Cat.No.: | BSM-0137 |
Product Name: | GSK-J1 (Free acid) |
CAS No.: | 1373422-53-7 |
Figure: |
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Synonyms: | N-[2-(2-Pyridinyl)-6-(1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl)-4-pyrimidinyl]-β-alanine |
Description: | GSK-J1 is a potent and selective inhibitor of jumonji H3K27 histone demethylases JMJD3 and UTX (IC₅₀ = 60 nM, human JMJD3). This is the first known inhibitor selective for the H3K27me3-specific JMJ subfamily which binds to the active catalytic site of the enzyme. The COOH group confers cell impermeability and as such is useful as a standard in in vitro assays. A cell permeable ethyl ester analog is also available. |
Appearance: | Pale yellow powder. |
Molecular Weight: | 398.45 |
Purity: | ≥98% by TLC |
Storage: | -20°C |
Targets: | JMJD3/UTX |
Molecular Formula: | C22H23N5O2 |
MDL Number: | MFCD22683851 |
Solubility: | DMSO (~ 20 mg/ml) |
Shipping Conditions: | Gel Pack |
Warning: | For Research Use Only! Not For Use in Humans. |
Product Types | ||
◆ Bioactive Small Molecules | ||
BSM-0027 | UNC0321 (trifluoroacetate salt) | Inquiry |
◆ Antibodies | ||
EAb-0072 | JMJD6 Polyclonal Antibody | Inquiry |
EAb-0074 | JMJD2c Polyclonal Antibody | Inquiry |
EAb-0075 | JMJD2b Polyclonal Antibody | Inquiry |
EAb-0076 | JMJD2A Polyclonal Antibody | Inquiry |
Related Gene / Proteins | |||
JMJD | JMJD1A | JMJD1B | JMJD1C |
JMJD2 | JMJD2A | JMJD2B | JMJD2C |
JMJD2D | JMJD2E | JMJD2F | JMJD3 |
JMJD4 | JMJD5 | JMJD6 | UTF1 |
UTX |
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