1-(3,4-dichlorophenyl)-2-[4-[(1-ethyl-3-piperidyl)amino]-6-methyl-pyrimidin-2-yl]guanidine manufacturers
- SKOG102
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- $2180.00
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2026-05-11
- CAS:21062-28-2
- Purity:
- Supply Ability: 10g
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| | 1-(3,4-dichlorophenyl)-2-[4-[(1-ethyl-3-piperidyl)amino]-6-methyl-pyrimidin-2-yl]guanidine Basic information |
| | 1-(3,4-dichlorophenyl)-2-[4-[(1-ethyl-3-piperidyl)amino]-6-methyl-pyrimidin-2-yl]guanidine Chemical Properties |
| Boiling point | 573.54°C (rough estimate) | | density | 1.1768 (rough estimate) | | refractive index | 1.6300 (estimate) | | pka | 8.80±0.10(Predicted) |
| | 1-(3,4-dichlorophenyl)-2-[4-[(1-ethyl-3-piperidyl)amino]-6-methyl-pyrimidin-2-yl]guanidine Usage And Synthesis |
| Uses | SKOG102 is a potent OLIG2 inhibitor that is directly engaging OLIG2 and interferes with the ability of OLIG2 to bind DNA. SKOG102 can be used for the research of glioblastoma (GBM)[1]. | | in vivo | SKOG102 (10-20 mg/kg; i.p.) inhibits GBM4 tumor growth in mice[1].
SKOG102 (5 mg/kg; i.p.) accumulates in the tumor even over a relatively brief time period and the plasma and brain concentrations are almost identical at 4 hours after injection in mice[1]. | Animal Model: | NSG mice were inoculated in each flank with GBM4 cells[1] | | Dosage: | 10, 15, and 20 mg/kg; dissolved in solutol:PEG400:water (20%:40%:40%) | | Administration: | Intraperitoneal injection; first 2 weeks (from day 33 to 46) 10 mg/kg, third week (from day 47 to 54) 15 mg/kg, fourth week (from 55 to 66) first 3 days 20 mg/kg, 2 days break, then alternate days from day 60 to 66 | | Result: | Significantly attenuated tumor growth.
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| | References | [1] Tsigelny IF, et, al. Multiple spatially related pharmacophores define small molecule inhibitors of OLIG2 in glioblastoma. Oncotarget. 2017 Apr 4;8(14):22370-22384. DOI:10.18632/oncotarget.5633 |
| | 1-(3,4-dichlorophenyl)-2-[4-[(1-ethyl-3-piperidyl)amino]-6-methyl-pyrimidin-2-yl]guanidine Preparation Products And Raw materials |
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