Magrolimab
CAS No. 2169232-81-7
Magrolimab( —— )
Catalog No. M34758 CAS No. 2169232-81-7
Magrolimab (Hu5F9-G4) is a humanized anti-CD47 IgG4 monoclonal antibody that exhibits antitumor activity by blocking CD47 and binding primarily to the N-terminal pyroglutamate of CD47. It can be used in combination with other compounds for the treatment of recurrent myeloma.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 455 | Get Quote |
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| 10MG | 708 | Get Quote |
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| 25MG | 1064 | Get Quote |
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| 50MG | 1386 | Get Quote |
|
| 100MG | Get Quote | Get Quote |
|
| 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 NameMagrolimab
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NoteResearch use only, not for human use.
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Brief DescriptionMagrolimab (Hu5F9-G4) is a humanized anti-CD47 IgG4 monoclonal antibody that exhibits antitumor activity by blocking CD47 and binding primarily to the N-terminal pyroglutamate of CD47. It can be used in combination with other compounds for the treatment of recurrent myeloma.
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DescriptionMagrolimab (Hu5F9-G4) is a first-in-class humanized anti-CD47 IgG4 antibody with an anti-tumor activity.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number2169232-81-7
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Formula Weight
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Molecular Formula——
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Purity>98% (HPLC)
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Solubility——
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SMILES——
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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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praeruptorin C(b)
Praeruptorin C (Pra-C) an effective component in the root of Peucedanum praeruptorum dunn a traditional Chinese medicine may function in neuroprotection.?
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P-Cymene
P-cymene is a monoterpene that is?toluene?substituted by an isopropyl group at position 4. It has a role as a plant metabolite a volatile oil component and a human urinary metabolite. It is a member of toluenes and a monoterpene.
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alpha-Dihydroartemis...
Dihydroartemisinin is widely used as an intermediate in the preparation of other artemisinin-derived antimalarial drugs, is recommended as the first-line anti-malarial drug with low toxicity. Dihydroartemisinin possesses promising anticancer activities and induce cancer cell death through apoptotic pathways.
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