GR 125743

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Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: CAS:148547-33-5
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
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Products Intro: Product Name:GR 125743
CAS:148547-33-5
Purity:99.76% Package:1mg;36USD|2mg;51USD|5mg;80USD
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Products Intro: Product Name:GR 125743
CAS:148547-33-5
Package:10 mg;100 mg;2 mg;200 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Aladdin Scientific
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Products Intro: Product Name:GR 125743
CAS:148547-33-5
Purity:>=99% Package:$147.9/10mg;Bulk package Remarks:99%
Company Name: Ascent Scientific  
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Products Intro: Product Name:GR 125743
CAS:148547-33-5
Purity:>99% Package:10mg Remarks:5HT1B/1D antagonist

GR 125743 manufacturers

  • GR 125743
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  • $36.00 / 1mg
  • 2025-11-10
  • CAS:148547-33-5
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  • Purity: 99.76%
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GR 125743 Basic information
Product Name:GR 125743
Synonyms:GR 125743;Benzamide, N-[4-methoxy-3-(4-methyl-1-piperazinyl)phenyl]-3-methyl-4-(4-pyridinyl)-;h5-HT1B,cognitive disorder,h5-HT1D,cardiovascular,GR-125743,GR125743,inhibit,Parkinson's disease,5-HT Receptor,GR 125743,5-hydroxytryptamine Receptor,receptor,Inhibitor,Serotonin Receptor;GR 125743, 5-HT1B/1D antagonist;GR 125743, 10 mM in DMSO
CAS:148547-33-5
MF:C25H28N4O2
MW:416.52
EINECS:
Product Categories:Serotonin
Mol File:148547-33-5.mol
GR 125743 Structure
GR 125743 Chemical Properties
storage temp. 4°C, protect from light
solubility DMSO: 100 mg/mL (240.08 mM)
form Solid
color White to off-white
Safety Information
MSDS Information
GR 125743 Usage And Synthesis
UsesGR 125743 is a selective 5-HT1B/1D receptor antagonist, with pKis of 8.85 and 8.31 for wild-type h5-HT1B and wild-type h5-HT1D, respectively. GR 125743 is used for the research of Parkinson's disease and cardiovascular diseases[1][2].
in vivo

GR 125743 (0.3 mg/kg; i.p.) produces significant decreases in extracellular 5-HT in the frontal cortex of the conscious guinea pig[2].

Animal Model:Male Dunkin Hartley guinea-pigs (350-450 g)[2]
Dosage:0.3 mg/kg
Administration:Intraperitoneal injection
Result:Produced significant transient increases in extracellular 5-HT.
IC 50human 5-HT1B Receptor: 8.85 (pKi); human 5-HT1D Receptor: 8.31 (pKi)
References[1] T Wurch, et al. Induction of a high-affinity ketanserin binding site at the 5-Hydroxytryptamine(1B) receptor by modification of its carboxy-terminal intracellular portion. Characterization of human serotonin 1D and 1B receptors using [3H]-GR-125743, a novel radiolabelled serotonin 5HT1D/1B receptor antagonist. Biochem Pharmacol. 2000 May 1;59(9):1117-21. DOI:10.1016/s0006-2952(99)00416-5
[2] Roberts, C., et al. The role of 5-HT1B/1D receptors in the modulation of 5-hydroxytryptamine levels in the frontal cortex of the conscious guinea pig. European Journal of Pharmacology. 1997 May 12;326(1):23-30. DOI:10.1016/s0014-2999(97)00156-8
GR 125743 Preparation Products And Raw materials
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