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RAINEY MILLET, M.D.
M.D.
Obstetrics & Gynecology Physician
NPI: 1588800403IndividualAccepts Medicare
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
70153(AZ)
CMS Specialties
PrimaryOBSTETRICS/GYNECOLOGY
Education
TEXAS A & M UNIVERSITY SYSTEM, HSC, COLLEGE OF MEDICINE
Class of 2008
Research & Publications (13)
Design, synthesis and biological evaluation of substituted dioxodibenzothiazepines and dibenzocycloheptanes as farnesyltransferase inhibitors.
PMID 17827015·Bioorg Med Chem Lett·2007
7-preclinical
Pharmacomodulations around the 4-oxo-1,4-dihydroquinoline-3-carboxamides, a class of potent CB2-selective cannabinoid receptor ligands: consequences in receptor affinity and functionality.
PMID 17915849·J Med Chem·2007
7-preclinical
Synthesis of a novel conformationally restricted Val-Phe dipeptidomimetic.
PMID 15948143·J Pept Sci·2006
8-other
Solid-phase synthesis and pharmacological evaluation of a library of peptidomimetics as potential farnesyltransferase inhibitors: an approach to new lead compounds.
PMID 16647166·Eur J Med Chem·2006
8-other
Novel 4-oxo-1,4-dihydroquinoline-3-carboxamide derivatives as new CB2 cannabinoid receptors agonists: synthesis, pharmacological properties and molecular modeling.
PMID 16392793·J Med Chem·2006
8-other
Novel N-(4-Piperidinyl)benzamide antimalarials with mammalian protein farnesyltransferase inhibitory activity.
PMID 16204993·Chem Pharm Bull (Tokyo)·2005
7-preclinical
In vitro and in vivo evaluation of two rational-designed nonpeptidic farnesyltransferase inhibitors on HT29 human colon cancer cell lines.
PMID 16925112·Oncol Res·2005
7-preclinical
Synthesis of 5-nitro-2-furancarbohydrazides and their cis-diamminedichloroplatinum complexes as bitopic and irreversible human thioredoxin reductase inhibitors.
PMID 16250662·J Med Chem·2005
7-preclinical
Antitrypanosomal activities and cytotoxicity of 5-nitro-2-furancarbohydrazides.
PMID 12443785·Bioorg Med Chem Lett·2002
7-preclinical
Novel potent substance P and neurokinin A receptor antagonists. Conception, synthesis and biological evaluation of indolizine derivatives.
PMID 12110311·Bioorg Med Chem·2002
7-preclinical
A flexible approach to the design of new potent substance P receptor ligands.
PMID 11480541·J Pharm Pharmacol·2001
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 5533 E BELL ROAD, STE 103
SCOTTSDALE, AZ 85254 - Phone
- (602) 466-1111
Quick Facts
- NPI
- 1588800403
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 18
- Publications
- 13
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