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| Number | Title | Issue Date |
| 6583149 | Method for the treatment or prevention of viral infection using nucleoside analogues Compounds of formula I: ##STR1## wherein Y, X, R1 and Ra are defined herein are in methods for treating or preventing a viral infections selected from herpes simplex virus, varicella zoster virus, respiratory syncytial virus and cytomegalovirus infec... | 06/24/2003 |
| 6566365 | Method for the treatment of Flaviviridea viral infection using nucleoside analogues In accordance with the present invention there is provided a method for treating or preventing a Flaviviridea viral infection in a host comprising administering a therapeutically effective amount of at least one compound of formula (I) or (II) ##STR1... | 05/20/2003 |
| 6194576 | Process for preparing antiviral 2-phosponate nucleotide analogs Nucleotide analogues having the general formula (I) and pharmaceutically acceptable derivatives: ##STR1## wherein n is 0 or an integer; X is O or S, CH2, CH-halogen, CH--N3, or C.dbd.CH2 ; Q and U are independently selected fro... | 02/27/2001 |
| 6127540 | Antiviral compounds Nucleotide analogues having the general formula (I) and pharmaceutically acceptable derivatives: ##STR1## wherein n is 0 or an integer; X is O or S, CH2, CH--halogen, CH--N3, or C.dbd.CH2 ; Q and U are independently s... | 10/03/2000 |
| 6110923 | Method for treating cancer using novel substituted purinyl derivatives with immunomodulating activity The present invention covers a method of treatment of cancer, in particular, colon carcinoma, comprising the step of administering the compound N2-(6-dimethylamino purin-9-yl)-7-pentyloxycarbonyl-L-arginine in combination with 5-fluorouracil. The present ... | 08/29/2000 |
| 5994361 | Substituted purinyl derivatives with immunomodulating activity The present invention comprises a compound of formula I: ##STR1## R1 of Formula I is substituted amino represented by formula NR5 R6 wherein R5 and R6 are independently selected from the group co... | 11/30/1999 |
| 5955610 | Antiviral compounds Nucleotide analogues having the general formula (I) and pharmaceutically acceptable derivatives: ##STR1## wherein n is 0 or an integer; X is O or S, CH2, CH-halogen, CH--N3, or C.dbd.CH2 ; Q and U are independently se... | 09/21/1999 |
| 5457180 | Methods for producing linear thiopeptides using an amino acid ortho amino thioanilide compound The present invention provides methods for producing linear thiopeptides using an amino acid ortho amino thioanilide compound of formula (III) ##STR1## wherein R1 is selected from the group consisting of hydrogen or C1 -C4 | 10/10/1995 |
