TR201802543T4 - Telomeraz aktivitesinin artırılması ve hıv enfeksiyonunun tedavi edilmesi için bileşimler. - Google Patents

Telomeraz aktivitesinin artırılması ve hıv enfeksiyonunun tedavi edilmesi için bileşimler. Download PDF

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TR201802543T4
TR201802543T4 TR2018/02543T TR201802543T TR201802543T4 TR 201802543 T4 TR201802543 T4 TR 201802543T4 TR 2018/02543 T TR2018/02543 T TR 2018/02543T TR 201802543 T TR201802543 T TR 201802543T TR 201802543 T4 TR201802543 T4 TR 201802543T4
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compositions
telomerase
hiv infection
cells
telomerase activity
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B Harley Calvin
C Chin Allison
Akama Tsutomu
Yuk-Yu Ip Nancy
Wong Yung-Hou
Davi̇d M Miller-Martini Dr
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Telomerase Activation Sciences Inc
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Abstract

Mevcut buluş hücrelerde telomeraz aktivitesinin artırılması için yöntemler ve bileşimler ile ilgilidir. Bu tür bileşimler, topikal dahil farmasötik bileşimleri, ve nutrasötik bileşimleri içerir. Yöntemler ve bileşimler, bir hastanın hücresinde veya dokusunda telomeraz aktivitesindeki bir artış ile tedaviye tabi, örneğin, HIV enfeksiyonu, çeşitli dejeneratif hastalıklar, ve akut ve kronik deri rahatsızlıkları gibi hastalıkların tedavi edilmesinde faydalıdır. Bunlar, aynı zamanda, ex vivo hücre terapisi ve kök hücrelerin proliferasyonları gibi, kültür içerisindeki hücrelerin replikasyon kapasitesinin artırılmasında faydalıdır.

