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 |
| 2MG | 49 | In Stock |
|
| 5MG | 80 | In Stock |
|
| 10MG | 140 | In Stock |
|
| 25MG | 259 | In Stock |
|
| 50MG | 383 | In Stock |
|
| 100MG | 565 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameZL0580
-
NoteResearch use only, not for human use.
-
Brief DescriptionZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.
-
DescriptionZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.
-
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.
-
In Vivo——
-
Synonyms——
-
PathwayChromatin/Epigenetic
-
TargetEpigenetic Reader Domain
-
RecptorBRD4|HIV
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2377151-10-3
-
Formula Weight532.53
-
Molecular FormulaC25H23F3N4O4S
-
Purity>98% (HPLC)
-
SolubilityDMSO:250 mg/mL (469.46 mM; Need ultrasonic)
-
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
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
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.
molnova catalog
related products
-
GSK778 hydrochloride
GSK778 hydrochloride hydrochloride is a potent and selective BD1 bromodomain inhibitor of the BET proteins, with IC50s of 75 nM (BRD2 BD1), 41 nM (BRD3 BD1), 41 nM (BRD4 BD1), and 143 nM (BRDT BD1), respectively.
-
IRAK4-IN-1
IRAK4-IN-1 is an interleukin-1 receptor associated kinase 4 (IRAK4) inhibitor with an IC50 of 7 nM.
-
PBRM1-BD2-IN-2
PBRM1-BD2-IN-2, a selective and cell-active inhibitor of the polybromo-1 (PBRM1) bromodomain, exhibits binding affinity and inhibitory activity specifically targeting the PBRM1-BD2 domain, with Kd and IC50 values of 9.3 μM and 1.0 μM, respectively.
Cart
sales@molnova.com