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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
12 Results for "
CSNK1G2
" in MedChemExpress (MCE) Product Catalog:
Products (12)
12 Results for "CSNK1G2" in MCE Product Catalog:
2
2 Cited Publications
Research Areas:
HS-276 is an orally active, potent and highly selective TAK1 inhibitor, with a Ki of 2.5 nM. HS-276 shows significant inhibition of TAK1, CLK2, GCK, ULK2, MAP4K5, IRAK1, NUAK, CSNK1G2, CAMKKβ-1, and MLK1, with IC50 values of 8.25, 29, 33, 63, 125, 264, 270, 810, 1280, and 5585 nM, respectively. HS-276 reduces the expression of TNF, IL-6, and IL-1β. HS-276 can be used for rheumatoid arthritis (RA) research .
Cat. No.: HY-RS03249
Target:
Research Areas:
CSNK1G2 Human Pre-designed siRNA Set A contains three designed siRNAs for CSNK1G2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
Cat. No.: HY-RS27137
Target:
Research Areas:
Csnk1g2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Csnk1g2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
Cat. No.: HY-RS20628
Target:
Research Areas:
Csnk1g2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Csnk1g2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
Cat. No.: HY-P702667
Purity: ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: CSNK1G2; casein kinase 1 gamma 2; CK1G2
Species:
Source:
Cat. No.: HY-P705797
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CSNK1G2; casein kinase 1 gamma 2; CK1G2
Species:
Source:
Cat. No.: HY-P705798
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CSNK1G2; casein kinase 1 gamma 2; CK1G2
Species:
Source:
Cat. No.: HY-P72873
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: Casein kinase I isoform gamma-2;
CKI-gamma 2; CSNK1G2; CK1G2
Species:
Source:
Cat. No.: HY-147141A
Research Areas:
HS-276 hydrochloride is an orally active, potent and highly selective TAK1 inhibitor, with a Ki of 2.5 nM. HS-276 hydrochloride shows significant inhibition of TAK1, CLK2, GCK, ULK2, MAP4K5, IRAK1, NUAK, CSNK1G2, CAMKKβ-1, and MLK1, with IC50 values of 8.25, 29, 33, 63, 125, 264, 270, 810, 1280, and 5585 nM, respectively. HS-276 hydrochloride reduces the expression of TNF, IL-6, and IL-1β. HS-276 hydrochloride can be used for rheumatoid arthritis (RA) research .
Cat. No.: HY-147141B
Research Areas:
HS-276 formic is an orally active, potent and highly selective TAK1 inhibitor, with a Ki of 2.5 nM. HS-276 formic shows significant inhibition of TAK1, CLK2, GCK, ULK2, MAP4K5, IRAK1, NUAK, CSNK1G2, CAMKKβ-1, and MLK1, with IC50 values of 8.25, 29, 33, 63, 125, 264, 270, 810, 1280, and 5585 nM, respectively. HS-276 formic reduces the expression of TNF, IL-6, and IL-1β. HS-276 formic can be used for rheumatoid arthritis (RA) research .
Cat. No.: HY-184652
Target:
Research Areas:
LRRK2/JNK3-IN-1 is a brain-penetrant multi-target inhibitor of LRRK2 (including G2019S mutant and wild-type) and JNK3, with enzymatic IC50 values of 3.90 nM against LRRK2 G2019S, 3.24 nM against wild-type LRRK2, and 22.1 nM against JNK3. LRRK2/JNK3-IN-1 displays favorable selectivity in a 97-kinase profiling screen, and also shows inhibitory activity against JNK1, JNK2, and MKNK2. LRRK2/JNK3-IN-1 can be used for the research of Parkinson's disease .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
