MZ1, BRD4 degrader (TBI5090)
$108.00 – $351.00
| SKU | Stock | SIZE (mg) | Price | Quantity | ||
|---|---|---|---|---|---|---|
| TBI5090-1MG | Yes | 1 MG | $108.00 | |||
| TBI5090-5MG | Yes | 5 MG | $351.00 |
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Description
Product Details
Formal Name: (2S,4R)-1-((S)-2-(tert-Butyl)-17-((S)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)-4,16-dioxo-6,9,12-trioxa-3,15-diazaheptadecan-1-oyl)-4-hydroxy-N-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide
Molecular Formula: C49H60ClN9O8S2
Formula Weight: 1002.6
CAS Number: 1797406-69-9
Purity: >98%
Formulation: Powder
Solubility: Soluble in DMSO (up to at least 100 mg/ml)
Storage: -20°C
Stability: ≥ 2 years
Applications
BRD4 degrader
Functions
MZ1 consists of JQ1 tethered to a ligand for the E3 ubiquitin ligase VHL and is a selective degrader of the BET bromodomain protein BRD4. It rapidly and potently induces reversible, long-lasting and unexpectedly selective degradation of BRD4 over BRD2 and BRD3. It exerts anticancer effects in acute myeloid leukemia by targeting c-Myc and ANP32B. An important tool for studying the effects of BRD4 degradation in cancer therapy.
Application Procedures
First dissolved in DMSO (up to at least 100 mg/ml), then diluted to aqueous buffer. Solutions in DMSO may be stored at -20°C for up to 2 months.
Research use only.
Additional information
| SIZE (mg) | 1 MG, 5 MG |
|---|
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