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(+)-JQ-1 25 mg | 98.00%
TargetMol
![](https://smallmolecules.com/sm/wp-content/uploads/products/targetmol/12/1268524-70-4-300x184.png)
(+)-JQ1 is a BET bromodomain inhibitor (IC50: 77 nM/33 nM for BRD4 (1/2)).
More Information Supplier Page(+)-JQ-1 50 mg | 98.00%
TargetMol
![](https://smallmolecules.com/sm/wp-content/uploads/products/targetmol/12/1268524-70-4-300x184.png)
(+)-JQ1 is a BET bromodomain inhibitor (IC50: 77 nM/33 nM for BRD4 (1/2)).
More Information Supplier Page(+)-JQ-1 5 mg | 98.00%
TargetMol
![](https://smallmolecules.com/sm/wp-content/uploads/products/targetmol/12/1268524-70-4-300x184.png)
(+)-JQ1 is a BET bromodomain inhibitor (IC50: 77 nM/33 nM for BRD4 (1/2)).
More Information Supplier Page(+)-JQ-1 100 mg | 98.00%
TargetMol
![](https://smallmolecules.com/sm/wp-content/uploads/products/targetmol/12/1268524-70-4-300x184.png)
(+)-JQ1 is a BET bromodomain inhibitor (IC50: 77 nM/33 nM for BRD4 (1/2)).
More Information Supplier Page(+)-JQ-1-aldehyde 5 mg | Purity Not Available
TargetMol
(+)-JQ-1-aldehyde is the aldehyde derivative of (+)-JQ1, commonly used as a precursor for the synthesis of PROTACs targeting the BET bromine domain[1].
More Information Supplier Page(+)-JQ-1-aldehyde 10 mg | Purity Not Available
TargetMol
(+)-JQ-1-aldehyde is the aldehyde derivative of (+)-JQ1, commonly used as a precursor for the synthesis of PROTACs targeting the BET bromine domain[1].
More Information Supplier Page(+)-JQ-1-aldehyde 25 mg | Purity Not Available
TargetMol
(+)-JQ-1-aldehyde is the aldehyde derivative of (+)-JQ1, commonly used as a precursor for the synthesis of PROTACs targeting the BET bromine domain[1].
More Information Supplier Page(+)-JQ-1-aldehyde 50 mg | Purity Not Available
TargetMol
(+)-JQ-1-aldehyde is the aldehyde derivative of (+)-JQ1, commonly used as a precursor for the synthesis of PROTACs targeting the BET bromine domain[1].
More Information Supplier Page(+)-JQ-1-aldehyde| ChemScene 10mg | >98%
ChemScene
(+)-JQ-1-aldehyde is the aldehyde form of (+)-JQ1. (+)-JQ-1-aldehyde can be uesd as a precursor to synthesize PROTACs, which targets BET bromodomains.
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