BTO-1

BTO-1
  • CAS No.:40647-02-7

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
  3. The purchaser must not use this product, or supply it to another party, for personal consumption, sports or fitness, weight loss, health supplements, food, or animal feed.
Other grades of this product :
BTO-1 Basic information
Product Name:BTO-1
Synonyms:BTO-1;5-Cyano-7-nitro-2-benzothiazolecarboxamide-3-oxide;Polo-like Kinase Inhibitor II, BTO-1;Polo-like Kinase Inhibitor II, BTO-1 - CAS 40647-02-7 - Calbiochem
CAS:40647-02-7
MF:C9H4N4O4S
MW:264.22
EINECS:
Product Categories:
Mol File:40647-02-7.mol
BTO-1 Chemical Properties
storage temp. 2-8°C
solubility H2O: <2ML/mL
form solid
color tan
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36/37
WGK Germany 3
MSDS Information
BTO-1 Usage And Synthesis
UsesBTO-1 is a benzothiazolo-N-oxide Plk1 inhibitor.
General DescriptionA cell-permeable benzothiazolo-N-oxide compound that targets the ATP-binding pocket of polo-like kinase and is shown to inhibit Plk1 kinase activity in cell-free kinase assays (IC50 = 8.0 μM) and suppress the phosphorylation of cellular Plk1 substrate Cdc25C in rat kangaroo kidney-derived PTK cells (75% inhibition at 6.3 μM). BTO-1 treatment of cultured cells results in mitosis defects consistent with loss-of-Plk1 phenotypes seen in Plk1 RNAi-treated U20S cells, including the appearance of monopolar spindles and the reduction of γ-tubulin at the centrosomes. Plk1 inhibition by BTO-1 in HeLa cells results in a blockage of Rho and Rho-GEF recruitment, which is essential for the assembly of a functional contractile ring.
Biochem/physiol ActionsBTO-1 is a polo-like kinase (Plk) inhibitor.
BTO-1 Preparation Products And Raw materials

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