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Curcumin Extract Powder General Health Lean Factor 1 lb
Curcumin Extract Powder General Health Lean Factor
Curcumin Extract Powder General Health Lean Factor
Curcumin Extract Powder General Health Lean Factor 4 oz

Curcumin Extract Powder

$39.99 $45.99

Product Overview

With more than 1000 published studies and over 7000 published articles curcumin extract is one of the most well researched medicinal plant extracts to date and one of nature's most powerful healers. One of the active ingredient in turmeric is curcumin. Turmeric has been used for over 2500 years in India, where it is eaten daily as a common spice in the diet. When taken with some form of fat and/or pepper it will increase the bioavailability by as much as 100 times.

Our Curcumin Extract Powder is a 95% extract (30:1 ratio) meaning each serving contains an 95% concentration of Curcuminoids.

Turmeric is a member of the curcuma botanical group which is a part of the ginger family of herbs known as zingiberaceae. On average 2-4% of curcumin is what you naturally find in turmeric in its whole root form. While turmeric has many powerful active constituents, curcumin, is the one that modern science has taken quite an interest in.  It is believed and well documented that turmeric in either its standardized form with a minimum of 95% of this active ingredient or whole form (usually added to either a fat or pepper extract) is a major key in supporting optimal wellness. Much of today’s science is focused on the ability for the body to have a healthy inflammation response and its relationship to disease.  This is where turmeric is believed to be of great value and the research clearly back this up 100%.

The research on curcumin shows it’s ability to support the body in multiple ways. First, it may support the body’s ability to modulate 700 different genes. As a part of that modulation process, it may support over 160 different physiological pathways. Next, by possibly supporting the body’s ability to make cell membranes more orderly, it may have a direct effect on signaling specific types of molecules. This signal reaction has shown to possibly interact directly with how cell survival proteins maintain integrity under extreme cellular distress. Curcumin’s ability to cross the blood-brain barrier has sparked much research into its ability to possibly support healthy neurological function. There are several characteristics that make this possible. It’s natural antioxidant compounds (ORAC score of 160,000) and its ability to support a healthy inflammation response, in and of itself, may support the function of a healthy brain.  

Additionally, curcumin may support the body’s ability to help prevent the production of beta-amyloids. This is accomplished in several ways. It may reduce levels of pro-inflammatory signaling molecules that promote beta-amyloids. It may limit oxidation of crucial fats and proteins which trigger enzymes involved in beta amyloid formation. It may support cleanup of existing beta amyloid deposits. Because curcumin is nontoxic and does not adversely affect healthy cells; it leaves this compound open for much more research on its potential uses.  

With the research showing the potential for close to 600 therapeutic effects of curcumin (according to greenmedinfo) it would only seem natural that there was proof in the pudding to support this. As a part of this research it was shown that curcumin has the potential to compete with with some of the heavy hitters in the pharmaceutical industry. A 2008 study that compared curcumin with Lipitor was published in Drugs R&D showed that curcuminoids may support the body’s ability to have healthy endothelial function equally effective as the drug.  A 1999 study published in the Journal of Phytotherapy Research found similar positive results between a corticosteroid drug and curcumin. According to this study, the curcumin was found to work in a safer fashion when supporting inflammatory eye issues.  Another study showed its potential as an alternative therapy to dexamethasone by possibly protecting against lung transplant injuries without the side effects. In a 2011 antidepressant study published in the, Journal of Acta Poloniae Pharmaceutica, found curcumin may have worked, equally as well as, the top drugs like prozac through supporting healthy levels of serotonin and dopamine.  This study took 60 patients and divided them into 3 groups. The first one took 20 mgs of Prozac every morning. The second group took 1000 mgs of curcumin and the third group took both. Evaluations after 2, 4, and 6 weeks showed that the group which took both the prozac and curcumin had 77.8% of participants responded well to the treatment. This was compared to 62.5% for the curcumin group and 64.7% for the prozac groups alone. It was concluded that curcumin may be a good add on therapy for major depression. A 2009 study comparing metformin with curcumin published in the Journal of Biochemical and Biophysical Research Communications showed that curcumin may support the body’s ability to increase glucose uptake just as well as the metformin.  

