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Bd1047 dihydrobromide

Manufactured by Merck Group

BD1047 dihydrobromide is a laboratory chemical compound used in research and development. It is a specific antagonist for the sigma-1 receptor. The core function of BD1047 dihydrobromide is to selectively bind to and block the sigma-1 receptor, which is involved in various physiological and pathological processes.

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3 protocols using bd1047 dihydrobromide

1

Methamphetamine Toxicity Mitigation

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Methamphetamine hydrochloride was purchased from Sigma-Aldrich (St. Louis, MO). M100907 was synthesized by Kenner Rice (Ullrich and Rice, 2000 (link)). BD 1047 dihydrobromide was purchased from Sigma-Aldrich. M100907 was dissolved in sterile water with dropwise addition of 0.1 N hydrochloric acid and sonication until it dissolved. All other drugs were dissolved in physiological saline. All drugs were administered by intraperitoneal (IP) injection at a volume of 0.01 ml per g body weight of each mouse. All doses are reported in the salt form 30 minutes prior to treatment with METH at 78 mg/kg (LD67), mice were administered M100907 (1 and10 mg/kg), BD 1047 (10 mg/kg), or a combination of M100907 (1 mg/kg) and BD 1047 (10 mg/kg), which we subsequently refer to as M100907/BD 1047 (1/10 mg/kg).
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2

In Vitro Cocaine Neuroinflammation Study

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Cocaine hydrochloride and BD1047 dihydrobromide (a highly selective putative Sig1R antagonist) were purchased from Sigma Aldrich (St. Louis, MO.), PRE-084 (2-(4-Morpholinethyl)-1 phenylcyclohexanecarboxylate hydrochloride) at 99.9% purity was obtained from Tocris Pharmaceuticals (Avonmouth, Bristol, UK). The cocaine dose selected for this study (10μM) was based on our previous studies and other viability assays (Zenón-Meléndez et al., 2014 (link)).
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3

Evaluating Cocaine and Sigma-1 Receptor Antagonist Effects

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Cocaine hydrochloride and BD1047 dihydrobromide (a highly selective putative Sig1R antagonist) were purchased from Sigma Aldrich (St. Louis, MO.), PRE-084 (2-(4-Morpholinethyl)-1 phenylcyclohexanecarboxylate hydrochloride) at 99.9% purity was obtained from Tocris Pharmaceuticals (Avonmouth, Bristol, UK). The cocaine dose selected for this study (10 μM) was based on our previous studies and other viability assays (Zenón et al. 2014 (link)).
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