Skip to main navigation
Skip to search
Skip to main content
Johns Hopkins University Home
Home
Profiles
Research units
Research output
Search by expertise, name or affiliation
An improved synthesis of a selective αvβ
3
-integrin antagonist cyclo(-RGDfK-)
X. Dai, Z. Su,
J. O. Liu
Research output
:
Contribution to journal
›
Article
›
peer-review
35
Scopus citations
Overview
Fingerprint
Fingerprint
Dive into the research topics of 'An improved synthesis of a selective αvβ
3
-integrin antagonist cyclo(-RGDfK-)'. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Medicine & Life Sciences
cyclo-DfKRG
100%
cyclo(arginyl-glycyl-aspartyl-phenylalanyl-valyl)
97%
Solid-Phase Synthesis Techniques
75%
Cyclic Peptides
67%
Integrins
44%
Peptides
30%
Apoptosis
28%
Blood Vessels
27%
Pharmaceutical Preparations
19%
Chemical Compounds
Pentapeptide
57%
Cyclic Peptide
54%
Antagonist
43%
Drug
24%
Purity
23%
Reaction Yield
19%