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Details

Stereochemistry RACEMIC
Molecular Formula C23H24N2O
Molecular Weight 344.4495
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TAN-67

SMILES

CN1CC[C@@]2(CC3=NC4=C(C=CC=C4)C=C3C[C@H]2C1)C5=CC=CC(O)=C5

InChI

InChIKey=LEPBHAAYNPPRRA-WMZHIEFXSA-N
InChI=1S/C23H24N2O/c1-25-10-9-23(18-6-4-7-20(26)13-18)14-22-17(12-19(23)15-25)11-16-5-2-3-8-21(16)24-22/h2-8,11,13,19,26H,9-10,12,14-15H2,1H3/t19-,23+/m0/s1

HIDE SMILES / InChI

Molecular Formula C23H24N2O
Molecular Weight 344.4495
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.7 nM [EC50]
Substance Class Chemical
Created
by admin
on Wed Apr 02 11:21:44 GMT 2025
Edited
by admin
on Wed Apr 02 11:21:44 GMT 2025
Record UNII
UY7TB22PB7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SB-205607
Preferred Name English
TAN-67
Code English
PHENOL, 3-((4AR,12AS)-1,3,4,5,12,12A-HEXAHYDRO-2-METHYLPYRIDO(3,4-B)ACRIDIN-4A(2H)-YL)-, REL-
Systematic Name English
PHENOL, 3-(1,3,4,5,12,12A-HEXAHYDRO-2-METHYLPYRIDO(3,4-B)ACRIDIN-4A(2H)-YL)-, TRANS-
Systematic Name English
REL-3-((4AR,12AS)-1,3,4,5,12,12A-HEXAHYDRO-2-METHYLPYRIDO(3,4-B)ACRIDIN-4A(2H)-YL)PHENOL
Systematic Name English
SB205607
Code English
REL-(4AS,12AR)-4A-(3-HYDROXYPHENYL)-2-METHYL-1,2,3,4,4A,5,12,12A-OCTAHYDROPYRIDO(3,4-B)ACRIDINE
Systematic Name English
Code System Code Type Description
FDA UNII
UY7TB22PB7
Created by admin on Wed Apr 02 11:21:44 GMT 2025 , Edited by admin on Wed Apr 02 11:21:44 GMT 2025
PRIMARY
EPA CompTox
DTXSID201018434
Created by admin on Wed Apr 02 11:21:44 GMT 2025 , Edited by admin on Wed Apr 02 11:21:44 GMT 2025
PRIMARY
CAS
148545-09-9
Created by admin on Wed Apr 02 11:21:44 GMT 2025 , Edited by admin on Wed Apr 02 11:21:44 GMT 2025
PRIMARY
WIKIPEDIA
TAN-67
Created by admin on Wed Apr 02 11:21:44 GMT 2025 , Edited by admin on Wed Apr 02 11:21:44 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> AGONIST