Pyridostatin
CAS No. 1085412-37-8
Pyridostatin( —— )
Catalog No. M10334 CAS No. 1085412-37-8
Pyridostatin Trifluoroacetate Salt is a G-quadruplexe stabilizer with Kd of 490 nM in a cell-free assay.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 67 | In Stock |
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| 10MG | 102 | In Stock |
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| 25MG | 181 | In Stock |
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| 50MG | 282 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NamePyridostatin
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NoteResearch use only, not for human use.
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Brief DescriptionPyridostatin Trifluoroacetate Salt is a G-quadruplexe stabilizer with Kd of 490 nM in a cell-free assay.
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DescriptionPyridostatin Trifluoroacetate Salt is a G-quadruplexe stabilizer with Kd of 490 nM in a cell-free assay, which targets a series of proto-oncogenes including c-kit, K-ras and Bcl-2.
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In VitroPyridostatin (RR82) (10 μM; 48 hours) induces cell cycle arrest. Pyridostatin is a very selective G-quadruplex DNA-binding small molecule designed to form a complex with and stabilize G-quadruplex structure. Pyridostatin causes neurite retraction, synaptic loss, and dose-dependent neuronal death. In cultured primary neurons, Pyridostatin induces the formation of DNA DSBs. Remarkably, Pyridostatin (1-5 μM, overnight) down regulates the BRCA1 protein, a protein that guards and repairs the neuronal genome, at the transcriptional level. They are for reference only.Pyridostatin:Cell Viability Assay Cell Line:Over 60 different cancer cell lines Concentration:10 μM Incubation Time:48 hours Result:Predominantly accumulated in the G2 phase of the cell cycle over 60 different cancer cell lines.
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In Vivo——
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Synonyms——
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PathwayCell Cycle/DNA Damage
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TargetDNA/RNA Synthesis
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RecptorG-quadruplexe
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number1085412-37-8
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Formula Weight596.64
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Molecular FormulaC31H32N8O5
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Purity>98% (HPLC)
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SolubilityEthanol: 30 mg/mL 30; Water: 100 mg/mL 100; DMSO: 100 mg/mL 100
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SMILESNCCOC1=CC(=NC(=C1)C(=O)NC1=NC2=CC=CC=C2C(OCCN)=C1)C(=O)NC1=NC2=CC=CC=C2C(OCCN)=C1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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NSAH?
NSAH is a nonnucleoside inhibitor of human ribonucleotide reductase (hRR).with cell-free IC50 of 32 μM and cell-based IC50 of ~250 nM, respectively.A unique nonnucleoside small-molecule hRR inhibitor, naphthyl salicylic acyl hydrazone (NSAH), using virtual screening, binding affinity, inhibition, and cell toxicity assays.?NSAH binds to hRRM1 with an apparent dissociation constant of 37 μM, and steady-state kinetics reveal a competitive mode of inhibition.?
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Calcium folinate
Leucovorin Calcium is a reduced folic acid.
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UNC6852
UNC6852 contains an EED ligand (IC50 = 247 nM) and a von Hippel-Lindau ligand and is a selective polycomb repressive complex 2 (PRC2) degrader based on PROTAC.
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