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Valecobulin hydrochloride

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Catalog No. T13278Cas No. 1240321-53-2
Alias CKD-516 hydrochloride

Valecobulin hydrochloride (CKD-516 hydrochloride) is the valine prodrug and vasoblocker of S516. Valecobulin hydrochloride (CKD-516 hydrochloride) has a potent inhibitory effect on β-tubulin polymerization and has significant anti-tumor activity against solid tumors in mice and humans.

Valecobulin hydrochloride

Valecobulin hydrochloride

🥰Excellent
Purity: 98.63%
Catalog No. T13278Alias CKD-516 hydrochlorideCas No. 1240321-53-2
Valecobulin hydrochloride (CKD-516 hydrochloride) is the valine prodrug and vasoblocker of S516. Valecobulin hydrochloride (CKD-516 hydrochloride) has a potent inhibitory effect on β-tubulin polymerization and has significant anti-tumor activity against solid tumors in mice and humans.
Pack SizePriceAvailabilityQuantity
1 mg$81In Stock
5 mg$173In Stock
10 mg$273In Stock
25 mg$452In Stock
50 mg$636In Stock
100 mg$858In Stock
200 mg$1,150In Stock
1 mL x 10 mM (in DMSO)$218In Stock
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Purity:98.63%
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Product Introduction

Bioactivity
Description
Valecobulin hydrochloride (CKD-516 hydrochloride) is the valine prodrug and vasoblocker of S516. Valecobulin hydrochloride (CKD-516 hydrochloride) has a potent inhibitory effect on β-tubulin polymerization and has significant anti-tumor activity against solid tumors in mice and humans.
In vivo
METHODS: Nude mice carrying human colonic HCT116 and human colonic overexpression of the P-gp transporter HCT15 were treated with Valecobulin hydrochloride (CKD-516 hydrochloride) (5 mg/kg and 10 mg/kg, intraperitoneal injection, Q4D 4).
RESULTS The IR of Valecobulin hydrochloride (CKD-516 hydrochloride) in HCT116 nude mice was 36% and 65%, respectively, and tumor growth was significantly inhibited in a dose-dependent manner; Valecobulin hydrochloride (CKD-516 hydrochloride) also showed resistance to MDR The potent antitumor activity of positive cell lines (HCT15), with IRs of 12% and 5%, respectively. [2]
AliasCKD-516 hydrochloride
Chemical Properties
Molecular Weight573.06
FormulaC26H29ClN6O5S
Cas No.1240321-53-2
SmilesCl.COc1cc(cc(OC)c1OC)C(=O)c1ccc(cc1-n1cncn1)-c1csc(NC(=O)[C@@H](N)C(C)C)n1
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 125 mg/mL (218.13 mM), Sonication is recommended.
H2O: 50 mg/mL (87.25 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM1.7450 mL8.7251 mL17.4502 mL87.2509 mL
5 mM0.3490 mL1.7450 mL3.4900 mL17.4502 mL
10 mM0.1745 mL0.8725 mL1.7450 mL8.7251 mL
20 mM0.0873 mL0.4363 mL0.8725 mL4.3625 mL
50 mM0.0349 mL0.1745 mL0.3490 mL1.7450 mL
DMSO
1mg5mg10mg50mg
100 mM0.0175 mL0.0873 mL0.1745 mL0.8725 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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