Introduction:Basic information about CAS 300586-90-7|OAC1, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | OAC1 |
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| CAS Number | 300586-90-7 | Molecular Weight | 237.257 |
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| Density | 1.4±0.1 g/cm3 | Boiling Point | 386.6±22.0 °C at 760 mmHg |
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| Molecular Formula | C14H11N3O | Melting Point | / |
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| MSDS | / | Flash Point | 187.6±22.3 °C |
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Names
| Name | oac1 |
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| Synonym | More Synonyms |
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OAC1 BiologicalActivity
| Description | OAC1 is a Octamer-binding transcription factor 4 (Oct4)-activating compound; enhances the iPSC reprogramming efficiency and accelerated the reprogramming process.IC50 value: Target: Oct4 activatorin vitro: OAC1 enhances the formation of Oct4-GFP+ colonies and accelerates the dynamics of reprogramming. OAC1 enhanced reprogramming efficiency through a mechanism that is independent of endogenous Oct4 promoter demethylation. OAC1 enhanced reprogramming efficiency through a mechanism that is distinct from suppressing p53-p21 expression. Luciferase assay revealed that OAC1 had no effect on Topflash activity, although BIO activated the Topflash reporter potently. OAC1 functions through a mechanism that is independent of the Wnt signaling. |
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| Related Catalog | Signaling Pathways >>Stem Cell/Wnt >>Oct3/4Research Areas >>Others |
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| References | [1]. Li W, et al. Identification of Oct4-activating compounds that enhance reprogramming efficiency. Proc Natl Acad Sci U S A. 2012 Dec 18;109(51):20853-8. |
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Chemical & Physical Properties
| Density | 1.4±0.1 g/cm3 |
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| Boiling Point | 386.6±22.0 °C at 760 mmHg |
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| Molecular Formula | C14H11N3O |
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| Molecular Weight | 237.257 |
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| Flash Point | 187.6±22.3 °C |
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| Exact Mass | 237.090210 |
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| PSA | 57.78000 |
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| LogP | 1.19 |
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| Vapour Pressure | 0.0±0.9 mmHg at 25°C |
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| Index of Refraction | 1.755 |
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| InChIKey | HWJRIFZDXJKJJN-UHFFFAOYSA-N |
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| SMILES | O=C(Nc1cc2cc[nH]c2cn1)c1ccccc1 |
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Safety Information
| RIDADR | NONH for all modes of transport |
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Synonyms
| N-(1H-Pyrrolo[2,3-c]pyridin-5-yl)benzamide |
| Benzamide, N-1H-pyrrolo[2,3-c]pyridin-5-yl- |