WO2014052225A1 - Composition for prostatic hyperplasia and prostate cancer - Google Patents

Composition for prostatic hyperplasia and prostate cancer Download PDF

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Publication number
WO2014052225A1
WO2014052225A1 PCT/US2013/061143 US2013061143W WO2014052225A1 WO 2014052225 A1 WO2014052225 A1 WO 2014052225A1 US 2013061143 W US2013061143 W US 2013061143W WO 2014052225 A1 WO2014052225 A1 WO 2014052225A1
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Prior art keywords
tea
composition
extracts
prostate
prostate cancer
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PCT/US2013/061143
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French (fr)
Inventor
Shiming Li
Qiang Wu
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Shiming Li
Qiang Wu
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Publication of WO2014052225A1 publication Critical patent/WO2014052225A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A61K31/3533,4-Dihydrobenzopyrans, e.g. chroman, catechin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • A61K36/82Theaceae (Tea family), e.g. camellia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/88Liliopsida (monocotyledons)
    • A61K36/889Arecaceae, Palmae or Palmaceae (Palm family), e.g. date or coconut palm or palmetto

Definitions

  • This invention relates to a composition and method for the treatment of prostate diseases, such as, benign prosthetic hyperplasia, hereinafter referred to as "BPH " .
  • Benign proetatsc hyperplasia or 8PH a gradual enlargement of the prostate, Is the most common benign proliferative disorder of unknown etiology found in men, affecting- at least 80% of all men over age 50 years old. An enlarged prostate Is not cancer. There is no evidence that BPH leads to prostate cancer. However, symptoms of both disorders are similar, and it is possible to have BPH and prostate cancer at the same time. Deregulation of testosterone's conversion to dmydrotesfosterone (DHT) by 5 alpha-reductase Is the key step in the development of BPH.
  • DHT dmydrotesfosterone
  • Elevated DHT ievels correlate with the pathogenesis and progression of androgen-dependent diseases such as prostate cancer and BPH.
  • the relationship between prostate cancer and androgens is concluded to be U-shaped, with both extremes of androgen concentrations being associated with increased risk of invasive cancer.
  • 8PH has been treated with Sa-reductase inhibitors such as sa palmetto extracts, In which the conversion of testosterone to DHT Is blocked. Hence, the DHT ievei available to prostate tissue Is lowered.
  • Drugs for BPH treatment also include alpha-adrenerglc receptor
  • dietary supplements for promoting prostate health include horbal agents saw palmetto extracts (SPEp rye grass pollen extract, pygeum, lycopone from tomato (peel) extraels : and extracts from
  • EC1. 14 99,9 EC4. 1.2.30 is the microsomal cytochrome P45G-dep@ndeni rnono-oxygenase which catalyzes doth l/a-hydroxylation and ciaavage of the C1?,20-3 ⁇ 4ide chain during the conversion of 21 -carbon steroids pregnenolone (human) and progesterone (rat) to the 19-carbon androgens
  • the present invention comprises compositions of compounds which are useful for promoting prostate health, treating prostate diseases Including enlarged prostate, prostatitis, benign prosthetic hyperplasia and prostate cancer.
  • the com osition of the present invention may be obtained either by ⁇ 1 ⁇ extraction from natural products such as tea, saw palmetto, fruits and/or vegetables as weii as animal and vegetable oils or (2) by chemical synthesis from compounds o tained from natural products. More particularly, the synthesized compounds of the invention are obtained from the chemical or enzymatic reaction between fatty acids and polyphenols or benzotroplone derivative that have phenolic groups to produce esters which exhibit the properties of the Inventive composition.
  • the inventive compositions are administered to a human subject diagnosed with/and or suffering from a prostate disease in an anti-prostate disease effective amount of the inventive composition.
  • the natural product combination of the present Invention preferably is comprised of tea extracts and sa palmetto extracts.
  • Suitable tea extracts include green tea extracts, black tea extracts or both.
  • the efficacious compounds in tea extracts are tea polyphenols including green tea
  • Suitable black tea polyphenols Include thea iavlns and ihearub!gins..
  • Theaflav!ns include theaflavin (TFI) ; theaflavln-B-monogailte (IF 2a or TF2, ⁇ S f eaflavsn-3' «moncgai!ate CTF2b or TF2h, theafIavin-3,3 -digallate ⁇ TF3) 5 isotheaflavins, theaflagaliins. fbeafiavates, fheaiiavlc acids, theanap thoquinone.
  • Theafubigins include bistheaflavins t thead;ben£otroplones : theatribenzotropoiones ; dehydrotheatlavins, EGCG dlmer and oiicopolymers, Iheasinensins., and atheogallimn.
  • POISJ Green tee eatechins and black tea theafiavins can inhibit CYP1 , and or Inhibit both CYP17 and Sa ⁇ reductase ; which consequently inhibit the production of testosterone and DHT that are responsible for prostate cancer promotion.
  • the green tea component EGCG end black tea component Theaflavln-3-O-monoqallate can in ibi human prostate carcinoma INCaP cells.