Description

Tarifname içerisinde atifta bulunulan patent dökümanlari: Tarifnamede belirtilen patentlestirilmemis literatür: ° ALLSOPP, R.C. et al. Telomere shortening is associated With cell division in vitro and in vivo. Exp. Cell Res., September 1995, vol. 220 (1), ° ALLSOPP, R.C. et al. Telomerase is required to slow telomere shortening and extend replicative lifespan of HSC during serial transplantation. Blood (e- ° BODNAR, A.G. et al. Extension of life-span by introduction of telomerase into normal human cells. Science, 16 ° CHIU, C.P. et al. Replicative senescence and cell immortality: the role of telomeres and telomerase. Proc.
Soc. Exp. Biol. Med., February 1997, ° HARLE-BACHOR, C. et al.
Telomerase activity in the regenerative basal layer of the epidermis inhuman skin and in immortal and carcinoma- derived skin keratinocytes. Proc Natl Acad Sci USA, 25 June 1996, vol. 93 - HARLEY, C.B. et al. Telomeres fibroblasts. Nature, 31 May 1990, vol.
° HARLEY, C.B. et al. Telomerase, cell iminortality, and cancer. Cold Spring Harb. Symp. Quaiit. Biol., - HARLEY, C.B. et al. Telomeres and telomerase in aging and cancer. Curr.
Opin Genet. Dev., April 1995, vol. 5 and cancer. Important Adv. Oncol., o DAGARAG, M. et al. Differential iinpairment of lytic and cytokine functions in senescent human immunodeficiency virus type 1-specific cytotox T lymphocytes. J. Virol., March 2003, - FARWELL, D.G. et al. Genetic and epigenetic changes in human epithelial cells immortalized by telomerase.
American Journal of Pathology, May ° FUJIMOTO, R. et al. Expression of telomerase components in oral keratinocytes and squamous cell carcinomas. Oral Oncology, February o FUNK, WALTER D. et al.
Telomerase expression restores derinal integrity to in vitro-aged fibroblasts in a reconstituted skin model. Experimental Cell Research, ° LEE, K.M. et al. Immortalization With telomerase of the Nestin-positive cells of the human pancreas. Biochem Biophys Res Commun, 21 February 0 LUDWIG, A. et al. Ribozyme cleavage of telomerase mRNA sensitizes breast epithelial cells to inhibitors of topoisomerase. Cancer Res., 2001, vol. 61, ° MATTSON, M.P. Emerging neuroprotective strategies for A12heimer”s disease: dietary restriction, telomerase activation, and stem cell therapy. Exp 502 [0005] - MORALES, C. P. et al. Absence of cancer-associated changes in human fibroblasts immortalized With telomerase. Nature Genetics, January 1999, vol. 21 (1), 115-8 [0005] telomeres. Ciba Found. Symp., 1997, - HARLEY, C.B. Telomerase is not an ° HENDERSON, S. et :11. In situ analysis of changes in telomere size during replicative aging and cell transformation. J. Cell Biol., July 1996, o JIANG, X.R. et al. Telomerase expression in human somatic cells does not induce changes associated with a transformed phenotype. Nature Genetics, January 1999, vol. 21 (1), 1 1 1-4 [0005] - KANG, M.K. et al. Replicative senescence of normal human oral keratinocytes is associated With the loss shortening of telomeres. Cell Growth & Differentiation, January 1998, vol. effects of ginsenoside-Rgl on p561ck kinase and cell proliferation in J urkat T cells. Korean J. Ginseng Sci., - Selected non-timber forest products With medicinal applications from J ilin Province in China. HUANG, Y. et al. Conference Title: Forest communities in the third millennium: Linking research, business, and policy toward a sustainable non-timber forest product sector; Kenora, Ontario, Canada, 1-4 October, 1999. General Research Station, USDA Forest . KANEKO, M. et al. Accelerated recovery from cyclophosphamide- induced leukopenia in mice administered a Japanese ethical herbal drug, Hochu-ekki-to. lmmunopharmacology, 1999, vol. 44 0 OH, H. ; SCHNEIDER, MD. The emerging role of telomerase in cardiac muscle cell growth and survival. J Mol Cell Cardiol, July 2002, vol. 34 (7), 717-24 [0005] ° SIMONSEN, J.L. et al. Telomerase expression extends the proliferative life-span and maintains the osteogenic stromal cells. Nat Biotechnol, June 2002, vol. o THOMAS, M. ; YANG, L. ; functional tissue from transplanted adrenocortical cells expressing telomerase reverse transcriptase. Nat Biotechnol, January activates telomerase and delays endothelial cell senescence. Circ. Res., ° YANG, J. et al. Telomerized human microvasculature is functional in vivo.
Nature Biotechnology (United States), - YANG, J. et al. Human endothelial cell life extension by telomerase expression. J. Biol. Chein., 10 - YUDOH, K. et al. Reconstituting telomerase activity using the telomerase catalytic subunit prevents the telomere shorting and replicative senescence in human osteoblasts. J. Bore and Mineral 0 BEDIR, E. et al. lmmunostimulatory effects of cycloartane-type triterpene glycosides from Astragalus Species.
Biol & Pharm Bull, 2000, vol. 23 (7), 834-7 tetracyclic triterpenes (argentatins A, B and D) on the estradiol receptor of - KINJO, J. et al. Anti-herpes virus activity of fabaceous triterpenoidal saponins. Biological pharinaceutical - KHUSHBAKTOVA, Z. A. et al. lnfluence of cycloartanes from plants of synthetic analogs on the contractive function of the myocarbium and the activity 0fNa,K-ATPase. Chem. Nat.
- LEE, Y.J. et al. Ginsenoside-Rgl, one of the major active molecules from Panax ginseng, is a functional ligand of glucocorticoid receptor. Mol Cell Endocrinol, October 1997, vol. 133 (2), 135-40 [0007] - LIU, P. et al. Effect of ginsenosides Rbl , Rgl, Rhl and Re en proliferation of cells in vitro. Tianran Chanwu haemolytic activities of 47 saponins derived from medicinal and food plants.
- PISTELLI, L. et al. Antimicrobial and antifungal activity of crude extracts and isolated saponins from Astragalus verrucosus. Fitoterapia, 2002, vol. 73 ginsenoside Re on the proliferation of murine bone marrow cells. Baiqiuen Yike Daxue Xuebao, 1997, vol. 23 (2), - WANG, Y-P. et al. Effect of astragaloside IV on T,B lymphocyte proliferation and peritoneal macrophage function in mice. Acta Pharmacologica triterpene derivatives from plants hormone-dependent tumors of human breast. Medical Science Research, 0 CHEN, X. et al. Protective effect of ginsenoside Rgl on dopamin-induced apoptotis in PC12 cells. Acta Pharmacol Sinica, 2001, vol. 22 (8), ° ZHANG W.J. et al. Regulation of the fibrinolytic potential of cultured human umbilical vein endothelial cells: astragaloside IV downregulates plasminogen activator inhibitor-l and upregulates tissue-type plasminogen activator expression. Journal of Vascular 80 [0007] 0 ZI-PU, L. ; QIAN, C. Effects of astragaloside IV on myocardial calcium transport and cardiac function in ischemic rats. Acta Pharmacol Sin, ° ROKIA et al. Pharmazie, 1993, vol. 0 LONKOVA. Phytochemistry, 1997, inhibit the effects of a tumor promoter, and sitostero] and betulinic acid inhibit tumor formation in mouse skin two- Stage carcinogenesis. Oncology, stimulatory effects of ginseng saponins on proliferation and DNA synthesis of human vascular endothelial cells and skin fibroblasts in relation to cytokines or growth factors. Nissei Byoin Igaku o P-H WANG et al. J. Chinese Chem.
° OH; SCHNEIDER.J Mol Cell - MATTSON. Exp Gerontol., vol. 35 - SIMONSEN et al. Nat Biotechnol, - THOMAS et al. Nat Biotechnol, Sciences. Williams & Wilkins, 1995 SEKILLERDEKI YAZILARIN ANLAMLARI A : Astragalosid IV B = Astragenol C = Sikloastragenol D = Astragalosid IV 16-011 E : Ginsenosid RHl F :1 Bilesiginin Insan Keratinositlerinde Telomeraz Aktivitesi Üzerindeki Etkisi G = Telomeraz Aktivitesi (% KTRL) H = Konsantrasyon (ug/ml) Üzerindeki Etkisi J :Doz (HM) K = Yaslanan Eriskin Keratinositlerde Yara Iyilesmesinin Hizlanmasi L = Kontrol R = Genç Keratinositlerde Yara Iyilesmesinin Hizlanmasi S = Yaslanan Keratinositlerde Yara Iyilesmesinin Hizlanmasi T :Yaslanan Keratinositlerde Yara Iyilesmesi U = Açik Yara (% KTRL) 9 &ama N 1555 0.. Nm v de To Nmoö 5.0 Nmood Awimon. m0& "%555 .ninbvmâkân ü 8:20 + g.. __2 giii even_ mâxmllol

