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

Details

Stereochemistry ABSOLUTE
Molecular Formula C22H25N3O3.C4H6O6
Molecular Weight 529.539
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SOLYPERTINE TARTRATE

SMILES

O[C@H]([C@@H](O)C(O)=O)C(O)=O.COC1=C(C=CC=C1)N2CCN(CCC3=CNC4=C3C=C5OCOC5=C4)CC2

InChI

InChIKey=FDYHSJCNTRLQCR-LREBCSMRSA-N
InChI=1S/C22H25N3O3.C4H6O6/c1-26-20-5-3-2-4-19(20)25-10-8-24(9-11-25)7-6-16-14-23-18-13-22-21(12-17(16)18)27-15-28-22;5-1(3(7)8)2(6)4(9)10/h2-5,12-14,23H,6-11,15H2,1H3;1-2,5-6H,(H,7,8)(H,9,10)/t;1-,2-/m.1/s1

HIDE SMILES / InChI

Molecular Formula C22H25N3O3
Molecular Weight 379.4522
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C4H6O6
Molecular Weight 150.0868
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Solypertine (WIN-18413-2) is an antiadrenergic drug. Solypertine selectively blocked the conditioned avoidance response in rats. Solypertine potentiated hexobarbitone sleeping time, caused hypothermia and afforded protection from amphetamine toxicity inaggregated mice.

CNS Activity

Curator's Comment: Solypertine selectively blocked the conditioned avoidance response in rats. Solypertine potentiated hexobarbitone sleeping time, caused hypothermia and afforded protection from amphetamine toxicity inaggregated mice.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pyscho-sedative properties of three indolyl-ethyl-piperazine derivatives.
1966 Jan
Patents

Sample Use Guides

Mice: LD50 = 81.5 mg/kg. Solypertine (WIN-18413-2) in doses of 4 and 8 mg/kg, caused behavioural depression and apathy in the cats.
Route of Administration: Intraperitoneal
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:11:46 UTC 2023
Edited
by admin
on Fri Dec 15 15:11:46 UTC 2023
Record UNII
LGH2D06D4K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SOLYPERTINE TARTRATE
USAN  
USAN  
Official Name English
WIN-18413-2
Code English
5H-1,3-DIOXOLO(4,5-F)INDOLE, 7-(2-(4-(2-METHOXYPHENYL)-1-PIPERAZINYL)ETHYL)-, (R-(R*,R*))-2,3-DIHYDROXYBUTANEDIOATE (1:1)
Common Name English
7-[2-[4-(O-Methoxyphenyl)-1-piperazinyl]ethyl]-5H-1,3-dioxolo-[4,5-f]-indole tartrate (1:1)
Common Name English
WIN 18,413-2
Code English
SOLYPERTINE TARTRATE [USAN]
Common Name English
NSC-107432
Code English
Classification Tree Code System Code
NCI_THESAURUS C29710
Created by admin on Fri Dec 15 15:11:46 UTC 2023 , Edited by admin on Fri Dec 15 15:11:46 UTC 2023
NCI_THESAURUS C66883
Created by admin on Fri Dec 15 15:11:46 UTC 2023 , Edited by admin on Fri Dec 15 15:11:46 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C152391
Created by admin on Fri Dec 15 15:11:46 UTC 2023 , Edited by admin on Fri Dec 15 15:11:46 UTC 2023
PRIMARY
NSC
107432
Created by admin on Fri Dec 15 15:11:46 UTC 2023 , Edited by admin on Fri Dec 15 15:11:46 UTC 2023
PRIMARY
PUBCHEM
267773
Created by admin on Fri Dec 15 15:11:46 UTC 2023 , Edited by admin on Fri Dec 15 15:11:46 UTC 2023
PRIMARY
FDA UNII
LGH2D06D4K
Created by admin on Fri Dec 15 15:11:46 UTC 2023 , Edited by admin on Fri Dec 15 15:11:46 UTC 2023
PRIMARY
CAS
5591-43-5
Created by admin on Fri Dec 15 15:11:46 UTC 2023 , Edited by admin on Fri Dec 15 15:11:46 UTC 2023
PRIMARY
ChEMBL
CHEMBL1739674
Created by admin on Fri Dec 15 15:11:46 UTC 2023 , Edited by admin on Fri Dec 15 15:11:46 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY