1. Cell Cycle/DNA Damage
  2. CDK
  3. PROTAC CDK9 degrader-6

PROTAC CDK9 degrader-6 is a PROTAC targeting to CDK9 sepcifically. PROTAC CDK9 degrader-6 mediates CDK9 degradation via the proteasome. PROTAC CDK9 degrader-6 degrades CDK9 with DC50s of 0.10 μM and 0.14 μM for the CDK942 and CDK955 isoforms, respectively.

For research use only. We do not sell to patients.

PROTAC CDK9 degrader-6 Chemical Structure

PROTAC CDK9 degrader-6 Chemical Structure

CAS No. : 2935587-91-8

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Description

PROTAC CDK9 degrader-6 is a PROTAC targeting to CDK9 sepcifically. PROTAC CDK9 degrader-6 mediates CDK9 degradation via the proteasome. PROTAC CDK9 degrader-6 degrades CDK9 with DC50s of 0.10 μM and 0.14 μM for the CDK942 and CDK955 isoforms, respectively[1].

IC50 & Target[1]

CDK942

0.03 μM (DC50)

CDK955

0.05 μM (DC50)

In Vitro

PROTAC CDK9 degrader-6 (compound 16) (1 μM; 6 h) decreases the protein level of MCL2, and competely degrades CDK9 in MV411 cells[1].
PROTAC CDK9 degrader-6 (1 μM; 1-6 h) time-dependently decreases the protein level of MCL2, and CDK9, and remaines suppression for 24 h[1].

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

Western Blot Analysis[1]

Cell Line: MV411 cells
Concentration: 1 μM
Incubation Time: 1 h, 2 h, 4 h, 6 h
Result: Degraded CDK9 starting at 2 h incubation and reaching a plateau at 4 h.
Remained suppressed for 24 h with some recurrence at 48 h after finished treatment.
Molecular Weight

878.80

Formula

C42H49Cl2N9O8

CAS No.
SMILES

O=C(NCCCCCCCCCCC(N1CCC(CC1)NC(C2=NNC=C2NC(C3=C(C=CC=C3Cl)Cl)=O)=O)=O)CNC4=CC=CC(C(N5C6CCC(NC6=O)=O)=O)=C4C5=O

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

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PROTAC CDK9 degrader-6
Cat. No.:
HY-149963
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