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Details

Stereochemistry RACEMIC
Molecular Formula C18H26N2S
Molecular Weight 302.477
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TANDAMINE

SMILES

CCN1C2=C(C=CC=C2)C3=C1C(C)(CCN(C)C)SCC3

InChI

InChIKey=BRPOADLGOFPKKJ-UHFFFAOYSA-N
InChI=1S/C18H26N2S/c1-5-20-16-9-7-6-8-14(16)15-10-13-21-18(2,17(15)20)11-12-19(3)4/h6-9H,5,10-13H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C18H26N2S
Molecular Weight 302.477
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Tandamine was developed as a selective serotonin reuptake inhibitor for the treatment of depression. Tandamine participated in clinical trials in hospitalized depressed patients, where it showed that the well-tolerated drug could be of some benefit for retarded depressions. In addition, was found in human volunteers, that tandamine possessed significant anticholinergic activity, to reduce appetite and to produce sedation. However, this drug has never been marketed.

Approval Year

PubMed

PubMed

TitleDatePubMed
The effects of tandamine, a new potential antidepressant agent, on biogenic amine uptake mechanisms and related activities.
1976 May 15
Effects of tandamine and pirandamine, new potential antidepressants, on the brain uptake of norepinephrine and 5-hydroxytryptamine and related activities.
1976 May 5
Effects of tandamine and pirandamine, selective blockers of biogenic amine uptake mechanisms, on gastric acid secretion and ulcer formation in the rat.
1977 Apr 15
Clinical pharmacological studies of tandamine, a potential antidepressive drug.
1977 Mar 23
Effect of acute and chronic treatment of tandamine, a new heterocyclic antidepressant, on biogenic amine metabolism and related activities.
1979 Sep
Patents

Sample Use Guides

In Vivo Use Guide
was administered in doses from 75 to 200 mg to a group of 20 hospitalized depressed patients.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:13:54 UTC 2023
Edited
by admin
on Sat Dec 16 02:13:54 UTC 2023
Record UNII
6L5FH5A43E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TANDAMINE
INN  
INN  
Official Name English
1-(2-(DIMETHYLAMINO)ETHYL)-9-ETHYL-1,3,4,9-TETRAHYDRO-1-METHYLTHIOPYRANO(3,4-B)-INDOLE
Systematic Name English
THIOPYRANO(3,4-B)INDOLE-1-ETHANAMINE, 9-ETHYL-1,3,4,9-TETRAHYDRO-N,N,1-TRIMETHYL-
Systematic Name English
tandamine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C265
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
Code System Code Type Description
EVMPD
SUB10828MIG
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
PUBCHEM
39187
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
ChEMBL
CHEMBL2110652
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
INN
3639
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
NCI_THESAURUS
C152506
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
CAS
42408-80-0
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
FDA UNII
6L5FH5A43E
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
EPA CompTox
DTXSID70866094
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
MESH
C021259
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
WIKIPEDIA
TANDAMINE
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
SMS_ID
100000082403
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
DRUG BANK
DB09192
Created by admin on Sat Dec 16 02:13:54 UTC 2023 , Edited by admin on Sat Dec 16 02:13:54 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY