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Details

Stereochemistry ACHIRAL
Molecular Formula C13H18Br2N2O
Molecular Weight 378.103
Optical Activity NONE
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMBROXOL

SMILES

NC1=C(Br)C=C(Br)C=C1CN[C@H]2CC[C@H](O)CC2

InChI

InChIKey=JBDGDEWWOUBZPM-XYPYZODXSA-N
InChI=1S/C13H18Br2N2O/c14-9-5-8(13(16)12(15)6-9)7-17-10-1-3-11(18)4-2-10/h5-6,10-11,17-18H,1-4,7,16H2/t10-,11-

HIDE SMILES / InChI

Molecular Formula C13H18Br2N2O
Molecular Weight 378.103
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:43:02 UTC 2023
Edited
by admin
on Fri Dec 15 15:43:02 UTC 2023
Record UNII
200168S0CL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMBROXOL
INN   MI   WHO-DD  
INN  
Official Name English
ambroxol [INN]
Common Name English
Ambroxol [WHO-DD]
Common Name English
TABCIN
Brand Name English
AMBROXOL [MI]
Common Name English
TRANS-4-((2-AMINO-3,5-DIBROMOBENZYL)AMINO)CYCLOHEXANOL
Systematic Name English
4-HYDROXYDEMETHYLBROMHEXINE, TRANS-
Common Name English
Classification Tree Code System Code
WHO-ATC R03CC63
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
FDA ORPHAN DRUG 262308
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
NCI_THESAURUS C74536
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
NCI_THESAURUS C29767
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
WHO-VATC QR05CB06
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
WHO-ATC R05CB06
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
Code System Code Type Description
DRUG CENTRAL
147
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
NCI_THESAURUS
C74262
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
MERCK INDEX
m1650
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY Merck Index
CAS
18683-91-5
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
RXCUI
625
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY RxNorm
MESH
D000551
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
EVMPD
SUB05397MIG
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
SMS_ID
100000087650
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
WIKIPEDIA
AMBROXOL
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
EPA CompTox
DTXSID8022583
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
DRUG BANK
DB06742
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
FDA UNII
200168S0CL
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
INN
3692
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
ChEMBL
CHEMBL153479
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
ECHA (EC/EINECS)
242-500-3
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
DAILYMED
200168S0CL
Created by admin on Fri Dec 15 15:43:02 UTC 2023 , Edited by admin on Fri Dec 15 15:43:02 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
PARENT -> METABOLITE ACTIVE
When bromhexine is administered orally, the systemic exposure to ambroxol is much lower (;8-fold; Liu et al., 2010), but since the true molecular action of these agents is not entirely known, it cannot be ascertained whether bromhexine or ambroxol, or both, contribute to activity. Ambroxol has also been associated with a reduction in throat pain, which has triggered investigation into the activity of it and bromhexine at sodium channels (such as NaV1.8 and the tetrodotoxin sensitive channel; Leffler et al., 2010).
MAJOR
PLASMA
Related Record Type Details
ACTIVE MOIETY