Page last updated: 2024-09-04

vx 497 and bms-337197

vx 497 has been researched along with bms-337197 in 3 studies

Compound Research Comparison

Studies
(vx 497)
Trials
(vx 497)
Recent Studies (post-2010)
(vx 497)
Studies
(bms-337197)
Trials
(bms-337197)
Recent Studies (post-2010) (bms-337197)
2537600

Protein Interaction Comparison

ProteinTaxonomyvx 497 (IC50)bms-337197 (IC50)
Inosine-5'-monophosphate dehydrogenase 2Homo sapiens (human)0.015

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Barrish, JC; Bednarz, MS; Berry, KK; Chen, BC; Cheney, DL; Dhar, TG; Fleener, CA; Gu, HH; Guo, J; Harper, TW; Hollenbaugh, DL; Iwanowicz, EJ; Liu, C; MacMaster, JF; McIntyre, KW; Miller, LM; Pitts, WJ; Rouleau, KA; Shen, Z; Sherbina, NZ; Shuster, DJ; Tredup, JA; Watterson, SH; Witmer, MR; Zhao, R1
Ballentine, SK; Barrish, JC; Chen, P; Dhar, TG; Fleener, CA; Gu, HH; Hollenbaugh, DL; Iwanowicz, EJ; Norris, D; Rouleau, KA; Shen, Z; Townsend, R; Watterson, SH1
Beevers, RE; Buckley, GM; Davies, N; Fraser, JL; Galvin, FC; Hannah, DR; Haughan, AF; Jenkins, K; Mack, SR; Pitt, WR; Ratcliffe, AJ; Richard, MD; Sabin, V; Sharpe, A; Williams, SC1

Other Studies

3 other study(ies) available for vx 497 and bms-337197

ArticleYear
Discovery of N-[2-[2-[[3-methoxy-4-(5-oxazolyl)phenyl]amino]-5-oxazolyl]phenyl]-N-methyl-4- morpholineacetamide as a novel and potent inhibitor of inosine monophosphate dehydrogenase with excellent in vivo activity.
    Journal of medicinal chemistry, 2002, May-23, Volume: 45, Issue:11

    Topics: Animals; Antibody Formation; Arthritis, Experimental; Enzyme Inhibitors; Enzyme-Linked Immunosorbent Assay; IMP Dehydrogenase; Male; Mice; Mice, Inbred BALB C; Morpholines; Mycophenolic Acid; Oxazoles; Rats; Rats, Inbred Lew; Structure-Activity Relationship

2002
3-cyanoindole-based inhibitors of inosine monophosphate dehydrogenase: synthesis and initial structure-activity relationships.
    Bioorganic & medicinal chemistry letters, 2003, Oct-20, Volume: 13, Issue:20

    Topics: Catalysis; Enzyme Inhibitors; IMP Dehydrogenase; Indoles; Kinetics; Structure-Activity Relationship

2003
Low molecular weight indole fragments as IMPDH inhibitors.
    Bioorganic & medicinal chemistry letters, 2006, May-01, Volume: 16, Issue:9

    Topics: Carbamates; Crystallography, X-Ray; Enzyme Inhibitors; Hydrogen Bonding; IMP Dehydrogenase; Indoles; Models, Molecular; Molecular Structure; Molecular Weight; Oxazoles; Phenylurea Compounds; Sensitivity and Specificity; Structure-Activity Relationship

2006