Method of Using dihydro-resveratrol or its stilbenoid derivatives and/or chemical variants in treatments of fibrotic and diabetic conditions
US-2017290782-A1 · Oct 12, 2017 · US
US10017442B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10017442-B2 |
| Application number | US-201715849650-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 20, 2017 |
| Priority date | Jun 16, 2015 |
| Publication date | Jul 10, 2018 |
| Grant date | Jul 10, 2018 |
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The present invention relates to a polyphenol derivative of the stilbenoid family, namely trans-3,5,4′-trihydroxybibenzyl, also known as dihydro-resveratrol, as a remedial agent. In particular, the present invention presents the usage of dihydro-resveratrol or its derivatives/chemical variants in the manufacture of a medicament for the treatment of tumors or cancers. The dihydrostilbenes can be used in the treatment or delay of progression of a cancer in a patient or used in a pharmaceutical formulation for the aforementioned purposes.
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What we claim: 1. A method of treating colorectal, melanoma and pancreatic carcinoma by administering to a subject in need thereof an effective dosage of a compound of formula (2) 2. The method according to claim 1 wherein said compound is dihydro-resveratrol. 3. The method according to claim 1 wherein said compound is trans-3,5,4′-trihydroxybibenzyl. 4. The method according to claim 1 wherein said effective dosage ranges from 1.62 mg/kg to 8.13 mg/kg in body weight per day. 5. The method according to claim 1 wherein said effective dosage is 8.13 mg/kg in body weight per day. 6. The method according to claim 4 wherein said subject is human. 7. The method according to claim 5 wherein said subject is human. 8. The method according to claim 1 wherein said compound is administered in situ to site of the colorectal, melanoma and pancreatic carcinoma. 9. The method according to claim 8 wherein said compound is administered intraperitoneally to said subject in need thereof. 10. The method according to claim 1 wherein said subject is human. 11. The method according to claim 1 wherein the compound is administered every other day for an effective period of time. 12. The method according to claim 11 wherein said effective period of time is no less than 21 days.
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