PT91101A - Processo de preparacao de derivados lipidos de nucleosidos antivirais, de suspensoes de lipossomas e de composicoes farmaceuticas - Google Patents
Processo de preparacao de derivados lipidos de nucleosidos antivirais, de suspensoes de lipossomas e de composicoes farmaceuticasInfo
- Publication number
- PT91101A PT91101A PT9110189A PT9110189A PT91101A PT 91101 A PT91101 A PT 91101A PT 9110189 A PT9110189 A PT 9110189A PT 9110189 A PT9110189 A PT 9110189A PT 91101 A PT91101 A PT 91101A
- Authority
- PT
- Portugal
- Prior art keywords
- nucleoside
- antiviral
- compounds
- liposomes
- group
- Prior art date
Links
- 230000000840 anti-viral effect Effects 0.000 title abstract 6
- 239000002502 liposome Substances 0.000 title abstract 5
- 239000002777 nucleoside Substances 0.000 title abstract 5
- 150000002632 lipids Chemical class 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 3
- 125000003835 nucleoside group Chemical group 0.000 title abstract 3
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 239000000725 suspension Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 6
- 229940127073 nucleoside analogue Drugs 0.000 abstract 5
- 125000001805 pentosyl group Chemical group 0.000 abstract 4
- 150000003904 phospholipids Chemical class 0.000 abstract 3
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 abstract 2
- QXKAIJAYHKCRRA-BXXZVTAOSA-N D-ribonic acid Chemical group OC[C@@H](O)[C@@H](O)[C@@H](O)C(O)=O QXKAIJAYHKCRRA-BXXZVTAOSA-N 0.000 abstract 2
- 239000003443 antiviral agent Substances 0.000 abstract 2
- OPTASPLRGRRNAP-UHFFFAOYSA-N cytosine Chemical compound NC=1C=CNC(=O)N=1 OPTASPLRGRRNAP-UHFFFAOYSA-N 0.000 abstract 2
- 150000003833 nucleoside derivatives Chemical class 0.000 abstract 2
- FTSFSHHUBPYPIE-UHFFFAOYSA-N 5-(azidomethyl)-1h-pyrimidine-2,4-dione Chemical compound [N-]=[N+]=NCC1=CNC(=O)NC1=O FTSFSHHUBPYPIE-UHFFFAOYSA-N 0.000 abstract 1
- 208000030507 AIDS Diseases 0.000 abstract 1
- 229930024421 Adenine Natural products 0.000 abstract 1
- GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical compound NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 abstract 1
- 229930186217 Glycolipid Natural products 0.000 abstract 1
- 208000031886 HIV Infections Diseases 0.000 abstract 1
- 241000725303 Human immunodeficiency virus Species 0.000 abstract 1
- XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
- 108010067390 Viral Proteins Proteins 0.000 abstract 1
- 208000036142 Viral infection Diseases 0.000 abstract 1
- MKUXAQIIEYXACX-UHFFFAOYSA-N aciclovir Chemical compound N1C(N)=NC(=O)C2=C1N(COCCO)C=N2 MKUXAQIIEYXACX-UHFFFAOYSA-N 0.000 abstract 1
- 229960004150 aciclovir Drugs 0.000 abstract 1
- 229960000643 adenine Drugs 0.000 abstract 1
- 229940124522 antiretrovirals Drugs 0.000 abstract 1
- 239000003903 antiretrovirus agent Substances 0.000 abstract 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 abstract 1
- 125000000089 arabinosyl group Chemical group C1([C@@H](O)[C@H](O)[C@H](O)CO1)* 0.000 abstract 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 abstract 1
- 210000004027 cell Anatomy 0.000 abstract 1
- 239000003153 chemical reaction reagent Substances 0.000 abstract 1
- 230000008878 coupling Effects 0.000 abstract 1
- 238000010168 coupling process Methods 0.000 abstract 1
- 238000005859 coupling reaction Methods 0.000 abstract 1
- 229940104302 cytosine Drugs 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- 238000001647 drug administration Methods 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 230000003834 intracellular effect Effects 0.000 abstract 1
- 239000003446 ligand Substances 0.000 abstract 1
- 125000003473 lipid group Chemical group 0.000 abstract 1
- 210000002540 macrophage Anatomy 0.000 abstract 1
- 210000001616 monocyte Anatomy 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 abstract 1
- 102000004196 processed proteins & peptides Human genes 0.000 abstract 1
- 108090000765 processed proteins & peptides Proteins 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 230000010076 replication Effects 0.000 abstract 1
- 230000000717 retained effect Effects 0.000 abstract 1
- 230000001177 retroviral effect Effects 0.000 abstract 1
- 150000003408 sphingolipids Chemical class 0.000 abstract 1
- 230000009385 viral infection Effects 0.000 abstract 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21641288A | 1988-07-07 | 1988-07-07 | |
| US07/319,483 US4884863A (en) | 1989-03-06 | 1989-03-06 | Optical fiber splicing enclosure for installation in pedestals |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PT91101A true PT91101A (pt) | 1990-02-08 |
| PT91101B PT91101B (pt) | 1995-01-31 |
Family
ID=26910992
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT9110189A PT91101B (pt) | 1988-07-07 | 1989-07-07 | Processo de preparacao de derivados lipidos de nucleosidos antivirais, de suspensoes de lipossomas e de composicoes farmaceuticas |
Country Status (1)
| Country | Link |
|---|---|
| PT (1) | PT91101B (pt) |
-
1989
- 1989-07-07 PT PT9110189A patent/PT91101B/pt not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| PT91101B (pt) | 1995-01-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG3A | Patent granted, date of granting |
Effective date: 19940721 |
|
| PC3A | Transfer or assignment |
Free format text: 940906 VESTAR, INC. US |
|
| PC3A | Transfer or assignment |
Free format text: 970306 NEXSTAR PHARMACEUTICALS, INC. US |
|
| PC3A | Transfer or assignment |
Free format text: 20010912 CHIMERIX, INC. US |
|
| MM4A | Annulment/lapse due to non-payment of fees;searched & examined patent |
Free format text: MAXIMUM VALIDITY LIMIT REACHED Effective date: 20090721 |