Aminothiazole
CAS No. 96-50-4
Aminothiazole( Aminothiazole | 2-aminothiazole | Basedol | NSC 1900 | NSC-1900 | NSC1900 )
Catalog No. M16867 CAS No. 96-50-4
Aminothiazole(2-Aminothiazole) is a beginning point for synthesis of many compounds including sulfur drugs, biocides, fungicides, dyes and chemical reaction accelerators.
Purity : >98% (HPLC)
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Biological Information
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Product NameAminothiazole
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NoteResearch use only, not for human use.
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Brief DescriptionAminothiazole(2-Aminothiazole) is a beginning point for synthesis of many compounds including sulfur drugs, biocides, fungicides, dyes and chemical reaction accelerators.
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DescriptionAminothiazole(2-Aminothiazole) is a beginning point for synthesis of many compounds including sulfur drugs, biocides, fungicides, dyes and chemical reaction accelerators.(In Vitro):Aminothiazole can be used as a thyroid inhibitor in the research of hyperthyroidism and it has antibacterial activity.Aminothiazole can be used for the synthesis of antitubercular and antibacterial agents.
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In VitroAminothiazole can be used as a thyroid inhibitor in the research of hyperthyroidism and it has antibacterial activity.Aminothiazole can be used for the synthesis of antitubercular and antibacterial agents.
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In Vivo——
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SynonymsAminothiazole | 2-aminothiazole | Basedol | NSC 1900 | NSC-1900 | NSC1900
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number96-50-4
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Formula Weight100.14
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Molecular FormulaC3H4N2S
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Purity>98% (HPLC)
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SolubilityEthanol: 20 mg/mL (199.72 mM); Water: 20 mg/mL (199.72 mM); DMSO: 20 mg/mL (199.72 mM)
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SMILESNC1=NC=CS1
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Chemical Namethiazol-2-amine
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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AKOS025692697
AKOS025692697 is a biochemical.
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Guanosine 5'-monopho...
Guanosine monophosphate also known as guanylic acid or 5'-GMP belongs to the class of organic compounds known as purine ribonucleoside monophosphates. In particular L-Glutamic acid and guanosine monophosphate can be biosynthesized from xanthylic acid and L-glutamine; which is catalyzed by the enzyme GMP synthase.
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DCZ0415
DCZ0415 induces antimyeloma activity in vitro, in vivo and in primary cells of drug-resistant myeloma patients. DCZ0415 is a potent TRIP13 inhibitor that can impair the repair of non-homologous end junctions and inhibit NF-κB activity.DCZ0415 (10, 20 μM; 72 hours) showed a marked reduction in colony formation, indicating that it inhibited cell proliferation.