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ChemicalBook > Product Catalogue >Biochemical Engineering >Inhibitors >Cell Cycle >Aurora Kinase Inhibitors >Hesperadin

Hesperadin

Hesperadin Structure
  • ₹7300 - ₹27480
  • Product name: Hesperadin
  • CAS: 422513-13-1
  • MF: C29H32N4O3S
  • MW: 516.65
  • EINECS:200-258-5
  • MDL Number:MFCD18074526
  • Synonyms:(Z)-N-(2-oxo-3-(phenyl(4-(piperidin-1-ylmethyl)phenylamino)methylene)indolin-5-yl)ethanesulfonamide;Hesperadin Hesperadine;N-[2,3-Dihydro-2-oxo-3-[(3Z)-phenyl[[4-(1-piperidinylmethyl)phenyl]amino]methylene]-1H-indol-5-yl]ethanesulfonamide Hesperadin;Hesperadin, >=98%;Hesperadin;Hesperadin hydrochloride;N-[(3Z)-2-Oxo-3-[phenyl-[4-(piperidin-1-ylMethyl)anilino]Methylidene]-1H-indol-5-yl]ethanesulfonaMide;Hesperadine
3 prices
Selected condition:

Brand

  • TCI Chemicals (India)
  • Sigma-Aldrich(India)

Package

  • 5MG
  • 10MG
  • 50MG
  • ManufacturerTCI Chemicals (India)
  • Product numberH1708
  • Product descriptionHesperadin
  • Packaging10MG
  • Price₹7300
  • Updated2022-05-26
  • Buy
  • ManufacturerTCI Chemicals (India)
  • Product numberH1708
  • Product descriptionHesperadin
  • Packaging50MG
  • Price₹23800
  • Updated2022-05-26
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product number375680
  • Product descriptionHesperadin - CAS 422513-13-1 - Calbiochem Hesperadin primarily used in Inhibition.
  • Packaging5MG
  • Price₹27480
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
TCI Chemicals (India) H1708 Hesperadin 10MG ₹7300 2022-05-26 Buy
TCI Chemicals (India) H1708 Hesperadin 50MG ₹23800 2022-05-26 Buy
Sigma-Aldrich(India) 375680 Hesperadin - CAS 422513-13-1 - Calbiochem Hesperadin primarily used in Inhibition. 5MG ₹27480 2022-06-14 Buy

Properties

Melting point :228 °C
Density :1.326
storage temp. :Refrigerator
solubility :DMSO, Methanol
form :Solid
pka :9.14±0.20(Predicted)
color :Yellow
CAS DataBase Reference :422513-13-1

Safety Information

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Signal word:
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Description

Hesperadin is a multi-kinase inhibitor. It inhibits human Aurora kinase B (IC50 = 250 nM) and its T. brucei homolog Aurora kinase-1 (IC50 = 40 nM) in in vitro kinase assays. Hesperadin (1 μM) inhibits AMPK, LCK, MKK1, MAPKAP-K1, CHK1, and PHK in a panel of 25 kinases. It also inhibits MEKK2 in ATPase and transphosphorylation assays with IC50s of 60 and 34 nM, respectively. Hesperadin (50-100 nM) induces polyploidy and defects in cytokinesis and spindle assembly as well as inhibits proliferation of HeLa cells and overrides mitotic arrest induced by paclitaxel or monastrol . Hesperadin also induces toxicity in HepG2 cells with a toxic concentration (TC50) value of less than 0.2 μM. It inhibits replication of clinical isolates of influenza A and B viruses with EC50s ranging from 0.22 to 2.21 μM in a plaque formation assay. Hesperadin inhibits the growth of T. brucei, L. major promastigotes and amastigotes, and P. falciparum with EC50 values ranging from 0.01 to 2.37 μM, but has less activity against T. cruzi (EC50 = 39 μM).

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