精品trifluorothymidine（三氟胸腺嘧啶核苷）课件

Antiviral Agents GAO Fen-Fei Overview Viruses are obligate intracellular parasites; their replication depends primarily on synthetic processes of the host cell. Antiviral agents must either block viral entry into or exit from the cell or be active inside the host cell. Research in Antiviral Chemotherapy In the early 1950s, IdUR and Trifluorothymidine(三氟胸腺嘧啶核苷) In the mid 1970s, Adenine arabinoside (Vidarabine,ara-A,阿糖腺苷) In the late 1970s, Acyclovir (阿昔洛韦) With the appearance of AIDS epidemic in the 1990s, Inhibitor reverse transcriptase or the protease Antiretroviral (Anti-HIV) Agents The first available agents: Nucleoside analog class competitive inhibition of the viral reverse transcriptase Nonnucleoside reverse transcriptase inhibitors The protease inhibitors The combination of at least two antiretroviral agents (cocktail therapy) enhancing potency and delaying resistance 病毒 RNA 互补双螺 旋DNA 掺入宿主 基因组 反转录酶HIV整合酶 转录 翻译 多聚 蛋白 小分子功 能蛋白 HIV蛋白酶 Drugs NRTIs NNRTIs PIs Viral RNA double helix DNA Incorporated into host genome reverse transcriptase HIV integrase transcription translation Polyproteins Final structural proteins HIV protease Drugs NRTIs NNRTIs PIs Nucleoside Reverse Transcriptase Inhibitors Derivatives of Pyramine: AZT, ddC, d4T, 3TC Derivatives of Purine: ddI, ABC Mechanism of Action Competitive inhibition of HIV-1 reverse transcriptase; Incorporated into the growing viral DNA chain cause termination Drugs requires intracytoplasmic activation- - phosphorylation triphosphate form Most have activity against HIV-2 as well as HIV-1. Zidovudine Azidothymidine (叠氮胸腺嘧啶), AZT Deoxythymidine analog anti-HIV-1 and HIV-2 Well absorbed from the gut and distributed to most body tissues and fluids, including the cerebrospinal fluid. Eliminated primarily by renal excretion following glucuronidation in the liver. Decrease the rate of clinical disease progression and prolong survival. Treatment HIV-associated dementia(痴呆) and thrombocytopenia(血小板减少). Reduce the rate of vertical (mother-to- newborn) transmission of HIV. Adverse effect: myelosuppression(骨髓抑 制) anemia or neutropenia; gastrointestinal intolerance, headachs, insomnia(失眠) Zalcitabine (ddC) Cytosine analog Anti-HIV-1 Zalcitabine + Zidovudine + one protease inhibitor Long intracellular half-life of 10hs. Dose-dependent peripheral neuropathy. Contraindication to use with other drugs that may cause neuropathy. Stavudine Thymidne analog (d4T), not used with AZT because AZT may reduce the phosphorylation of d4T. Anti-HIV-1 and HIV-2 High oral bioavailability (86%) that is not food- dependent. Plasma protein binding is negligible, mean cerebrospinal fluid concentrations are 55% of those of plasma. Excretion is by active tubular secretion and glomerular filtration. Adverse effects: Dose-limiting toxicity is a dose-related peripheral sensory neuropathy. Pancreatitis, arthralgias(关节痛), elevation in serum aminotransferases(转氨酶). Didanosine (ddI) Synthetic analog of deoxyadenosine Plasma protein binding is low (5%), cerebrospinal fluid concentrations are 20% of serum concentrations. Eliminated by glomerular filtration and tubular secretion. Should be taken on an empty stomach. Anti-HIV activity of ddI is potentiated by hydroxyurea(羟基脲) due to a depletion of intracellular pools of dATP, so two agents is administered in combination. Adverse effects: Dose-dependent pancreatitis Painful peripheral distal neuropathy Diarrhea Hepatitis Esophageal ulceration(食管溃疡) Cardiomyopathy Central nervous system toxicity (headach, irritability, insomnia) Nonnucleoside reverse transcriptase inhibitors Including delavirdine, nevirapine, efavirenz. Bind directly to a site on the viral reverse transcriptase that is near to but distinct from the binding site of the NRTIs. Neither compete with nucleoside triphosphates nor require phosphorylation to be active. The binding to the enzymes active site results in blockade of RNA- and DNA-dependent DNA polymerase activities. Specific activity against HIV-1. Cross-resistance among this class of agents. The rapid emergence of resistance prohibits monotherapy