Back to Search
DAVID BOGER, M.D.
M.D.
Psychiatry Physician
NPI: 1609171016Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
248496(NY)
Research & Publications (20)
Discovery of inhibitors of aberrant gene transcription from Libraries of DNA binding molecules: inhibition of LEF-1-mediated gene transcription and oncogenic transformation.
PMID 19216569·J Am Chem Soc·2009
7-preclinical
The isolation, total synthesis and structure elucidation of chlorofusin, a natural product inhibitor of the p53-mDM2 protein-protein interaction.
PMID 19642417·Nat Prod Rep·2009
6-review
Blockade of endocannabinoid-degrading enzymes attenuates neuropathic pain.
PMID 19502530·J Pharmacol Exp Ther·2009
7-preclinical
Fundamental relationships between structure, reactivity, and biological activity for the duocarmycins and CC-1065.
PMID 19639994·J Med Chem·2009
6-review
Total synthesis of vinblastine, vincristine, related natural products, and key structural analogues.
PMID 19292450·J Am Chem Soc·2009
7-preclinical
Design, synthesis, and evaluation of an alpha-helix mimetic library targeting protein-protein interactions.
PMID 19334711·J Am Chem Soc·2009
7-preclinical
Characterization of lassa virus cell entry inhibitors: determination of the active enantiomer by asymmetric synthesis.
PMID 19428249·Bioorg Med Chem Lett·2009
8-other
Synthesis and evaluation of vancomycin aglycon analogues that bear modifications in the N-terminal D-leucyl amino acid.
PMID 19209892·J Med Chem·2009
8-other
CSI-FID: high throughput label-free detection of DNA binding molecules.
PMID 19435662·Bioorg Med Chem Lett·2009
8-other
Endocannabinoid modulation of scratching response in an acute allergenic model: a new prospective neural therapeutic target for pruritus.
PMID 19168707·J Pharmacol Exp Ther·2009
7-preclinical
Total synthesis and evaluation of iso-duocarmycin SA and iso-yatakemycin.
PMID 19154178·J Am Chem Soc·2009
7-preclinical
Structure-activity relationship studies of fostriecin, cytostatin, and key analogs, with PP1, PP2A, PP5, and( beta12-beta13)-chimeras (PP1/PP2A and PP5/PP2A), provide further insight into the inhibitory actions of fostriecin family inhibitors.
PMID 19592665·J Pharmacol Exp Ther·2009
4-observational
Correlation of inhibitor effects on enzyme activity and thermal stability for the integral membrane protein fatty acid amide hydrolase.
PMID 18644727·Bioorg Med Chem Lett·2008
7-preclinical
Total synthesis of chlorofusin, its seven chromophore diastereomers, and key partial structures.
PMID 18712872·J Am Chem Soc·2008
8-other
Yatakemycin: total synthesis, DNA alkylation, and biological properties.
PMID 18389136·Nat Prod Rep·2008
8-other
Exploration of a fundamental substituent effect of alpha-ketoheterocycle enzyme inhibitors: Potent and selective inhibitors of fatty acid amide hydrolase.
PMID 18639454·Bioorg Med Chem Lett·2008
8-other
Optimization of the central heterocycle of alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase.
PMID 18630870·J Med Chem·2008
7-preclinical
Unique small molecule entry inhibitors of hemorrhagic fever arenaviruses.
PMID 18474596·J Biol Chem·2008
7-preclinical
Asymmetric synthesis of inhibitors of glycinamide ribonucleotide transformylase.
PMID 18686942·J Med Chem·2008
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
- 138 W 25TH ST, SUITE 622
NEW YORK, NY 10001 - Phone
- (917) 574-7541
Quick Facts
- NPI
- 1609171016
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile