Cat No:BMSPEM-0002
OAC1 is an Oct4-activating compound used in induced pluripotent stem-cell research. In the presence of Oct4, Sox2, c-Myc, and Klf4, it increased and accelerated reprogramming 20-fold compared with the four factors alone. It induces Oct4, Sox2, Nanog, and Tet1 mRNA expression without affecting the p53–p21 or Wnt–β-catenin signaling pathways.
| Chemical Formula | C₁₄H₁₁N₃O |
| Molecular Weight | 237.26 g/mol |
| Storage Conditions | Store at −20°C. |
| Purity | ≥97% |
| Primary Application | Oct4 activation and induced pluripotent stem-cell reprogramming studies |
| English Synonyms | OAC-1; Oct4-activating compound 1; N-(1H-pyrrolo[2,3-c]pyridin-5-yl)benzamide |
| Molecular Type | Small molecule |
| Density | 1.4 |
| Solubility | DMSO: up to 23.73 mg/mL (100 mM); ethanol: up to 23.73 mg/mL (100 mM) |
| Melting Point | 197.05°C |
| Boiling Point | Approximately 386.6°C at 760 mmHg |
| Refractive Index | 1.76 |
| Sensitivity | Sensitive to light, air, and heat |
| PubChem SID | 528766462 |
| IUPAC Name | N-(1H-pyrrolo[2,3-c]pyridin-5-yl)benzamide |
| InChI | 1S/C14H11N3O/c18-14(10-4-2-1-3-5-10)17-13-8-11-6-7-15-12(11)9-16-13/h1-9,15H,(H,16,17,18) |
| InChI Key | HWJRIFZDXJKJJN-UHFFFAOYSA-N |
| SMILES | C1=CC=C(C=C1)C(=O)NC2=NC=C3C(=C2)C=CN3 |
| Isomeric SMILES | C1=CC=C(C=C1)C(=O)NC2=NC=C3C(=C2)C=CN3 |
| Reaxys RN | 32136747 |
| WGK Germany | 3 |
| Biochemical Mechanism | Oct4 activator. With Oct4, Sox2, c-Myc, and Klf4, OAC1 enhances and accelerates iPSC reprogramming 20-fold versus the four factors alone. It induces Oct4, Sox2, Nanog, and Tet1 mRNA expression and does not affect p53–p21 or Wnt–β-catenin signaling. |
| Action Type | Activator |
| Shipping Conditions | Ultra-low-temperature transport |
| Available Package Sizes | 5mg, 25mg, 100mg |
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