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Details

Stereochemistry RACEMIC
Molecular Formula C21H23N
Molecular Weight 289.414
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TACLAMINE

SMILES

[H][C@@]12CCCCN1C[C@@]3([H])C4=C(CCC5=CC=CC2=C35)C=CC=C4

InChI

InChIKey=BFHGFZIDLRXFJE-PMACEKPBSA-N
InChI=1S/C21H23N/c1-2-8-17-15(6-1)11-12-16-7-5-9-18-20-10-3-4-13-22(20)14-19(17)21(16)18/h1-2,5-9,19-20H,3-4,10-14H2/t19-,20-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H23N
Molecular Weight 289.414
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Taclamine is an isoquinoline derivative patented by Ayerst, McKenna and Harrison Ltd. as central nervous system depressant and anti-inflammatory agent. In preclinical models, Taclamine antagonizes the turnover of noradrenaline and dopamine in the rat brain during immobilization stress without effects on brain serotonin turnover

Approval Year

PubMed

PubMed

TitleDatePubMed
Effects of taclamine (AY-22,214), a new psychoactive agent, on catecholamine and serotonin metabolism.
1975 Jan
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:27:54 GMT 2023
Edited
by admin
on Fri Dec 15 18:27:54 GMT 2023
Record UNII
P98BJE9F79
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TACLAMINE
INN  
INN  
Official Name English
TACLAMINE, (4AS-TRANS)-ISOMER
Common Name English
taclamine [INN]
Common Name English
1H-BENZO(6,7)CYCLOHEPTA(1,2,3-DE)PYRIDO(2,1-A)ISOQUINOLINE, 2,3,4,4A,8,9,13B,14-OCTAHYDRO-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C78272
Created by admin on Fri Dec 15 18:27:54 GMT 2023 , Edited by admin on Fri Dec 15 18:27:54 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2111072
Created by admin on Fri Dec 15 18:27:54 GMT 2023 , Edited by admin on Fri Dec 15 18:27:54 GMT 2023
PRIMARY
EPA CompTox
DTXSID901043357
Created by admin on Fri Dec 15 18:27:54 GMT 2023 , Edited by admin on Fri Dec 15 18:27:54 GMT 2023
PRIMARY
EVMPD
SUB10795MIG
Created by admin on Fri Dec 15 18:27:54 GMT 2023 , Edited by admin on Fri Dec 15 18:27:54 GMT 2023
PRIMARY
NCI_THESAURUS
C152486
Created by admin on Fri Dec 15 18:27:54 GMT 2023 , Edited by admin on Fri Dec 15 18:27:54 GMT 2023
PRIMARY
FDA UNII
P98BJE9F79
Created by admin on Fri Dec 15 18:27:54 GMT 2023 , Edited by admin on Fri Dec 15 18:27:54 GMT 2023
PRIMARY
PUBCHEM
76968506
Created by admin on Fri Dec 15 18:27:54 GMT 2023 , Edited by admin on Fri Dec 15 18:27:54 GMT 2023
PRIMARY
SMS_ID
100000083013
Created by admin on Fri Dec 15 18:27:54 GMT 2023 , Edited by admin on Fri Dec 15 18:27:54 GMT 2023
PRIMARY
INN
3274
Created by admin on Fri Dec 15 18:27:54 GMT 2023 , Edited by admin on Fri Dec 15 18:27:54 GMT 2023
PRIMARY
CAS
34061-33-1
Created by admin on Fri Dec 15 18:27:54 GMT 2023 , Edited by admin on Fri Dec 15 18:27:54 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY