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Details

Stereochemistry RACEMIC
Molecular Formula C16H25N3O5
Molecular Weight 339.3868
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of XAMOTEROL

SMILES

OC(CNCCNC(=O)N1CCOCC1)COC2=CC=C(O)C=C2

InChI

InChIKey=DXPOSRCHIDYWHW-UHFFFAOYSA-N
InChI=1S/C16H25N3O5/c20-13-1-3-15(4-2-13)24-12-14(21)11-17-5-6-18-16(22)19-7-9-23-10-8-19/h1-4,14,17,20-21H,5-12H2,(H,18,22)

HIDE SMILES / InChI

Molecular Formula C16H25N3O5
Molecular Weight 339.3868
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 Fri Dec 15 16:07:52 UTC 2023
Edited
by admin
on Fri Dec 15 16:07:52 UTC 2023
Record UNII
7HE0JQL703
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
XAMOTEROL
INN   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
4-MORPHOLINECARBOXAMIDE, N-(2-((2-HYDROXY-3-(4-HYDROXYPHENOXY)PROPYL)AMINO)ETHYL)-, (±)-
Systematic Name English
XAMOTEROL [USAN]
Common Name English
ICI-118587
Code English
XAMOTEROL [MI]
Common Name English
4-MORPHOLINECARBOXAMIDE, N-(2-((2-HYDROXY-3-(4-HYDROXYPHENOXY)PROPYL)AMINO)ETHYL)-, (±)-
Common Name English
(±)-N-(2-((2-HYDROXY-3-(P-HYDROXYPHENOXY)PROPYL)AMINO)ETHYL)-4-MORPHOLINECARBOXAMIDE
Common Name English
xamoterol [INN]
Common Name English
Xamoterol [WHO-DD]
Common Name English
ICI-118,587
Code English
Classification Tree Code System Code
NCI_THESAURUS C48149
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
WHO-VATC QC01CX07
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
WHO-ATC C01CX07
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
Code System Code Type Description
WIKIPEDIA
XAMOTEROL
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
PUBCHEM
155774
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
USAN
U-92
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
EPA CompTox
DTXSID8045222
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
MESH
D017307
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
DRUG CENTRAL
2848
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
FDA UNII
7HE0JQL703
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
CAS
81801-12-9
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
ChEMBL
CHEMBL75753
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
SMS_ID
100000079329
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
MERCK INDEX
m11523
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C81344
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
INN
5271
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
EVMPD
SUB00092MIG
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
DRUG BANK
DB13781
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY
RXCUI
39801
Created by admin on Fri Dec 15 16:07:52 UTC 2023 , Edited by admin on Fri Dec 15 16:07:52 UTC 2023
PRIMARY RxNorm
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
SHORT-ACTING
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY