Drug intelligence / Profile preview

maritoclax

Development stage
Preclinical
Lead developer
Penn State College of Medicine
Modality
Small Molecules
Administration
Experimental; Likely In Vitro And Possibly In Vivo Preclinical Studies Only; No Established Clinical Route
01

Overview

**Maritoclax** (also known as marinopyrrole A) is a **natural product** isolated from marine Streptomyces species. It is a **small molecule inhibitor** that targets the anti-apoptotic protein **Mcl-1** (myeloid cell leukemia 1), a member of the Bcl-2 family of proteins. Maritoclax binds directly to Mcl-1, disrupts its interaction with the pro-apoptotic protein Bim, and induces proteasome-mediated degradation of Mcl-1. This leads to the induction of apoptosis, especially in cancer cells that rely heavily on Mcl-1 for survival. Maritoclax has shown particular effectiveness in sensitizing cancer cells (including melanoma, hematologic malignancies, and leukemia) to other therapies targeting Bcl-2 proteins (such as ABT-737), overcoming resistance associated with high Mcl-1 expression. It has also demonstrated antimicrobial activity, including activity against methicillin-resistant *Staphylococcus aureus*.[1][2][3][4][8]

Brand names
maritoclax
Other names
marinopyrrole A
02

Targets

MCL1 (Myeloid cell leukemia sequence 1)

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