Drug intelligence / Profile preview

c6 ceramide

Development stage
Unknown
Lead developer
PendreaBio
Modality
Small Molecules
Administration
Intravenous, Topical
01

Overview

C6 ceramide is a synthetic, cell-permeable analog of naturally occurring long-chain ceramides. It is more hydrophobic than shorter-chain analogs and closely mimics some biological effects of physiological ceramides. C6 ceramide acts by mediating diverse cellular activities, primarily inducing apoptosis (programmed cell death), arresting the cell cycle (notably at G0/G1), activating protein phosphatase 2A, and modulating MAP kinase pathways. It inhibits mitochondrial respiration and promotes cell death in a range of cancer cell lines, including cutaneous T cell lymphoma, breast, colon, and ovarian cancers. In addition, C6 ceramide suppresses insulin-induced tyrosine phosphorylation, inhibits glycoprotein trafficking, and affects neurite growth. It has been formulated into nanoliposomes (CNL) to improve its pharmacokinetics and cell delivery, with preclinical and early clinical studies focused on cancer therapy, notably for relapsed/refractory acute myeloid leukemia (AML) and advanced solid tumors.

Other names
N-hexanoyl-D-erythro-sphingosineN-(hexanoyl)sphing-4-enineC6CerC-6CerC 6CerC6 Ceramide (d18:1/6:0)
02

Targets

AKT (RAC-alpha serine/threonine-protein kinase)PP2A (Protein phosphatase 2A)SPT (Serine palmitoyltransferase)CTSD (Cathepsin D)

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