• synthesis
  • The method is based on the measurement of the incorporation of bromouridine (as the uridine analogue) into the nascent RNA during RNA synthesis inhibition (RSI) induced by the stalling of RNA polymerases at DNA lesions on the transcribed DNA strand, which triggers transcription-coupled nucleotide excision repair (TC-NER). (go.jp)
  • The synthesis of 5-methyl-MDA can be found online. (wikipedia.org)
  • In 1912 Dr. Anton Köllisch was requested to develop a patentable synthesis for 3-methyl-hydrastinine. (wikidoc.org)
  • chemical
  • To identify gene expression that can be closely involved in chemical-induced hepatocellular hypertrophy, the hepatic gene expression profile was assessed by cDNA microarray analysis in male F344 rats fed for 3 days, 4 weeks, and 13 weeks a diet containing a hepatocellular hypertrophy inducer, either phenobarbital (500 ppm), clofibrate (2,500 ppm), or piperonyl butoxide (20,000 ppm). (go.jp)
  • When we tested chemical agents (camptothecin, etoposide, 4-nitroquinoline-1-oxide, mitomycin C, methyl methanesulfonate, and cisplatin) in HeLa cells by the method, RSI indicative of genomic toxicity was observed in the nucleoli of the tested cells. (go.jp)
  • The designation of gamma butyrolactone or any other chemical as a listed chemical pursuant to subdivision 802(34) or 802(35) of Title 21 of the United States Code does not preclude a finding pursuant to this subdivision that the chemical is a controlled substance analogue. (ncleg.net)
  • 2014) 3-Naphthoylindazoles and 2-naphthoylbenzoimidazoles as novel chemical groups of synthetic cannabinoids: chemical structure elucidation, analytical characterists and identification of the first representatives in smoke mixtures. (blogspot.com)
  • 6-MAPDB (1-(2,3-dihydrobenzofuran-6-yl)-N-methylpropan-2-amine) is a chemical compound which might be an entactogenic drug. (wikipedia.org)
  • known
  • In his book PiHKAL (Phenethylamines i Have Known And Loved), the dosage range is listed as 150-230 mg and the duration is listed as 4-8 hours. (wikipedia.org)
  • legally
  • 5-Methyl-MDA is not scheduled at the federal level in the United States , but it is possible that 5-Methyl-MDA could legally be considered an analog of MDA , in which case, sales or possession could potentially be prosecuted under the Federal Analogue Act . (wikipedia.org)
  • safrole
  • Wacker oxidation of safrole to yield 3,4-methylenedioxyphenylpropan-2-one (MDP2P) followed by reductive amination or via reduction of its oxime. (wikipedia.org)
  • Safrole (4-allyl-1,2-methylenedioxybenzene or shikimol) is a phenylpropene. (wikipedia.org)
  • Safrole itself is an acetal which is readily hydrolysed in acidic solutions to give 4-allylpyrocatechol and formaldehyde (or formaldehyde polymers). (wikipedia.org)
  • effects
  • 3] The most common side effects are cardiovascular, such as fast or irregular heartbeat, and psychological, such as anxiety. (pearltrees.com)
  • substance
  • 3a) 'Commission' means the Commission for Mental Health, Developmental Disabilities, and Substance Abuse Services established under Part 4 of Article 3 of Chapter 143B of the General Statutes. (ncleg.net)
  • 4) 'Control' means to add, remove, or change the placement of a drug, substance, or immediate precursor included in Schedules I through VI of this Article. (ncleg.net)
  • 3. The physical appearance of the tablets, capsules or other finished product containing the substance is substantially identical to a specified controlled substance. (ncleg.net)
  • Maximum 3 years imprisonment Schedule IV: It is not an indictable offence to possess a Schedule IV substance for personal use. (wikipedia.org)
  • substances
  • 4] Circa 1993, the DEA added cathinone to the Controlled Substances Act's Schedule I. Dextroamphetamine. (pearltrees.com)
  • least
  • The DEA also reports that there have been at least 3 documented deaths involving AB-PINACA. (blogspot.com)
  • method
  • This is reduced to the 2-aminoindan following a modification of Nichols' earlier method from a paper discussing DOM analogues, using a Pd/C catalyst in glacial acetic acid with catalytic H2SO4. (wikipedia.org)
  • name
  • 3] It was used in the Soviet Union during the 1930s and 1940s as an anti-depressant (under the name Эфедрон-ephedrone). (pearltrees.com)
  • days
  • Reflux conditions were maintained for 3 days, and then after cooling in an ice bath, the excess hydride was destroyed with the careful addition of H2O. (psychotropicon.info)