Thalidomide-5-NH2-CH2-COOH
CAS No. 2412056-27-8
Thalidomide-5-NH2-CH2-COOH( (2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)glycine )
Catalog No. M28263 CAS No. 2412056-27-8
(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)glycine is a chemical compound.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 67 | Get Quote |
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| 5MG | 110 | Get Quote |
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| 10MG | 161 | Get Quote |
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| 25MG | 267 | Get Quote |
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| 50MG | 439 | Get Quote |
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| 100MG | 644 | Get Quote |
|
| 500MG | 1332 | Get Quote |
|
| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameThalidomide-5-NH2-CH2-COOH
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NoteResearch use only, not for human use.
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Brief Description(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)glycine is a chemical compound.
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Description(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)glycine is a chemical compound.
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In Vitro——
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In Vivo——
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Synonyms(2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)glycine
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PathwayOthers
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TargetOther Targets
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RecptorFAK|c-Src|PI3K|Rac1|MMP-2|MMP-9
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Research Area——
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Indication——
Chemical Information
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CAS Number2412056-27-8
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Formula Weight331.28
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Molecular FormulaC15H13N3O6
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 33.33 mg/mL (100.61 mM)
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SMILESOC(CNc(cc1)cc(C(N2C(CCC(N3)=O)C3=O)=O)c1C2=O)=O
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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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P110
Dynamin-related protein 1 (Drp1) inhibitor, inhibits Drp1 GTPase activity. Displays no effect on dynamin 1 or other mitochondrial dynamics-related proteins. Inhibits mitochondrial fission, dysfunction and reactive oxygen species (ROS) production in vitro. Reduces programmed cell death and improves cell viability by protecting mitochondrial integrity. Reduces mitochondrial fragmentation and mitochondrial ROS production in mouse model of Parkinson's disease. Cell permeable.
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Bragsin2
Bragsin2 is a hydration-resistant cell penetrant, selective and non-competitive inhibitor of Afr guanine nucleotide exchange factor BRAG2.
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BCAT-IN-4
BCAT-IN-4 is a potent BCAT inhibitor with an IC50 value of 2.35 μM for hBCATc. BCAT-IN-4 has anticancer activity and can be used to study pancreatic ductal adenocarcinoma.
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