Drug intelligence / Profile preview

d rhamnose β-hederin

Development stage
Preclinical
Modality
Small Molecules
Administration
Intraperitoneal
01

Overview

D rhamnose β-hederin (DRβ-H) is a novel oleanane-type triterpenoid saponin isolated from the traditional Chinese medicinal plant *Clematis ganpiniana*. It is currently in the preclinical research stage, primarily investigated for its anti-tumor activity in breast cancer. DRβ-H exerts its effects by inhibiting the PI3K/AKT signaling pathway and activating the ERK signaling pathway, leading to the induction of apoptosis via the mitochondrial pathway (regulating Bcl-2 family proteins and activating caspases). Additionally, it has been shown to inhibit cancer cell migration and invasion by upregulating RNPC1 and E-cadherin and suppressing tumor-derived exosome secretion. It also demonstrates potential in reversing chemoresistance to agents like docetaxel and adriamycin in breast cancer cells.

Other names
D rhamnose + β-hederinD Rhamnose β-hederin3β-[(α-L-arabinopyranosyl)-oxy] olean-12-en-28-oic acid
02

Targets

AKT (RAC-alpha serine/threonine-protein kinase)CDH1 (Cadherin-1)BCL-2 (BCL-2 family)MAPK3 (Mitogen-activated protein kinase 1)RBM38 (RNA-binding protein 38)CASP3 (Caspase-3)CASP9 (Caspase-9)PI3K (Phosphoinositide-3-kinase regulatory subunit 6)

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