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Thalidomide-O-C4-NH2 hydrochloride
CAS No. 2376990-29-1
Thalidomide-O-C4-NH2 hydrochloride( Thalidomide-linker 9 | Thalidomide-O-C4-NH2 hydrochloride )
Catalog No. M28663 CAS No. 2376990-29-1
Thalidomide-linker 9 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 29 | In Stock |
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| 25MG | 56 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameThalidomide-O-C4-NH2 hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionThalidomide-linker 9 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
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DescriptionThalidomide-linker 9 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
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In Vitro——
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In Vivo——
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SynonymsThalidomide-linker 9 | Thalidomide-O-C4-NH2 hydrochloride
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PathwayOthers
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TargetOther Targets
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RecptorCytochrome P450
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Research Area——
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Indication——
Chemical Information
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CAS Number2376990-29-1
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Formula Weight381.81
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Molecular FormulaC17H20ClN3O5
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C1N(C(CC2)C(NC2=O)=O)C(C3=C1C=CC=C3OCCCCN)=O.[H]Cl
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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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R715 TFA(185052-09-9...
Potent and selective bradykinin B1 receptor antagonist (pA2 = 8.49). Displays no activity at B2 receptors. Reduces mechanical hypernociception in a mouse model of neuropathic pain. Metabolically stable.
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IRBP(668-687) (TFA) ...
Interphotoreceptor retinoid-binding protein(668-687) TFA is the 668-687 amino acid residue of human Interphotoreceptor retinoid binding protein(IRBP), which can induce uveitis.
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3,5-Di-tert-butylben...
3,5-Di-tert-butylbenzaldehyde may be used in the synthesis of the following:5-p-pyridyl-15-(3,5-di-tert-butylphenyl)porphyrin via condensation reaction with 4-pyridinecarboxaldehyde and 2,2′-dipyrrylmethane.3,5-di-tert-butylphenyl-dipyrromethane via reaction with pyrrole in the presence of trifluoroacetic acid.3,5-di-tert-butyl-2-nitrobenzaldehyde via nitration reaction.
