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

Details

Stereochemistry RACEMIC
Molecular Formula C18H29NO3
Molecular Weight 307.4278
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTAMIRATE

SMILES

CCC(C(=O)OCCOCCN(CC)CC)C1=CC=CC=C1

InChI

InChIKey=DDVUMDPCZWBYRA-UHFFFAOYSA-N
InChI=1S/C18H29NO3/c1-4-17(16-10-8-7-9-11-16)18(20)22-15-14-21-13-12-19(5-2)6-3/h7-11,17H,4-6,12-15H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C18H29NO3
Molecular Weight 307.4278
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:06:19 UTC 2023
Edited
by admin
on Sat Dec 16 17:06:19 UTC 2023
Record UNII
M75MZG2236
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTAMIRATE
INN   MI   WHO-DD  
INN  
Official Name English
BUTAMIRATE [MI]
Common Name English
BENZENEACETIC ACID, .ALPHA.-ETHYL-2-(2-(DIETHYLAMINO)ETHOXY)ETHYL ESTER
Common Name English
butamirate [INN]
Common Name English
CODIMIN
Brand Name English
2-(2-(DIETHYLAMINO)ETHOXY)ETHYL 2-PHENYLBUTYRATE
Systematic Name English
Butamirate [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66917
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
WHO-VATC QR05DB13
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
WHO-ATC R05DB13
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
Code System Code Type Description
EVMPD
SUB06000MIG
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
RXCUI
19862
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID7048403
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
WIKIPEDIA
BUTAMIRATE
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
PUBCHEM
28892
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
ChEMBL
CHEMBL1332546
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
NCI_THESAURUS
C81596
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
MESH
C006841
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
DRUG BANK
DB13731
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
MERCK INDEX
m2786
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
242-005-2
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
DRUG CENTRAL
442
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
INN
2704
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
SMS_ID
100000088476
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
CAS
18109-80-3
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
FDA UNII
M75MZG2236
Created by admin on Sat Dec 16 17:06:20 UTC 2023 , Edited by admin on Sat Dec 16 17:06:20 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY