjust information to hide
4CompletedTreatmentEradication Therapy of Helicobacter Pylori1somestatusstop reasonjust information to hide
4CompletedTreatmentGastric Cancer1somestatusstop reasonjust information to hide
4CompletedTreatmentHelicobacter Pylori Eradication Antibiotic1somestatusstop reasonjust information to hide
4CompletedTreatmentInfections, Helicobacter1somestatusstop reasonjust information to hide

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
FormRouteStrength
Tablet, delayed release
TabletOral10.000 mg
Prices
Not Available
Patents
Not Available

Properties

State
Not Available
Experimental Properties
Not Available
Predicted Properties
PropertyValueSource
Water Solubility0.0934 mg/mLALOGPS
logP2.42ALOGPS
logP3.04Chemaxon
logS-3.6ALOGPS
pKa (Strongest Acidic)10.1Chemaxon
pKa (Strongest Basic)4.27Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count4Chemaxon
Hydrogen Donor Count1Chemaxon
Polar Surface Area72.8 Å2Chemaxon
Rotatable Bond Count5Chemaxon
Refractivity111.91 m3·mol-1Chemaxon
Polarizability40.08 Å3Chemaxon
Number of Rings4Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon
Predicted ADMET Features
Not Available

Spectra

Mass Spec (NIST)
Not Available
Spectra
SpectrumSpectrum TypeSplash Key
Predicted MS/MS Spectrum - 10V, Positive (Annotated)Predicted LC-MS/MSsplash10-014i-0009000000-7fbf6a09f131d79170b9
Predicted MS/MS Spectrum - 10V, Negative (Annotated)Predicted LC-MS/MSsplash10-00lr-0092000000-9cad0f2abf1c4526684d
Predicted MS/MS Spectrum - 20V, Positive (Annotated)Predicted LC-MS/MSsplash10-014r-1829000000-aa55f5375fbcec3d6bd5
Predicted MS/MS Spectrum - 20V, Negative (Annotated)Predicted LC-MS/MSsplash10-001i-0090000000-baacd3e61cd97d41621a
Predicted MS/MS Spectrum - 40V, Positive (Annotated)Predicted LC-MS/MSsplash10-0a4i-3911000000-9f0102168e5a368d9d19
Predicted MS/MS Spectrum - 40V, Negative (Annotated)Predicted LC-MS/MSsplash10-01q9-4950000000-b0a2707f780f7d21a932
Predicted 1H NMR Spectrum1D NMRNot Applicable
Predicted 13C NMR Spectrum1D NMRNot Applicable
Chromatographic Properties
Collision Cross Sections (CCS)
AdductCCS Value (Å2)Source typeSource
[M-H]-183.86113
predicted
DeepCCS 1.0 (2019)
[M+H]+186.2567
predicted
DeepCCS 1.0 (2019)
[M+Na]+192.50671
predicted
DeepCCS 1.0 (2019)

Drug created at October 20, 2016 21:06 / Updated at February 21, 2021 18:53