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Details

Stereochemistry ACHIRAL
Molecular Formula 2C19H20N2.C10H8O6S2
Molecular Weight 841.048
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEBHYDROLIN NAPADISILATE

SMILES

OS(=O)(=O)C1=CC=CC2=C1C=CC=C2S(O)(=O)=O.CN3CCC4=C(C3)C5=C(C=CC=C5)N4CC6=CC=CC=C6.CN7CCC8=C(C7)C9=C(C=CC=C9)N8CC%10=CC=CC=C%10

InChI

InChIKey=CJUOSBUQOWKEKJ-UHFFFAOYSA-N
InChI=1S/2C19H20N2.C10H8O6S2/c2*1-20-12-11-19-17(14-20)16-9-5-6-10-18(16)21(19)13-15-7-3-2-4-8-15;11-17(12,13)9-5-1-3-7-8(9)4-2-6-10(7)18(14,15)16/h2*2-10H,11-14H2,1H3;1-6H,(H,11,12,13)(H,14,15,16)

HIDE SMILES / InChI

Molecular Formula C19H20N2
Molecular Weight 276.3755
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C10H8O6S2
Molecular Weight 288.297
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Mebhydrolin (INN) or mebhydroline is a histamine H1-receptor antagonist. It is not available in the United States, but it is available in various other countries under the brand names Bexidal and Diazolin. It is used for symptomatic relief of allergic symptoms caused by histamine release, including nasal allergies and allergic dermatosis.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions
PubMed

PubMed

TitleDatePubMed
Cutaneous reaction to oral antihistamine.
2003 Mar
[Indole cleavage with mebhydroline by sodium periodate--part 2. Mechanism of the dilactam formation].
2006 May
Subcorneal pustular dermatosis: 50 years on.
2008 May

Sample Use Guides

Adults and children over 10 years 2-6 tablets daily Children from 5-10 years 2-4 tablets daily Children from 2-5 years 1-3 tablets daily Children up to 2 years 1-2 tablets daily Treatment should be given in several single doses daily.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:02:05 GMT 2023
Edited
by admin
on Fri Dec 15 19:02:05 GMT 2023
Record UNII
O5G04RB25M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEBHYDROLIN NAPADISILATE
JAN   WHO-DD  
Common Name English
MEBHYDROLIN NAPADISILATE [JAN]
Common Name English
Mebhydrolin napadisilate [WHO-DD]
Common Name English
MEBHYDROLINE 1,5-NAPHTHALENEDISULFONATE SALT
MI  
Common Name English
5-BENZYL-1,3,4,5-TETRAHYDRO-2-METHYL-2H-PYRIDO(4,3-B)INDOLE, 1,5-NAPHTHALENEDISULFONATE SALT
Common Name English
MEBHYDROLIN NAPADISYLATE
Common Name English
OMERIL
Brand Name English
DIAZOLINE
Systematic Name English
MEBHYDROLINE 1,5-NAPHTHALENEDISULFONATE SALT [MI]
Common Name English
FABAHISTIN
Brand Name English
Code System Code Type Description
ECHA (EC/EINECS)
228-170-3
Created by admin on Fri Dec 15 19:02:05 GMT 2023 , Edited by admin on Fri Dec 15 19:02:05 GMT 2023
PRIMARY
SMS_ID
100000086162
Created by admin on Fri Dec 15 19:02:05 GMT 2023 , Edited by admin on Fri Dec 15 19:02:05 GMT 2023
PRIMARY
CAS
6153-33-9
Created by admin on Fri Dec 15 19:02:05 GMT 2023 , Edited by admin on Fri Dec 15 19:02:05 GMT 2023
PRIMARY
PUBCHEM
22529
Created by admin on Fri Dec 15 19:02:05 GMT 2023 , Edited by admin on Fri Dec 15 19:02:05 GMT 2023
PRIMARY
ChEMBL
CHEMBL1625607
Created by admin on Fri Dec 15 19:02:05 GMT 2023 , Edited by admin on Fri Dec 15 19:02:05 GMT 2023
PRIMARY
RXCUI
22822
Created by admin on Fri Dec 15 19:02:05 GMT 2023 , Edited by admin on Fri Dec 15 19:02:05 GMT 2023
PRIMARY RxNorm
EPA CompTox
DTXSID3045566
Created by admin on Fri Dec 15 19:02:05 GMT 2023 , Edited by admin on Fri Dec 15 19:02:05 GMT 2023
PRIMARY
MESH
C025079
Created by admin on Fri Dec 15 19:02:05 GMT 2023 , Edited by admin on Fri Dec 15 19:02:05 GMT 2023
PRIMARY
FDA UNII
O5G04RB25M
Created by admin on Fri Dec 15 19:02:05 GMT 2023 , Edited by admin on Fri Dec 15 19:02:05 GMT 2023
PRIMARY
MERCK INDEX
m7109
Created by admin on Fri Dec 15 19:02:05 GMT 2023 , Edited by admin on Fri Dec 15 19:02:05 GMT 2023
PRIMARY Merck Index
EVMPD
SUB03103MIG
Created by admin on Fri Dec 15 19:02:05 GMT 2023 , Edited by admin on Fri Dec 15 19:02:05 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY