Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Ester doai
Reexamination Certificate
2003-05-22
2010-02-16
Hui, San-ming (Department: 1628)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Ester doai
C554S229000, C568S664000
Reexamination Certificate
active
07662852
ABSTRACT:
An antiviral preparation comprising as an active ingredient, a phorbol derivative of formula 1:wherein is R1is —(CH2)aX(CH2)bCH3, —(CH2)cX(CH2)dYCH3, —CO(CH2)eCH3or —(CH2)fCH3R2is —CO(CH2)nCH3, R3, R4and R5are hydrogen atom, or an aliphatic or aromatic carboxylic acid residue, X and Y are O or S, and each of a-f and n is a number, and having a specific safety index S.I.=CC50/EC50of 10 or more wherein EC50means a concentration at which HIV-1 induced cytopathogenic effect (CPE) in MT-4 cell is inhibited by 50%, and CC50means a concentration at which survival of MT-4 cell in a cell proliferation test is reduced by 50%. These preparations are particularly effective for human immuno-deficiency virus (HIV).
REFERENCES:
patent: 6268395 (2001-07-01), Hattori
patent: A-05-097888 (1993-04-01), None
patent: A-05-279329 (1993-10-01), None
patent: A-05-331067 (1993-12-01), None
patent: A-06-025158 (1994-02-01), None
patent: A-06-056825 (1994-03-01), None
patent: A-06-073004 (1994-03-01), None
patent: A-06-234641 (1994-08-01), None
patent: A-06-316524 (1994-11-01), None
patent: A-07-082292 (1995-03-01), None
patent: A-07-285877 (1995-10-01), None
patent: A-09-030974 (1997-02-01), None
patent: A-11-322789 (1999-11-01), None
patent: WO 01/82927 (2001-11-01), None
Raffanti S and Haas DW, Chapter 51 Antimicrobial Agents, “Goodman & Gilman's The Pharmacological Basis of Therapeutics, 10th ed.” Hardman JG, Limbird LE, and Goodman AG, Eds., McGraw-Hill, New York, 2001.
Carey FA and Sundberg RJ, Chapter 13, Section 13.1, “Advanced Organic Chemistry 3rd. Ed.”, Plenum Press, New York, 1990, pp. 678-686 provided.
Greene TW and Wuts PGM, “Protective Groups in Organic Synthesis,” John Wiley & Sons, Inc., New York, 1991, Chapter 2, pp. 10-13, 88, and 89 provided.
El-Mekkawy et al., “Inhibition of Cytopathic Effect of Human Immunodeficiency Virus Type-1 by Various Phorbol Derivatives,” Chem. Pharrn. Bull., 2002, vol. 50, No. 4, pp. 523-529.
El-Mekkawy et al., “12-O-Acetylphorbol-13-decanoate Potently Inhibits Cytopathic Effects of Human Immunodeficiency Virus Type 1 (HIV-1), without Activation of Protein Kinase C,” Chem. Pharm. Bull., 1999, vol. 47, No. 9, pp. 1346-1347.
El-Mekkawy et al., “Anti-HIV-1 phorbol esters from the seeds ofCroton tiglium,” Phytochemistry, 2000, vol. 53, No. 4, pp. 457-464.
Maio et al., “Regulation of Expression Driven by Human Immunodeficiency Virus Type 1 and Human T-Cell Leukemia Virus Type 1 and Human T-Cell Leukemia Virus Type I Long Terminal Repeats in Pluripotential Human Embryonic Cells,” J. Virol., 1988, vol. 62, No. 4, pp. 1398-1407.
Kinzel et al., “Stimulation of Choline Incorporation in Cell Cultures by Phorbol Derivatives and Its Correlation with Their Irritant and Tumor-Promoting Activity,” Cancer Research, 1979, vol. 39, No. 7, pp. 2743-2750.
Chem. Abstr., vol. 70, No. 4, 1969, pp. 359-360, abstract No. 70: 47626, Kreibich et al. “Chemistry of Phorbol. V. Phorbol Ethers,” Chemie, Biochemie. Biophysik. Biologie., 1968, vol. 23, No. 11, pp. 1444-1452.
Hattori Masao
Mori Masao
Nemoto Hideo
Saito Haruo
Yamamoto Naoiki
Hui San-ming
Lead Chemical Co., Ltd.
Oliff & Berridg,e PLC
Zarek Paul
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