Gut restricted-7
CAS No. 2553218-46-3
Gut restricted-7( GR-7 )
Catalog No. M26241 CAS No. 2553218-46-3
Gut restricted-7 (GR-7) is a covalent and orally active pan-bile salt hydrolase (BSH) inhibitor. It decreases gut bacterial BSHs and decreases deconjugated bile acid levels in the feces of mice.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 299 | Get Quote |
|
| 10MG | 479 | Get Quote |
|
| 25MG | 777 | Get Quote |
|
| 50MG | 1071 | Get Quote |
|
| 100MG | Get Quote | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameGut restricted-7
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NoteResearch use only, not for human use.
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Brief DescriptionGut restricted-7 (GR-7) is a covalent and orally active pan-bile salt hydrolase (BSH) inhibitor. It decreases gut bacterial BSHs and decreases deconjugated bile acid levels in the feces of mice.
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DescriptionGut restricted-7 (GR-7) is a covalent and orally active pan-bile salt hydrolase (BSH) inhibitor. It decreases gut bacterial BSHs and decreases deconjugated bile acid levels in the feces of mice.(In Vitro):Gut restricted-7 (60 μM) does not affect the epithelial barrier integrity of Caco-2 cells, suggesting that this compound is relatively nontoxic. Gut restricted-7 also does not affect microbial biomass.(In Vivo):The C57BL/6 mice fed with either powdered chow containing 0.09% Gut restricted-7 (w/w) for 1 d day or powdered chow alone. Gut restricted-7 significant inhibits the BSH activity in the feces of inhibitor-treated mice 8 h post-diet change. 20picomol/mg wet mass (~20 μM) of Gut restricted-7 in cecal contents is detected.
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In Vitro——
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In Vivo——
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SynonymsGR-7
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PathwayCell Cycle/DNA Damage
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TargetPotassium Channel
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RecptorCDK1| CDK2| CDK3| CDK5
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Research Area——
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Indication——
Chemical Information
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CAS Number2553218-46-3
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Formula Weight510.63
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Molecular FormulaC25H40FNaO6S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (489.59 mM)
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SMILESO=C(CF)CC[C@@H](C)[C@@]1([H])CC[C@@]2([H])[C@]3([H])[C@H](O)C[C@]4([H])C[C@H](OS(=O)(O[Na])=O)CC[C@]4(C)[C@@]3([H])CC[C@@]21C
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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.McMillin DW, Delmore J, Negri J et al. Molecular and cellular effects of multi-targeted cyclin-dependent kinase inhibition in myeloma: biological and clinical implications. Br J Haematol. 2011 Feb;152(4):420-32.
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