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Details

Stereochemistry RACEMIC
Molecular Formula C16H22Cl2N2O
Molecular Weight 329.265
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of U-47700

SMILES

CN(C)[C@H]1CCCC[C@@H]1N(C)C(=O)C2=CC(Cl)=C(Cl)C=C2

InChI

InChIKey=JGPNMZWFVRQNGU-GJZGRUSLSA-N
InChI=1S/C16H22Cl2N2O/c1-19(2)14-6-4-5-7-15(14)20(3)16(21)11-8-9-12(17)13(18)10-11/h8-10,14-15H,4-7H2,1-3H3/t14-,15-/m0/s1

HIDE SMILES / InChI
Molecular Formula C16H22Cl2N2O
Molecular Weight 329.265
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
139594
Substance Class Chemical
Created
by admin
on Sat Dec 16 11:21:48 UTC 2023
Edited
by admin
on Sat Dec 16 11:21:48 UTC 2023
Record UNII
6IY4WX208T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
U-47700
Code English
pinky
Common Name English
3,4-DICHLORO-N-(2-(DIMETHYLAMINO)CYCLOHEXYL)-N-METHYLBENZAMIDE
Systematic Name English
U4
Common Name English
pink heroin
Common Name English
BENZAMIDE, 3,4-DICHLORO-N-(2-(DIMETHYLAMINO)CYCLOHEXYL)-N-METHYL-, TRANS-
Systematic Name English
U-4
Common Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-U-47700
Created by admin on Sat Dec 16 11:21:48 UTC 2023 , Edited by admin on Sat Dec 16 11:21:48 UTC 2023
DEA NO. 9547
Created by admin on Sat Dec 16 11:21:48 UTC 2023 , Edited by admin on Sat Dec 16 11:21:48 UTC 2023
Code System Code Type Description
WIKIPEDIA
U-47700
Created by admin on Sat Dec 16 11:21:48 UTC 2023 , Edited by admin on Sat Dec 16 11:21:48 UTC 2023
PRIMARY
CAS
121348-98-9
Created by admin on Sat Dec 16 11:21:48 UTC 2023 , Edited by admin on Sat Dec 16 11:21:48 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
CAS
82657-23-6
Created by admin on Sat Dec 16 11:21:48 UTC 2023 , Edited by admin on Sat Dec 16 11:21:48 UTC 2023
PRIMARY
SMS_ID
100000167006
Created by admin on Sat Dec 16 11:21:48 UTC 2023 , Edited by admin on Sat Dec 16 11:21:48 UTC 2023
PRIMARY
FDA UNII
6IY4WX208T
Created by admin on Sat Dec 16 11:21:48 UTC 2023 , Edited by admin on Sat Dec 16 11:21:48 UTC 2023
PRIMARY
EPA CompTox
DTXSID001014181
Created by admin on Sat Dec 16 11:21:48 UTC 2023 , Edited by admin on Sat Dec 16 11:21:48 UTC 2023
PRIMARY
PUBCHEM
71719125
Created by admin on Sat Dec 16 11:21:48 UTC 2023 , Edited by admin on Sat Dec 16 11:21:48 UTC 2023
PRIMARY
EVMPD
SUB181325
Created by admin on Sat Dec 16 11:21:48 UTC 2023 , Edited by admin on Sat Dec 16 11:21:48 UTC 2023
PRIMARY
Related Record Type Details
MU-TYPE OPIOID RECEPTOR
TARGET -> AGONIST
Emax 85.9 percent of Fentanyl
EC50
MU-TYPE OPIOID RECEPTOR
TARGET -> AGONIST
BINDING
Ki
KAPPA-TYPE OPIOID RECEPTOR
TARGET->WEAK AGONIST
EC50
Structure of U-47700 S-isomer
ENANTIOMER -> RACEMATE
Related Record Type Details
Structure of N-DESMETHYL U-47700
METABOLITE INACTIVE -> PARENT
MAJOR
Structure of N‐Didesmethyl U‐47700
METABOLITE INACTIVE -> PARENT
MAJOR
Related Record Type Details
Structure of U-47700
ACTIVE MOIETY
NIH
NCATS
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