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Valrubicin PKC inhibitor

Cat.No.S9522

Valrubicin (AD-32) is a chemotherapy drug used to treat bladder cancer. This compound is a chemotherapy agent, inhibits TPA- and PDBu-induced PKC activation with IC50s of 0.85 and 1.25 μM, respectively.
Valrubicin PKC inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 723.64

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 723.64 Formula

C34H36F3NO13

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 56124-62-0 -- Storage of Stock Solutions

Synonyms AD-32 Smiles CCCCC(=O)OCC(=O)C1(CC(C2=C(C1)C(=C3C(=C2O)C(=O)C4=C(C3=O)C=CC=C4OC)O)OC5CC(C(C(O5)C)O)NC(=O)C(F)(F)F)O

Solubility

In vitro
Batch:

DMSO : 100 mg/mL (138.19 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 100 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
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Mechanism of Action

Targets/IC50/Ki
TPA-activated PKC [1]
(Cell-free assay)
0.85 μM
PDBu-activated PKC [1]
(Cell-free assay)
1.25 μM
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT01316874 Completed
Carcinoma in Situ|Bladder Cancer
Endo Pharmaceuticals
November 1993 Phase 2|Phase 3

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