CPS-11
CAS No. 145945-21-7
CPS-11( —— )
Catalog No. M33976 CAS No. 145945-21-7
CPS-11 (N-(Hydroxymethyl)thalidomide) is a Thalidomide analogue with significant antitumor activity, exhibiting a broader and more potent effect on the MM (multiple myeloma) cell line.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 603 | Get Quote |
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| 5MG | 847 | Get Quote |
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| 10MG | 1121 | Get Quote |
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| 25MG | 1454 | Get Quote |
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| 50MG | 1822 | Get Quote |
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| 100MG | 2250 | 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 NameCPS-11
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NoteResearch use only, not for human use.
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Brief DescriptionCPS-11 (N-(Hydroxymethyl)thalidomide) is a Thalidomide analogue with significant antitumor activity, exhibiting a broader and more potent effect on the MM (multiple myeloma) cell line.
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DescriptionCPS-11 (N-(Hydroxymethyl)thalidomide) a Thalidomide (HY-14658) analogue, is a potent anti-cancer agent. CPS-11 inhibits NF-κB, activates NFAT, and repress cytokine expression through elevated ROS. CPS-11 exhibits a wider activity spectrum and higher potency against MM (multiple myeloma) cell lines.
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In VitroCPS-11 abrogates ability of bone marrow stromal cells (BMSCs) to induce proliferation of MM cells, confirming its ability to target tumor cells in the bone marrow microenvironment.CPS-11 (0-200 μM, 0 or 4 h) shows virtually no effect on activation of p38 and only slight, transient activation of ATF2 and HSP27.CPS-11 (0-100 μM, 24 or 48 h) was no toxic to H157 cells, WT MEFs or the p38α-/- MEFs at doses as high as 100 μM.CPS-11 (50 μM, 24 or 48 h) does not induce apoptosis in H157 cells.Western Blot Analysis Cell Line:H157 cells, PC3 cells, HUVEC cells Concentration:0, 1, 5, 10, 20, 50, 100 and 200 μM Incubation Time:0, 15 min, 30 min, 1 h, 2 h, and 4 h Result:Showed virtually no effect on activation of p38 and only slight, transient activation of ATF2 and HSP27. Increased Akt phosphorylation within 15 minutes, and decreased Akt phosphorylation from 15 minutes to 4 hours.Cell Cytotoxicity Assay Cell Line:H157 cells, wild-type (WT) mouse embryonic fibroblasts (MEF) and p38α-/- MEF Concentration:0, 20, 50, and 100 μM Incubation Time:24 or 48 hours Result:Showed no toxic to H157 cells at doses as high as 100 μM and an incubation time of 48 hours. had no toxic effect on either the WT MEFs or the p38α-/- MEFs at doses as high as 100 μM.Apoptosis Analysis Cell Line:H157 cells Concentration:50 μM Incubation Time:24 or 48 hours Result:Did not induce apoptosis in H157 cells at either time point.
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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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RecptorReactive Oxygen Species | NF-κB | Dehydrogenase
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Research Area——
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Indication——
Chemical Information
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CAS Number145945-21-7
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Formula Weight288.26
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Molecular FormulaC14H12N2O5
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C1N(C(=O)C=2C1=CC=CC2)C3C(=O)N(CO)C(=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
1. Aragon-Ching JB, et al. Thalidomide analogues as anticancer drugs. Recent Pat Anticancer Drug Discov. 2007 Jun;2(2):167-74. ?
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