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Molybdenum disulfide | CAS:1317-33-5
Molybdenum disulfide
  • Name:Molybdenum disulfide
  • CAS:1317-33-5
  • Synonyms:Molybdenum disulphide
  • Molecular Formula:MoS2
  • Molecular Weight:160.07
  • EINESC:215-263-9

Description

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Safety

SDS/MSDS S22;S24/25

SDS

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Peer-Reviewed Papers
Synthesis and evaluation of heteroaryl-ketone derivatives as a novel class of VEGFR-2 inhibitors.Eugene L Piatnitski Chekler et al.Bioorganic & medicinal chemistry letters, 18(15), 4344-4347 (2008-07-22) Discovery of a novel class of PPARdelta partial agonists.Barry G Shearer et al.Bioorganic & medicinal chemistry letters, 18(18), 5018-5022 (2008-08-30) Meanwell, N., A.; et al. Bioorganic & Medicinal Chemistry Letters, 20, 1460-1460 (2010) Engineering Styrene Monooxygenase for Biocatalysis: Reductase-Epoxidase Fusion Proteins.Thomas Heine et al.Applied biochemistry and biotechnology, 181(4), 1590-1610 (2016-11-11) Indole ring oxidation by activated leukocytes prevents the production of hypochlorous acid.V F Ximenes et al.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 38(11), 1575-1583 (2005-11-01) Synthesis of 3,3-diindolyl oxyindoles efficiently catalysed by FeCl3 and their in vitro evaluation for anticancer activity.Ahmed Kamal et al.Bioorganic & medicinal chemistry letters, 20(17), 5229-5231 (2010-08-03) Fluorescence of protonated excited-state forms of 5-hydroxytryptamine (serotonin) and related indoles.R F Chen Proceedings of the National Academy of Sciences of the United States of America, 60(2), 598-605 (1968-06-01) Tryptophan 2,3-dioxygenase (TDO) inhibitors. 3-(2-(pyridyl)ethenyl)indoles as potential anticancer immunomodulators.Eduard Dolusić et al.Journal of medicinal chemistry, 54(15), 5320-5334 (2011-07-06) Identification of potent ITK inhibitors through focused compound library design including structural information.Matthias Herdemann et al.Bioorganic & medicinal chemistry letters, 20(23), 6998-7003 (2010-10-23) Synthesis and evaluation of 3-aroylindoles as anticancer agents: metabolite approach.Yu-Shan Wu et al.Journal of medicinal chemistry, 52(15), 4941-4945 (2009-07-10)
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