VTP50469
- Product Name
- VTP50469
- CAS No.
- 2169916-18-9
- Chemical Name
- VTP50469
- Synonyms
- VTP50469;VTP50469, 10 mM in DMSO;5-Fluoro-N,N-diisopropyl-2-((4-(7-((trans-4-(methylsulfonamido)cyclohexyl)methyl)-2,7-diazaspiro[3.5]nonan-2-yl)pyrimidin-5-yl)oxy)benzamide;Benzamide, 5-fluoro-N,N-bis(1-methylethyl)-2-[[4-[7-[[trans-4-[(methylsulfonyl)amino]cyclohexyl]methyl]-2,7-diazaspiro[3.5]non-2-yl]-5-pyrimidinyl]oxy]-;Menin-MLL,leukemia,survival,VTP 50469,Epigenetic Reader Domain,antiproliferative,Apoptosis,Inhibitor,protein-protein,VTP-50469,inhibit,VTP50469,differentiation
- CBNumber
- CB75839891
- Molecular Formula
- C32H47FN6O4S
- Formula Weight
- 630.82
- MOL File
- 2169916-18-9.mol
VTP50469 Property
- Boiling point:
- 735.2±70.0 °C(Predicted)
- Density
- 1.28±0.1 g/cm3(Predicted)
- solubility
- DMSO: Soluble: =10 mg/ml
Ethanol: Sparingly soluble: 1-10 mg/ml - form
- Solid
- pka
- 10.97±0.40(Predicted)
- color
- White to light yellow
- InChIKey
- ADHHOUXZPBYYSU-YOCNBXQISA-N
- SMILES
- C(N(C(C)C)C(C)C)(=O)C1=CC(F)=CC=C1OC1=CN=CN=C1N1CC2(CCN(C[C@@H]3CC[C@@H](NS(C)(=O)=O)CC3)CC2)C1
N-Bromosuccinimide Price
- Product number
- CS-0077527
- Product name
- VTP50469
- Purity
- 99.41%
- Packaging
- 5mg
- Price
- $450
- Updated
- 2021/12/16
- Product number
- CS-0077527
- Product name
- VTP50469
- Purity
- 99.41%
- Packaging
- 10mg
- Price
- $780
- Updated
- 2021/12/16
- Product number
- CS-0077527
- Product name
- VTP50469
- Purity
- 99.41%
- Packaging
- 50mg
- Price
- $2150
- Updated
- 2021/12/16
- Product number
- CS-0077527
- Product name
- VTP50469
- Purity
- 99.41%
- Packaging
- 100mg
- Price
- $2850
- Updated
- 2021/12/16
- Product number
- 012382
- Product name
- VTP50469
- Packaging
- 003
- Price
- $3600
- Updated
- 2021/12/16
VTP50469 Chemical Properties,Usage,Production
Uses
VTP50469 is a potent, highly selective and orally active Menin-MLL interaction inhibitor with a Ki of 104 pM. VTP50469 has potently anti-leukemia activity[1][2].
in vivo
VTP50469 (15-60 mg/kg; oral administration; twice a day; for 28 days; NSG mice) treatment is highly efficacious across all dosage levels and all treatment groups have a significant survival advantage. Mice dosed at 30 and 60 mg/kg VTP50469 extends survival advantage[1].
| Animal Model: | Unconditioned immunodeficient (NSG) mice with MV4;11 cells[1] |
| Dosage: | 15 mg/kg, 30 mg/kg, and 60 mg/kg |
| Administration: | Oral administration; twice a day; for 28 days |
| Result: | Was highly efficacious across all dosage levels and all treatment groups had a significant survival advantage over the control group. |
References
[1] Krivtsov AV, et al. A Menin-MLL Inhibitor Induces Specific Chromatin Changes and Eradicates Disease in Models of MLL-Rearranged Leukemia. Cancer Cell. 2019 Dec 9;36(6):660-673.e11. DOI:10.1016/j.ccell.2019.11.001
[2] Andrei V. Krivtsov, et al. Abstract 4958: VTP50469 is a novel, orally available menin-MLL1 inhibitor effective against MLL-rearranged and NPM1-mutant leukemia. Cancer Resceach. July 2018.Volume 78, Issue 13 Supplement.
VTP50469 Preparation Products And Raw materials
Raw materials
Preparation Products
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