  • a recent double-blind study far 200 individuals was carried out wherein 100 individual took SOOmq of green tea polyphenols and another 100
  • PC!ITJ Tea polyphenols particularly EGCG, EGG. EC in green tea extracts and black tea polyphenols such as theaflavins ; i.e. Theaflsvin, Tfteafiavin-3- monogallate i Theafiavin-S'-- monogai!ate and ThealiavlmS ⁇ -dsgailate etc b nzotropofone derivatives have strong anil- Inflammatory activity Tea polyphenols can down-regulate the expression of Cox-2, INOS, TNF-a. MFKS, IU. IL-8, lL-8 ( ICA&M , p53, im ki ase, AP-i Inflammation genes and inhibit protein activity. Also, tea polyphenols can induce cancer cell apoptosis.
  • tea polyphenols can induce cancer cell apoptosis.
  • 100183 Saw palmetto extracts suitable for use in the present invention ma be obtained by the extraction of saw palmetto berry, leaves and plants using both organic and water as solvents such as ethyl acetate, ettianol, methanol liquid carbon dsoxlde, acetone or mixtures of solvents.
  • esters has the formula:
  • the polyphenols may be from EC EGG, EGG, EGCG, GC 5 GCG
  • the fatty acids may be from saw palmetto (including lauric acid, n nstic acid, palmitic sold, stearic acid, eapric acid, caprylic acid, oleic acid, fin ieic acid. Unolenlo acid, and other fatty acids and fatty alcohols and sterols in saw palmetto), pygeum, folium urtloae, dandelion, juniper berry, rhisome phragrnifls (reed root). couehgrass, coucngrass root (tea root; and fatty acids from other plant extracts.
  • saw palmetto including lauric acid, n nstic acid, palmitic sold, stearic acid, eapric acid, caprylic acid, oleic acid, fin ieic acid. Unolenlo acid, and other fatty acids and fatty alcohols and sterols in saw palmet
  • the compounds synthesized also include the esters formed from fatty acids and enzotropione derivatives that have phenolic group(s).
  • esters include mixtu e of esters formed by treating tea extracts and saw palmetto extracts in a certain ratio with acids and or enzymes that can catalyze the ester synthesis,
  • the polyphenols also Include flavonosds, such as f avonolds from fruits, for example, apple, citrus fruits and citrus peels, blue berry, and cranberry, and/or vegetables, such as, onion, broccoli, tomato, carrots and the like.
  • flavonosds such as f avonolds from fruits, for example, apple, citrus fruits and citrus peels, blue berry, and cranberry
  • vegetables such as, onion, broccoli, tomato, carrots and the like.
  • the sources of fatty acids include sa palmetto, pygeum, folium
  • amines and anilines also can be used to synthesize amides from fatty acids and these amines and anilines, such as celliam;ne from Rhixoma phragmltis.
  • the combination formulas composed of combination of tea extracts and other one or more plant extracts .e.g., saw palmetto extracts, the formed compounds (esters and amides) between the fatty acids and polyphenols (and also amines and anilines from some plants) can promote prostate health and treat prostate diseases including enlarged prostata, prostatitis, benign prostatic hyperplasia ⁇ BPH ⁇ and prostate cancer,
  • the resulting combination formula is expected to treat BPH and prevention and treatment of prostata cancer by s nsrglstiealy inhibiting Sa-reductase by saw palmetto extracts and tea polyphenols; b inhibiting CYP17 f17a-hydroxyiase/C1T ; 20- lyase) by thea!lsylns and thearubiglns m black tea extracts and eatechins in green tea extracts; by inhibiting the growth of prostate cancer celis ⁇ LNCaP) and further decreasing the level of androgen receptor and the decrease of PSA secretion: and by strong anthlnflammatlon and apoptotic activity of tea polyphenols,
  • the extract may be prepared by extraction from water, eihanoL mixture of water and ethanol, ethyl acetate., methanol or mix ure of methanol and water.
  • the extraction Is carried out for rom 5-60 minutes and repealed 2-3 times.
  • the extraction temperature range from ambient temperature to 100 °C. the temperature as even higher, 120 e C to 140 ; € when pressure was applied In the extraction process.
  • the pressure can be as high as 100 aim (1500 psl).
  • composition of the invention may be administered to a human subject diagnosed with a prostate disease in an antlprostate disease effective amount by Intravenous injection, subcutaneous injection, intramuscular Injection , topical application, oral administration in liquid or tablet form or other conventions forms of medicinal administration, e.g., nasal injection or inhalation via drops or spray..,
  • An Important aspect in treating BPH and prostate cancer prevention and treatment is the combination of tea ⁇ black tea and green tea) extracts and saw palmetto extracts m various proportions., suet; as 10%-9S
  • Tea extracts can be green tea extract , black tea extracts or the mixture of green tea extracts and black, tea extracts ;n various proportion of each tea extracts
  • the tea polyphenols, or catechsn content of green tea extracts range from I %-99% and the content of theaiiavins in black tea extracts range f om S%- 90%.
  • Black tea extracts can contain thearublgins range from 5% ⁇ 80%. All proportions expressed herein are on a weight/weight basis.

