U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C8H11N7S
Molecular Weight 237.285
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMBAZONE

SMILES

NC(=N)NN=C1C=CC(C=C1)=NNC(N)=S

InChI

InChIKey=MLMFUKWWZIZRHX-UWRPRBHNSA-N
InChI=1S/C8H11N7S/c9-7(10)14-12-5-1-3-6(4-2-5)13-15-8(11)16/h1-4H,(H4,9,10,14)(H3,11,15,16)/b12-5-,13-6+

HIDE SMILES / InChI

Molecular Formula C8H11N7S
Molecular Weight 237.285
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Ambazone (1,4-benzoquinone guanylhydrazone thiosemicarbazone) is an antibacterial agent. It exerts antitumor activity both in vitro and in vivo. Ambazone is indicated in the treatment of infections of the mouth and throat, including tonsillitis, gingivitis, stomatitis, as well as after tonsillectomy, after tooth extraction.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

Faringosept (ambazone 10 mg). 3-5 tablets daily for 3-4 days. The tablets should be sucked slowly. The tablets should not be swallowed but allowed to slowly dissolve in the mouth. Use 15-30 minutes after a meal; after using the preparation, do not eat or drink fluids for 2-3 hours.
Route of Administration: Topical
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:44:57 GMT 2023
Edited
by admin
on Sat Dec 16 17:44:57 GMT 2023
Record UNII
BYK4592A3Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMBAZONE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
ambazone [INN]
Common Name English
AMBAZONE [MI]
Common Name English
FARINGOSEPT
Brand Name English
AMBAZONE [MART.]
Common Name English
Ambazone [WHO-DD]
Common Name English
HYDRAZINECARBOTHIOAMIDE, 2-(4-(2-(AMINOIMINOMETHYL)HYDRAZINYLIDENE)-2,5-CYCLOHEXADIEN-1-YLIDENE)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C28394
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
NCI_THESAURUS C274
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
WHO-VATC QR02AA01
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
WHO-ATC R02AA01
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
Code System Code Type Description
FDA UNII
BYK4592A3Q
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
NCI_THESAURUS
C72627
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
MERCK INDEX
m552
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY Merck Index
EVMPD
SUB12841MIG
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
MESH
C037931
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
WIKIPEDIA
AMBAZONE
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
DRUG BANK
DB13697
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
CAS
539-21-9
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
SMS_ID
100000077683
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID3046407
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
DRUG CENTRAL
145
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-713-0
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
INN
822
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
PUBCHEM
1549158
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
ChEMBL
CHEMBL2103762
Created by admin on Sat Dec 16 17:44:58 GMT 2023 , Edited by admin on Sat Dec 16 17:44:58 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SOLVATE->ANHYDROUS
Related Record Type Details
ACTIVE MOIETY