(+)-JQ1 carboxylic acid
Tocris Bioscience, part of Bio-Techne | Catalog # 6588
Carboxylic acid-functionalized BET bromodomain inhibitor; target ligand for PROTACs
Discontinued Product
6588 has been discontinued.
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Key Product Details
Description
Carboxylic acid-functionalized BET bromodomain inhibitor; target ligand for PROTACs
Product Description
(+)-JQ1 carboxylic acid is a BET bromodomain inhibitor (+)-JQ1 (Cat. No. 4499) with a carboxylic acid functional group for conjugation reactions. Can be used as a precursor to PROTAC® Degraders that targets BET bromodomains after conjugation to a linker and E3 ligase ligand.PROTAC® is a registered trademark of Arvinas Operations, Inc., and is used under license.
Product Specifications
Molecular Weight
400.88
Formula
C19H17ClN4O2S
Storage
Store at -20°C
Purity
≥98% (HPLC)
Chemical Name
(6S)-4-(4-Chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid
CAS Number
202592-23-2
PubChem ID
66828107
InChI Key
LJOSBOOJFIRCSO-AWEZNQCLSA-N
SMILES
OC(C[C@@H]1N=C(C2=CC=C(Cl)C=C2)C3=C(SC(C)=C3C)N4C1=NN=C4C)=O
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 40.09 | 100 | |
| Ethanol | 40.09 | 100 |
Preparing Stock Solutions
for (+)-JQ1 carboxylic acid
The following data is based on the product molecular weight 400.88
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.49 mL | 12.47 mL | 24.95 mL |
| 5 mM | 0.50 mL | 2.49 mL | 4.99 mL |
| 10 mM | 0.25 mL | 1.25 mL | 2.49 mL |
| 50 mM | 0.05 mL | 0.25 mL | 0.50 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Zengerle Selective small molecule induced degradation of the BET bromodomain protein BRD4. ACS Chem Biol. 2015 PMID: 26035625
- Gadd Structural basis of PROTAC cooperative recognition for selective protein degradation. Nat.Chem.Biol. 2017 PMID: 28288108
- Winter DRUG DEVELOPMENT. Phthalimide conjugation as a strategy for in vivo target protein degradation. Science 2015 PMID: 25999370
Product Specific Notices for (+)-JQ1 carboxylic acid
For research use only
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