Back to Search
EDWARD HILLARD, M.D.
M.D.
Specialist
NPI: 1760455950Individual
Specialties, Licenses & Credentials
SpecialistPrimary
Specialist
Code: 174400000X
6906(AL)
Research & Publications (20)
Electrochemical parameters and techniques in drug development, with an emphasis on quinones and related compounds.
PMID 18535688·Chem Commun (Camb)·2008
6-review
The influence of phenolic hydroxy substitution on the electron transfer and anti-cancer properties of compounds based on the 2-ferrocenyl-1-phenyl-but-1-ene motif.
PMID 17992292·Dalton Trans·2007
8-other
A series of unconjugated ferrocenyl phenols: prospects as anticancer agents.
PMID 16892391·ChemMedChem·2006
8-other
Ferrocene-mediated proton-coupled electron transfer in a series of ferrocifen-type breast-cancer drug candidates.
PMID 16312004·Angew Chem Int Ed Engl·2005
8-other
Role of aromatic substituents on the antiproliferative effects of diphenyl ferrocenyl butene compounds.
PMID 19662309·Dalton Trans·2009
7-preclinical
A [3]ferrocenophane polyphenol showing a remarkable antiproliferative activity on breast and prostate cancer cell lines.
PMID 19526991·J Med Chem·2009
8-other
Structural and biological investigation of ferrocene-substituted 3-methylidene-1,3-dihydro-2H-indol-2-ones.
PMID 19173072·Dalton Trans·2009
7-preclinical
Synthesis and structure-activity relationships of ferrocenyl tamoxifen derivatives with modified side chains.
PMID 19053086·Chemistry·2009
8-other
The presence of a ferrocenyl unit on an estrogenic molecule is not always sufficient to generate in vitro cytotoxicity.
PMID 17022106·ChemMedChem·2006
8-other
Metal complex SERMs (selective oestrogen receptor modulators). The influence of different metal units on breast cancer cell antiproliferative effects.
PMID 16402138·Dalton Trans·2006
4-observational
Modification of the estrogenic properties of diphenols by the incorporation of ferrocene. Generation of antiproliferative effects in vitro.
PMID 15943467·J Med Chem·2005
8-other
Selective estrogen receptor modulators in the ruthenocene series. Synthesis and biological behavior.
PMID 15828819·J Med Chem·2005
8-other
New chemistry of the triply bonded divanadium (V2 4+) unit and reduction to an unprecedented V2 3+ core.
PMID 12971778·Inorg Chem·2003
8-other
Observation of symmetry lowering and electron localization in the doublet-states of a spin-frustrated equilateral triangular lattice: Cu3(O2C16H23) x 1.2C6H12.
PMID 12720427·J Am Chem Soc·2003
8-other
Applications of high-field (W-band) EPR to M-M bonded units (M = Cr, Mo): the first confirmed oxidation of a Cr2 4+ paddlewheel complex to a stable isostructural Cr2 5+ product.
PMID 12611500·Inorg Chem·2003
8-other
A highly reduced v(2)(3+) unit with a metal-metal bond order of 3.5.
PMID 12590512·J Am Chem Soc·2003
8-other
The first dirhodium tetracarboxylate molecule without axial ligation: new insight into the electronic structures of molecules with importance in catalysis and other reactions.
PMID 12010037·J Am Chem Soc·2002
8-other
The lengths of molybdenum to molybdenum quadruple bonds: correlations, explanations, and corrections.
PMID 11978114·Inorg Chem·2002
8-other
Filling a void: isolation and characterization of tetracarboxylato dimolybdenum cations.
PMID 11896734·Inorg Chem·2002
8-other
Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions.
PMID 10741955·Am J Hum Genet·2000
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 900 ANNA AVE
TUSCALOOSA, AL 35401 - Phone
- (205) 758-6611
Quick Facts
- NPI
- 1760455950
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile