MS-417
CAS No. 916489-36-6
MS-417( GTPL-7512 )
Catalog No. M16583 CAS No. 916489-36-6
MS-417 (GTPL-7512) is a highly specific BET bromodomain inhibitor that binds to BRD4-BD1 and BRD4 BD2 with Kd of 36.1 uM and 25.4 uM respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 40 | Get Quote |
|
| 5MG | 65 | Get Quote |
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| 10MG | 102 | Get Quote |
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| 25MG | 176 | Get Quote |
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| 50MG | 267 | Get Quote |
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| 100MG | 462 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameMS-417
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NoteResearch use only, not for human use.
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Brief DescriptionMS-417 (GTPL-7512) is a highly specific BET bromodomain inhibitor that binds to BRD4-BD1 and BRD4 BD2 with Kd of 36.1 uM and 25.4 uM respectively.
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DescriptionMS-417 (GTPL-7512) is a highly specific BET bromodomain inhibitor that binds to BRD4-BD1 and BRD4 BD2 with Kd of 36.1 uM and 25.4 uM respectively; shows 100-200-fold weaker affinity for CBP, BRD7, or BPTF, and no binding affinity for many other bromodomains; blocks BRD4 binding to the acetylated NF-κB, effectively attenuates NF-κB transcriptional activation of proinflammatory genes in kidney cells treated with TNFα or infected by HIV; ameliorates inflammation and kidney injury in HIV-1 transgenic mice.
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In Vitro——
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In Vivo——
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SynonymsGTPL-7512
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PathwayChromatin/Epigenetic
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TargetBromodomain
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RecptorBromodomain
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Research Area——
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Indication——
Chemical Information
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CAS Number916489-36-6
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Formula Weight414.908
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Molecular FormulaC20H19ClN4O2S
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Purity>98% (HPLC)
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SolubilityEthanol : 50 mg/mL 120.51 mM
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SMILESCC1=C(SC2=C1C(=N[C@H](C3=NN=C(N32)C)CC(=O)OC)C4=CC=C(C=C4)Cl)C
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Chemical NameMethyl 2-[(6S,Z)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl]acetate
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. Zhang G, et al. J Biol Chem. 2012 Aug 17;287(34):28840-51.
2. Boehm D, et al. Cell Cycle. 2013 Feb 1;12(3):452-62.
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