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
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-;
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/18680446Curator'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/
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18680446
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.
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CNS Activity
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL2179 |
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Target ID: GO:0043129 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | MUCOSOLVAN Approved UseMUCOSOLVAN (ambroxol hydrochloride) is indicated for secretolytic therapy in acute and chronic bronchopulmonary diseases associated with abnormal mucus secretion and impaired mucus transport. |
PubMed
Title | Date | PubMed |
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Neltenexine tablets in smoking and non-smoking patients with COPD. A double-blind, randomised, controlled study versus placebo. | 2001 Aug |
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Oral neltenexine in patients with obstructive airways diseases: an open, randomised, controlled comparison versus sobrerol. | 2001 Aug |
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Attenuation by ambroxol of monochloramine-enhanced gastric carcinogenesis: a possible prevention against Helicobacter pylori-associated gastric carcinogenesis. | 2001 Jul 26 |
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Transport properties of ionic drugs in the ammonio methacrylate copolymer membranes. | 2001 Mar |
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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 |
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The predictive value of asthma medications to identify individuals with asthma--a study in German general practices. | 2001 Nov |
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Enhanced resistance to Sendai virus infection in DBA/2J mice with a botanical drug combination (Sinupret). | 2001 Sep |
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Immunoassay screening of lysergic acid diethylamide (LSD) and its confirmation by HPLC and fluorescence detection following LSD ImmunElute extraction. | 2002 Apr |
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Pharmacokinetic properties of single-dose loratadine and ambroxol alone and combined in tablet formulations in healthy men. | 2003 Aug |
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Determination of ambroxol in human plasma using LC-MS/MS. | 2003 Jun 1 |
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In vitro inhibition of human neutrophil histotoxicity by ambroxol: evidence for a multistep mechanism. | 2003 Oct |
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[Protective effects of ambroxol on lung injury during cardiacpulmonary bypass in patients undergoing valve replacement]. | 2004 Dec |
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[Management of extensive burn accompanying severe inhalation injury]. | 2004 May |
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[Oxidative and anti-oxidative effects of ambroxol on acute hydrochloric acid-induced lung injury in rats]. | 2004 Oct |
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Determination of ambroxol in an automated multi-pumping pulsed flow system. | 2005 Apr |
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Adsorptive stripping voltammetric determination of ambroxol. | 2005 Mar |
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Differences in tidal breathing between infants with chronic lung diseases and healthy controls. | 2005 Sep 8 |
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Determination of ambroxol hydrochloride, methylparaben and benzoic acid in pharmaceutical preparations based on sequential injection technique coupled with monolithic column. | 2006 Feb 13 |
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Proteases essential for human influenza virus entry into cells and their inhibitors as potential therapeutic agents. | 2007 |
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Solid-state chemistry of ambroxol theophylline-7-acetate. | 2007 May |
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Action of neltenexine on anion secretion in human airway epithelia. | 2007 May 18 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugs.com/ambroxol.html
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
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26560688
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
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186010
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236595
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0HM1E174TN
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96989-76-3
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DB13141
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SUB12842MIG
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DTXSID60914235
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100000089018
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ACTIVE MOIETY
PARENT (SALT/SOLVATE)
SUBSTANCE RECORD