• N&PD Moderators: Skorpio | thegreenhand

The Neuroscience and Pharmacology Quick Question Thread

*NOTE* Before posting, convert the structure to a SMILES string and run it through Pubchem - https://pubchem.ncbi.nlm.nih.gov

It also shows SIMILER structures and compounds which your material is a substructure of. Pubchem provides REFERENCE.

It's also worth reading Shulgin's work. The ONLY place a halogen goes onto a PEA is at the para position.
 
I just read that antisense peptids show interesting effects and also often also active at the same target as the sense peptides. Does anybody knows more about this?

A review about them, didn’t read it yet:

 
Can someone point me to why indole is most reactive on the 3 position?
 
Can someone point me to why indole is most reactive on the 3 position?



Nucleophilicity of Indole Derivatives:  Activating and Deactivating Effects Based on Proton Affinities and Electron Density Properties
Nicolás Otero, Marcos Mandado, and Ricardo A. Mosquera
View Author Information
Cite this: J. Phys. Chem. A 2007, 111, 25, 5557–5562
Publication Date:June 1, 2007
 
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