Claims (5)

ISTEMLER
1. Formül 1 ile gösterilen, bir HIV enfeksiyonun tedavisinde kullanim amaçli, etkili miktarda izole bir bilesik olup: X1, hidroksidir veya ß-D-glukopiranoziddir, 10 X2, hidroksidir veya ß-D-glukopiranoziddir, ve X3, hidroksidir; OR', hidroksidir; R2, 9. karbon ile birlikte kayiiasmis bir siklopropil halkasi 15 olusturur; ve 2 9. ve 11. karbonlar arasindaki bir tekli bagi gösterir.
2. Bir HIV enfeksiyonun tedavisinde kullanim amaçli, etkili miktarda astragalosid IV 16-0ndur.
3. Bir farmas'otik bilesim olup, söz konusu bilesim, farmasötik açidan kabul edilebilir bir tasiyici içerisinde, astragalosid IV 16-011, sikloastragenol 6-ß-D-glukopiranozid ve sikloastragenol 3-ß-D- ksilopiranozid içerisinden seçilen bir bilesigi içerir.
4. Bir farmasötik bilesim olup, söz konusu bilesim, sikloastragenol, astragenol, astragalosid IV 16-0n, sikloastragenol 6-ß-D- glukopiranozid ve sikloastragenol 3-ß-D-ksilopiranozid içerisinden seçilen izole bir bilesigin bir topikal formülasyonunu içerir.
5. Istem 4'e göre bilesim olup, burada, söz konusu bilesik belirtilen formülasyonda en az %0,1 (agirlik/hacim) konsantrasyonunda bulunur.
TR2018/02543T 2003-06-23 2004-06-23 Telomeraz aktivitesinin artırılması ve hıv enfeksiyonunun tedavi edilmesi için bileşimler. TR201802543T4 (tr)

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