Abstract

A composition and method for the treatment of prostate diseases, such as, benign prosthetic hyperplasia, hereinafter referred to as "BΡΗ" is disclosed. The composition of the present invention may be obtained either by (1) extraction from natural products such as tea, saw palmetto, fruits and/or vegetables as well as animal and vegetable oils or (2) by chemical synthesis from compounds obtained from natural products. Methods for preparing and using the inventive composition are also disclosed.

Description

COMPOSITION FOR PROSTATIC HYPERPLASIA AND PROSTATE CANCER
Figure imgf000002_0001
10 031 (1 ) F eld of the Invention
[ 0041 This invention relates to a composition and method for the treatment of prostate diseases, such as, benign prosthetic hyperplasia, hereinafter referred to as "BPH".
POOS] (2) Description of Related Art
0)006] Benign proetatsc hyperplasia or 8PH, a gradual enlargement of the prostate, Is the most common benign proliferative disorder of unknown etiology found in men, affecting- at least 80% of all men over age 50 years old. An enlarged prostate Is not cancer. There is no evidence that BPH leads to prostate cancer. However, symptoms of both disorders are similar, and it is possible to have BPH and prostate cancer at the same time. Deregulation of testosterone's conversion to dmydrotesfosterone (DHT) by 5 alpha-reductase Is the key step in the development of BPH. Elevated DHT ievels correlate with the pathogenesis and progression of androgen-dependent diseases such as prostate cancer and BPH. The relationship between prostate cancer and androgens is concluded to be U-shaped, with both extremes of androgen concentrations being associated with increased risk of invasive cancer. 8PH has been treated with Sa-reductase inhibitors such as sa palmetto extracts, In which the conversion of testosterone to DHT Is blocked. Hence, the DHT ievei available to prostate tissue Is lowered.
[000?! Drugs for BPH treatment also include alpha-adrenerglc receptor
blockers. Up to now, dietary supplements for promoting prostate health include horbal agents saw palmetto extracts (SPEp rye grass pollen extract, pygeum, lycopone from tomato (peel) extraels: and extracts from
pomegranates.
|0008J Recent studies show t at tea extracts exhibit anti-cancer properties against prostate cancer. The growth of prostate cancer is dependent of male sex hormones, such as testosterone and 5a~dlhydrotesiostefone (DH ), The known treatment of prostate cancer Is generally an effort to block the synthesis and action of androgens. In the biosynthesis of androgens, a crucial enzyme, 17a- hydroxyiase/Cl / JOPyase (CYP17,
EC1. 14 99,9 EC4. 1.2.30), is the microsomal cytochrome P45G-dep@ndeni rnono-oxygenase which catalyzes doth l/a-hydroxylation and ciaavage of the C1?,20-¾ide chain during the conversion of 21 -carbon steroids pregnenolone (human) and progesterone (rat) to the 19-carbon androgens
dehyoroaplandrosterone and androstenedscne; respectively. Current drug and surgery treatments are directed to eliminating testosterone production which Is about (90%) from testes out not that produced Py the adrenal route { 10%}.
! Sum a ^^^
|O01 C¾ We have discovered a composition which exhibits strong protective eftectsfcr prostate and effectively cure prostate diseases such as benign prostatic hyperplasia (8PH) and prostate cancer. Mere particularly, the present invention comprises compositions of compounds which are useful for promoting prostate health, treating prostate diseases Including enlarged prostate, prostatitis, benign prosthetic hyperplasia and prostate cancer. O011] The com osition of the present invention may be obtained either by {1} extraction from natural products such as tea, saw palmetto, fruits and/or vegetables as weii as animal and vegetable oils or (2) by chemical synthesis from compounds o tained from natural products. More particularly, the synthesized compounds of the invention are obtained from the chemical or enzymatic reaction between fatty acids and polyphenols or benzotroplone derivative that have phenolic groups to produce esters which exhibit the properties of the Inventive composition.
