Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

V Aldrich

Showing results (1-10 of 87) with videos related to

Pageof 9
Sort By:
International Journal of Peptide and Protein Research|July 1, 1993
Comparison of methods for the Fmoc solid-phase synthesis and cleavage of a peptide containing both tryptophan and arginineH Choi, J V Aldrich
Organic Letters|February 28, 2003
A solid-phase synthetic strategy for labeled peptides: synthesis of a biotinylated derivative of the delta opioid receptor antagonist TIPP (Tyr-Tic-Phe-Phe-OH)Vivek Kumar, Jane V Aldrich
The Journal of Peptide Research : Official Journal of the American Peptide Society|August 29, 2000
A solid-phase synthetic strategy for the preparation of peptide-based affinity labels: synthesis of dynorphin A analogsL Leelasvatanakij, J V Aldrich
Handbook of Experimental Pharmacology|August 31, 2021
Peptide Kappa Opioid Receptor Ligands and Their Potential for Drug DevelopmentJane V Aldrich, Jay P McLaughlin
Drug Discovery Today. Technologies|January 15, 2013
Opioid Peptides: Potential for Drug DevelopmentJane V Aldrich, Jay P McLaughlin
International Journal of Peptide and Protein Research|March 1, 1994
Side-product formation during cyclization with HBTU on a solid supportS C Story, J V Aldrich
International Journal of Peptide and Protein Research|January 1, 1992
Preparation of protected peptide amides using the Fmoc chemical protocol. Comparison of resins for solid phase synthesisS C Story, J V Aldrich
The AAPS Journal|May 12, 2009
Peptide kappa opioid receptor ligands: potential for drug developmentJane V Aldrich, Jay P McLaughlin
The Journal of Organic Chemistry|December 28, 2019
Optimized Ring Closing Metathesis Reaction Conditions To Suppress Desallyl Side Products in the Solid-Phase Synthesis of Cyclic Peptides Involving Tyrosine(<i>O</i>-allyl)Solomon A Gisemba, Jane V Aldrich
Journal of Medicinal Chemistry|August 23, 2002
Solid phase synthesis and evaluation of Tyr-Tic-Phe-Phe(p-NHCOCH(2)Br) ([Phe(p-bromoacetamide)(4)]TIPP), a potent affinity label for delta opioid receptorsVivek Kumar, Thomas F Murray, Jane V Aldrich
Pageof 9

Showing results (1-10 of 87) with videos related to

Sort By:
Pageof 9
International Journal of Peptide and Protein Research|July 1, 1993
Comparison of methods for the Fmoc solid-phase synthesis and cleavage of a peptide containing both tryptophan and arginineH Choi, J V Aldrich
Organic Letters|February 28, 2003
A solid-phase synthetic strategy for labeled peptides: synthesis of a biotinylated derivative of the delta opioid receptor antagonist TIPP (Tyr-Tic-Phe-Phe-OH)Vivek Kumar, Jane V Aldrich
The Journal of Peptide Research : Official Journal of the American Peptide Society|August 29, 2000
A solid-phase synthetic strategy for the preparation of peptide-based affinity labels: synthesis of dynorphin A analogsL Leelasvatanakij, J V Aldrich
Handbook of Experimental Pharmacology|August 31, 2021
Peptide Kappa Opioid Receptor Ligands and Their Potential for Drug DevelopmentJane V Aldrich, Jay P McLaughlin
Drug Discovery Today. Technologies|January 15, 2013
Opioid Peptides: Potential for Drug DevelopmentJane V Aldrich, Jay P McLaughlin
International Journal of Peptide and Protein Research|March 1, 1994
Side-product formation during cyclization with HBTU on a solid supportS C Story, J V Aldrich
International Journal of Peptide and Protein Research|January 1, 1992
Preparation of protected peptide amides using the Fmoc chemical protocol. Comparison of resins for solid phase synthesisS C Story, J V Aldrich
The AAPS Journal|May 12, 2009
Peptide kappa opioid receptor ligands: potential for drug developmentJane V Aldrich, Jay P McLaughlin
The Journal of Organic Chemistry|December 28, 2019
Optimized Ring Closing Metathesis Reaction Conditions To Suppress Desallyl Side Products in the Solid-Phase Synthesis of Cyclic Peptides Involving Tyrosine(<i>O</i>-allyl)Solomon A Gisemba, Jane V Aldrich
Journal of Medicinal Chemistry|August 23, 2002
Solid phase synthesis and evaluation of Tyr-Tic-Phe-Phe(p-NHCOCH(2)Br) ([Phe(p-bromoacetamide)(4)]TIPP), a potent affinity label for delta opioid receptorsVivek Kumar, Thomas F Murray, Jane V Aldrich
Pageof 9