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Mycophenolate Mofetil
CAS No. 128794-94-5
Mycophenolate Mofetil( RS 61443 )
Catalog No. M11174 CAS No. 128794-94-5
Mycophenolate Mofetil(RS 61443) is a non-competitive, selective and reversible inhibitor of inosine monophosphate dehydrogenase I/II with IC50 of 39 nM and 27 nM, respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 48 | In Stock |
|
| 25MG | 29 | In Stock |
|
| 50MG | 38 | In Stock |
|
| 100MG | 59 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 147 | In Stock |
|
| 1G | 219 | In Stock |
|
Biological Information
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Product NameMycophenolate Mofetil
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NoteResearch use only, not for human use.
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Brief DescriptionMycophenolate Mofetil(RS 61443) is a non-competitive, selective and reversible inhibitor of inosine monophosphate dehydrogenase I/II with IC50 of 39 nM and 27 nM, respectively.
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DescriptionMycophenolate Mofetil(RS 61443) is a non-competitive, selective and reversible inhibitor of inosine monophosphate dehydrogenase I/II with IC50 of 39 nM and 27 nM, respectively.(In Vitro):The inosine monophosphate dehydrogenase is an important enzyme in the de novo synthesis of guanosine nucleotides in T and B lymphocytes.
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In VitroThe inosine monophosphate dehydrogenase is an important enzyme in the de novo synthesis of guanosine nucleotides in T and B lymphocytes.
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In Vivo——
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SynonymsRS 61443
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PathwayOthers
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TargetOther Targets
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RecptorInosine monophosphate dehydrogeN/Ase II | Inosine monophosphate dehydrogeN/Ase I
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number128794-94-5
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Formula Weight433.49
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Molecular FormulaC??H??NO?
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Purity>98% (HPLC)
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SolubilityDMSO: 86 mg/mL (198.38 mM)
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SMILESO=C(OCCN1CCOCC1)CC/C(C)=C/CC2=C(O)C3=C(COC3=O)C(C)=C2OC
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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. nakanishi, T., et al., Effect of the inosine 5'-monophosphate dehydrogenase inhibitor BMS-566419 on rat cardiac allograft rejection. Int Immunopharmacol, 2010. 10(1): p. 91-7.
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