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Details

Stereochemistry ACHIRAL
Molecular Formula C9H9N3S.ClH
Molecular Weight 227.714
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMIPHENAZOLE HYDROCHLORIDE

SMILES

Cl.NC1=NC(N)=C(S1)C2=CC=CC=C2

InChI

InChIKey=AGSXNJJBDIOXIP-UHFFFAOYSA-N
InChI=1S/C9H9N3S.ClH/c10-8-7(13-9(11)12-8)6-4-2-1-3-5-6;/h1-5H,10H2,(H2,11,12);1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C9H9N3S
Molecular Weight 191.253
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Amiphenazole, a respiratory stimulant, can be used parenteral and oral. Nicholas Laboratories marketed it under the trade name Daptazole. It was used to treat chronic respiratory failure, by increasing ventilation and by reduction of the pCO2 in some patients. Increased ventilation was brought about by an increase in tidal volume rather than an increase in respiratory rate. In combination with bemegride, amiphenazole was used as an antidote for barbiturate, glutethimide overdose, as well as poisoning from other sedative drugs. Now, this drug is used very rarely, because it replaced by more effective drugs.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Daptazole

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Barbiturate poisoning treated with amiphenazole and bemegride.
1956 Nov 10
Treatment of glutethimide poisoning with bemegride and amiphenazole.
1957 Feb 23
Amiphenazole and morphine in production of analgesia.
1958 Aug 9
Massive doses of bemegride and amiphenazole in treatment of barbiturate poisoning.
1958 Mar 29
Use of amiphenazole in respiratory failure.
1962 Jan 27

Sample Use Guides

oral: 100 mg (Daptazole 100) intravenous: 100, 150 mg intramuscular: 75, 100 mg
Route of Administration: Other
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 14:59:07 GMT 2023
Edited
by admin
on Fri Dec 15 14:59:07 GMT 2023
Record UNII
W6W4748LIO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMIPHENAZOLE HYDROCHLORIDE
MART.   WHO-DD  
Common Name English
5-PHENYLTHIAZOLE-2,4-DIAMINE HYDROCHLORIDE
Systematic Name English
AMIPHENAZOLE HCL
Common Name English
NSC-35538
Code English
Amiphenazole hydrochloride [WHO-DD]
Common Name English
AMIPHENAZOLE HYDROCHLORIDE [MART.]
Common Name English
Code System Code Type Description
FDA UNII
W6W4748LIO
Created by admin on Fri Dec 15 14:59:07 GMT 2023 , Edited by admin on Fri Dec 15 14:59:07 GMT 2023
PRIMARY
EVMPD
SUB00473MIG
Created by admin on Fri Dec 15 14:59:07 GMT 2023 , Edited by admin on Fri Dec 15 14:59:07 GMT 2023
PRIMARY
PUBCHEM
24276
Created by admin on Fri Dec 15 14:59:07 GMT 2023 , Edited by admin on Fri Dec 15 14:59:07 GMT 2023
PRIMARY
NSC
35538
Created by admin on Fri Dec 15 14:59:07 GMT 2023 , Edited by admin on Fri Dec 15 14:59:07 GMT 2023
PRIMARY
SMS_ID
100000085159
Created by admin on Fri Dec 15 14:59:07 GMT 2023 , Edited by admin on Fri Dec 15 14:59:07 GMT 2023
PRIMARY
CAS
7635-50-9
Created by admin on Fri Dec 15 14:59:07 GMT 2023 , Edited by admin on Fri Dec 15 14:59:07 GMT 2023
SUPERSEDED
CAS
942-31-4
Created by admin on Fri Dec 15 14:59:07 GMT 2023 , Edited by admin on Fri Dec 15 14:59:07 GMT 2023
PRIMARY
ECHA (EC/EINECS)
213-389-9
Created by admin on Fri Dec 15 14:59:07 GMT 2023 , Edited by admin on Fri Dec 15 14:59:07 GMT 2023
PRIMARY
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