Vincent J. Colandrea, Ph.D.

Affiliations: 
2002 Rutgers University, New Brunswick, New Brunswick, NJ, United States 
Area:
Organic Chemistry
Google:
"Vincent Colandrea"
Mean distance: (not calculated yet)
 

Parents

Sign in to add mentor
Leslie S. Jimenez grad student 2002 Rutgers, New Brunswick
 (I. Progress toward the synthesis of mitomycin C. II. Synthesis and reactions of C(2)-symmetric vinylsulfonium salts.)
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Wilson JE, Kurukulasuriya R, Reibarkh M, et al. (2016) Discovery of Novel Indoline Cholesterol Ester Transfer Protein Inhibitors (CETP) through a Structure-Guided Approach. Acs Medicinal Chemistry Letters. 7: 261-5
Neelamkavil SF, Agrawal S, Bara T, et al. (2016) Discovery of MK-8831, A Novel Spiro-Proline Macrocycle as a Pan-Genotypic HCV-NS3/4a Protease Inhibitor. Acs Medicinal Chemistry Letters. 7: 111-6
Vachal P, Miao S, Pierce JM, et al. (2012) 1,3,8-Triazaspiro[4.5]decane-2,4-diones as efficacious pan-inhibitors of hypoxia-inducible factor prolyl hydroxylase 1-3 (HIF PHD1-3) for the treatment of anemia. Journal of Medicinal Chemistry. 55: 2945-59
Yan L, Colandrea VJ, Hale JJ. (2010) Prolyl hydroxylase domain-containing protein inhibitors as stabilizers of hypoxia-inducible factor: small molecule-based therapeutics for anemia. Expert Opinion On Therapeutic Patents. 20: 1219-45
Du W, Jewell JP, Lin LS, et al. (2009) Synthesis and evaluation of N-[(1S,2S)-3-(4-chlorophenyl)-2-(3-cyanophenyl)-1-methylpropyl]-2-methyl-2-aminopropanamide as human cannabinoid-1 receptor (CB1R) inverse agonists. Bioorganic & Medicinal Chemistry Letters. 19: 5195-9
Armstrong HE, Galka A, Lin LS, et al. (2007) Substituted acyclic sulfonamides as human cannabinoid-1 receptor inverse agonists. Bioorganic & Medicinal Chemistry Letters. 17: 2184-7
Colandrea VJ, Legiec IE, Huo P, et al. (2006) 2,5-Disubstituted pyrrolidine carboxylates as potent, orally active sphingosine-1-phosphate (S1P) receptor agonists. Bioorganic & Medicinal Chemistry Letters. 16: 2905-8
Colandrea VJ, Rajaraman S, Jimenez LS. (2003) Synthesis of the mitomycin and FR900482 ring systems via dimethyldioxirane oxidation. Organic Letters. 5: 785-7
Stearns RA, Miller RR, Tang W, et al. (2002) The pharmacokinetics of a thiazole benzenesulfonamide beta 3-adrenergic receptor agonist and its analogs in rats, dogs, and monkeys: improving oral bioavailability. Drug Metabolism and Disposition: the Biological Fate of Chemicals. 30: 771-7
Biftu T, Feng DD, Liang GB, et al. (2000) Synthesis and SAR of benzyl and phenoxymethylene oxadiazole benzenesulfonamides as selective beta3 adrenergic receptor agonist antiobesity agents. Bioorganic & Medicinal Chemistry Letters. 10: 1431-4
See more...