Finally, a study was done with 45 patients to evaluate curcumin to support the inflammation process associated with rheumatoid arthritis. The patients were randomly put into 3 groups. Group one received 500 mg of curcumin daily, group two received the curcumin and 50 mgs daily of the drug diclofenac, and, group three received only the drug. This study lasted 8 weeks where the patients were evaluated based on an activity score and blood work was done both before and after the 8 week period. The results of this study were quite impressive because it showed specific practical advantages of the herb over the drug. Every patient in group one stated that overall they hurt less and had significant improvement in their activity scores (group one had a 44.5% improvement, group 2 a 44.4% improvement and group 3 42.1% improvement). Group one had 93% less swelling and tenderness  compared to the other groups that saw a 73% and 33% improvement. The blood marker results were in alignment with these statements as well, proving it was not just the patient’s feelings. The exciting results showed curcumin alone to be more effective than the drug alone and the drug combined with the herb. The group with the combination had no additional benefit by adding on the drug.

This is all just the tip of the iceberg! Curcumin has a very impressive track record for long term results and safety as well. Curcumin is a clear and simple choice whether being used as an extract or added to your food to possibly support optimal health.

Some possible traditional uses of 95% Curcumin Extract Powder may include:

  • May support a healthy immune system response
  • May support healthy brain functions
  • Possibly helps support the production of glutathione, the body's "master antioxidant"
  • May support healthy cell replication
  • May support healthy bones, joints & overall skeletal system
  • May support blood vessel health
  • May support healthy lipid levels
  • May support neurological health
  • May support healthy liver function
  • May support skin health from ultraviolet B radiation (UVB) damage
  • May support a healthy digestive system
  • May support healthy memory function especially when combined with green tea
  • Possible natural antiseptic & antibacterial agent, may be useful in disinfecting cuts & burns
  • May support a healthy circulatory system
  • May maintain cell integrity when threatened by occasional environmental stressors
  • May support heart health
  • May support your overall eye health
  • May support skin health
  • Possibly provides the antioxidants you need to help support your cells against excessive oxidation & free radicals
  • May support healthy blood sugar levels already within the normal range
  • May support the neurological system's healthy response to stress
  • Possibly helps body maintain healthy cells and support against free radicals

Constituents of Curcumin Extract include:

  • Phytochemicals: Alpha-Alantone, Alpha-Terpineol, Arabinose, AR-Turmerone, Arabinose, Azulene, Bisabolene, Cinnamic-Acid, Curcumin, Curlone, L-Alpha-Cumcumene, L-Beta-Curcumene, Turmerone, Zingiberene
  • Essential Oils: Beta-Pinene, Caryophyllene, Cineole, Curcumene, Curcumenol, Curdione, Eugenol,  Limonene, Linalol, Terpinene, Trepineol   

For additional constituent information, visit:

Suggested Use: Mix ½ to 1 teaspoon with your favorite juice or add to your favorite smoothie.

Mixing Suggestions: To increase flavor and nutritional profile combine with our organic ginger, piperine extract and coconut oil.

Botanical Name: Curcuma Longa.

Other Names: Indian saffron, Curcumin, Jiang Huang, Ukon, Goeratji, Kakoenji, Koenjet, Kondin, Kunir, Kunyit, Oendre, Rame, Renet, Temu kuning, Temu kunyit, Tius, Terra Merita, Safran Boubou, Safran De Malabar, Safran Des Indes.

Parts Used: Turmeric Root.

Ingredients: Curcumin Extract standardized to 95% Curcuminoids.

Origin: Grown and extracted in China. Packaged with care in Florida, USA.

Lean Factor strives to offer the highest quality organically grown, raw, vegan, gluten free, non-GMO products available and exclusively uses low temperature drying techniques to preserve all the vital enzymes and nutrients. Our 95% Curcumin Extract Powder passes our strict quality assurance which typically includes testing for botanical identity, heavy metals, chemicals and microbiological contaminants. offers 95% Curcumin Extract Powder packaged in airtight stand-up, resealable foil pouches for optimum freshness. Once opened, just push the air out of the pouch before resealing it in order to preserve maximum potency. Keep your 95% Curcumin Extract Powder in a cool, dark, dry place.

