Mebhydrolin

This drug entry is astuband has not been fully annotated. It is scheduled to be annotated soon.

Identification

Summary

Mebhydrolinis an antihistamine indicated in the treatment of allergies.

Generic Name
Mebhydrolin
DrugBank Accession Number
DB13808
Background

Not Available

Type
Small Molecule
Groups
Experimental
Structure
Weight
Average: 276.383
Monoisotopic: 276.162648652
Chemical Formula
C19H20N2
Synonyms
  • Mebhydrolin

Pharmacology

Indication

Not Available

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Associated Conditions
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
Pathway Category
Mebhydrolin H1-Antihistamine Action Drug action
Pharmacogenomic Effects/ADRsBrowse all" title="" id="snp-actions-info" class="drug-info-popup" href="javascript:void(0);">
Not Available

Interactions

Drug InteractionsLearn More" title="" id="structured-interactions-info" class="drug-info-popup" href="javascript:void(0);">
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.
Drug Interaction
Droxidopa The therapeutic efficacy of Droxidopa can be increased when used in combination with Mebhydrolin.
Ephedrine The therapeutic efficacy of Ephedrine can be increased when used in combination with Mebhydrolin.
Epinephrine The therapeutic efficacy of Epinephrine can be increased when used in combination with Mebhydrolin.
Levonordefrin The therapeutic efficacy of Levonordefrin can be increased when used in combination with Mebhydrolin.
Norepinephrine The therapeutic efficacy of Norepinephrine can be increased when used in combination with Mebhydrolin.
Protokylol The therapeutic efficacy of Protokylol can be increased when used in combination with Mebhydrolin.
Racepinephrine The therapeutic efficacy of Racepinephrine can be increased when used in combination with Mebhydrolin.
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Food Interactions
Not Available

Products

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Product Ingredients
Ingredient UNII CAS InChI Key
Mebhydrolin napadisylate O5G04RB25M 6153-33-9 CJUOSBUQOWKEKJ-UHFFFAOYSA-N

Categories

ATC Codes
R06AX15 — Mebhydrolin
Drug Categories
Chemical TaxonomyProvided byClassyfire
Description
This compound belongs to the class of organic compounds known as n-alkylindoles. These are compounds containing an indole moiety that carries an alkyl chain at the 1-position.
Kingdom
Organic compounds
Super Class
Organoheterocyclic compounds
Class
Indoles and derivatives
Sub Class
N-alkylindoles
Direct Parent
N-alkylindoles
Alternative Parents
3-alkylindoles/Aralkylamines/Substituted pyrroles/Benzene and substituted derivatives/Heteroaromatic compounds/Trialkylamines/Azacyclic compounds/Organopnictogen compounds/Hydrocarbon derivatives
Substituents
3-alkylindole/Amine/Aralkylamine/Aromatic heteropolycyclic compound/Azacycle/Benzenoid/Heteroaromatic compound/Hydrocarbon derivative/Indole/Monocyclic benzene moiety
Molecular Framework
Aromatic heteropolycyclic compounds
External Descriptors
Not Available
Affected organisms
Not Available

Chemical Identifiers

UNII
9SUK9B7XVY
CAS number
524-81-2
InChI Key
FQQIIPAOSKSOJM-UHFFFAOYSA-N
InChI
InChI = 1 s / C19H20N2 / c1 -20-12-11-19-17(14-20)16-9-5-6-10-18(16)21(19)13-15-7-3-2-4-8-15/h2-10H,11-14H2,1H3
IUPAC Name
5-benzyl-2-methyl-1H,2H,3H,4H,5H-pyrido[4,3-b]indole
SMILES
CN1CCC2=C(C1)C1=CC=CC=C1N2CC1=CC=CC=C1

References

General References
  1. FDA Thailand Product Information: MYDOLIN (mebhydrolin) capsule [Link]
Human Metabolome Database
HMDB0240237
ChemSpider
21129
RxNav
29411
ChEBI
135144
ChEMBL
CHEMBL1625607
ZINC
ZINC000000001651
Wikipedia
Mebhydrolin

Clinical Trials

Clinical TrialsLearn More" title="" id="clinical-trials-info" class="drug-info-popup" href="javascript:void(0);">
Phase Status Purpose Conditions Count

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
Form Route Strength
Tablet, film coated Oral
Tablet, coated
Tablet
Suspension
Tablet 50 mg
Capsule 50 mg
Prices
Not Available
Patents
Not Available

Properties

State
Not Available
Experimental Properties
Not Available
Predicted Properties
Property Value Source
Water Solubility 0.0367 mg/mL ALOGPS
logP 3.69 ALOGPS
logP 3.69 Chemaxon
logS -3.9 ALOGPS
pKa (Strongest Basic) 7.2 Chemaxon
Physiological Charge 1 Chemaxon
Hydrogen Acceptor Count 1 Chemaxon
Hydrogen Donor Count 0 Chemaxon
Polar Surface Area 8.17 Å2 Chemaxon
Rotatable Bond Count 2 Chemaxon
Refractivity 88.49 m3·mol-1 Chemaxon
Polarizability 32.54 Å3 Chemaxon
Number of Rings 4 Chemaxon
Bioavailability 1 Chemaxon
Rule of Five Yes Chemaxon
Ghose Filter Yes Chemaxon
Veber's Rule Yes Chemaxon
MDDR-like Rule No Chemaxon
Predicted ADMET Features
Not Available

Spectra

Mass Spec (NIST)
Not Available
Spectra
Spectrum Spectrum Type Splash Key
Predicted GC-MS Spectrum - GC-MS Predicted GC-MS Not Available
Predicted MS/MS Spectrum - 10V, Positive (Annotated) Predicted LC-MS/MS Not Available
Predicted MS/MS Spectrum - 20V, Positive (Annotated) Predicted LC-MS/MS Not Available
Predicted MS/MS Spectrum - 40V, Positive (Annotated) Predicted LC-MS/MS Not Available
Predicted MS/MS Spectrum - 10V, Negative (Annotated) Predicted LC-MS/MS Not Available
Predicted MS/MS Spectrum - 20V, Negative (Annotated) Predicted LC-MS/MS Not Available
Predicted MS/MS Spectrum - 40V, Negative (Annotated) Predicted LC-MS/MS Not Available

Drug created at June 23, 2017 20:49 / Updated at May 21, 2021 10:23