2. PROTAC Epigenetics Cell Cycle/DNA Damage Apoptosis
  3. PROTACs HDAC Apoptosis
  4. PROTAC HDAC6 degrader 1

PROTAC HDAC6 degrader (Compound A6) is a potent and selective PROTAC HDAC6 degrader with a DC50 of 3.5 nM. PROTAC HDAC6 degrader shows promising antiproliferative activity via inducing apoptosis in myeloid leukemia cell lines.

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PROTAC HDAC6 degrader 1 Chemical Structure

PROTAC HDAC6 degrader 1 Chemical Structure

CAS No. : 2785404-76-2

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PROTAC HDAC6 degrader 1 Related Antibodies

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Description

PROTAC HDAC6 degrader (Compound A6) is a potent and selective PROTAC HDAC6 degrader with a DC50 of 3.5 nM. PROTAC HDAC6 degrader shows promising antiproliferative activity via inducing apoptosis in myeloid leukemia cell lines[1].

IC50 & Target[1]

HDAC6

3.5 nM (DC50)

HDAC6

4.86 nM (IC50)

HDAC1

0.1 μM (IC50)

In Vitro

PROTAC HDAC6 degrader (Compound A6) (0.1-10 μM; 6 h) does not degrade HDAC1 but displays inhibitory activity toward HDAC1. PROTAC HDAC6 degrader demonstrates potent HDAC6 degradation as well as hyperacetylation of α-tubulin in U266 and HL-60 cells, confirming that the activity is not restricted to leukemia cell lines[1].
PROTAC HDAC6 degrader (0.5-50 μM) inhibits leukemia cells viability with log IC50 values of 1.2-1.7 μM[1].
PROTAC HDAC6 degrader (8-24 μM; 48 h) induces MOLM13 cell apoptosis and arrests cell cycle at sub-G1 phase[1].

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

PROTAC HDAC6 degrader 1 Related Antibodies

Western Blot Analysis[1]

Cell Line: HL-60 cells
Concentration: 100 nM, 1 μM, 10 μM
Incubation Time: 6 h
Result: Degraded HDAC6 but not HDAC1. Induced hyperacetylation of α-tubulin and caused hyperacetylation of histone H3.

Cell Viability Assay[1]

Cell Line: Acute myeloid leukemia or AML (HL-60, Kasumi, THP-1, HL-60, SKNO1, and MOLM13) and B-cell acute lymphoblastic leukemia or B-ALL (REH and 697)
Concentration: 0.5-50 μM
Incubation Time: 72 h
Result: Inhibited cell viability with log IC50 values of 1.2-1.7 μM.

Apoptosis Analysis[1]

Cell Line: MOLM13
Concentration: 8, 16 and 24 μM
Incubation Time: 48 h
Result: Induced caspase 3/7-dependent apoptosis in dose-dependent fashion.

Cell Cycle Analysis[1]

Cell Line: MOLM13
Concentration: 8, 16 and 24 μM
Incubation Time: 48 h
Result: Induced a dose-dependent increase in the sub-G1 fraction with a concomitant reduction of cell population in G2/M phase.
Molecular Weight

734.80

Formula

C37H46N6O10
CAS No.
SMILES

O=C(C1=CC=C(C=C1)NC(CCCCCCCNC(COC2=CC=CC(C(N3C4CCC(NC4=O)=O)=O)=C2C3=O)=O)=O)NCCCCCCC(NO)=O
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
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PROTAC HDAC6 degrader 1 Related Classifications

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

PROTAC HDAC6 degrader 12785404-76-2PROTACsHDACApoptosisHistone deacetylasesHL-60U266leukemiaMOLM13Inhibitorinhibitorinhibit

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