{0812] In the method of the present invention, the inventive compositions are administered to a human subject diagnosed with/and or suffering from a prostate disease in an anti-prostate disease effective amount of the inventive composition.
Figure imgf000004_0001
| δΊ | The natural product combination of the present Invention preferably is comprised of tea extracts and sa palmetto extracts. Suitable tea extracts Include green tea extracts, black tea extracts or both. The efficacious compounds in tea extracts are tea polyphenols including green tea
polyphenols and black tea polyphenols. Green tea polyphenols suitable for use in the present invention Include catechins such as ( )-catechin; {-)- catechin. epicatechln (EC), eplgallocatechln (EGC): eplcateohln gallte (EGG), epigallocatechin gai!ate iEGCG), gailocatechin (GC gallocateehln gailate (GCG), catechin vallate (CG) and gallic acid. Suitable black tea polyphenols Include thea iavlns and ihearub!gins.. Theaflav!ns include theaflavin (TFI); theaflavln-B-monogailte (IF 2a or TF2,}S f eaflavsn-3'«moncgai!ate CTF2b or TF2h, theafIavin-3,3 -digallate {TF3)5 isotheaflavins, theaflagaliins. fbeafiavates, fheaiiavlc acids, theanap thoquinone. and methylated theaflavin derivatives etc that have a common com of he bensoiropo!eme s ruc ural moiety, Theafubigins Include bistheaflavinst thead;ben£otroplones: theatribenzotropoiones; dehydrotheatlavins, EGCG dlmer and oiicopolymers, Iheasinensins., and atheogallimn.
POISJ Green tee eatechins and black tea theafiavins can inhibit CYP1 , and or Inhibit both CYP17 and Sa~reductase; which consequently inhibit the production of testosterone and DHT that are responsible for prostate cancer promotion. Also the green tea component EGCG end black tea component Theaflavln-3-O-monoqallate can in ibi human prostate carcinoma INCaP cells. A recent double-blind study far 200 individuals was carried out wherein 100 individual took SOOmq of green tea polyphenols and another 100
Individuals took a placebo. After 12 months, only 3% of patients In the green tea catechin group developed prostate cancer, whereas the rate of cancer development m the placebo taking Individuals was 30%. This study clearly showed the in vivo efficacy of green tea eatechins for prostate cancer prevention effect,
1001 SJ Theatlavins In black tea; especially Theaflavm-3.3! digaHatei were found to inhibit Sa- reductasehand cause an associate decrease In the growth OfLNCaP prostate cancer cells, which are sensitive to androgens. With black tea consumption, decrease In androgen receptor level and decrease in secretion of prostate specific antigen (PSA) was observed.
PC!ITJ Tea polyphenols, particularly EGCG, EGG. EC in green tea extracts and black tea polyphenols such as theaflavins; i.e. Theaflsvin, Tfteafiavin-3- monogallatei Theafiavin-S'-- monogai!ate and ThealiavlmS^-dsgailate etc b nzotropofone derivatives have strong anil- Inflammatory activity Tea polyphenols can down-regulate the expression of Cox-2, INOS, TNF-a. MFKS, IU. IL-8, lL-8( ICA&M , p53, im ki ase, AP-i Inflammation genes and inhibit protein activity. Also, tea polyphenols can induce cancer cell apoptosis.
100183 Saw palmetto extracts suitable for use In the present invention ma be obtained by the extraction of saw palmetto berry, leaves and plants using both organic and water as solvents such as ethyl acetate, ettianol, methanol liquid carbon dsoxlde, acetone or mixtures of solvents.
1001 ¾ This natural product combination formula Includes comprised tea
extracts, sa palmetto extracts, pygeum, folium urtloae, dandelion, juniper berry, rhixome phragmltis (reed root), couchgrass, and couchgrass root (tea root). An ester formed from the chemical reaction or enzymatic reaction between tea polyphenols and fatty acids are esters has the formula:
Figure imgf000006_0001
[0 03 The polyphenols may be from EC EGG, EGG, EGCG, GC5 GCG
