KW-2478

Modify Date: 2024-02-03 21:14:11

KW-2478 Structure
KW-2478 structure
Common Name KW-2478
CAS Number 819812-04-9 Molecular Weight 574.662
Density 1.2±0.1 g/cm3 Boiling Point 746.9±60.0 °C at 760 mmHg
Molecular Formula C30H42N2O9 Melting Point N/A
MSDS N/A Flash Point 405.5±32.9 °C

 Use of KW-2478


KW-2478 is an inhibitor of Hsp90α, with an IC50 of 3.8 nM, and has antitumor activity against various human hematological tumor cells.

 Names

Name 2-[2-ethyl-3,5-dihydroxy-6-[3-methoxy-4-(2-morpholin-4-ylethoxy)benzoyl]phenyl]-N,N-bis(2-methoxyethyl)acetamide
Synonym More Synonyms

 KW-2478 Biological Activity

Description KW-2478 is an inhibitor of Hsp90α, with an IC50 of 3.8 nM, and has antitumor activity against various human hematological tumor cells.
Related Catalog
Target

HSP90α:3.8 nM (IC50)

In Vitro KW-2478 is an inhibitor of Hsp90, with an IC50 of 3.8 nM for Hsp90α. KW-2478 shows anti-proliferative activity against multiple myeloma (MM) and non-Hodgkin’s lymphoma (NHL), with GI50s of 0.30 μM (OPM-2/GFP), 0.34 μM (KMS-11), 0.39 μM (RPMI 8226), 0.12 μM (NCI-H929), 0.36 μM (Raji), 0.098 μM (SR), and 0.33 μM μM (SC-1). KW-2478 also inhibits the transcription of c-Maf and Cyclin D1 genes by mainly suppressing the function of Cdk9[1].
In Vivo KW-2478 (25-200 mg/kg, i.v.) inhibits tumor growth in combined immunodeficiency (SCID) mice bearing NCI-H929 cells, without body weight loss. KW-2478 (100 mg/kg, i.v.) causes degradation of the Hsp90 client proteins (IGF-1Rβ, c-Raf-1, Cdk9) levels and dephosphorylated Erk1/2 proteins in NCI-H929 tumors of mice[1].
Cell Assay The cells are plated into 96-well plates and treated with KW-2478. After 72 hours of cultivation, cell viability is determined using WST-1. WST reagent is added to the wells, followed by incubation for 4 hours at 37°C. After that, the absorbance at 450 nm with reference at 650 nm is measured with a microplate spectrophotometer[1].
Animal Admin Mice[1] Severe combined immunodeficient (SCID) mice are intraperitoneally injected with anti-asialo GM1 antibody. The next day, all mice are subcutaneously inoculated with NCI-H929 cells (1×107 cells) suspended in PBS containing 50% of Matrigel. After 10 days, tumor volume is measured using the Antitumor test system II, a computer-operated system including software and instruments. SCID mice with tumors (190 to 290 mm3) are selected. After randomly grouping, saline (vehicle) or KW-2478 is intravenously administered to mice once or twice daily for 5 days. 17-AAG is intravenously administered to mice. Tumor volume is calculated by the Anti-tumor test system II as follows: Tumor volume=DL×DS×DS×1/2. Fourteen days after the initial administration, blood samples of each mouse are obtained, followed by measurement of serum M protein (Ig kappa chain) with Human Kappa-b&f ELISA Quantitation Kit. The statistical analysis is performed using SAS software[1].
References

[1]. Nakashima T, et al. New molecular and biological mechanism of antitumor activities of KW-2478, a novel nonansamycin heat shock protein 90 inhibitor, in multiple myeloma cells. Clin Cancer Res. 2010 May 15;16(10):2792-802.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 746.9±60.0 °C at 760 mmHg
Molecular Formula C30H42N2O9
Molecular Weight 574.662
Flash Point 405.5±32.9 °C
Exact Mass 574.289001
PSA 127.23000
LogP 2.99
Vapour Pressure 0.0±2.6 mmHg at 25°C
Index of Refraction 1.560
Storage condition -20℃

 Synonyms

cc-326
pound not KW2478 pound not KW 2478
QC-7253
UNII-QY50S617NM
2-(2-Ethyl-3,5-dihydroxy-6-{3-methoxy-4-[2-(4-morpholinyl)ethoxy]benzoyl}phenyl)-N,N-bis(2-methoxyethyl)acetamide
Benzeneacetamide, 2-ethyl-3,5-dihydroxy-N,N-bis(2-methoxyethyl)-6-[3-methoxy-4-[2-(4-morpholinyl)ethoxy]benzoyl]-
KW-2478
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