Brazilian Honeybees
50 to 55%
Resins of vegetable sources
Bee wax
8 to 10%
Essencial oils
In minor quantities, we can find fatty acids, organic acids, aminoacids, vitamins and minerals.
  • Antimicrobial  
• Antifungal
• Antivirotic
• Anti-protozoan
• Bactericidal and Bacteriostatic
• Anesthetic
• Anti-inflammatory
• Antioxidant
• Cicatrization agent and
Tissue regeneration
• Anti-septic and hipotensives
• Gingivitis treatment
• Hepatoprotection activity and anti-ulcer agent
• Immune System stimulant
• Anti-tumor activity


- Inside the cells: where the queen puts its eggs, and worker bees deposits honey, propolis is used to make it stronger and for desinfection;

- In openings: Avoiding invaders like ants, beetles, and mites entrance to prejudice the hive integrity,
contaminating it;

- In hive cleaning: when an invader is neutralized inside the hive, and it cannot be brought out by the bees, they cover it with propolis, to avoid putrefaction, and consequent hive contamination.

For these reasons, the greeks named this substance as


"in favor" of the "city" or - in favor of the hive.

Propolis' Biological Activity
Antitumor Activity of Artepillin-C


- Hayashibara Biochemical Laboratory Counselor
- Kawasaki Medical School Emeritus Professor

Recently, when the reaching limits of western medical science have being pointed out, expectation on oriental medical science and popular medical therapy increases. And propolis - which has an old history in Europe as a traditional popular medicine, is receiving now strong interest.


Many bioactive substances from propolis have been discovered and reported. We also have demonstrated the results of our research concerning the macrophage activity and bactericidal activity so far. But this time, squeezing focus to the cell-killing effect, in result of repeating examination, we succeed to isolate Artepillin-C. In this substance, other than active macrophage activation and bactericidal action, we have verified a superior antitumor effect on each kind of cultured cancer cells and in transplanted tumor cells in a mouse.


The Artepillin-C prepared for this experience was obtained from an ethanolic extraction of brazilian propolis. Its structural and chemical formula are as shown on the attached figure. (figure 1)

Figure 1 - Artepillin-C structural and chemical formula

This substance is not water soluble, and initially, we dissolved it in ethanol and added to the culture solution, but later, we developed also a water soluble solution which we are using now.


1. Inhibition effect on the multiplication of culture tumor cells


First, as a fundamental experiment, Artepillin-C was added to culture cancer cells. We examined its effects.


The prepared cancer cells were:

- Human malignant tumor cells (6 kinds - lung cancer, stomach cancer, liver cell cancer etc.);
- Human Leukemia cell and Lymph malignant tumor (4 kinds – Lymph Leukemia, Myeloid Leukemia, Monocyte Leukemia, etc.);
- Rat origin cells (liver cell cancer);
- Mouse origin cells (3 kinds - Colon cancer, Malignant Melanoma, Fibroblast tumor etc.);
- Normal cells (Mouse origin fibroblast cells)

As result, remarkable multiplication control were shown in most of the above mentioned cancer cells at 10~100μg/mL of Artepillin-C concentration. (figure 2 and picture 1). In most cases, 3 or 4 days after Artepillin-C addition, cancer cells were extinct.

Figure 2 - Artepillin-C's Depression Effect on culture tumor cells




Picture 1 - Artepillin-C`s process multiplication depression effect on cancer cells
  Human lung cancer cells Human lung cancer cells
  not processed - 24 hours Artepillin-C 100 μg processed - 24 hours remarkable cell damage
  Human stomach cancer cells Human stomach cancer cells
  not processed - 24 hours Artepillin-C 100 μg processed - 24 hours notorious cancer cells necrosis
However, even acknowledging the remarkable cell-killing effect we couldn’t use it in the organism if it prejudices also healthy cells. Then, we prepared a comparative experiment with healthy cells, and as result, obtained that the shorter the cell cycle, the higher is the cell-killing effect.

Comparing with normal cells, cells that suffered mutation are very fast and at the same time has as characteristic that it multiplies limitlessly. Artepillin-C does with these cells, that keep multiplying in a short period of time, a selective cell-killing-and-wounding (sharp-shooting).

To elucidate the reason of this, measuring the influence on DNA synthesized at cell division time, it was proven that the DNA synthesis was obstructed when the tumor cells multiplication was remarkable.

