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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)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 500MG | 37 | In Stock |
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| 1G | Get Quote | In Stock |
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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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FAPI-2
FAPI-2 is a specific inhibitor of fibroblast-activated protein based on the radiotracer FAP labeling. It has anticancer activity and can be used in the study of pancreatic cancer.
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ELA-32 (human)
Potent, high affinity apelin receptor agonist (IC50 = 0.27 nM; Kd = 0.51 nM). Exhibits no binding GPR15 and GPR25. Activates the PI3K/AKT pathway and promotes self-renewal of hESCs via cell-cycle progression and protein translation. Also potentiates the TGFβ pathway, priming hESCs toward the endoderm lineage. Stimulates angiogenesis in HUVEC cells. Relaxes mouse aortic vessels. Functions as an anorexigenic hormone through activation of the AVP and CRH neurons in the PVN.
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Oxypaeoniflorin
Oxypaeoniflorin is a natural product derived from Radix Paeoniae Rubra and Radix Paeoniae Alba.
