1. PROTAC Epigenetics
  2. PROTACs Histone Methyltransferase
  3. CARM1 degrader-1

CARM1 degrader-1 is a CARM1 PROTAC degrader (DC50 = 8.1 nM) with high selectivity over other protein arginine methyltransferases. CARM1 degrader-1 degrades CARM1 in a VHL- and proteasome-dependent manner. CARM1 degrader-1 downregulates the methylation level of CARM1 substrates in cell-based assays. CARM1 degrader-1 inhibits cancer cell migration in cell-based assays. CARM1 degrader-1 can be used for the research of breast cancer.
(Pink: CARM1 ligand (HY-114965); Blue: VHL ligand (HY-112078); Black: linker).

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

CARM1 degrader-1

CARM1 degrader-1 Chemical Structure

CAS No. : 3032785-00-2

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Description

CARM1 degrader-1 is a CARM1 PROTAC degrader (DC50 = 8.1 nM) with high selectivity over other protein arginine methyltransferases. CARM1 degrader-1 degrades CARM1 in a VHL- and proteasome-dependent manner. CARM1 degrader-1 downregulates the methylation level of CARM1 substrates in cell-based assays. CARM1 degrader-1 inhibits cancer cell migration in cell-based assays. CARM1 degrader-1 can be used for the research of breast cancer[1]. (Pink: CARM1 ligand (HY-114965); Blue: VHL ligand (HY-112078); Black: linker).

IC50 & Target[1]

CARM1

8.1 nM (DC50)

In Vitro

CARM1 degrader-1 (compound 3b) (6.25-500 nM, 0.1-10 μM; 1-48 h) potently degrades CARM1 in MCF7 cells with a DC50 of 8.1 nM and 97% maximal degradation, achieving significant degradation within 2 h and sustaining it for up to 48 h[1].
CARM1 degrader-1 (0.5 μM; 24 h) degrades CARM1 in MCF7 cells in a CARM1-binding-, VHL-, proteasome-, and neddylation-dependent manner[1].
CARM1 degrader-1 (0.01-10 μM, 25 nM; 4-24 h) exerts highly selective degradation of CARM1 over PRMT1, PRMT6, and PRMT5 in MCF7 cells, with minimal off-target proteome effects[1].
CARM1 degrader-1 (0.1-10 μM, 0.5 μM; 2-48 h) potently inhibits asymmetric dimethylation of CARM1 substrates BAF155 and PABP1 in MCF7, BT474, and MDA-MB-231 breast cancer cells, with at least 100-fold greater functional potency than the CARM1 inhibitor TP-064 in MCF7 cells[1].
CARM1 degrader-1 (0.5 μM; 20 h) potently inhibits migration of MDA-MB-231 triple-negative breast cancer cells[1].
CARM1 degrader-1 potently degrades CARM1 in MCF10A normal human mammary epithelial cells[1].
CARM1 degrader-1 (7 days) does not inhibit proliferation of MCF7, MCF10A, or MDA-MB-231 cells[1].

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

Cell Viability Assay[1]

Cell Line: MDA-MB-231 triple-negative breast cancer cells
Concentration: 0.5 μM
Incubation Time: 20 h
Result: Reduced the migration area to ~15% of DMSO-treated controls.
Showed significant inhibition compared to DMSO.

Western Blot Analysis[1]

Cell Line: MCF7 cells
Concentration: 0.1 μM, 0.5 μM, 1 μM
Incubation Time: 24 h
Result: Exerted highly degradation of CARM1.
Molecular Weight

1279.68

Formula

C71H98N12O8S

CAS No.
SMILES

O=C([C@H]1N(C([C@@H](NC(CN2CCN(CC3CCN(CC4CCN(C(COC5=CC=C(OC6=CC=CC(C(N(C)CC7=CC(C8CCN(CCNC)CC8)=NC=C7)=O)=C6)C=C5)=O)CC4)CC3)CC2)=O)C(C)(C)C)=O)C[C@H](O)C1)N[C@H](C9=CC=C(C%10=C(C)N=CS%10)C=C9)C

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

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CARM1 degrader-1
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HY-156152
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