For example, the obstruction on DNA synthesis in human leukemia cells at the concentration of 100μg/mL was remarkable , and in mouse melanoma cells even more remarkable, but in case of normal fibroblasts, old cells and cells where DNA synthesis was static, the damage on DNA was minor.


This fact tells the possibility that, Artepillin-C’s does minor damage in normal healthy cells (culture cells), which have a loose multiplication speed comparing to cancer cells, and that in fast advance and easily spread cancer cells, it demonstrates the stronger depression effect, proportionally.


2. Cancer multiplication control experiment on mouse.


In parallel to the above experiments done in this laboratory, an experiment with transplanted cancer cells on mature mouse was done. The transplant were prepared with human origin lung cancer, stomach cancer, liver cancer cells; mouse origin colon cancer; and rat origin liver cancer cells.


Among mice which received the transplants, one group was left as control, and on the other group 500μg of Artepillin-C was injected in each one, with one day gap. Observation of the process was done. One of the examples of it are shown in the pictures. (picture 2 ~ 5)


This is the mouse which received a transplant of human lung cancer cells. In the ones that nothing was injected, the cancer cells multiplied and formed a lump. In relation with it, the ones injected with Artepillin-C, the tumor divided itself into small tumors and its growing wasn`t visible. (pictures 2 and 3)

  Picture 2 - Picture 3 -
  Human lung cancer tumor transpalnted in a nude mouse Injecting Artepillin-C in this tumor and it stopped growing
In those injected with Artepillin-C during the tumor growing, it eventually suffer necrosis and fell off. (pictures 4 and 5)
  Picture 4 - Picture 5 -
  Grown tumor injected with Artepillin-C, most of it suffered necrosis (black section) This tumor eventually fell off, forming a clot where the tumor was.

The dissection result – In all tumor cell cases, Artepillin-C`s effect caused the nucleus denaturation by melting and concentration (picture 6), the nucleus fragmentation (picture 7), the natural death of a small group (picture 8), the solidification and necrosis of a extensive and large group (picture 9), clearly demonstrating it’s depression on multiplication of cancer cells effect.

Pictures 6 ~ 9 - Effect of Artepillin-C on transplanted human lung cancer cells
  Picture 6 - Picture 7 -
  Nucleus denaturation and melting Nucleus fragmentation
  Picture 8 - Picture 9 -
  Natural death of a small group fragmentation and necrosis of a large group

3. Damaged section restoration phenomena.


There is another point that should be observed here. In the group of mouse which received for a long time Artepillin-C, lymphocytes infiltrates the surroundings of cancer cells that suffered necrosis, and furthermore, the collagen from the cellular matrix encloses it, advancing in the restoring process of the damaged section by the cancer (healing the wound). (picture 10 and 11)

  Picture 10 -
  With collagen multiplication, cancer cells are enclosured (cancer nest surrounded like an island. - * sign)
  Picture 11 -  

With the macrophages and lymphocytes multiplication, collagen multiplication advances (zoom of the area with ↓ sign on picture 10)


This fact demonstrates that by Artepillin-C`s effect, collagen multiplication is promoted, stopping cancer multiplication and converting it in an island, and as result, makes it possible to the organism to coexist with the cancer for a long time.

This way Artepillin-C extinguishing selectively cancer cells, plus – without collateral effects, and in addition, increasing immunity activity, enclosing cancer cells, and restoring the damaged section. Accepting that we have demonstrated and verified many anti-cancer activities, we furthermore, continue to research and develop minute and multilaterally.

- Tetsuo Kimoto
  1945 – Graduated at Okayama University, Medicine College
  1954 – Became PhD in Medicine
  1958 – Became Medical Department Lecturer at Okayama University

1962 to 1965 – Scholarship in the USA (Rosewell Park Memorial Laboratory), in the returning year became Assistant Professor of the Medical Department of Okayama University.

  1972 – Became Professor at Kawasaki Medical School.
  1976 – Director of the Kawasaki University Organized Culture Imunity Center
  1990 – Nominated Emeritus Professor of Kawasaki Medical School. Professor at the Kawasaki College of Allied Health Professions, successive services at the Kawasaki University of Medical Welfare.

Since 1995 – Counselor of Hayashibara Biochemical Laboratory Ltd.
Published in December 1st, 2001 - in “Propolis Kenkou Tokuhon 1” from the series “Health Science” magazine, volume 3, pages 45~48 – by Touyou Igakusha Ltd.

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