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BP 897 hydrochloride

Catalog No. T14767   CAS 314776-92-6

BP 897 is a potent and selective agonist of dopamine D3 receptor and it is a weak dopamine D2 receptor antagonist, with Kis of 0.92 nM and 61 nM for D3 and D2 receptors. Which shows low affinities at D1 and D4 receptors (Kis, 3 and 0.3 μM, respectively).

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BP 897 hydrochloride Chemical Structure
BP 897 hydrochloride, CAS 314776-92-6
Pack Size Availability Price/USD Quantity
1 mg In stock $ 147.00
2 mg In stock $ 198.00
5 mg In stock $ 313.00
10 mg In stock $ 488.00
25 mg In stock $ 785.00
50 mg In stock $ 1,120.00
100 mg In stock $ 1,480.00
500 mg In stock $ 2,950.00
1 mL * 10 mM (in DMSO) In stock $ 359.00
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Purity: 98.00%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description BP 897 is a potent and selective agonist of dopamine D3 receptor and it is a weak dopamine D2 receptor antagonist, with Kis of 0.92 nM and 61 nM for D3 and D2 receptors. Which shows low affinities at D1 and D4 receptors (Kis, 3 and 0.3 μM, respectively).
Targets&IC50 D1:3 μM, D4:0.3 μM(ki), D3:(ki)0.92 nM, D2:61 nM(ki)
In vitro BP 897 inhibits forskolin-induced cyclic AMP accumulation with an EC50 of 1.0 ± 0.3?nM, and increases mitogenesis, another D3-receptor-mediated response (EC50 = 3 ± 1?nM) in NG 108-15 cells expressing the human D3 receptor. However, BP 897 (1?μM) does not inhibit cyclic AMP accumulation or trigger mitogenesis in cells expressing the D2 receptor[1]. With a 70 times lower affinity at the D2 receptor (Ki, 61 nM). BP 897 also weakly binds to α1 and α2 adrenergic receptors (Ki = 60 and 83?nM, respectively), 5HT1A and 5HT7 receptors (Ki = 84 and 345?nM, respectively), and has negligible affinities (Ki > 1?μM) at muscarinic, histamine and opiate receptors.
In vivo BP 897 (0, 0.05, 0.5, 1?mg/kg) inhibits cocaine-seeking behaviour that depends upon the presentation of drug-associated cues, without having any intrinsic, primary rewarding effects[1]. BP 897 binds to D2-receptor in mouse striatum with an ED50 of 15?mg/kg, and the D3-receptor occupancy is blow 0.5?mg/kg.
Molecular Weight 454
Formula C26H32ClN3O2
CAS No. 314776-92-6

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 9 mg/mL (19.82 mM)

TargetMolReferences and Literature

1. Pilla M, et al. Selective inhibition of cocaine-seeking behaviour by a partial dopamine D3 receptor agonist. Nature. 1999 Jul 22;400(6742):371-5.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Anti-Neurodegenerative Disease Compound Library GPCR Compound Library Neurotransmitter Receptor Compound Library Anti-Parkinson's Disease Compound Library Bioactive Compounds Library Max NO PAINS Compound Library Bioactive Compound Library Neuronal Signaling Compound Library

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Keywords

BP 897 hydrochloride 314776-92-6 GPCR/G Protein Neuroscience Dopamine Receptor Inhibitor inhibit stimuli BP-897 behaviour BP897 Hydrochloride addiction rewarding BP 897 BP-897 Hydrochloride BP 897 Hydrochloride cocaine drug-seeking motivational BP897 inhibitor

 

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