Efficient and Scalable Enantioselective Synthesis of a Key Intermediate for Rimegepant: An Oral CGRP Receptor Antagonist
Saved in:
Main Authors: | Zhonghua Luo (Author), Guodong Sun (Author), Guowei Wang (Author), Xin Zhang (Author), Yang Zhang (Author), Ji Zhang (Author) |
---|---|
Format: | Book |
Published: |
Georg Thieme Verlag KG,
2024-03-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Antagonism of CGRP Signaling by Rimegepant at Two Receptors
by: Kylie S. Pan, et al.
Published: (2020) -
An Overview of the Synthesis of Hexafluoroisopropanol and Its Key Intermediates
by: Guihua Luo, et al.
Published: (2024) -
Lipidated Calcitonin Gene-Related Peptide (CGRP) Peptide Antagonists Retain CGRP Receptor Activity and Attenuate CGRP Action In Vivo
by: Aqfan Jamaluddin, et al.
Published: (2022) -
Enantioselective Synthesis, Enantiomeric Separations and Chiral Recognition
Published: (2020) -
Rimegepant as an acute treatment in a refractory migraine patient non-responder to two anti-CGRP monoclonal antibodies and triptans: Case report and pharmacological considerations
by: Andrea Burgalassi, et al.
Published: (2024)