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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H26N4O
Molecular Weight 338.4466
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LISURIDE

SMILES

[H][C@@]12CC3=CNC4=CC=CC(=C34)C1=C[C@@H](CN2C)NC(=O)N(CC)CC

InChI

InChIKey=BKRGVLQUQGGVSM-KBXCAEBGSA-N
InChI=1S/C20H26N4O/c1-4-24(5-2)20(25)22-14-10-16-15-7-6-8-17-19(15)13(11-21-17)9-18(16)23(3)12-14/h6-8,10-11,14,18,21H,4-5,9,12H2,1-3H3,(H,22,25)/t14-,18+/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H26N4O
Molecular Weight 338.4466
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:00:20 UTC 2023
Edited
by admin
on Fri Dec 15 15:00:20 UTC 2023
Record UNII
E0QN3D755O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LISURIDE
INN   MI   WHO-DD  
INN  
Official Name English
Lisuride [WHO-DD]
Common Name English
LYSURIDE
Common Name English
lisuride [INN]
Common Name English
3-(9,10-DIDEHYDRO-6-METHYLERGOLIN-8.ALPHA.-YL)-1,1-DIETHYLUREA
Systematic Name English
LISURIDE [MI]
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 316610
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
WHO-VATC QG02CB02
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
WHO-ATC G02CB02
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
NCI_THESAURUS C38149
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
WHO-ATC N02CA07
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
WHO-VATC QN02CA07
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C82247
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
EVMPD
SUB08535MIG
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
WIKIPEDIA
LISURIDE
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
PUBCHEM
28864
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
CAS
18016-80-3
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
ECHA (EC/EINECS)
241-925-1
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
DRUG CENTRAL
1588
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
FDA UNII
E0QN3D755O
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
ChEMBL
CHEMBL157138
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
IUPHAR
43
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
LACTMED
Lisuride
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
DRUG BANK
DB00589
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
CHEBI
51164
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
INN
3065
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
MERCK INDEX
m6844
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY Merck Index
RXCUI
6446
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY RxNorm
MESH
D008090
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
EPA CompTox
DTXSID3023217
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
SMS_ID
100000082525
Created by admin on Fri Dec 15 15:00:20 UTC 2023 , Edited by admin on Fri Dec 15 15:00:20 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY