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Details

Stereochemistry ACHIRAL
Molecular Formula C13H18Br2N2O.C9H10N4O4
Molecular Weight 616.303
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMBROXOL ACEFYLLINATE

SMILES

CN1C2=C(N(CC(O)=O)C=N2)C(=O)N(C)C1=O.NC3=C(Br)C=C(Br)C=C3CN[C@H]4CC[C@H](O)CC4

InChI

InChIKey=IPUHJDQWESJTGD-PFWPSKEQSA-N
InChI=1S/C13H18Br2N2O.C9H10N4O4/c14-9-5-8(13(16)12(15)6-9)7-17-10-1-3-11(18)4-2-10;1-11-7-6(8(16)12(2)9(11)17)13(4-10-7)3-5(14)15/h5-6,10-11,17-18H,1-4,7,16H2;4H,3H2,1-2H3,(H,14,15)/t10-,11-;

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including http://adisinsight.springer.com/drugs/800035262 | https://www.ncbi.nlm.nih.gov/pubmed/23158495 | https://www.ncbi.nlm.nih.gov/pubmed/18482096 | https://www.ncbi.nlm.nih.gov/pubmed/19578116 | http://zywiebio.com/drug-development/therapeutic-areas-of-interest/gaucher-disease/

Ambroxol, a substituted benzylamine, is an active metabolite of bromhexine, which is itself a synthetic derivative of vasicine, the active principle extracted from the plant species Adhatoda vasica. Ambroxol is an expectorant exerting mucokinetic properties, mucociliary activity, stimulation of surfactant production, anti-inflammatory and antioxidative actions and the local anaesthetic effect. Ambroxol was discovered at and has been manufactured by Dr. Karl Thomae GmbH, a division of Boehringer Ingelheim. The ambroxol patent is expired and the drug is available as a generic product from many different companies. Ambroxol was originally developed by Boehringer Ingelheim as a OTC therapy for respiratory disorders related to excessive mucus. Ambroxol's indication is secretolytic therapy in acute and chronic bronchopulmonary diseases associated with abnormal mucus secretion and impaired mucus transport. Boehringer Ingelheim markets the product under various brand names such as Mucosolvan® and Lasolvan®. Ambroxol was identified and found to be a pH-dependent, mixed-type inhibitor of glucocerebrosidase (GCase). Its inhibitory activity was maximal at neutral pH, found in the endoplasmic reticulum, and undetectable at the acidic pH of lysosomes. The pH dependence of Ambroxol to bind and stabilize the enzyme was confirmed. Ambroxol increases both the lysosomal fraction and the enzymatic activity of several mutant GCase variants. This profile of Ambroxol would allow to bind and stabilize GCase in the endoplasmic reticulum (thus preventing its degradation within endoplasmic reticulum), but without affecting GCase in the lysosomes (thus allowing it to degrade glucosylceramide). Indeed, studies showed that Ambroxol treatment significantly increased N370S and F213I mutant GCase activity and protein levels in fibroblasts originally obtained from Gaucher patients. Gaucher's disease is caused by the deficiency of glucocerebrosidase; ambroxol is a chaperone that acts by binding to and stabilising glucocerebrosidase. Zywie (formerly ExSAR Corporation) and Belrose Pharma are developing ambroxol hydrochloride (BEL 0218) for the treatment of type III Gaucher's disease. .

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
MUCOSOLVAN

Approved Use

MUCOSOLVAN (ambroxol hydrochloride) is indicated for secretolytic therapy in acute and chronic bronchopulmonary diseases associated with abnormal mucus secretion and impaired mucus transport.
PubMed

