ONC206

ONC206 is a selective antagonist of DRD2/3/4 with broad-spectrum anti-tumor activity.

ONC206 Chemical Structure

ONC206 Chemical Structure

CAS: 1638178-87-6

Selleck's ONC206 has been cited by 2 publications

Purity & Quality Control

Batch: Purity: 99.93%
99.93

ONC206 Related Products

Choose Selective Dopamine Receptor Inhibitors

Biological Activity

Description ONC206 is a selective antagonist of DRD2/3/4 with broad-spectrum anti-tumor activity.
Targets
DRD2 [1]
In vitro
In vitro

ONC206 is a ClpP agonist regarding the requirement of high doses (50–130 mg/kg) to achieve in vivo efficacy. [2]

Cell Research Cell lines SUM159 and MDA‐MB‐231 (WT and CLPP‐KO) cell lines
Concentrations --
Incubation Time 72 h
Method

Cells were treated with indicated drug concentrations for 72 h and imaged following addition of Hoechst stain.

(Data sourced from selleck products)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT04732065 Recruiting
Diffuse Midline Glioma (DMG)|Glioblastoma|Recurrent Ependymoma|Recurrent Malignant Central Nervous System Neoplasm|Spinal Cord Glioma|World Health Organization (WHO) Grade III Glioma|CNS Tumor|Central Nervous System Tumor
Sabine Mueller MD PhD|Chimerix|Mithil Prasad Foundation|Storm the Heavens Fund|The ChadTough Defeat DIPG Foundation|National Cancer Institute (NCI)|University of California San Francisco
August 23 2021 Phase 1
NCT04541082 Recruiting
Central Nervous System Neoplasms|Glioblastoma|Gliosarcoma Adult|Anaplastic Oligodendroglioma|Anaplastic Astrocytoma|Pilocytic Astrocytoma|Oligodendroglioma|Gliomatosis Cerebri|Pleomorphic Xanthoastrocytoma|Anaplastic Pleomorphic Xanthoastrocytoma|Diffuse Midline Glioma H3 K27M-Mutant|Ependymoma|Ependymoma Anaplastic|Medulloblastoma|Teratoid Rhabdoid Tumor|Neuroectodermal Tumors Primitive|Neuroectodermal Tumors|Anaplastic Meningioma|Atypical Meningioma|Choroid Plexus Neoplasms|Pineal Tumor|Diffuse Astrocytoma|Glial Tumor
Chimerix|National Institutes of Health (NIH)
October 26 2020 Phase 1

Chemical Information & Solubility

Molecular Weight 408.44 Formula

C23H22F2N4O

CAS No. 1638178-87-6 SDF --
Smiles FC1=CC(=C(CN2C(=O)C3=C(CCN(CC4=CC=CC=C4)C3)N5CCN=C25)C=C1)F
Storage (From the date of receipt) 3 years -20°C powder

In vitro
Batch:

DMSO : 82 mg/mL ( (200.76 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 27 mg/mL

Water : Insoluble


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In vivo
Batch:

Add solvents to the product individually and in order.


In vivo Formulation Calculator

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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.

Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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