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CINDY NATIVI, DO
DO
Student in an Organized Health Care Education/Training Program
NPI: 1952140352Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (19)
Pyrrolic tripodal receptors effectively recognizing monosaccharides. Affinity assessment through a generalized binding descriptor.
PMID 17362009·J Am Chem Soc·2007
8-other
Cyclic glycopeptidomimetics through a versatile sugar-based scaffold.
PMID 19395262·Bioorg Med Chem Lett·2009
8-other
Biotin-tagged probes for MMP expression and activation: design, synthesis, and binding properties.
PMID 19275207·Bioconjug Chem·2009
8-other
Inhibition and dispersion of Pseudomonas aeruginosa biofilms by glycopeptide dendrimers targeting the fucose-specific lectin LecB.
PMID 19101469·Chem Biol·2008
8-other
Synthesis, conformational studies, binding assessment and liposome insertion of a thioether-bridged mimetic of the antigen GM3 ganglioside lactone.
PMID 17705308·Chembiochem·2007
8-other
A tricatecholic receptor for carbohydrate recognition: synthesis and binding studies.
PMID 17444686·J Org Chem·2007
8-other
Exploring the subtleties of drug-receptor interactions: the case of matrix metalloproteinases.
PMID 17269766·J Am Chem Soc·2007
8-other
A high-affinity carbohydrate-containing inhibitor of matrix metalloproteinases.
PMID 16892399·ChemMedChem·2006
8-other
A self-assembled pyrrolic cage receptor specifically recognizes beta-glucopyranosides.
PMID 16986191·Angew Chem Int Ed Engl·2006
8-other
O-Methylglucogalloyl esters: synthesis and evaluation of their antimycotic activity.
PMID 16005221·Bioorg Med Chem Lett·2005
8-other
Design in silico, synthesis and binding evaluation of a carbohydrate-based scaffold for structurally novel inhibitors of matrix metalloproteinases.
PMID 15977273·Chembiochem·2005
8-other
A new tripodal receptor for molecular recognition of monosaccharides. A paradigm for assessing glycoside binding affinities and selectivities by 1H NMR spectroscopy.
PMID 15600348·J Am Chem Soc·2004
8-other
A new scaffold for the stereoselective synthesis of alpha-O-linked glycopeptide mimetics.
PMID 15373507·J Org Chem·2004
8-other
Totally stereoselective synthesis of 1,3-disaccharides through Diels-Alder reactions.
PMID 14575481·J Org Chem·2003
8-other
Conformational evaluation of some 4-deoxyhex-4-enopyranose derivatives and their use in the preparation of a previously undescribed class of 3-thio-L-sorbopyranosides and their 6-C-methoxy analogues.
PMID 12526836·Carbohydr Res·2003
8-other
Design, synthesis and biological activity of carbohydrate-containing peptidomimetics as new ligands for the human tachykinin NK-2 receptor.
PMID 12161112·Bioorg Med Chem Lett·2002
7-preclinical
Regiocontrolled synthesis of enantiopure 3,3'-thiosubstituted biphenyls.
PMID 11925205·J Org Chem·2002
8-other
Induction of a preferred sense of twist in flexible diphenyls by carbohydrate scaffolds. Synthesis of two "naked" ellagitannin analogous.
PMID 11749607·J Org Chem·2001
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1731 E 120TH ST
LOS ANGELES, CA 90059 - Phone
- (323) 563-9363
Quick Facts
- NPI
- 1952140352
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 19
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