green tea eafec ns, ΤΡ TF2a If 2b TP 3, theaflavina. The fatty acids may be from saw palmetto (including lauric acid, n nstic acid, palmitic sold, stearic acid, eapric acid, caprylic acid, oleic acid, fin ieic acid. Unolenlo acid, and other fatty acids and fatty alcohols and sterols in saw palmetto), pygeum, folium urtloae, dandelion, juniper berry, rhisome phragrnifls (reed root). couehgrass, coucngrass root (tea root; and fatty acids from other plant extracts.
[0021] The compounds synthesized also include the esters formed from fatty acids and enzotropione derivatives that have phenolic group(s).
[§S2¾ The esters include mixtu e of esters formed by treating tea extracts and saw palmetto extracts in a certain ratio with acids and or enzymes that can catalyze the ester synthesis,
023 The polyphenols also Include flavonosds, such as f avonolds from fruits, for example, apple, citrus fruits and citrus peels, blue berry, and cranberry, and/or vegetables, such as, onion, broccoli, tomato, carrots and the like.
[00241 The sources of fatty acids include sa palmetto, pygeum, folium
urticae, dandelion, juniper berry, rhizome pnrsgmiils (reed root), couohgrass, couohgrass root (te root), coffee (ohlorogenlc acids and csffelc acids etc), fish oil, pumpkin seed oils, te ,e.g,, gallic acid and the like,
|0S2Sj Besides polyphenols, some amines and anilines also can be used to synthesize amides from fatty acids and these amines and anilines, such as celliam;ne from Rhixoma phragmltis.
[0020] The combination formulas composed of combination of tea extracts and other one or more plant extracts .e.g., saw palmetto extracts, the formed compounds (esters and amides) between the fatty acids and polyphenols (and also amines and anilines from some plants) can promote prostate health and treat prostate diseases including enlarged prostata, prostatitis, benign prostatic hyperplasia {BPH} and prostate cancer,
[002?] By combining the saw palmetto extracts and tea extracts, the resulting combination formula is expected to treat BPH and prevention and treatment of prostata cancer by s nsrglstiealy inhibiting Sa-reductase by saw palmetto extracts and tea polyphenols; b inhibiting CYP17 f17a-hydroxyiase/C1T;20- lyase) by thea!lsylns and thearubiglns m black tea extracts and eatechins in green tea extracts; by inhibiting the growth of prostate cancer celis{LNCaP) and further decreasing the level of androgen receptor and the decrease of PSA secretion: and by strong anthlnflammatlon and apoptotic activity of tea polyphenols,
fSOtS] Different species of green tea (Camellia ssnensis)may be used to
prepare the inventive oo nposion, These include Chinese tea. Camellia sinensis vat. sinensis, and , Assam tea. Camellia sinensis var. assarnlca.
|0Θ2§] The extract may be prepared by extraction from water, eihanoL mixture of water and ethanol, ethyl acetate., methanol or mix ure of methanol and water. The extraction Is carried out for rom 5-60 minutes and repealed 2-3 times. The extraction temperature range from ambient temperature to 100 °C. the temperature as even higher, 120 eC to 140 ;€ when pressure was applied In the extraction process. The pressure can be as high as 100 aim (1500 psl).
O03 ¾ The composition of the invention may be administered to a human subject diagnosed with a prostate disease in an antlprostate disease effective amount by Intravenous injection, subcutaneous injection, intramuscular Injection , topical application, oral administration in liquid or tablet form or other conventions forms of medicinal administration, e.g., nasal injection or inhalation via drops or spray..,
18031] An Important aspect in treating BPH and prostate cancer prevention and treatment is the combination of tea {black tea and green tea) extracts and saw palmetto extracts m various proportions., suet; as 10%-9S
(welghi/ elg t) saw palmetto and 90%- 5% ( e;oht/weig t) tea extracts. Tea extracts can be green tea extract , black tea extracts or the mixture of green tea extracts and black, tea extracts ;n various proportion of each tea extracts The tea polyphenols, or catechsn content of green tea extracts range from I %-99% and the content of theaiiavins in black tea extracts range f om S%- 90%. Black tea extracts can contain thearublgins range from 5% ~ 80%. All proportions expressed herein are on a weight/weight basis.

