OAC1

Synonyms: BAS 00287861

OAC1 (Oct4-activating compound 1, BAS 00287861) can enhance the efficiency of reprogramming. OAC1 can activate both Oct4 and Nanog promoter-driven luciferase reporter genes.

OAC1 Chemical Structure

OAC1 Chemical Structure

CAS: 300586-90-7

Selleck's OAC1 has been cited by 3 publications

Purity & Quality Control

Batch: S721701 DMSO] 47 mg/mL] false] Ethanol] 21 mg/mL] false] Water] Insoluble] false Purity: 99.21%
99.21

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Biological Activity

Description OAC1 (Oct4-activating compound 1, BAS 00287861) can enhance the efficiency of reprogramming. OAC1 can activate both Oct4 and Nanog promoter-driven luciferase reporter genes.
Targets
Oct4 [1]
In vitro
In vitro OAC1 at 1 μM enhances reprogramming efficiency by activating both Oct4 and Nanog promoter-driven luciferase reporter genes. Furthermore, OAC1 enhances the pluripotent stem cells (iPSC) reprogramming efficiency and accelerates the reprogramming process in the quartet reprogramming factors (Oct4, Sox2, c-Myc, and Klf4) treated mouse embryonic fibroblasts (MEFs). The iPSC colonies derived using OAC1 along with the quartet factors exhibits typical ESC morphology, gene-expression pattern, and developmental potential. OAC1 seems to enhance reprogramming efficiency via increasing transcription of the Oct4-Nanog-Sox2 triad and Tet1, a gene known to be involved in DNA demethylation. While it doesn’t inhibit the p53-p21 pathway or activate the Wnt-β-catenin signaling. OAC1 may be used to enhance the reprogramming of somatic cells to a pluripotent state. [1]
Cell Research Cell lines Human ESCs transfected with human Oct4 and Nanog luciferase reporter genes
Concentrations ~1 μM
Incubation Time 24 h
Method The Oct4-luc or Nanog-luc cells are treated with compound OAC1 at 1 μM concentration. Luciferase reporter assays are performed 24 h after OAC1 treatment.
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT01161836 Completed
Advanced Solid Tumors
Sanofi
July 2010 Phase 1

Chemical Information & Solubility

Molecular Weight 237.26 Formula

C14H11N3O

CAS No. 300586-90-7 SDF Download OAC1 SDF
Smiles C1=CC=C(C=C1)C(=O)NC2=NC=C3C(=C2)C=CN3
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 47 mg/mL ( (198.09 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 21 mg/mL

Water : Insoluble


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In vivo
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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.

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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.

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