Sources & References

1. Ammon, H.P. and M.A. Wahl. 1991. Pharmacology of Curcuma longa . Planta Med 57(1):1"“7

2. Ammon, H.P., M.I. Anazodo, H. Safayhi, B.N. Dhawan, R.C. Srimal. 1992. Curcumin: a potent inhibitor of leukotriene B4 formation in rat peritoneal polymorphonuclear neutrophils. Planta Med 58(2):226

3. Ayurvedic Pharmacopoeia of India (API). 1989. New Delhi: Government of India"”Ministry of Health and Family Welfare"”Department of Health. 45"“46

4. Baumann, J.C., K. Heintze, H.W. Muth. 1971. Klinisch-experimentelle untersuchungen der gallen-, pankreas- und magensaftsekretion unter den phytocholagogen wirkstoffen einer Carduus marianus "“Chelidonium "“Curcuma suspension [Clinico-experimental studies on the secretion of bile, pancreatic and gastric juice under the influence of phytocholagogous agents of a suspension of Carduus marianus, Chelidonium and Curcuma] Arzneimforsch 21(1):98"“101

5. Baumann, J.C. 1975. Ãœber die wirkung von Chelidonium , Curcuma , Absinth und Carduus marianus auf die galle-und pankreassekretion bei hepatopathien [Effect of Chelidonium , Curcuma , Absinth and Carduus marianus on the bile and pancreatic secretion in liver diseases]. Med Monatsschr 29(4):173"“180

6. Braun, R. et al. 1997. Standardzulassungen für Fertigarzneimittel"”Text and Kommentar . Stuttgart: Deutscher Apotheker Verlag

7. Budavari, S. (ed.). 1996. The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals , 12th ed. Whitehouse Station, N.J.: Merck & Co., Inc. 450, 1674

8. But, P.P.H. et al. (eds.). 1997. International Collation of Traditional and Folk Medicine . Singapore: World Scientific. 207"“208

9. Charles, V. and S.X. Charles. 1992. The use and efficacy of Azadirachta indica ADR ("˜Neem') and Curcuma longa ("˜Turmeric') in scabies. A pilot study. Trop Geogr Med 44(1"“2):178"“181

10. Gonda, R., M. Tomoda, K. Takada, N. Ohara, N. Shimizu. 1992. The core structure of ukonan A, a phagocytosis-activating polysaccharide from the rhizome of Curcuma longa , and immunological activities of degradation products. Chem Pharm Bull (Tokyo) 40(4):990"“993

11. Gonda, R., M. Tomoda, N. Ohara, K. Takada. 1993. Arabinogalactan core structure and immunological activities of ukonan C, an acidic polysaccharide from the rhizome of Curcuma longa . Biol Pharm Bull 16(3):235"“238

12. Hastak, K. et al. 1997. Effect of turmeric oil and turmeric oleoresin on cytogenetic damage in patients suffering from oral submucous fibrosis. Cancer Lett 116(2):265"“269

13. Iwu, M.M. 1993. Handbook of African Medicinal Plants . Boca Raton: CRC Press. 164"“166

14. The Japanese Standards for Herbal Medicines (JSHM). 1993. Tokyo: Yakuji Nippo, Ltd. 279

15. Kapoor, L.D. 1990. CRC Handbook of Ayurvedic Medicinal Plants. Boca Raton: CRC Press. 149"“150

16. Kiso, Y., Y. Suzuki, N. Watanabe, Y. Oshima, H. Hikino. 1983. Antihepatotoxic principles of Curcuma longa rhizomes. Planta Med 49(3):185"“187

17. Kiuchi, F. et al. 1993. Nematocidal activity of turmeric: synergistic action of curcuminoids. Chem Pharm Bull (Tokyo) 41(9):1640"“1643

18. Kositchaiwat, C., S. Kositchaiwat, J. Havanondha. 1993. Curcuma longa Linn. in the treatment of gastric ulcer comparison to liquid antacid: a controlled clinical trial. J Med Assoc Thai 76(11):601"“605

19. Leung, A.Y. and S. Foster. 1996. Encyclopedia of Common Natural Ingredients Used in Food, Drugs and Cosmetics , 2nd ed. New York: John Wiley & Sons, Inc. 499"“501

20. McGuffin, M., C. Hobbs, R. Upton, A. Goldberg. 1997. American Herbal Product Association's Botanical Safety Handbook. Boca Raton: CRC Press. 39

21. Nadkarni, K.M. 1976. Indian Materia Medica . Bombay: Popular Prakashan. 414"“418

22. Polasa, K., T.C. Raghuram, T.P. Krishna, K. Krishnaswamy. 1992. Effect of turmeric on urinary mutagens in smokers. Mutagenesis 7(2):107"“109