Claims

O 2014/052225 What is claimed is:
1. A composition comprising a combination of extract of tea and a mixture of fatty acids obtained from natural products.
. The composition of claim 1 wherein the tea is selected from the group consisting of green tea and black tea.
3. The composition -of claim 1 wherein the fatt acid is obtained from saw palmetto extract.
4. the composition of claim 1 hsc contains an anti-prostate disease effective amount of a compound having the structure:
Figure imgf000010_0001
5. a compound having the structure:
Figure imgf000010_0002
6. A method for making the composition of claim 1 comprising extracting tea and saw palmetto, respectively, with a solvent and combining the thus obtained extracts.
7. A method for m king the composition of claim 1 comprising reacting an extract of tea with f¾ity acids at a temperature and for a time sufficient to produce an ester therefrom:.
8. A met od for the therapeutic treatment of a human diagnosed it prostate disease c m isng administering an anti-prostate disease effective amount of the composition of clam 1 to the human.
PCT/US2013/061143 2012-09-25 2013-09-23 Composition for prostatic hyperplasia and prostate cancer WO2014052225A1 (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104189690A (en) * 2014-08-22 2014-12-10 兰州古驰生物科技有限公司 Traditional Chinese medicine preparation for relieving male prostatitis symptoms and proliferation
EP3720462A4 (en) * 2017-10-19 2021-12-22 Yale University Inhibition of androgen receptor by extracts of medicinal herbs and compositions thereof
CN114377107A (en) * 2022-01-14 2022-04-22 完美(广东)日用品有限公司 Application of sea-buckthorn seed meal protein peptide in preparation of medicine for preventing and treating prostatic hyperplasia

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011123942A1 (en) * 2010-04-08 2011-10-13 Genesis Group Inc. Fatty acid derivatives of catechins and methods of their use
WO2012061790A1 (en) * 2010-11-04 2012-05-10 Genyous Biomed International Combination therapy for prostate cancer using botanical compositions and bicalutamide
US8221803B1 (en) * 2007-06-25 2012-07-17 OncoNatural Solutions, Inc. Composition for prostate health

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8221803B1 (en) * 2007-06-25 2012-07-17 OncoNatural Solutions, Inc. Composition for prostate health
WO2011123942A1 (en) * 2010-04-08 2011-10-13 Genesis Group Inc. Fatty acid derivatives of catechins and methods of their use
WO2012061790A1 (en) * 2010-11-04 2012-05-10 Genyous Biomed International Combination therapy for prostate cancer using botanical compositions and bicalutamide

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104189690A (en) * 2014-08-22 2014-12-10 兰州古驰生物科技有限公司 Traditional Chinese medicine preparation for relieving male prostatitis symptoms and proliferation
EP3720462A4 (en) * 2017-10-19 2021-12-22 Yale University Inhibition of androgen receptor by extracts of medicinal herbs and compositions thereof
US11839639B2 (en) 2017-10-19 2023-12-12 Yale University Inhibition of androgen receptor by extracts of medicinal herbs and compositions thereof
CN114377107A (en) * 2022-01-14 2022-04-22 完美(广东)日用品有限公司 Application of sea-buckthorn seed meal protein peptide in preparation of medicine for preventing and treating prostatic hyperplasia
CN114377107B (en) * 2022-01-14 2023-09-05 完美(广东)日用品有限公司 Application of sea buckthorn seed meal protein peptide in preparation of medicine for preventing and treating prostatic hyperplasia

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