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Details

Stereochemistry ACHIRAL
Molecular Formula C15H19N3O
Molecular Weight 257.3309
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CP-94253

SMILES

CCCOC1=CC=C2NC=C(C2=N1)C3=CCNCC3

InChI

InChIKey=KWQWBZIGHIOKIO-UHFFFAOYSA-N
InChI=1S/C15H19N3O/c1-2-9-19-14-4-3-13-15(18-14)12(10-17-13)11-5-7-16-8-6-11/h3-5,10,16-17H,2,6-9H2,1H3

HIDE SMILES / InChI

Molecular Formula C15H19N3O
Molecular Weight 257.3309
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P08908
Gene ID: 3350.0
Gene Symbol: HTR1A
Target Organism: Homo sapiens (Human)
89.0 nM [Ki]
Target ID: P28222
Gene ID: 3351.0
Gene Symbol: HTR1B
Target Organism: Homo sapiens (Human)
2.0 nM [Ki]
Target ID: P28221
Gene ID: 3352.0
Gene Symbol: HTR1D
Target Organism: Homo sapiens (Human)
49.0 nM [Ki]
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:41:09 GMT 2023
Edited
by admin
on Sat Dec 16 17:41:09 GMT 2023
Record UNII
FYC6YY5RYL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CP-94253
Code English
1H-Pyrrolo[3,2-b]pyridine, 5-propoxy-3-(1,2,3,6-tetrahydro-4-pyridinyl)-
Systematic Name English
5-Propoxy-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-pyrrolo[3,2-b]pyridine
Systematic Name English
CP94253
Code English
Code System Code Type Description
FDA UNII
FYC6YY5RYL
Created by admin on Sat Dec 16 17:41:09 GMT 2023 , Edited by admin on Sat Dec 16 17:41:09 GMT 2023
PRIMARY
PUBCHEM
4029677
Created by admin on Sat Dec 16 17:41:09 GMT 2023 , Edited by admin on Sat Dec 16 17:41:09 GMT 2023
PRIMARY
EPA CompTox
DTXSID10470073
Created by admin on Sat Dec 16 17:41:09 GMT 2023 , Edited by admin on Sat Dec 16 17:41:09 GMT 2023
PRIMARY
WIKIPEDIA
CP-94253
Created by admin on Sat Dec 16 17:41:09 GMT 2023 , Edited by admin on Sat Dec 16 17:41:09 GMT 2023
PRIMARY
CAS
131084-35-0
Created by admin on Sat Dec 16 17:41:09 GMT 2023 , Edited by admin on Sat Dec 16 17:41:09 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
TARGET -> AGONIST
TARGET -> AGONIST