PubMed

TitleDatePubMed
Neltenexine tablets in smoking and non-smoking patients with COPD. A double-blind, randomised, controlled study versus placebo.
2001 Aug
Oral neltenexine in patients with obstructive airways diseases: an open, randomised, controlled comparison versus sobrerol.
2001 Aug
Attenuation by ambroxol of monochloramine-enhanced gastric carcinogenesis: a possible prevention against Helicobacter pylori-associated gastric carcinogenesis.
2001 Jul 26
Transport properties of ionic drugs in the ammonio methacrylate copolymer membranes.
2001 Mar
Validation of an HPLC method for the quantification of ambroxol hydrochloride and benzoic acid in a syrup as pharmaceutical form stress test for stability evaluation.
2001 Mar
The predictive value of asthma medications to identify individuals with asthma--a study in German general practices.
2001 Nov
Enhanced resistance to Sendai virus infection in DBA/2J mice with a botanical drug combination (Sinupret).
2001 Sep
Immunoassay screening of lysergic acid diethylamide (LSD) and its confirmation by HPLC and fluorescence detection following LSD ImmunElute extraction.
2002 Apr
Pharmacokinetic properties of single-dose loratadine and ambroxol alone and combined in tablet formulations in healthy men.
2003 Aug
Determination of ambroxol in human plasma using LC-MS/MS.
2003 Jun 1
In vitro inhibition of human neutrophil histotoxicity by ambroxol: evidence for a multistep mechanism.
2003 Oct
[Protective effects of ambroxol on lung injury during cardiacpulmonary bypass in patients undergoing valve replacement].
2004 Dec
[Management of extensive burn accompanying severe inhalation injury].
2004 May
[Oxidative and anti-oxidative effects of ambroxol on acute hydrochloric acid-induced lung injury in rats].
2004 Oct
Determination of ambroxol in an automated multi-pumping pulsed flow system.
2005 Apr
Adsorptive stripping voltammetric determination of ambroxol.
2005 Mar
Differences in tidal breathing between infants with chronic lung diseases and healthy controls.
2005 Sep 8
Determination of ambroxol hydrochloride, methylparaben and benzoic acid in pharmaceutical preparations based on sequential injection technique coupled with monolithic column.
2006 Feb 13
Proteases essential for human influenza virus entry into cells and their inhibitors as potential therapeutic agents.
2007
Solid-state chemistry of ambroxol theophylline-7-acetate.
2007 May
Action of neltenexine on anion secretion in human airway epithelia.
2007 May 18
Patents

Sample Use Guides

In Vivo Use Guide
Adults: daily dose of 30 mg (one Ambroxol tablet ) to 120 mg (4 Ambroxol tablets) taken in 2 to 3 divided doses Children up to 2 years: half a teaspoonful Ambroxol syrup twice daily Children 2 - 5 years: half a teaspoonful Ambroxol syrup 3 times daily Children over 5 years: One teaspoonful Ambroxol syrup 2-3 times daily.
Route of Administration: Oral
Ambroxol exerted a biphasic response in surfactant secretion, with a significant increase at low concentrations (1 - 10 uM) and an inhibition at high concentrations (≥ 0.1 mM), which is beyond reported plasma Ambroxol concentrations in blood
Name Type Language
AMBROXOL ACEFYLLINATE
MART.   WHO-DD  
Common Name English
Ambroxol Theophyllinate [WHO-DD]
Common Name English
ACEBROPHYLLINE
Common Name English
AMBROMUCIL
Common Name English
7H-PURINE-7-ACETIC ACID, 1,2,3,6-TETRAHYDRO-1,3-DIMETHYL-2,6-DIOXO-, COMPD. WITH TRANS-4-(((2-AMINO-3,5-DIBROMOPHENYL)METHYL)AMINO)CYCLOHEXANOL (1:1)
Systematic Name English
AMBROXOL THEOPHYLLINATE
Common Name English
BRONCOMNES
Common Name English
SURFOLASE
Common Name English
CYCLOHEXANOL, 4-(((2-AMINO-3,5-DIBROMOPHENYL)METHYL)AMINO)-, TRANS-, MONO(1,2,3,6-TETRAHYDRO-1,3-DIMETHYL-2,6-DIOXO-7H-PURINE-7-ACETATE) (SALT)
Systematic Name English
AMBROXOL ACEFYLLINATE [MART.]
Common Name English
AMBROXOL-THEOPHYLLINE-7-ACETATE
Common Name English
Ambroxol acefyllinate [WHO-DD]
Common Name English
Code System Code Type Description
RXCUI
186010
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
ALTERNATIVE
RXCUI
236595
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY RxNorm
FDA UNII
0HM1E174TN
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
CAS
96989-76-3
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
DRUG BANK
DB13141
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
EVMPD
SUB12842MIG
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
EPA CompTox
DTXSID60914235
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY
SMS_ID
100000089018
Created by admin on Fri Dec 15 19:14:33 GMT 2023 , Edited by admin on Fri Dec 15 19:14:33 GMT 2023
PRIMARY