| Identification | Back Directory | [Name]
BD 1008 Dihydrobromide | [CAS]
138356-09-9 | [Synonyms]
BD-1008 HBr
BD 1008 (hydrobromide)
N-[2-(3,4-Dichlorophenyl)ethyl]-N-Methyl-1-pyrrolidineethanaMine DihydrobroMide | [Molecular Formula]
C15H22Cl2N2 | [MDL Number]
MFCD00209903 | [MOL File]
138356-09-9.mol | [Molecular Weight]
301.255 |
| Chemical Properties | Back Directory | [storage temp. ]
Store at -20°C | [solubility ]
Soluble in H2O | [form ]
solid | [color ]
White to off-white | [Water Solubility ]
Soluble to 50 mM in water |
| Hazard Information | Back Directory | [Uses]
An α receptor antagonist, attenuating the biochemical effects of cocaine. Also studied was this compounds ability to prevent neuropathic pain following chemotherapy. | [Biological Activity]
bd 1008 dihydrobromide is a potent and selective ligand for σ-receptor with ki values of 2 and 8 nm for σ-1 receptor and σ-2 receptor, respectively [1].σ-receptor is a type of opioid receptor. there are two subtypes of σ-receptor: σ-1 and σ-2 [2].bd 1008 dihydrobromide is a potent and selective σ-receptor ligand. bd1008 showed high affinity to sites labeled by 4-[125i]pemp with ki value of 5.06 nm in guinea pig brain membranes. in mcf-7 breast cancer and melanoma (a375) cells, 4-[125i]pemp inhibited the binding of bd1008 with ki value of 11 nm in a dose-dependent way [2]. in xenopus oocytes coexpressed n-methyl-d-aspartate (nmda) receptor (nr) 1a with either nr2a, 2b or 2c, bd1008 inhibited nmda-activated membrane current responses with ic50 values of 62, 18 and 120 μm for nr1a/2a, nr1a/2b and nr1a/2c respectively, which were due to direct effects on the receptor channel complex [3].in mice, bd1008 (1 mg/kg) inhibited cocaine-induced locomotor activity with ed50 value increased from 6.50 mg/kg to 11.19 mg/kg [1]. | [References]
[1]. mccracken ka, bowen wd, matsumoto rr. novel sigma receptor ligands attenuate the locomotor stimulatory effects of cocaine. eur j pharmacol, 1999, 365(1): 35-38.
[2]. john cs, gulden me, vilner bj, et al. synthesis, in vitro validation and in vivo pharmacokinetics of [125i]n-[2-(4-iodophenyl)ethyl]-n-methyl-2-(1-piperidinyl) ethylamine: a high-affinity ligand for imaging sigma receptor positive tumors. nucl med biol, 1996, 23(6): 761-766.
[3]. whittemore er, ilyin vi, woodward rm. antagonism of n-methyl-d-aspartate receptors by sigma site ligands: potency, subtype-selectivity and mechanisms of inhibition. j pharmacol exp ther, 1997, 282(1): 326-338. |
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