with any of the NNRTIs. No cross-resistance between the NNRTIs and the NRTIs or the protease inhibitors. Oral bioavailability is high. Metabolized by the CYP3A P450 isoform, excreted in the urine. Adverse effects: skin rash Protease inhibitors Including ritonavir, nelfinavir, saquinavir, indinavir and amprenavir. Gag and Gag-Pol gene Polyproteins, Immature budding particles translate Final structural proteins, Mature virioncore protease Combination therapy with other agents is recommended to avoid emergence of resistance, because of specific genotypic alterations. Adverse effect: Syndrome of altered body fat distribution (buffalo hump and truncal obesity, with facial and peripheral atrophy) Insulin resistance Hyperlipidemia(高脂血症) Others Antiviral Agents Including: Nucleoside antiviral agents Nonnucleoside antiviral agents Immune enhancement agent Mechanism of action: Compete the receptors, eg: Heparin, Polysaccharide Block viral adsorption to and penetration into host cells and uncoating of viral nucleic acid, eg: amantadine Block viral biosynthesis, eg: idoxuridine Enhance the host immune activity, eg: interferon Nucleoside Antiviral Agents Including Purine-nucleoside and Pyrimidine-nucleoside Drugs requires intracytoplasmic activation- - phosphorylation triphosphate form competitive inhibition of viral DNA polymerase. Incorporated into the growing viral DNA chain cause termination Acyclovir (ACV) An acyclic guanosine derivative Pharmacological effects: Against HSV-1 and HSV-2 and against varicella-zoster virus, Epstein-Barr virus and cytomegalovirus. Mechanism: Three phosphorylation steps for activation. First converted to the monophosphate derivative by the virus-specified thymidine kinase;（selective activation） Then to the di- and triphosphate compounds by hosts cellular enzymes. Acyclovir triphosphate inhibits viral DNA synthesis by two mechanisms: Competitive inhibition of deoxyGTP for the viral DNA polymerase, with binding to the DNA template as an irreversible complex; Incorporation into the viral DNA chain termination Resistance HSV or VZV alteration in either the viral thymidine kinase or the DNA polymerase resistance Cross-resistance to valacyclovir(伐昔洛韦), famciclovir(泛昔洛韦), and ganciclovir(更昔洛 韦). Agents such as foscarnet(膦甲酸), cidofovir(西 多福韦), and trifluridine(三氟尿苷) do not require activation by viral thymidine kinase and thus have preserved activity against the most prevalent acyclovir-resistant strains. Pharmacokinetics Available in oral, intravenous, and topical formulations. Oral bioavailability is 15-20%. Plasma protein binding is low, diffuses into most tissues and body fluids. Cleared primarily by glomerular filtration and tubular secretion. Clinical uses Treatment of HSV infection first selection Topical acyclovir is much less effective than oral therapy for primary HSV infection. It is of no benefit in treating recurrences. VZV is less susceptible to acyclovir than HSV, high doses are required. Adverse reactions Nausea, diarrhea, headach Intravenous infusion renal insufficiency or neurologic toxicity Valacyclovir The L-valyl ester of acyclovir It is rapidly converted to acyclovir after oral administration, achieving serum levels three to five times greater than those achieved with oral acyclovir. Ganciclovir An acyclic guanosine(鸟苷) analog Against CMV is up to 100 times greater than that of acyclovir. Adverse reactions: Myelosuppression(骨髓抑制), particularly neutropenia(嗜中性白血球减少症) Trifluridine(曲氟尿苷) Trifluorothymidine(三氟胸腺嘧啶核苷), Fluorinated pyrimidine nucleoside. Against HSV-1, HSV-2, vaccinia(牛痘), and some adenoviruses(腺病毒). Incorporation of trifluridine triphosphate into both viral and cellular DNA prevents its systemic use. Therapy for keratoconjunctivitis(角膜结膜炎) and for recurrent epithelial keratitis due to HSV-1 and HSV-2. Topical application, alone or in combination with interfon alfa, has been used successfully in treatment of acyclovir -resistant HSV infections. Vidarabine, ara-A Adenosine analog Against HSV, VZV, CMV, HBV and some RNA viruses. Phosporylated intracellular by host enzymes to form ara-ATP, incorporated into