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

Details

Stereochemistry RACEMIC
Molecular Formula C21H23N.ClH
Molecular Weight 325.875
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TACLAMINE HYDROCHLORIDE

SMILES

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

InChI

InChIKey=LOSFVNFVCCXCEN-FKLPMGAJSA-N
InChI=1S/C21H23N.ClH/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;1H/t19-,20-;/m0./s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C21H23N
Molecular Weight 289.414
Charge 0
Count
Stereochemistry RACEMIC
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
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:02:45 GMT 2023
Edited
by admin
on Fri Dec 15 15:02:45 GMT 2023
Record UNII
0R94K6TJ5B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TACLAMINE HYDROCHLORIDE
USAN  
USAN  
Official Name English
AY-22214
Code English
TACLAMINE HYDROCHLORIDE [USAN]
Common Name English
AY-22,214
Code English
1H-BENZO(6,7)CYCLOHEPTA(1,2,3-DE)PYRIDO(2,1-A)ISOQUINOLINE, 2,3,4,4A,8,9,13B,14-OCTAHYDRO-, HYDROCHLORIDE
Common Name English
TACLAMINE HYDROCHLORIDE, (4AS-TRANS)-ISOMER (±)-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C78272
Created by admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C152487
Created by admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
PRIMARY
FDA UNII
0R94K6TJ5B
Created by admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
PRIMARY
ChEMBL
CHEMBL2111072
Created by admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
PRIMARY
EPA CompTox
DTXSID70955619
Created by admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
PRIMARY
MESH
C010342
Created by admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
PRIMARY
PUBCHEM
76968505
Created by admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
PRIMARY
CAS
34061-34-2
Created by admin on Fri Dec 15 15:02:45 GMT 2023 , Edited by admin on Fri Dec 15 15:02:45 GMT 2023
PRIMARY
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