Zobrazeno 1 - 10
of 79
pro vyhledávání: '"Scott S. Mitchell"'
Publikováno v:
Journal of pharmaceutical and biomedical analysis. 198
This paper describes a sensitive and selective method for the simultaneous determination of bispinacolato diboron (B
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 198:113987
This paper describes a sensitive and selective method for the simultaneous determination of bispinacolato diboron (B2Pin2) and tetrahydroxy diboron (B2(OH)4) in a small molecule Active Pharmaceutical Ingredient (API) by gas chromatography - mass spec
Autor:
Saskia T. C. Neuteboom, Scott S Mitchell, Barbara C. M. Potts, Jianlin Xu, Gordafaried Deyanat-Yazdi, Sy Teisan, Ta-Hsiang Chao, Katherine Anne Reed, Rama Rao Manam, Kin S. Lam
Publikováno v:
Journal of Natural Products. 70:269-276
Salinosporamide A (NPI-0052; 3), a highly potent inhibitor of the 20S proteasome, is currently in phase I clinical trials for the treatment of cancer. During the course of purifying multigram quantities of 3 from Salinispora tropica fermentation extr
Autor:
Ginger Tsueng, Jianlin Xu, Scott S Mitchell, Barbara C. M. Potts, Katherine A. McArthur, Kin S. Lam
Publikováno v:
The Journal of Antibiotics. 60:13-19
We examined the effects of halogens on the production of salinosporamide A (NPI-0052) by the obligate marine actinomycete Salinispora tropica NPS465, specifically the production of analogs containing halogens other than chlorine. Adding NaF, NaBr and
Autor:
Gordafaried Deyanat-Yazdi, Ta-Hsiang Chao, Paul R. Jensen, Bao Mai, Kin S. Lam, Barbara C. M. Potts, Michael A. Palladino, William Fenical, Saskia T. C. Neuteboom, Katherine Anne Reed, Benjamin Nicholson, Scott S Mitchell, Rama Rao Manam, Venkat R. Macherla
Publikováno v:
Journal of Medicinal Chemistry. 48:3684-3687
Salinosporamide A (1, NPI-0052) is a potent proteasome inhibitor in development for treating cancer. In this study, a series of analogues was assayed for cytotoxicity, proteasome inhibition, and inhibition of NF-kappaB activation. Marked reductions i
Publikováno v:
Tetrahedron. 55:10887-10892
Four novel diterpenoids, spongiabutenolides A – D (2–5), all of which contain a γ-hydroxybutenolide moiety, have been isolated from a Philippines marine sponge of the genus Spongia. The structures of spongiabutenolides A – D (2–5) and the me
Publikováno v:
The Journal of Organic Chemistry. 64:1626-1629
Polyalkyl pyran-4-ones 1a-c were irradiated in methanol or ethanol. Although the expected solvent trapping products 3 could be observed, extended irradiation times allowed exclusive formation of secondary photoproducts 4 and 5 in combined yields of 3
Publikováno v:
Journal of Natural Products. 67:1400-1402
During the course of our screening program designed to discover novel anticancer and anti-infective agents from marine microorganisms, a strain of Streptomyces aureoverticillatus (NPS001583) isolated from a marine sediment was found to produce a nove
Publikováno v:
Tetrahedron Letters. 34:4583-4586
Fused bicyclic 4-pyrones were prepared by condensation of enamines derived from cyclic ketones with diketene or substituted 1,3-dioxin-4-ones. Photolysis in a hydroxylic medium led to bicyclo[n3.0]alkenones bearing oxygenation at both angular positio
Publikováno v:
ChemInform. 24
Fused bicyclic 4-pyrones were prepared by condensation of enamines derived from cyclic ketones with diketene or substituted 1,3-dioxin-4-ones. Photolysis in a hydroxylic medium led to bicyclo[n3.0]alkenones bearing oxygenation at both angular positio