ZL0580
CAS No. 2377151-10-3
ZL0580( —— )
Catalog No. M24093 CAS No. 2377151-10-3
ZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 93 | In Stock |
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| 5MG | 73 | In Stock |
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| 10MG | 117 | In Stock |
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| 25MG | 188 | In Stock |
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| 50MG | 277 | In Stock |
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| 100MG | 412 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameZL0580
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NoteResearch use only, not for human use.
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Brief DescriptionZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.
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DescriptionZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.
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In VitroCell Viability Assay Cell Line:HIV-infected human CD4+ T cells.Concentration:0-8 μM.Incubation Time:2 days.Result:Suppress HIV in primary CD4+ T cell.Single treatment (8 μM) led to almost completed loss of productive HIV infection in CD4+ T cells.RT-PCR Cell Line:PBMCs of viremic HIV-infected individuals.Concentration:8 μM.Incubation Time:2 days.Result:Suppresses HIV transcription ex vivo in PBMCs of viremic HIV-infected individuals.Cell Cytotoxicity Assay Cell Line:J-Lat cells. Concentration:0-80 μM.Incubation Time:1 and 3 days.Result:Did not cause significant cell death at concentrations below 40 μM.Treatment of J-Lat cells with ZL0580 (10 μM) also did not cause significant cell death on days 2, 7, and 14 compared with NC in both PMA-activated and unstimulated cells.
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In Vivo——
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Synonyms——
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PathwayChromatin/Epigenetic
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TargetEpigenetic Reader Domain
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RecptorBRD4|HIV
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Research Area——
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Indication——
Chemical Information
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CAS Number2377151-10-3
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Formula Weight532.53
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Molecular FormulaC25H23F3N4O4S
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Purity>98% (HPLC)
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SolubilityDMSO:250 mg/mL (469.46 mM; Need ultrasonic)
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SMILESC1C[C@H](N(C1)S(=O)(=O)C2=CC=C(C=C2)NC(=O)NC3=CC=C(C=C3)C(F)(F)F)C(=O)NC4=CC=CC=C4
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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.Niu Q, et al. Structure-guided drug design identifies a BRD4-selective small molecule that suppresses HIV. J Clin Invest. 2019 Jul 22;129(8):3361-3373.
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