6 Results for "

KDM5D

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "KDM5D" in MCE Product Catalog:

9
9 Publications Verification
Cat. No.: HY-102047B
CAS No.: 2448475-08-7
Purity:  98.11%
Target:  

Histone Demethylase

Research Areas:  

Cancer

KDOAM-25 citrate is a potent and highly selective histone lysine demethylases 5 (KDM5) inhibitor with IC50s of 71 nM, 19 nM, 69 nM, 69 nM for KDM5A, KDM5B, KDM5C, KDM5D, respectively. KDOAM-25 citrate increases global H3K4 methylation at transcriptional start sites and impairs proliferation in multiple myeloma MM1S cells .
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Cat. No.: HY-RS07221
Research Areas:  

Others

KDM5D Human Pre-designed siRNA Set A contains three designed siRNAs for KDM5D gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-102047
CAS No.: 2230731-99-2
Target:  

Histone Demethylase

Research Areas:  

Cancer

KDOAM-25 is a potent and highly selective histone lysine demethylases 5 (KDM5) inhibitor with IC50s of 71 nM, 19 nM, 69 nM, 69 nM for KDM5A, KDM5B, KDM5C, KDM5D, respectively. KDOAM-25 increases global H3K4 methylation at transcriptional start sites and impairs proliferation in multiple myeloma MM1S cells .
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Cat. No.: HY-RS23621
Research Areas:  

Others

Kdm5d Rat Pre-designed siRNA Set A contains three designed siRNAs for Kdm5d gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS17171
Research Areas:  

Others

Kdm5d Mouse Pre-designed siRNA Set A contains three designed siRNAs for Kdm5d gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-102047A
Target:  

Histone Demethylase

Research Areas:  

Cancer

KDOAM-25 trihydrochloride is a potent and highly selective histone lysine demethylases 5 (KDM5) inhibitor with IC50s of 71 nM, 19 nM, 69 nM, 69 nM for KDM5A, KDM5B, KDM5C, KDM5D, respectively. KDOAM-25 trihydrochloride increases global H3K4 methylation at transcriptional start sites and impairs proliferation in multiple myeloma MM1S cells .
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