23. Rao, C.V., A. Rivenson, B. Simi, B.S. Reddy. 1995. Chemoprevention of colon carcinogenesis by dietary curcumin, a naturally occurring plant phenolic compound. Cancer Res 55(2):259"“266

24. Roth, G.N., A. Chandra, M.G. Nair. 1998. Novel bioactivities of Curcuma longa constituents. J Nat Prod 61(4):542"“545

25. Schulz, V., R. Hänsel, V.E. Tyler. 1998. Rational Phytotherapy: A Physicians' Guide to Herbal Medicine. New York: Springer

26. Selvam, R., L. Subramanian, R. Gayathri, N. Angayarkanni. 1995. The anti-oxidant activity of turmeric (Curcuma longa). J Ethnopharmacol 47(2):59"“67

27. Srinivas, L. and V.K. Shalini. 1991. DNA damage by smoke: protection by turmeric and other inhibitors of ROS. Free Radic Biol Med 11(3):277"“283

28. Srinivas, L., V.K. Shalini, M. Shylaja. 1992. Turmerin: a water-soluble antioxidant peptide from turmeric (Curcuma longa ). Arch Biochem Biophys 292(2):617"“623

29. Srivastava, K.C. 1989. Extracts from two frequently consumed spices"”cumin (Cucinum cyminum ) and turmeric (Curcuma longa )"”inhibit platelet aggregation and alter eicosanoid biosynthesis in human blood platelets Prostaglandins Leukot Essent Fatty Acids 37(1):57"“64

30. Srivastava, R., M. Dikshit, R.C. Srimal, B.N. Dhawan. 1985. Anti-thrombotic effect of curcumin. Thrombosis Res 40(3):413"“417

31. Srivastava, R., V. Puri, R.C. Srimal, B.N. Dhawan. 1986. Effect of curcumin on platelet aggregation and vascular prostacyclin synthesis. Arzneimforsch 36(4):715"“717

32. Stansbury, J.E. 1999. Cancer prevention diet"”the potential of protective phytochemicals. Nutrition Science News 4(8):380"“386

33. Subramanian, M., M. Sreejayan, N. Rao, T.P. Devasagayam, B.B. Singh. 1994. Diminution of singlet oxygen-induced DNA damage by curcumin and related antioxidants. Mutat Res 311(2):249"“255

34. Thamlikitkul, V. et al. 1989. Randomized double blind study of Curcuma domestica Val. for dyspepsia. J Med Assoc Thai 72(11):613"“620

35. Tu, G. (ed.). 1992. Pharmacopoeia of the People's Republic of China (English Edition 1992). Beijing: Guangdong Science and Technology Press. 202"“203

36. Tyler, V.E. 1994. Herbs of Choice: The Therapeutic Use of Phytomedicinals . New York: Pharmaceutical Products Press

37. Yen, K.Y. 1992. The Illustrated Chinese Materia Medica"”Crude and Prepared. Taipei, Taiwan: SMC Publishing, Inc. 82

38. Ferreira, L.A. et al. 1992. Antivenom and biological effects of ar -turmerone isolated from Curcuma longa Toxicon 30(10):1211"“1218

39. Jentzsch, K., T. Gonda, H. Höller. 1959. Papierchromatographische Unterscheidung von Curcuma domestica Val. und Curcuma xanthorrhiza Roxb. Pharm Acta Helv 34(4):181"“188

40. Jiangsu Institute of Modern Medicine. 1977. Zhong Yao Da Ci Dian (Encyclopedia of Chinese Materia Medica), Vol. 3. Shanghai: Shanghai Scientific and Technical Publications

41. Leung, A.Y. 1984. Chinese Herbal Remedies . New York: Universe Books. [Republished as: Chinese Healing Foods and Herbs. 1993. Glen Rock: AYSL Corp.]

42. Qureshi, S., A.H. Shah, A.M. Ageel. 1992. Toxicity studies on Alpinia galanga and Curcuma longa . Planta Med 58(2):124"“127

43. Randhawa, G.S. and R.K. Mahey. 1988. Herbs, Spices, and Medicinal Plants: Recent Advances in Botany, Horticulture, and Pharmacology , Vol. 3. Phoenix: Oryx Press

44. Srimal, R.C. and B.N. Dhawan. 1973. Pharmacology of diferuloyl methane (curcumin), a non-steroidal anti-inflammatory agent. J Pharm Pharmacol 25(6):447"“452




































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