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JQ-1 (carboxylic acid)

6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 4-(4-chlorophenyl)-2,3,9-triMethyl-, (6S)-

CAS: 202592-23-26

Molecular Formula: C19H17ClN4O2S

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JQ-1 (carboxylic acid) - Names and Identifiers

Name 6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 4-(4-chlorophenyl)-2,3,9-triMethyl-, (6S)-
Synonyms (+)-JQ1 (free acid)
JQ-1 (carboxylic acid)
(+)-JQ-1 CARBOXYLIC ACID
2-Methyl-5-trifluoroMethyl-2H-pyrazol-3-ylaMine
6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 4-(4-chlorophenyl)-2,3,9-triMethyl-, (6S)-
CAS 202592-23-26

JQ-1 (carboxylic acid) - Physico-chemical Properties

Molecular FormulaC19H17ClN4O2S
Molar Mass400.88
Density1.51±0.1 g/cm3(Predicted)
Boling Point661.6±65.0 °C(Predicted)
pKa4.11±0.10(Predicted)
Storage ConditionSealed in dry,Store in freezer, under -20°C
Physical and Chemical PropertiesBioactive JQ-1 carboxylic acid is a ()-JQ1 derivative (a BET bromine domain inhibitor). JQ-1 carboxylic acid can be used as a precursor for synthetic PROTACs, targeting BET-bromine domain.
UseUse of a highly efficient selective and cell-permeable BRD4 inhibitor.

JQ-1 (carboxylic acid) - In vitro study

( )-JQ-1 is a potent, specific, and reversible BET bromodomain inhibitor, with IC 50 s of 77 and 33 nM for the first and second bromodomain (BRD4(1/2)). ( )-JQ-1 also activates autophagy.

Last Update:2024-04-10 22:29:15
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