User:Etienne Robillard/Notebook/Schiff base
< User:Etienne Robillard | Notebook
Introduction to Schiff bases
- Insert text here in scientifically acceptable way (ie: without grammar errors) to explain the functions and basics of Schiff base formation. 
Schiff bases conjugated pharmacological intermediates and N-substituted heterocyclics carbenes
- Present summarly the basic psychopharmacological aspects/functions of imine in a biological system .
- pharmacological intermediates (N-substituted heterocyclics)
- Nucleophilic carbonyl addition
- PS: Yb(OTf)3 route to 1,2,3,4-tetrahydroisoquinolines derivatives.
- Micheal addition=>PS (Pictet-Spengler asymmetric synthesis of 1,2,3,4-tetrahydroisoquinolines)
Schiff bases as quorum sensing molecules (AHL) and Serine-dependent osmolitic regulators/ATP synthase
- Question 1 : In your own words, explain at least 2 functions of the envZ/30C6HSL (ATP-dependent) synthetase in E. coli.
- Question 2 : How is EnvZ relevant to CES (ADA) and specifically the CAMK2G gene?
- Note: Further info on Phenylmethylamine substituted beta-amyloid ligands (APP) are here.
- Question 3 (bonus question) : In your own words, describe the role of a synthase enzyme (without the help of Wikipedia!) in the phosphorylation of ATP.
Formation of phenylmethylamine as the tautomeric form of a ethyl-methyl carbanion
- For the long story, see Phenylmethylamine: A nucleophilic Schiff base where the N-substituted anion is fused to a benzene ring (?) to yield a enamine. See also Ethanamine. Note that the C=N double bond is the result (product) of asymmetric synthesis (Micheal addition) in presence of a organometal catalyst.
- assert biological relevance of Parkinson disease  as the result of prolonged 1,2,3,4-tetrahydroisoquinolines derivatives absorption: A 2-phenylmethylamine-specific enatiomer ?
- Additional data is provided in EC 22.214.171.124 to confirm a solid link between Parkinson disease and novel tetrahydroisoquinolines derivatives. -- Check this. -ER
- tristable PD riboswitch abstrachachachatization: Check/verify the tri-stable RNA polymerase repressor functions (LuxR) and AHL evidences in the design of Schiff base conjugated (6xHis tag) psychochemicals to induce (lazy) light-activated mRNA transcription and metabolism. -ER
- Verify this lazy RNA polymerase function: 2ATP+CO2->Ph2CO<=>2(N+2(R)+OH) -ER
- carbanion = cyanide anion
The Monsanto connection: Troika acids
- US6218563 (cyanophosphonamides as recombinant polyhistidine tag)
- US5935542 (cyanophosphonate derivatives compounds as a n-substituted Schiff base) (ie: for binding ca2+/mg2+ ions to a recombinant "fusion" protein...)