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VER49009

Catalog No. T2268Cas No. 940289-57-6
Alias VER-49009, VER 49009, CCT0129397

VER49009 (CCT0129397) is an effective HSP90 inhibitor(IC50 =25 nM, Kd=78 nM).

VER49009

VER49009

Purity: 100%
Catalog No. T2268Alias VER-49009, VER 49009, CCT0129397Cas No. 940289-57-6
VER49009 (CCT0129397) is an effective HSP90 inhibitor(IC50 =25 nM, Kd=78 nM).
Pack SizePriceAvailabilityQuantity
1 mg$55In Stock
2 mg$77In Stock
5 mg$113In Stock
10 mg$176In Stock
25 mg$297In Stock
50 mg$497In Stock
100 mg$677In Stock
1 mL x 10 mM (in DMSO)$97In Stock
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Purity:100%
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Product Introduction

Bioactivity
Description
VER49009 (CCT0129397) is an effective HSP90 inhibitor(IC50 =25 nM, Kd=78 nM).
Targets&IC50
HSP90:25 nM
In vitro
In the human ovarian tumor model, intraperitoneal injection of VER-49009 (4 mg/kg) can induce the dissociation of HSP90 and ERBB2. In athymic mice, intravenous injection of VER-49009 (20 mg/kg) demonstrates efficacy.
In vivo
VER-49009 can induce the dissociation of HSP72 and HSP27 from their binding proteins, leading to cell cycle arrest. In recombinant yeast Hsp90 protein (IC50 = 167 nM), VER-49009 inhibits the endogenous ATPase activity. During the treatment of liver fibrosis, VER-49009 induces the accumulation of hepatic stellate cells (CFSC) in the G2 phase, inhibiting cell growth.
Kinase Assay
Fluorescence Polarization Assay: Binding of HSP90 inhibitors to human full-length recombinant HSP90β is determined by a competitive binding fluorescence polarization assay, using a fluorescent pyrazole resorcinol probe.
Cell Research
Antiproliferative effects are measured using the sulforhodamine B assay. HUVEC sensitivity is determined by an alkaline phosphatase method. (Only for Reference)
AliasVER-49009, VER 49009, CCT0129397
Chemical Properties
Molecular Weight387.82
FormulaC19H18ClN3O4
Cas No.940289-57-6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: < 1 mg/mL (insoluble or slightly soluble)
DMSO: 71 mg/mL (183.1 mM)
Ethanol: < 1 mg/mL (insoluble or slightly soluble)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.5785 mL12.8926 mL25.7852 mL128.9258 mL
5 mM0.5157 mL2.5785 mL5.1570 mL25.7852 mL
10 mM0.2579 mL1.2893 mL2.5785 mL12.8926 mL
20 mM0.1289 mL0.6446 mL1.2893 mL6.4463 mL
50 mM0.0516 mL0.2579 mL0.5157 mL2.5785 mL
100 mM0.0258 mL0.1289 mL0.2579 mL1.2893 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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