Buy bromadol bdpc online

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Buy bromadol bdpc online

Buy bromadol bdpc online (systematic name 4-(4-bromophenyl)-4-(dimethylamino)-1-(2-phenylethyl)cyclohexanol; also known
as bromadol) is a potent narcotic analgesic with a distinctive arylcyclohexylamine chemical structure. It was developed
by Daniel Lednicer at Upjohn in the 1970s. Initial studies estimated that it was around 10,000 times the strength
of morphine in animal models. However, later studies using more modern techniques assigned a value of 504 times the
potency of morphine for the more active trans-isomer.

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To date, it is unknown if this drug (BDPC) has been used by humans, however, it was seized along with three kilograms
of acetylfentanyl in an April 25, 2013 police action in Montreal, Canada, and has reportedly continued to be available
on the designer drug black market internationally. Analogues where the para-bromine is replaced by chlorine or
CH3 retain similar activity, as does the meta-hydroxy derivative.

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Compound trans-4-(p-bromophenyl)-4-(dimethylamino)-1-(2-thiophene2-yl-ethyl)-cyclohexanol (C8813), structurally
unrelated to morphine, ((BDPC) is a novel analgesic. The present study examined the antinociceptivepioid receptor
selectivity and in vitro activity of C8813. The antinociceptive activity was evaluated using mouse hot plate and acetic
acid writhing tests.

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Compound trans-4-(p-bromophenyl)-4-(dimethylamino)-1-(2-thiophene2-yl-ethyl)-cyclohexanol (C8813), structurally
unrelated to morphine, ((BDPC) is a novel analgesic. The present study examined the antinociceptivepioid recepto
electivity and in vitro activity of C8813. The antinociceptive activity was evaluated using mouse hot plate and acetic
acid writhing tests.

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Buy bromadol bdpc online (3), also referred to as BDPC (trans-4-(p-bromophenyl)-4-( Buy bromadol bdpc online )-1-phenethylcyclohexanol), was
among the most potent and efficacious compounds studied here. Using a standard mouse hot plate assay, Liu et al.
(2003). previously suggested that the analgesic potency of bromadol may
be around 2.9 times that of fentanyl (Sharma
et al. 2019). The herein reported in vitro potencies for Barr2 and mini-Gi recruitment echo this, as the EC 50 values
for bromadol were 7.6-and 10.8-fold lower than those obtained for fentanyl using the same respective assays

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However, as discussed further, it remains difficult to directly compare in vivo analgesic potency to in vitro potency
values. Interestingly, the in vivo antinociceptive potency reported by Liu et al. (2003) was greater than what may be
expected based on opioid receptor binding affinity data (Sharma et al. 2019). Although determination of binding
affinity wa
e of the
rent study, the high in vitro effic
y and potency at MOR reported here may

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