Drug intelligence / Profile preview

minnelide

Development stage
Phase 2
Lead developer
Minneamrita Therapeutics
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Metabolically Activated Prodrugs → Prodrugs/Conditional Activator Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

Minnelide is a water-soluble prodrug of triptolide, a diterpene triepoxide derived from the Chinese herb Tripterygium wilfordii (thunder god vine). Upon administration, Minnelide is rapidly converted in the body to its active form, triptolide. Triptolide exerts potent anticancer effects by inhibiting heat shock protein 70 (HSP70), leading to disruption of cancer cell survival pathways and induction of apoptosis. Additional mechanisms include inhibition of MYC-driven transcriptional programs and suppression of NF-κB-mediated expression of pro-survival genes. Minnelide has demonstrated preclinical and early clinical activity against various solid tumors—including pancreatic cancer, gastric cancer (including advanced gastric cancer), colorectal cancer, adenosquamous carcinoma of the pancreas (ASCP), non-small cell lung cancer (NSCLC), and acute myeloid leukemia—by reducing tumor growth and promoting tumor cell death. It is being developed primarily as an antineoplastic agent for refractory or relapsed cancers[2][3][4][5][6][8].

Brand names
Minnelide
Other names
water-soluble triptolide prodrug
02

Targets

NF-κBHsp70 (70 kDa heat shock protein)MYC (MYC proto-oncogene protein)

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