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Details

Stereochemistry RACEMIC
Molecular Formula C20H20ClN5O3S2
Molecular Weight 477.988
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SURICLONE

SMILES

CN1CCN(CC1)C(=O)OC2N(C(=O)C3=C2SCCS3)C4=CC=C5C=CC(Cl)=NC5=N4

InChI

InChIKey=RMXOUBDDDQUBKD-UHFFFAOYSA-N
InChI=1S/C20H20ClN5O3S2/c1-24-6-8-25(9-7-24)20(28)29-19-16-15(30-10-11-31-16)18(27)26(19)14-5-3-12-2-4-13(21)22-17(12)23-14/h2-5,19H,6-11H2,1H3

HIDE SMILES / InChI

Molecular Formula C20H20ClN5O3S2
Molecular Weight 477.988
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Suriclone is a dithiinopyrrole derivative patented by Rhone-Poulenc S. A. as a sedative and anxiolytic drug. The mechanism of action by which suriclone produces it's sedative and anxiolytic effects is by modulating GABAA receptors, although suriclone is more subtype-selective than most benzodiazepines. In clinical trials, Suriclone shows a significant anxiolytic effect. The most common adverse reaction was dizziness.

Approval Year

PubMed

PubMed

TitleDatePubMed
Objective markers of drug effects on brain function from recordings of scalp potential in healthy volunteers.
2002 Dec
Patents

Patents

Sample Use Guides

0.1, 0.2 and 0.4 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:19:49 GMT 2023
Edited
by admin
on Fri Dec 15 18:19:49 GMT 2023
Record UNII
LNC9G689VR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SURICLONE
INN   MART.   MI  
INN  
Official Name English
RP-31264
Code English
SURICLONE [MI]
Common Name English
RP 31264
Code English
1-PIPERAZINECARBOXYLIC ACID, 4-METHYL-, 6-(7-CHLORO-1,8-NAPHTHYRIDIN-2-YL)-2,3,6,7-TETRAHYDRO-7-OXO-5H-1,4-DITHIINO(2,3-C)PYRROL-5-YL ESTER
Systematic Name English
CELEXANE
Brand Name English
SURIL
Brand Name English
SURICLONE [MART.]
Common Name English
suriclone [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28197
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
NCI_THESAURUS C29710
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
Code System Code Type Description
CAS
53813-83-5
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
EVMPD
SUB10782MIG
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
MESH
C037283
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
WIKIPEDIA
SURICLONE
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
NCI_THESAURUS
C96876
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
MERCK INDEX
m949
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY Merck Index
ChEMBL
CHEMBL2105561
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
EPA CompTox
DTXSID20866362
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
PUBCHEM
40903
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
SMS_ID
100000082987
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
INN
4701
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
ECHA (EC/EINECS)
258-794-1
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
FDA UNII
LNC9G689VR
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
PRIMARY
CAS
104355-41-1
Created by admin on Fri Dec 15 18:19:49 GMT 2023 , Edited by admin on Fri Dec 15 18:19:49 GMT 2023
SUPERSEDED
Related Record Type Details
ACTIVE MOIETY