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Details

Stereochemistry RACEMIC
Molecular Formula C19H28N4O2
Molecular Weight 344.4512
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ADB-PINACA

SMILES

CCCCCN1N=C(C(=O)NC(C(N)=O)C(C)(C)C)C2=C1C=CC=C2

InChI

InChIKey=FWTARAXQGJRQKN-UHFFFAOYSA-N
InChI=1S/C19H28N4O2/c1-5-6-9-12-23-14-11-8-7-10-13(14)15(22-23)18(25)21-16(17(20)24)19(2,3)4/h7-8,10-11,16H,5-6,9,12H2,1-4H3,(H2,20,24)(H,21,25)

HIDE SMILES / InChI

Molecular Formula C19H28N4O2
Molecular Weight 344.4512
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:09:08 GMT 2025
Edited
by admin
on Mon Mar 31 23:09:08 GMT 2025
Record UNII
U1Q4F41C9U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DEA NO. 7035
Preferred Name English
ADB-PINACA
Common Name English
1H-INDAZOLE-3-CARBOXAMIDE, N-(1-(AMINOCARBONYL)-2,2-DIMETHYLPROPYL)-1-PENTYL-
Systematic Name English
N-(1-AMINO-3,3-DIMETHYL-1-OXOBUTAN-2-YL)-1-PENTYL-1H-INDAZOLE-3-CARBOXAMIDE
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-ADB-PINACA
Created by admin on Mon Mar 31 23:09:08 GMT 2025 , Edited by admin on Mon Mar 31 23:09:08 GMT 2025
DEA NO. 7035
Created by admin on Mon Mar 31 23:09:08 GMT 2025 , Edited by admin on Mon Mar 31 23:09:08 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID301010007
Created by admin on Mon Mar 31 23:09:08 GMT 2025 , Edited by admin on Mon Mar 31 23:09:08 GMT 2025
PRIMARY
FDA UNII
U1Q4F41C9U
Created by admin on Mon Mar 31 23:09:08 GMT 2025 , Edited by admin on Mon Mar 31 23:09:08 GMT 2025
PRIMARY
CAS
1633766-73-0
Created by admin on Mon Mar 31 23:09:08 GMT 2025 , Edited by admin on Mon Mar 31 23:09:08 GMT 2025
PRIMARY
WIKIPEDIA
ADB-PINACA
Created by admin on Mon Mar 31 23:09:08 GMT 2025 , Edited by admin on Mon Mar 31 23:09:08 GMT 2025
PRIMARY
PUBCHEM
86280478
Created by admin on Mon Mar 31 23:09:08 GMT 2025 , Edited by admin on Mon Mar 31 23:09:08 GMT 2025
PRIMARY
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ACTIVE MOIETY