This indazole is substituted at R3 having a carboxamide group. The terminal amine of the carboxamide is bonded to some substituted propyl chain having an aminocarbonyl group at R1 plus a methyl group at R2. Most of these recreational substances had been originally synthesised for biomedical and therapeutic investigation, but https://fubinaca-k264073.thekatyblog.com/29999815/a-review-of-emb-fubinaca