(E/Z)-BCI phosphatase inhibitor

Cat.No.S0056

(E/Z)-BCI (BCI, NSC 150117) is an inhibitor of dual specific phosphatase 1/6 (DUSP1/DUSP6) and mitogen-activated protein kinase with EC50 of 13.3 μM and 8.0 μM for DUSP6 and DUSP1 in cells, respectively. (E)-BCI induces apoptosis via generation of reactive oxygen species (ROS) and activation of intrinsic mitochondrial pathway in H1299 lung cancer cells.
(E/Z)-BCI phosphatase inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 317.42

Quality Control

Batch: S005601 DMSO]63 mg/mL]false]Ethanol]20 mg/mL]false]Water]Insoluble]false Purity: 99.89%
99.89

Chemical Information, Storage & Stability

Molecular Weight 317.42 Formula

C22H23NO

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 15982-84-0 -- Storage of Stock Solutions

Synonyms BCI, NSC 150117 Smiles C1CCC(CC1)NC2C3=CC=CC=C3C(=O)C2=CC4=CC=CC=C4

Solubility

In vitro
Batch:

DMSO : 63 mg/mL (198.47 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 20 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
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Mechanism of Action

Targets/IC50/Ki
ROS [1]
DUSP1 [1]
(Cell-free assay)
8.0 μM(EC50)
DUSP6 [1]
(Cell-free assay)
13.3 μM(EC50)
References

Clinical Trial Information

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

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05470478 Not yet recruiting
Spinal Cord Injury|Amyotrophic Lateral Sclerosis|Brain Stem Infarctions|Locked-in Syndrome|Muscular Dystrophy
VA Office of Research and Development
September 1 2024 Not Applicable
NCT06231628 Not yet recruiting
Imaging Guided|Percutaneous Cementoplasty|Pelvic Bone Metstasis
Assiut University
February 2024 Not Applicable

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