![Pharmaceuticals | Free Full-Text | A Review of Synthetic Access to Therapeutic Compounds Extracted from Psilocybe Pharmaceuticals | Free Full-Text | A Review of Synthetic Access to Therapeutic Compounds Extracted from Psilocybe](https://pub.mdpi-res.com/pharmaceuticals/pharmaceuticals-16-00040/article_deploy/html/images/pharmaceuticals-16-00040-g001-550.jpg?1672209238)
Pharmaceuticals | Free Full-Text | A Review of Synthetic Access to Therapeutic Compounds Extracted from Psilocybe
![Psilocin – The “real deal” or an extraction byproduct - Gutman - Journal of Forensic Sciences - Wiley Online Library Psilocin – The “real deal” or an extraction byproduct - Gutman - Journal of Forensic Sciences - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/572742e3-4948-4ce8-bb05-bf8067069813/jfo15167-fig-0006-m.jpg)
Psilocin – The “real deal” or an extraction byproduct - Gutman - Journal of Forensic Sciences - Wiley Online Library
Synthesis, Structural Characterization, and Pharmacological Activity of Novel Quaternary Salts of 4-Substituted Tryptamines | ACS Omega
![Active Metabolite of Aeruginascin (4-Hydroxy-N,N,N-trimethyltryptamine): Synthesis, Structure, and Serotonergic Binding Affinity. - Abstract - Europe PMC Active Metabolite of Aeruginascin (4-Hydroxy-N,N,N-trimethyltryptamine): Synthesis, Structure, and Serotonergic Binding Affinity. - Abstract - Europe PMC](https://europepmc.org/articles/PMC7365549/bin/ao0c02208_0001.jpg)
Active Metabolite of Aeruginascin (4-Hydroxy-N,N,N-trimethyltryptamine): Synthesis, Structure, and Serotonergic Binding Affinity. - Abstract - Europe PMC
![Structure–Activity Relationships for Psilocybin, Baeocystin, Aeruginascin, and Related Analogues to Produce Pharmacological Effects in Mice | ACS Pharmacology & Translational Science Structure–Activity Relationships for Psilocybin, Baeocystin, Aeruginascin, and Related Analogues to Produce Pharmacological Effects in Mice | ACS Pharmacology & Translational Science](https://pubs.acs.org/cms/10.1021/acsptsci.2c00177/asset/images/medium/pt2c00177_0002.gif)
Structure–Activity Relationships for Psilocybin, Baeocystin, Aeruginascin, and Related Analogues to Produce Pharmacological Effects in Mice | ACS Pharmacology & Translational Science
Concise Synthesis of N,N-Dimethyltryptamine and 5-Methoxy-N,N-dimethyltryptamine Starting with Bufotenine from Brazilian Anadena
![Molecules | Free Full-Text | A Comprehensive Analysis of the Metal–Nitrile Bonding in an Organo-Diiron System Molecules | Free Full-Text | A Comprehensive Analysis of the Metal–Nitrile Bonding in an Organo-Diiron System](https://www.mdpi.com/molecules/molecules-26-07088/article_deploy/html/images/molecules-26-07088-g011.png)
Molecules | Free Full-Text | A Comprehensive Analysis of the Metal–Nitrile Bonding in an Organo-Diiron System
![Active Metabolite of Aeruginascin (4-Hydroxy-N,N,N-trimethyltryptamine): Synthesis, Structure, and Serotonergic Binding Affinity | ACS Omega Active Metabolite of Aeruginascin (4-Hydroxy-N,N,N-trimethyltryptamine): Synthesis, Structure, and Serotonergic Binding Affinity | ACS Omega](https://pubs.acs.org/cms/10.1021/acsomega.0c02208/asset/images/medium/ao0c02208_0003.gif)
Active Metabolite of Aeruginascin (4-Hydroxy-N,N,N-trimethyltryptamine): Synthesis, Structure, and Serotonergic Binding Affinity | ACS Omega
![Pharmaceuticals | Free Full-Text | A Review of Synthetic Access to Therapeutic Compounds Extracted from Psilocybe Pharmaceuticals | Free Full-Text | A Review of Synthetic Access to Therapeutic Compounds Extracted from Psilocybe](https://www.mdpi.com/pharmaceuticals/pharmaceuticals-16-00040/article_deploy/html/images/pharmaceuticals-16-00040-g002.png)
Pharmaceuticals | Free Full-Text | A Review of Synthetic Access to Therapeutic Compounds Extracted from Psilocybe
![4-acetoxy DMT (fumarate) (4-acetoxy-N,N-Dimethyltryptamine, O-Acetylpsilocin, Psilacetin, CAS Number: 1217230-42-6) | Cayman Chemical 4-acetoxy DMT (fumarate) (4-acetoxy-N,N-Dimethyltryptamine, O-Acetylpsilocin, Psilacetin, CAS Number: 1217230-42-6) | Cayman Chemical](https://www.caymanchem.com/images/catalog/screen/35188.png)