Lanatoside C

Lanatoside C has been studied in 3 papers since 2025: none in people yet, 1 in animals, 1 in cells, 1 review; 2 in the past year. The research so far is in animals and cells. The newest story, Nov 10, 2026: “Drug may target lab-grown human cells with reduced TET2 gene function”.

Intervention

3 papers study it5 findingsUpdated

PubChem

1 new paper in 30 daysSee all 3 papers on lanatoside C

At a glance

The findings reach mice, none yet in people. 2 independent labs in 1 country.

None of its findings points the other way.

Cells and mice: a single group. Worms or flies and humans: nothing yet.
  • 2 independent labs in 1 country
  • Funders: Ministry of Science and ICT, South Korea and others
  • Animals1
  • Cells1

What did studies of lanatoside C find?

5

Studies of lanatoside C measured 5 outcomes, among them relative donor-derived monocyte and neutrophil frequencies, macrophage apoptosis and apoptosis.

Relative donor-derived monocyte and neutrophil frequencies

downin mice1

1 study
  1. Lanatoside C decreases relative donor-derived monocyte and neutrophil frequencies in mice (partial donor-cell reconstitution model with Tet2-deficient donor-cell recipients).

    “Lanatoside C reduced relative donor‐derived monocyte and neutrophil frequencies in Tet2‐deficient donor‐cell recipients”

    Animalspartial donor-cell reconstitution model with Tet2-deficient donor-cell recipients

    Drug may target lab-grown human cells with reduced TET2 gene function

    Advanced science (Weinheim, Baden-Wurttemberg, Germany)

More on Relative donor-derived monocyte and neutrophil frequencies

macrophage apoptosis

upin cells1

1 study
  1. Lanatoside C induces macrophage apoptosis in cells (TET2-deficient macrophages compared with control cells).

    “The cardiac glycoside Lanatoside C preferentially induces mitochondrial depolarization and apoptosis in TET2 ‐deficient macrophages, with substantially smaller effects in control cells.”

    CellsTET2-deficient macrophages compared with control cellsmacrophage

    Drug may target lab-grown human cells with reduced TET2 gene function

    Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Apoptosis

upin human cells1

1 study
  1. Lanatoside C increases apoptosis in senescent HUVECs.

    “We found that Lana C depolarized and acidified senescent human umbilical vein endothelial cells (HUVECs), making them susceptible to apoptosis.”

    Cellsin senescent HUVECs

    Lanatoside C, a Novel Senolytic, Ameliorates Atherosclerosis in Mice

    Aging and disease

More on Apoptosis

Atherosclerotic lesion formation

downin mice1

1 study
  1. Lanatoside C decreases atherosclerotic lesion formation in ApoE-/- or Ldlr-/- knockout mice.

    “Lana C significantly ameliorated the senescence burden and the formation of atherosclerotic lesions in apolipoprotein E (ApoE-/-) or low-density lipoprotein receptor (Ldlr-/-) knockout mice.”

    Animalsin ApoE-/- or Ldlr-/- knockout mice

    Lanatoside C, a Novel Senolytic, Ameliorates Atherosclerosis in Mice

    Aging and disease

Senescence burden

downin mice1

1 study
  1. Lanatoside C decreases senescence burden in ApoE-/- or Ldlr-/- knockout mice.

    “Lana C significantly ameliorated the senescence burden and the formation of atherosclerotic lesions in apolipoprotein E (ApoE-/-) or low-density lipoprotein receptor (Ldlr-/-) knockout mice.”

    Animalsin ApoE-/- or Ldlr-/- knockout mice

    Lanatoside C, a Novel Senolytic, Ameliorates Atherosclerosis in Mice

    Aging and disease

More on Senescence burden

Latest

Dec 2025: 0Jan 2026: 0Feb 2026: 0Mar 2026: 0Apr 2026: 0May 2026: 1Jun 2026: 0Jul 2026: 0Aug 2026: 0Sep 2026: 0Oct 2026: 0Nov 2026: 12 papers in 12 months
Advanced Science

Drug may target lab-grown human cells with reduced TET2 gene function

A 48-hour screen of 489 compounds identified lanatoside C as a candidate for preferentially killing human immune cells with reduced TET2 gene function.A 48-hour screen of 489 compounds identified lanatoside C as a candidate for preferentially killing human immune cells with reduced TET2 gene function.

Human cell studyInterventions