CMLD-2
CAS No. 958843-91-9
CMLD-2( —— )
Catalog No. M34849 CAS No. 958843-91-9
CMLD-2 is an inhibitor of HuR-ARE interaction (Ki: 350 nM) that competitively binds HuR protein and disrupts its interaction with adenine element-rich (ARE) mRNA targets.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 258 | In Stock |
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| 5MG | 235 | In Stock |
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| 10MG | 392 | In Stock |
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| 25MG | 642 | In Stock |
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| 50MG | 877 | In Stock |
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| 100MG | 1181 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | 2353 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameCMLD-2
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NoteResearch use only, not for human use.
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Brief DescriptionCMLD-2 is an inhibitor of HuR-ARE interaction (Ki: 350 nM) that competitively binds HuR protein and disrupts its interaction with adenine element-rich (ARE) mRNA targets.
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DescriptionCMLD-2, an inhibitor of HuR-ARE interaction, competitively binds HuR protein disrupting its interaction with adenine-uridine rich elements (ARE)-containing mRNAs (Ki=350 nM). CMLD-2 induces apoptosis exhibits antitumor activity in different cancer cells as colon, pancreatic, thyroid and lung cancer cell lines. Hu antigen R (HuR) is an RNA binding protein, can regulate target mRNAs stability and translation.
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In VitroCell Viability Assay Cell Line:SW1736, 8505C, BCPAP and K1 cells Concentration:1, 5, 10, 25, 35, 50, 75 μM Incubation Time:24, 48, 72 hours Result:Reduced the viability of all the four cell lines when used at 35, 50 and 75?μM concentration and at different time points.Apoptosis AnalysisCell Line:H1299, A549, H1975, HCC827, MRC-9 and CCD16 cells Concentration:20, 30 μM Incubation Time:24, 48 hours Result:Marked activated the caspase-9 and -3 in lung tumor cells.Induce the cleavage of PARP in lung tumor cells.Significantly increased the annexin-V-positive staining in lung tumor cells.Cell Cycle Analysis Cell Line:H1299, A549, MRC-9 and CCD16 cells Concentration:30 μM Incubation Time:24, 48 hours Result:Induced greater G1 phase cell cycle arrest in H1299 and A549 cells than in MRC-9 and CCD16 cells.Western Blot Analysis Cell Line:H1299, A549, H1975, HCC827, CCD16 and MRC-9 cells Concentration:20, 30 μM Incubation Time:24, 48 hours Result:Diminished protein expression of HuR, Bcl-2, Cyclin E and Bcl-XL and increased expression of p27 and BAX in lung tumor cells.
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In Vivo——
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Synonyms——
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PathwayApoptosis
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TargetApoptosis
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RecptorApoptosis | HuR
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Research Area——
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Indication——
Chemical Information
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CAS Number958843-91-9
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Formula Weight513.58
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Molecular FormulaC31H31NO6
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (97.36 mM; Ultrasonic )
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SMILESCOc1ccc(cc1)C(CC(=O)N1CCCC1)c1c(OC)cc(OC)c2c(cc(=O)oc12)-c1ccccc1
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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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DB2313
DB2313 is a potent transcription factor PU.1 inhibitor, IC50=14 nM. DB2313 disrupts the interaction of PU.1 with target gene promoters. DB2313 induces apoptosis of acute myeloid leukemia (AML) cells, and has anticancer effects
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Hinokitiol
Hinokitiol (4-Isopropyltropolone;β-Thujaplicin) is a tropolone-related natural compound that can induces apoptosis and cell cycle arrest.
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