M. Young

发表

Biphenylsulfonamide endothelin receptor antagonists. 4. Discovery of N-[[2'-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1'-biphenyl]- 2-yl]methyl]-N,3,3-trimethylbutanamide (BMS-207940), a highly potent and orally active ET(A) selective antagonist.

Ping Chen, S. Spergel, S. Chong, 2003, Journal of medicinal chemistry.

Bacterial production of 7-formamidocephalosporins. Isolation and structure determination.

M. Young, R. Sykes, C. Cimarusti, 1984, The Journal of antibiotics.

Phosphinyl acid-based bisubstrate analog inhibitors of Ras farnesyl protein transferase.

M. Barbacid, B. Seizinger, M. Young, 1995, Journal of medicinal chemistry.

Synthesis of 6-methylthiopenicillins and 7-heteroatom-substituted cephalosporins.

M. Young, P. Funke, J. E. Dolfini, 1973, The Journal of organic chemistry.

BMS-200475, a novel carbocyclic 2′-deoxyguanosine analog with potent and selective anti-hepatitis B virus activity in vitro

O. Kocy, M. Young, R. Colonno, 1997 .

Synthesis of 2-, 4-, and 7-methylthio-substituted cephalosporins

M. Young, P. Funke, J. E. Dolfini, 1979 .

Synthesis of SQ-33,054, a novel cyclobutane nucleoside with potent antiviral activity

M. Young, G. Bisacchi, R. Zahler, 1989 .

Monobactams. The conversion of 6-APA to (S)-3-amino-2-oxoazetidine-1-sulfonic acid and its 3 (RS)-methoxy derivative

M. Young, D. Floyd, H. W. Chang, 1982 .

Synthesis of 2-, 4-, and 7-methylthio-substituted cephalosporins

M. Young, P. Funke, J. E. Dolfini, 1979 .

Oxidation of organic compounds with cerium(IV). IX. Formation of 2-methyltetrahydrofuran by oxidation of 1-pentanol☆

M. Young, W. S. Trahanovsky, Paul M. Nave, 1969 .

(±)-(1α,2β,3α)-9-[2,3-bis(hydroxymethyl)cyclobutyl]guanine [(±)-BHCG or SQ 33 054]: A potent and selective inhibitor of herpesviruses

M. Young, J. Clark, K. Mazina, 1990 .

Diastereomeric 7-ureidoacetyl cephalosporins. I. Superiority of 7alpha-H-L-isomers over D-isomers.

M. Young, H. Schneider, H. Basch, 1978, The Journal of antibiotics.

Analysis of diastereomeric 7-ureidoacetamido cephalosporins by high-performance liquid chromatography

M. Young, 1978 .

Broad-spectrum antiviral activity of the acyclic guanosine phosphonate (R,S)-HPMPG.

M. Young, K. Mazina, M. Haffey, 1988, Antiviral research.

Synthesis and antiviral activity of 1-cyclobutyl-5-(2-bromovinyl)uracil nucleoside analogues and related compounds.

M. Young, G. Bisacchi, J. Tino, 1992, Journal of medicinal chemistry.

Diastereomeric 7-ureidoacetyl cephalosporins. II. 7beta [[[(Aminocarbonyl) amino]-2-thienylacetyl] amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl) thio] methyl]-8-oxo-5-thia-1-azabicyclo [4.2.0] oct-2-ene-2-carboxylic acid.

M. Young, M. Ondetti, J. E. Dolfini, 1978, Journal of antibiotics (Tokyo. 1968).

Hydroxamic acid-based bisubstrate analog inhibitors of Ras farnesyl protein transferase.

M. Young, E. Gordon, S. Robinson, 1996, Journal of medicinal chemistry.

Broad-spectrum antiviral activity of the acyclic guanosine phosphonate (R,S)-HPMPG.

M. Young, K. Mazina, M. Haffey, 1988, Antiviral research.