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

Details

Stereochemistry UNKNOWN
Molecular Formula C19H25NO2
Molecular Weight 299.4073
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NYLIDRIN

SMILES

CC(CCC1=CC=CC=C1)NC(C)C(O)C2=CC=C(O)C=C2

InChI

InChIKey=PTGXAUBQBSGPKF-UHFFFAOYSA-N
InChI=1S/C19H25NO2/c1-14(8-9-16-6-4-3-5-7-16)20-15(2)19(22)17-10-12-18(21)13-11-17/h3-7,10-15,19-22H,8-9H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C19H25NO2
Molecular Weight 299.4073
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:35:38 UTC 2023
Edited
by admin
on Sat Dec 16 16:35:38 UTC 2023
Record UNII
695DKH33EI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NYLIDRIN
HSDB   MI   VANDF  
Common Name English
P-HYDROXY-.ALPHA.-(1-((1-METHYL-3-PHENYLPROPYL)AMINO)ETHYL)BENZYL ALCOHOL
Common Name English
BUPHENIN
Common Name English
BENZENEMETHANOL, 4-HYDROXY-.ALPHA.-(1-((1-METHYL-3-PHENYLPROPYL)AMINO)ETHYL)-
Systematic Name English
BUPHENINE
INN   WHO-DD  
INN  
Official Name English
Buphenine [WHO-DD]
Common Name English
NYLIDRIN [VANDF]
Common Name English
buphenine [INN]
Common Name English
NYLIDRIN [MI]
Common Name English
NYLIDRIN [HSDB]
Common Name English
Classification Tree Code System Code
WHO-ATC C04AA02
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
WHO-ATC G02CA02
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
NCI_THESAURUS C48149
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
WHO-VATC QC04AA02
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
WHO-VATC QG02CA02
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
Code System Code Type Description
RXCUI
7595
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY RxNorm
ChEMBL
CHEMBL114655
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
HSDB
3137
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
DRUG CENTRAL
1976
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
WIKIPEDIA
Nylidrin
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
MESH
D009756
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
NCI_THESAURUS
C81642
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
SMS_ID
100000088448
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
ECHA (EC/EINECS)
207-182-2
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
DRUG BANK
DB06152
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
EVMPD
SUB05981MIG
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
MERCK INDEX
m8091
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY Merck Index
FDA UNII
695DKH33EI
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
EPA CompTox
DTXSID4023387
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
CAS
447-41-6
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
PUBCHEM
4567
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
INN
461
Created by admin on Sat Dec 16 16:35:38 UTC 2023 , Edited by admin on Sat Dec 16 16:35:38 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY