Pomalidomide-PEG2-CO2H
CAS No. 2140807-17-4
Pomalidomide-PEG2-CO2H( Pomalidomide-PEG2-C2-acid | Pomalidomide 4'-PEG2-acid )
Catalog No. M28267 CAS No. 2140807-17-4
Pomalidomide-PEG2-CO2H is a synthetic E3 ligase ligand-linker conjugate containing a Pomalidomide-based cereblon ligand and a 2-unit PEG linker.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 54 | Get Quote |
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| 10MG | 79 | Get Quote |
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| 25MG | 132 | Get Quote |
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| 50MG | 237 | Get Quote |
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| 100MG | 347 | Get Quote |
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| 200MG | 518 | 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 NamePomalidomide-PEG2-CO2H
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NoteResearch use only, not for human use.
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Brief DescriptionPomalidomide-PEG2-CO2H is a synthetic E3 ligase ligand-linker conjugate containing a Pomalidomide-based cereblon ligand and a 2-unit PEG linker.
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DescriptionPomalidomide-PEG2-CO2H is a synthetic E3 ligase ligand-linker conjugate containing a Pomalidomide-based cereblon ligand and a 2-unit PEG linker.(In Vitro):PROTACs contain two distinct ligands, one for the E3 ubiquitin ligase and the other for the target protein, linked by a linker.
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In Vitro——
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In Vivo——
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SynonymsPomalidomide-PEG2-C2-acid | Pomalidomide 4'-PEG2-acid
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PathwayOthers
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TargetOther Targets
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RecptorEGFR
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Research Area——
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Indication——
Chemical Information
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CAS Number2140807-17-4
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Formula Weight433.41
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Molecular FormulaC20H23N3O8
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 62.5 mg/mL (144.21 mM)
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SMILESO=C(O)CCOCCOCCNC1=CC=CC=2C(=O)N(C(=O)C12)C3C(=O)NC(=O)CC3
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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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Deoxyribonuclease I
Deoxyribonuclease I (DNase I) is an enzyme commonly used to purify proteins with potential anti-inflammatory and anticancer activity and can be used to study bacterial and fungal infections.
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Quin C1
Quin C1 is a selective and potent formylpeptide receptor 2 (FPR2/ALX) agonist with anti-inflammatory activity, inhibits neutrophil and lymphocyte production in BALF, and reduces the expression of TNF-α, IL-1β, KC, and TGF-β1.Quin C1 is used in the study of lung injury.
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PACAP (6-38), human,...
PACAP (6-38), human, ovine, rat is a potent antagonist of PACAP 38. PACAP (6-38) is much more potent and selective than PACAP (6-27) in the inhibition of PACAP-27-stimulated pituitary adenylate cyclase.
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