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Histone Demethylase

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Histone Demethylase

Chemical Structure Cat. No. Product Name CAS No.
Trans-2-Phenylcyclopropylamine hemisulfate salt Chemical Structure
BCP15493 Trans-2-Phenylcyclopropylamine hemisulfate salt 13492-01-8
Tranylcypromine hemisulfate is an irreversible, nonselective MAO inhibitor used in the treatment of depression.
Seclidemstat Chemical Structure
BCP29581 Seclidemstat 1423715-37-0
Seclidemstat is an antineoplastic drug candidate.
AS-8351 Chemical Structure
BCP29140 AS-8351 796-42-9
AS-8351 induces reprogramming of human fetal lung fibroblasts into functional cardiomyocytes.
KDM4B-IN-B3 Chemical Structure
BCP29547 KDM4B-IN-B3 2003260-55-5
KDM4B-IN-B3 is a potent KDM4B inhibitor with an IC50 of 10 nM.
OG-L002 Chemical Structure
BCP12278 OG-L002 1357302-64-7
OG-L002 is a potent LSD1 inhibitor that has been found to inhibit herpes simplex virus (HSV) immediate early gene expression and viral yield in vitro and suppresses HSV primary infection in vivo.
Vafidemstat Chemical Structure
BCP29383 Vafidemstat 1357362-02-7
Vafidemstat, also known as ORY 2001, is a lysine-specific histone demethylase (LSD1) inhibitor.
RN-1 Chemical Structure
BCP20812 RN-1 1781835-13-9
Potent lysine specific demethylase 1 (LSD1) inhibitor (IC50 = 70 nM). Exhibits selectivity for LSD1 over MAO-A and MAO-B (IC50 values are 0.51 and 2.79 μM for MAO-A and MAO-B, respectively). Impairs long-term, but not short-term memory in mice. Brain penetrant following systemic administration.
Miconazole nitrate Chemical Structure
BCP13696 Miconazole nitrate 22832-87-7
Miconazole Nitrate is an imidazole antifungal agent.
Epoxiconazole Chemical Structure
BCP14362 Epoxiconazole 135319-73-2
Epoxiconazole is a 14-α demethylase inhibitor that inhibits ergosterol synthesis and fungal cell wall formation.
KDOAM-25 Chemical Structure
BCP25150 KDOAM-25 KDOAM-25
KDOAM-25, also known as GTPL8576, is a selective inihbitor of the KDM5 family histone demethylases JARID1A, JARID1B, JARID1C and JARID1D with IC50 values < 60 nM.
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