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Details

Stereochemistry RACEMIC
Molecular Formula C16H25NO2.C6H8O7
Molecular Weight 455.4987
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTETAMATE CITRATE

SMILES

OC(=O)CC(O)(CC(O)=O)C(O)=O.CCC(C(=O)OCCN(CC)CC)C1=CC=CC=C1

InChI

InChIKey=VVNURWKSPYZZCI-UHFFFAOYSA-N
InChI=1S/C16H25NO2.C6H8O7/c1-4-15(14-10-8-7-9-11-14)16(18)19-13-12-17(5-2)6-3;7-3(8)1-6(13,5(11)12)2-4(9)10/h7-11,15H,4-6,12-13H2,1-3H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)

HIDE SMILES / InChI

Molecular Formula C6H8O7
Molecular Weight 192.1235
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C16H25NO2
Molecular Weight 263.3752
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Butetamate is a cough suppressant. It exerts antispasmodic, bronchodilator and anticholinergic properties.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
HELIPHENICOL

Approved Use

Acute cough due to variety of causes, especially dry cough, suppression of preoperative and postoperative cough in surgery and bronchoscopy. whooping cough.

Sample Use Guides

Solution containing 3 mg/ml butetamate citrate. Children: 1 ml/kg/day. Adults: 10 ml every 6 hours.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:48:20 GMT 2023
Edited
by admin
on Fri Dec 15 17:48:20 GMT 2023
Record UNII
70430R0X79
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTETAMATE CITRATE
MART.   WHO-DD  
Common Name English
BUTETHAMATE CITRATE [MI]
Common Name English
BUTETAMATE CITRATE [MART.]
Common Name English
BENZENEACETIC ACID, .ALPHA.-ETHYL-, 2-(DIETHYLAMINO)ETHYL ESTER, 2-HYDROXY-1,2,3-PROPANETRICARBOXYLATE (1:1)
Common Name English
NSC-11781
Code English
Butetamate citrate [WHO-DD]
Common Name English
Code System Code Type Description
SMS_ID
100000084859
Created by admin on Fri Dec 15 17:48:20 GMT 2023 , Edited by admin on Fri Dec 15 17:48:20 GMT 2023
PRIMARY
EVMPD
SUB00915MIG
Created by admin on Fri Dec 15 17:48:20 GMT 2023 , Edited by admin on Fri Dec 15 17:48:20 GMT 2023
PRIMARY
ECHA (EC/EINECS)
237-671-6
Created by admin on Fri Dec 15 17:48:20 GMT 2023 , Edited by admin on Fri Dec 15 17:48:20 GMT 2023
PRIMARY
CAS
3639-12-1
Created by admin on Fri Dec 15 17:48:20 GMT 2023 , Edited by admin on Fri Dec 15 17:48:20 GMT 2023
PRIMARY
MERCK INDEX
m2795
Created by admin on Fri Dec 15 17:48:20 GMT 2023 , Edited by admin on Fri Dec 15 17:48:20 GMT 2023
PRIMARY Merck Index
PUBCHEM
117176
Created by admin on Fri Dec 15 17:48:20 GMT 2023 , Edited by admin on Fri Dec 15 17:48:20 GMT 2023
PRIMARY
CAS
13900-12-4
Created by admin on Fri Dec 15 17:48:20 GMT 2023 , Edited by admin on Fri Dec 15 17:48:20 GMT 2023
NON-SPECIFIC STOICHIOMETRY
RXCUI
235943
Created by admin on Fri Dec 15 17:48:20 GMT 2023 , Edited by admin on Fri Dec 15 17:48:20 GMT 2023
PRIMARY RxNorm
NSC
11781
Created by admin on Fri Dec 15 17:48:20 GMT 2023 , Edited by admin on Fri Dec 15 17:48:20 GMT 2023
PRIMARY
FDA UNII
70430R0X79
Created by admin on Fri Dec 15 17:48:20 GMT 2023 , Edited by admin on Fri Dec 15 17:48:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID40930276
Created by admin on Fri Dec 15 17:48:20 GMT 2023 , Edited by admin on Fri Dec 15 17:48:20 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY