MDPBP (Chinese Wikipedia)
Analysis of information sources in references of the Wikipedia article "MDPBP" in Chinese language version.
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archive.org (Global: 6th place; Chinese: 2nd place)
- Westphal F, Junge T, Klein B, Fritschi G, Girreser U. Spectroscopic characterization of 3,4-methylenedioxypyrrolidinobutyrophenone: a new designer drug with α-pyrrolidinophenone structure. Forensic Science International. June 2011, 209 (1–3): 126–32. PMID 21316166. doi:10.1016/j.forsciint.2011.01.016.
doi.org (Global: 2nd place; Chinese: 5th place)
- Kolanos R, Solis E, Sakloth F, De Felice LJ, Glennon RA. "Deconstruction" of the abused synthetic cathinone methylenedioxypyrovalerone (MDPV) and an examination of effects at the human dopamine transporter. ACS Chemical Neuroscience. December 2013, 4 (12): 1524–9. PMC 3867964
. PMID 24116392. doi:10.1021/cn4001236. - Westphal F, Junge T, Klein B, Fritschi G, Girreser U. Spectroscopic characterization of 3,4-methylenedioxypyrrolidinobutyrophenone: a new designer drug with α-pyrrolidinophenone structure. Forensic Science International. June 2011, 209 (1–3): 126–32. PMID 21316166. doi:10.1016/j.forsciint.2011.01.016.
espacenet.com (Global: 950th place; Chinese: 938th place)
worldwide.espacenet.com
- DE 1545591,Koeppe H, Zeile K, Ludwig G,「Verfahren zur Herstellung von α-Aminoketonen mit heterocyclischer Aminogruppe」,发表于28 May 1965,发行于7 August 1969,指定于Boehringer Ingelheim
nih.gov (Global: 5th place; Chinese: 3rd place)
ncbi.nlm.nih.gov
- Kolanos R, Solis E, Sakloth F, De Felice LJ, Glennon RA. "Deconstruction" of the abused synthetic cathinone methylenedioxypyrovalerone (MDPV) and an examination of effects at the human dopamine transporter. ACS Chemical Neuroscience. December 2013, 4 (12): 1524–9. PMC 3867964 . PMID 24116392. doi:10.1021/cn4001236.
- Westphal F, Junge T, Klein B, Fritschi G, Girreser U. Spectroscopic characterization of 3,4-methylenedioxypyrrolidinobutyrophenone: a new designer drug with α-pyrrolidinophenone structure. Forensic Science International. June 2011, 209 (1–3): 126–32. PMID 21316166. doi:10.1016/j.forsciint.2011.01.016.