MST-312
CAS No. 368449-04-1
MST-312( Telomerase Inhibitor IX )
Catalog No. M28357 CAS No. 368449-04-1
MST-312 is an inhibitor of telomerase and can be used in studies about cancer, such as multiple myeloma.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 31 | In Stock |
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| 5MG | 50 | In Stock |
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| 10MG | 87 | In Stock |
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| 25MG | 177 | In Stock |
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| 50MG | 330 | In Stock |
|
| 100MG | 491 | 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 NameMST-312
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NoteResearch use only, not for human use.
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Brief DescriptionMST-312 is an inhibitor of telomerase and can be used in studies about cancer, such as multiple myeloma.
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DescriptionMST-312 is an inhibitor of telomerase and can be used in studies about cancer, such as multiple myeloma.(In Vitro):In U-266 cells, MST-312 (2 μM) upregulates the pro-apoptotic gene Bax and down-regulates the anti-apoptotic gene Bcl-2 and suppresses the expression of c-Myc and hTERT genes. MST-312 (2-8 μM) reduces cellular viability in a dose dependent and time-dependent manner. MST-312 (2-8 μM) induces cell apoptosis in a dose-dependent manner.
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In VitroCell Viability Assay Cell Line:U-266 cells Concentration:2~8 μM Incubation Time:0~72 hours Result:The viability of U-266 cells was substantially decreased in a dose dependent and time-dependent manner, in response to exposure to MST-312.Apoptosis Analysis Cell Line:U-266 cells Concentration:2~8 μM Incubation Time:48 hours Result:Induced cell apoptosis in a dose-dependent manner.RT-PCR Cell Line:U-266 cells Concentration:2 μM Incubation Time:48 hours Result:Up-regulated the pro-apoptotic gene Bax and down-regulated the anti-apoptotic gene Bcl-2 and suppressed the expression of c-Myc and hTERT genes.
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In Vivo——
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SynonymsTelomerase Inhibitor IX
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PathwayCell Cycle/DNA Damage
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TargetTelomerase
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RecptorE3 Ligase Ligand-Linker Conjugate
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Research Area——
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Indication——
Chemical Information
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CAS Number368449-04-1
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Formula Weight380.356
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Molecular FormulaC20H16N2O6
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 125 mg/mL (328.64 mM)
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SMILESOc1cccc(C(=O)Nc2cccc(NC(=O)c3cccc(O)c3O)c2)c1O
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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
1.Qiu X, et al. Jiang B. Chemoselective Synthesis of Lenalidomide-Based PROTAC Library Using Alkylation Reaction. Org Lett. 2019;21(10):3838-3841.
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