1. Cell Cycle/DNA Damage Epigenetics Apoptosis
  2. HDAC Apoptosis
  3. Chlamydocin (purity≥70%)

Chlamydocin (purity≥70%), a fungal metabolite, is a highly potent HDAC inhibitor, with an IC50 of 1.3 nM. Chlamydocin (purity≥70%) exhibits potent antiproliferative and anticancer activities. Chlamydocin (purity≥70%) induces apoptosis by activating caspase-3.

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Chlamydocin (purity≥70%)

Chlamydocin (purity≥70%) Chemical Structure

CAS No. : 53342-16-8

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Description

Chlamydocin (purity≥70%), a fungal metabolite, is a highly potent HDAC inhibitor, with an IC50 of 1.3 nM. Chlamydocin (purity≥70%) exhibits potent antiproliferative and anticancer activities. Chlamydocin (purity≥70%) induces apoptosis by activating caspase-3[1].

IC50 & Target[1]

HDAC

1.3 nM (IC50)

In Vitro

Chlamydocin (purity≥70%) is originally isolated from the fungus Diheterospora chlamydosporia. Chlamydocin (purity≥70%) exhibits a broad spectrum of antiproliferative activity toward various cancer cell lines, irrespective of their p53 status. The antiproliferative activity of Chlamydocin (purity≥70%) is accompanied by accumulation of hyperacetylated histones H3 and H4, induction of p21cip1/waf1, and accumulation of cells in G2/M phase of the cell cycle[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

526.62

Formula

C28H38N4O6

CAS No.
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Purity & Documentation
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Chlamydocin (purity≥70%)
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HY-P2228
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