both viral and cellular DNA. excessive toxicity Rapidly metobolized to hypoxanthine arabinoside. Instability and toxicity limited its clinical utility. Topical application for acute keratoconjunctivitis(角膜结膜炎), superficial keratitis(表皮角膜炎), and recurrent epithelial keratitis due to HSV-1 and HSV-2. Intravenous for treatment of HSV encephalitis, neonatal herpes, and VZV infection in immunocompromised patients. Idoxuridine Competitive inhibition of thymidylic acid synthase block DNA synthesis. No effect on RNA virus. Only topical application because of its greater side effects in systemic application. Treatment of ocular or dermal infections due to herpesvirus or cowpox virus, especially acute epithelial keratitis due to herpesvirus. Ribavirin (Virazole) Guanosine analog. Phosphorylated intracellularly by host cell enzymes. Mechanism: to interfere with the synthesis of guanosine triphosphate, to inhibit capping of viral messenger RNA, and to inhibit the viral RNA-dependent RNA polymerase of certain viruses. Ribavirin triphosphate inhibits the replication of a wide range of DNA and RNA viruses, including influenza A and B, parainfluenza(副流感病毒), respiratory syncytial virus（呼吸道合胞病毒）, paramyxoviruses(副粘病毒), HCV（丙肝病毒）, and HIV-1. Lamivudine (3TC) Cytosine analog Against HIV-1, synergistic with a variety of antiretroviral nucleoside analogs, including zidovudine and stavudine. Treatment of chronic hepatitis B infection. Oral bioavailability exceeds 80% and is not food- dependent. The majority of lamivudine is eliminated unchanged in the urine. Nonnucleoside Antiviral Agents Including: Rimantadine and Amantadine Foscarnet Rimantadine and Amantadine Rimantadine is Amantadines methyl derivative. Cyclic amines. Inhibit uncoating of the viral RNA of influenza A within infected host cells. Prevention of influenza A virus infection. Reduce the duration of symptoms of influenza when administered within 48h of onset. Adverse effects: gastrointestinal intolerance, central nervous system complaints (nervous, difficulty in concentrating, lightheadedness) Foscarnet An inorganic(无机的) pyrophosphate(焦磷 酸盐) compound. Inhibit viral DNA polymerase, RNA polymerase, and HIV reverse transcriptase directly, without activation by phosphorylation. Against HSV, VZV, CMV, EBV, HHV-6, HHV-8, and HIV. Poor oral bioavailability. Only intravenous administration. CMV retinitis(视网膜炎) and acyclovir- resistant HSV infection. Immune Enhancement Agent Interferon a group of endogenous proteins that exert complex antiviral, immunoregulatory, and antiproliferative activities through cellular metabolic processes involving synthesis of both RNA and protein. Although not specifically antiviral, they appear to function by causing elaboration of effector proteins in infected cells, resulting in inhibition of viral pentration and uncoating, mRNA synthesis and translating, or virion assembly and release. Classified on the basis of the cell types from which they were derived: Interferon （type ）：leukocyte（白细胞） Interferon （type ）：fibroblast（成纤维细 胞） Interferon （type ）：immune cell（免疫细 胞） Three known enzymes are induced by interferons: A protein kinase that leads to phosphorylation of elongation factor 2, resulting in inhibition of peptide chain initiation; Oligoisoadenylate synthase (寡腺苷酸合酶), which leads to activation of a ribonuclease (RNA酶) and degradation of viral mRNA; A phosphodiesterase (磷酸二酯酶) that can degrade the terminal nucleotides of tRNA, inhibiting peptide elongation. Treatment of chronic hepatitis C, AIDS- associated Kaposis sarcoma, hairy cell leukemia, and chronic myelogenous leukemia (骨 髓性白血病), malignant melanoma (恶性黑色素瘤), condylomata acuminata (尖锐湿疣), relapsing multiple sclerosis (复发的多发性硬化症). Toxicities: neutropenia(嗜中性白血球减少症), anemia, thrombocytopenia(血小板减少), elevated aminotransferase levels(转氨酶升高), flu-like symptoms (including fever, chills, headache, myalgias肌痛, fatigue疲乏) Polyinosinic Polycytidylic Acid Synthetic doublestranded RNA (dsRNA). Inducer of interferon. Immune enhancement and broad spectrum antiviral effects. allergic reaction. 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