ABT 724 trihydrochloride
CAS No. 587870-77-7
ABT 724 trihydrochloride( —— )
Catalog No. M27497 CAS No. 587870-77-7
ABT 724 trihydrochloride is an effective and selective agonist of the D4 receptor (EC50 = 12.4 nM, 14.3 nM, and 23.2 nM for human, rat and ferret, respectively). ABT-724 trihydrochloride can be used in erectile dysfunction studies.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 35 | In Stock |
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| 5MG | 32 | In Stock |
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| 10MG | 56 | In Stock |
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| 25MG | 122 | In Stock |
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| 50MG | 184 | In Stock |
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| 100MG | 276 | In Stock |
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| 200MG | 411 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameABT 724 trihydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionABT 724 trihydrochloride is an effective and selective agonist of the D4 receptor (EC50 = 12.4 nM, 14.3 nM, and 23.2 nM for human, rat and ferret, respectively). ABT-724 trihydrochloride can be used in erectile dysfunction studies.
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DescriptionABT 724 trihydrochloride is an effective and selective agonist of the D4 receptor (EC50 = 12.4 nM, 14.3 nM, and 23.2 nM for human, rat and ferret, respectively). ABT-724 trihydrochloride can be used in erectile dysfunction studies.(In Vitro):A weak affinity to 5-HT1A receptors (Ki = 2780 nM) is observed. ABT 724 trihydrochloride(10 μM) exhibits a selective biochemical profile, as indicated by a lack of binding affinity for >70 neurotransmitter/uptake/ion channels including D2, D3, or D5 receptors. ABT 724 trihydrochloride(10 μM) does not inhibit the PDE activity of PDE1, PDE5, or PDE6.(In Vivo):In male adult Wistar rats, ABT 724 trihydrochloride (8.8 μg/kg; s.c.) treatment facilitated penile erection in a dose-dependent manner.
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In VitroABT-724 exhibits a selective biochemical profile, as indicates by a lack of binding affinity for >70 neurotransmitter/uptake/ion channels including D2, D3, or D5 receptors up to a 10 μM concentration. A weak affinity to 5-HT1A receptors (Ki = 2780 nM) is observed. ABT-724 does not inhibit the PDE activity of PDE1, PDE5, or PDE6 at 10 μM concentrations.
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In VivoABT-724 (8.8 μg/kg; subcutaneous injection; daily; for 5 days; male adult Wistar rats) treatment dose-dependently facilitates penile erection when given s.c. to conscious rats. Animal Model:Male adult Wistar rats (~300 g) Dosage:8.8 μg/kg Administration:Subcutaneous injection; daily; for 5 days Result:Dose-dependently facilitated penile erection.
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Synonyms——
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PathwayGPCR/G Protein
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TargetDopamine Receptor
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RecptorM4 mAChR
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Research Area——
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Indication——
Chemical Information
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CAS Number587870-77-7
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Formula Weight402.7
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Molecular FormulaC17H22Cl3N5
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : ≥ 100 mg/mL (248.29 mM))
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SMILESC1CN(CCN1CC2=NC3=CC=CC=C3N2)C4=CC=CC=N4.Cl.Cl.Cl
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Lei Zhang, et al. 5,7-dihydro-pyrrolo-pyridine derivatives for treating neurological and neurodegenerative diseases. WO2018002760A1
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