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 |
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| 25MG | 29 | In Stock |
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| 50MG | 38 | In Stock |
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| 100MG | 59 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 147 | In Stock |
|
| 1G | 219 | In Stock |
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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
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26Rfa, Hypothalamic ...
This human neuropeptide of the RFamide peptide family with orexigenic activity may be also involved in the control of feeding behavior. The 26RFa gene is exclusively expressed in the ventromedial hypothalamic nucleus and in the lateral hypothalamic area. The primary structures of human, rat, and frog 26RFa exhibit ≈80% identity. Other data suggest also the potential role of the 26RFa peptide in the control of the gonadotropic axis.
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DiMNF
DiMNF is a selective aryl hydrocarbon receptor (AHR) modulator. It also suppresses the expression of CD55 and CD46 induced by IL-1β in an inflammatory tumor cell microenvironment.
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Gastric Inhibitory P...
Gastric Inhibitory Polypeptide (1-30) (porcine)
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