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Details

Stereochemistry ACHIRAL
Molecular Formula C18H19ClN4.ClH
Molecular Weight 363.284
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of L-745870 HYDROCHLORIDE

SMILES

Cl.ClC1=CC=C(C=C1)N2CCN(CC3=CNC4=C3C=CC=N4)CC2

InChI

InChIKey=GFFJYISJZJIKAF-UHFFFAOYSA-N
InChI=1S/C18H19ClN4.ClH/c19-15-3-5-16(6-4-15)23-10-8-22(9-11-23)13-14-12-21-18-17(14)2-1-7-20-18;/h1-7,12H,8-11,13H2,(H,20,21);1H

HIDE SMILES / InChI

Molecular Formula C18H19ClN4
Molecular Weight 326.823
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
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
1.0 nM [IC50]
PubMed

PubMed

TitleDatePubMed
Comparative molecular field analysis of dopamine D4 receptor antagonists including 3-[4-(4-chlorophenyl)piperazin-1-ylmethyl]pyrazolo[1,5-a]pyridine (FAUC 113), 3-[4-(4-chlorophenyl)piperazin-1-ylmethyl]-1H-pyrrolo-[2,3-b]pyridine (L-745,870), and clozapine.
2001 Apr 12
Synthesis of potent and selective dopamine D(4) antagonists as candidate radioligands.
2001 Jun 4
Evidence for regulation of body temperature in rats by dopamine D2 receptor and possible influence of D1 but not D3 and D4 receptors.
2003 Jun
Pharmacological and functional characterisation of dopamine D4 receptors in the rat retina.
2003 Jun
Facilitatory effect of the dopamine D4 receptor agonist PD168,077 on memory consolidation of an inhibitory avoidance learned response in C57BL/6J mice.
2003 Jun 16
Effects of L-745,870, a dopamine D4 receptor antagonist, on naloxone-induced morphine dependence in mice.
2004 Oct
Regulation of working memory by dopamine D4 receptor in rats.
2004 Sep
Dopamine D4 receptors inhibit depolarization-induced [3H]GABA release in the rat subthalamic nucleus.
2004 Sep 13
Tonic modulation of inhibition by dopamine D4 receptors in the rat hippocampus.
2005
2-[4-(3,4-Dimethylphenyl)piperazin-1-ylmethyl]-1H benzoimidazole (A-381393), a selective dopamine D4 receptor antagonist.
2005 Jul
A dopamine D4 receptor antagonist attenuates ischemia-induced neuronal cell damage via upregulation of neuronal apoptosis inhibitory protein.
2005 Jul
The combination of nicotine with the D2 antagonist raclopride or the weak D4 antagonist L-745,870 generates a clozapine-like facilitation of NMDA receptor-mediated neurotransmission in pyramidal cells of the rat medial prefrontal cortex.
2005 Jun
D2 dopamine receptor subtype-mediated hyperactivity and amphetamine responses in a model of ADHD.
2010 Jan
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 14:38:22 GMT 2023
Edited
by admin
on Sat Dec 16 14:38:22 GMT 2023
Record UNII
X2UD7T27FU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
L-745870 HYDROCHLORIDE
Code English
3-((4-(4-CHLOROPHENYL)-1-PIPERAZINYL)METHYL)-1H-PYRROLO(2,3-B)PYRIDINE HYDROCHLORIDE
Systematic Name English
1H-PYRROLO(2,3-B)PYRIDINE, 3-((4-(4-CHLOROPHENYL)-1-PIPERAZINYL)METHYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
PUBCHEM
11957618
Created by admin on Sat Dec 16 14:38:22 GMT 2023 , Edited by admin on Sat Dec 16 14:38:22 GMT 2023
PRIMARY
CAS
1173023-36-3
Created by admin on Sat Dec 16 14:38:22 GMT 2023 , Edited by admin on Sat Dec 16 14:38:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID101016928
Created by admin on Sat Dec 16 14:38:22 GMT 2023 , Edited by admin on Sat Dec 16 14:38:22 GMT 2023
PRIMARY
FDA UNII
X2UD7T27FU
Created by admin on Sat Dec 16 14:38:22 GMT 2023 , Edited by admin on Sat Dec 16 14:38:22 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE