OAC1 300586-90-7
Product Description
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Molecular Weight: 237.26 OAC1 (Oct4-activating compound 1) can enhance the efficiency of reprogramming.
Biological Activity
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.
Protocol(Only for Reference)
Cell Assay: [1]
Conversion of different model animals based on BSA (Value based on data from FDA Draft Guidelines)
For example, to modify the dose of resveratrol used for a mouse (22.4 mg/kg) to a dose based on the BSA for a rat, multiply 22.4 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for resveratrol of 11.2 mg/kg.
Chemical Information
Contact us if you need more details on OAC1. We are ready to answer your questions on packaging, logistics, certification or any other aspects about 300586-90-7 OAC1、300586-90-7. If these products fail to match your need, please contact us and we would like to provide relevant information.
Molecular Weight: 237.26 OAC1 (Oct4-activating compound 1) can enhance the efficiency of reprogramming.
Biological Activity
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.
Protocol(Only for Reference)
Cell Assay: [1]
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. |
Conversion of different model animals based on BSA (Value based on data from FDA Draft Guidelines)
Species | Baboon | Dog | Monkey | Rabbit | Guinea pig | Rat | Hamster | Mouse |
Weight (kg) | 12 | 10 | 3 | 1.8 | 0.4 | 0.15 | 0.08 | 0.02 |
Body Surface Area (m2) | 0.6 | 0.5 | 0.24 | 0.15 | 0.05 | 0.025 | 0.02 | 0.007 |
Km factor | 20 | 20 | 12 | 12 | 8 | 6 | 5 | 3 |
Animal A (mg/kg) = Animal B (mg/kg) multiplied by | Animal B Km |
Animal A Km |
For example, to modify the dose of resveratrol used for a mouse (22.4 mg/kg) to a dose based on the BSA for a rat, multiply 22.4 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for resveratrol of 11.2 mg/kg.
Rat dose (mg/kg) = mouse dose (22.4 mg/kg) × | mouse Km(3) | = 11.2 mg/kg |
rat Km(6) |
Chemical Information
Molecular Weight (MW) | 237.26 |
---|---|
Formula | C14H11N3O |
CAS No. | 300586-90-7 |
Storage | 3 years -20℃Powder |
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6 months-80℃in solvent (DMSO, water, etc.) | |
Synonyms | BAS 00287861 |
Solubility (25°C) * | In vitro | DMSO | 47 mg/mL (198.09 mM) |
---|---|---|---|
Water | <1 mg/mL ( | ||
Ethanol | 21 mg/mL (88.51 mM) | ||
Chemical Name | Benzamide, N-1H-pyrrolo[2,3-c]pyridin-5-yl- |
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Contact us if you need more details on OAC1. We are ready to answer your questions on packaging, logistics, certification or any other aspects about 300586-90-7 OAC1、300586-90-7. If these products fail to match your need, please contact us and we would like to provide relevant information.
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