637360-23-7

Upstream product

• 823-85-8 4-fluorophenyhydrazine hydrochloride 
• 637362-28-8 1-[(E)-3-(4-chloro-phenyl)-allyl]-piperidin-4-one 
• 177-11-7 4,4-ethylenedioxy-piperidine 
• 103979-29-9 (E)-1-(4-chlorophenyl)-3-chloropropene 

Downstream Products

• 637361-79-6 1-[carboxylic acid (2-methoxyethyl)amide]-5-chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,4'-piperidine] 
• 637359-71-8 (E)-(1'-(3-(4-chlorophenyl)allyl)-5-fluorospiro[indoline-3,4'-piperidin]-1-yl)(2-chloropyridin-4-yl)methanone 

Relevant academic research and scientific papers

Do spiroindolines have the potential to replace vesamicol as lead compound for the development of radioligands targeting the vesicular acetylcholine transporter?

The vesicular acetylcholine transporter (VAChT) is an important target for in vivo imaging of neurodegenerative processes using positron emission tomography (PET). So far the development of VAChT PET radioligands is based on the single known lead compound

SPIROINDOLINEPIPERIDINE DERIVATIVES

Insecticidal, acaricidal, nematicidal or molluscicidal compounds of formula (I) wherein Y is a single bond, C=O, C=S or C=(O)q where q is 0, 1 or 2; and R1, R2, R3, R4, R8, R9 an