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Details

Stereochemistry ACHIRAL
Molecular Formula C21H23ClN6
Molecular Weight 394.901
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PF-184563

SMILES

CN1CC2=NN=C(C3CCN(CC3)C4=CC=CC=N4)N2C5=CC=C(Cl)C=C5C1

InChI

InChIKey=LXHAZNJVVVBJIF-UHFFFAOYSA-N
InChI=1S/C21H23ClN6/c1-26-13-16-12-17(22)5-6-18(16)28-20(14-26)24-25-21(28)15-7-10-27(11-8-15)19-4-2-3-9-23-19/h2-6,9,12,15H,7-8,10-11,13-14H2,1H3

HIDE SMILES / InChI

Molecular Formula C21H23ClN6
Molecular Weight 394.901
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:56:56 UTC 2023
Edited
by admin
on Sat Dec 16 16:56:56 UTC 2023
Record UNII
UQ326LKZ43
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PF-184563
Code English
8-CHLORO-5-METHYL-1-(3,4,5,6-TETRAHYDRO-2H-(1,2)BIPYRIDINYL-4-YL)-5,6-DIHYDRO-4H-2,3,5,10B-TETRAAZABENZO(E)AZULENE
Systematic Name English
4H-(1,2,4)TRIAZOLO(4,3-A)(1,4)BENZODIAZEPINE, 8-CHLORO-5,6-DIHYDRO-5-METHYL-1-(1-(2-PYRIDINYL)-4-PIPERIDINYL)-
Systematic Name English
8-CHLORO-5,6-DIHYDRO-5-METHYL-1-(1-(2-PYRIDINYL)-4-PIPERIDINYL)-4H-(1,2,4)TRIAZOLO(4,3-A)(1,4)BENZODIAZEPINE
Systematic Name English
12-chloro-8-methyl-3-[1-(pyridin-2-yl)piperidin-4-yl]-2,4,5,8-tetraazatricyclo[8.4.0.0?,?]tetradeca-1(10),3,5,11,13-pentaene
Systematic Name English
PF184563
Code English
Code System Code Type Description
PUBCHEM
11237434
Created by admin on Sat Dec 16 16:56:56 UTC 2023 , Edited by admin on Sat Dec 16 16:56:56 UTC 2023
PRIMARY
CAS
748806-39-5
Created by admin on Sat Dec 16 16:56:56 UTC 2023 , Edited by admin on Sat Dec 16 16:56:56 UTC 2023
PRIMARY
WIKIPEDIA
PF-184563
Created by admin on Sat Dec 16 16:56:56 UTC 2023 , Edited by admin on Sat Dec 16 16:56:56 UTC 2023
PRIMARY
FDA UNII
UQ326LKZ43
Created by admin on Sat Dec 16 16:56:56 UTC 2023 , Edited by admin on Sat Dec 16 16:56:56 UTC 2023
PRIMARY
EPA CompTox
DTXSID601029792
Created by admin on Sat Dec 16 16:56:56 UTC 2023 , Edited by admin on Sat Dec 16 16:56:56 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
ANTAGONIST