| Stem definition | Drug id | CAS RN |
|---|---|---|
| uridine derivatives used as antiviral agents and as antineoplastics | 4220 | 3424-98-4 |
| Dose | Unit | Route |
|---|---|---|
| 0.60 | g | O |
| Property | Value | Reference |
|---|---|---|
| BA (Bioavailability) | 68 % | Kim MT, Sedykh A, Chakravarti SK, Saiakhov RD, Zhu H |
| S (Water solubility) | 66.80 mg/mL | Bocci G, Oprea TI, Benet LZ |
| BDDCS (Biopharmaceutical Drug Disposition Classification System) | 3 | Bocci G, Oprea TI, Benet LZ |
| fu (Fraction unbound in plasma) | 1 % | Kawashima H, Watanabe R, Esaki T, Kuroda M, Nagao C, Natsume-Kitatani Y, Ohashi R, Komura H, Mizuguchi K |
| Date | Agency | Company | Orphan |
|---|---|---|---|
| April 24, 2007 | EMA | ||
| Oct. 25, 2006 | FDA | NOVARTIS |
| MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
|---|---|---|---|---|---|---|
| Drug resistance | 97.63 | 91.29 | 20 | 145 | 22913 | 63465944 |
| MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
|---|---|---|---|---|---|---|
| Blood creatine phosphokinase increased | 152.55 | 72.89 | 50 | 665 | 44807 | 34911409 |
| Drug resistance | 117.27 | 72.89 | 36 | 679 | 25891 | 34930325 |
| Hepatitis B DNA increased | 92.70 | 72.89 | 15 | 700 | 550 | 34955666 |
| Myalgia | 85.43 | 72.89 | 39 | 676 | 84071 | 34872145 |
| MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
|---|---|---|---|---|---|---|
| Blood creatine phosphokinase increased | 203.28 | 62.78 | 57 | 694 | 66033 | 79677604 |
| Drug resistance | 118.42 | 62.78 | 34 | 717 | 42179 | 79701458 |
| Hepatitis B DNA increased | 106.46 | 62.78 | 16 | 735 | 799 | 79742838 |
| Viral mutation identified | 93.95 | 62.78 | 18 | 733 | 3840 | 79739797 |
| Myalgia | 91.15 | 62.78 | 41 | 710 | 185600 | 79558037 |
| Pathogen resistance | 90.50 | 62.78 | 22 | 729 | 14320 | 79729317 |
None
| Source | Code | Description |
|---|---|---|
| ATC | J05AF11 | ANTIINFECTIVES FOR SYSTEMIC USE ANTIVIRALS FOR SYSTEMIC USE DIRECT ACTING ANTIVIRALS Nucleoside and nucleotide reverse transcriptase inhibitors |
| FDA MoA | N0000009947 | Nucleoside Reverse Transcriptase Inhibitors |
| FDA EXT | N0000175459 | Nucleoside Analog |
| MeSH PA | D000890 | Anti-Infective Agents |
| MeSH PA | D000998 | Antiviral Agents |
| MeSH PA | D004791 | Enzyme Inhibitors |
| MeSH PA | D019384 | Nucleic Acid Synthesis Inhibitors |
| FDA EPC | N0000175656 | Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor |
| CHEBI has role | CHEBI:36044 | antiviral drugs |
| CHEBI has role | CHEBI:59897 | reverse transcriptase inhibitors |
| Disease | Relation | SNOMED_ID | DOID |
|---|---|---|---|
| Chronic type B viral hepatitis | indication | 61977001 | |
| Myositis | contraindication | 26889001 | DOID:633 |
| Kidney disease | contraindication | 90708001 | DOID:557 |
| Lactic acidosis | contraindication | 91273001 | DOID:3650 |
| Disorder of muscle | contraindication | 129565002 | DOID:423 |
| Steatosis of liver | contraindication | 197321007 | |
| Peripheral nerve disease | contraindication | 302226006 | |
| Breastfeeding (mother) | contraindication | 413712001 |
None
None
| Dissociation level | Dissociation constant | Type (acidic/basic) |
|---|---|---|
| pKa1 | 9.46 | acidic |
| pKa2 | 13.02 | acidic |
| pKa3 | 13.7 | acidic |
| Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Patent number | Patent expiration date | Patent use |
|---|---|---|---|---|---|---|---|---|---|---|
| 600MG | TYZEKA | NOVARTIS | N022011 | Oct. 25, 2006 | DISCN | TABLET | ORAL | 7589079 | Sept. 11, 2023 | TREATMENT OF CHRONIC HEPATITIS B IN ADULT PATIENTS |
| 600MG | TYZEKA | NOVARTIS | N022011 | Oct. 25, 2006 | DISCN | TABLET | ORAL | 7858594 | Sept. 11, 2023 | TREATMENT OF CHRONIC HEPATITIS B IN ADULT PATIENTS |
| 100MG/5ML | TYZEKA | NOVARTIS | N022154 | April 28, 2009 | DISCN | SOLUTION | ORAL | 7858594 | Sept. 11, 2023 | TREATMENT OF CHRONIC HEPATITIS B IN ADULT PATIENTS |
None
| Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
|---|---|---|---|---|---|---|---|---|---|
| Protein P | Polyprotein | INHIBITOR | EC50 | 5.89 | DRUG LABEL | DRUG LABEL | |||
| Capsid protein | Unclassified | EC50 | 6.09 | CHEMBL |
| ID | Source |
|---|---|
| 4025782 | VUID |
| N0000179779 | NUI |
| D06675 | KEGG_DRUG |
| 4025782 | VANDF |
| C1453933 | UMLSCUI |
| CHEBI:63624 | CHEBI |
| LLT | PDB_CHEM_ID |
| CHEMBL374731 | ChEMBL_ID |
| D000077712 | MESH_DESCRIPTOR_UI |
| DB01265 | DRUGBANK_ID |
| 8296 | INN_ID |
| 2OC4HKD3SF | UNII |
| 159269 | PUBCHEM_CID |
| 474128 | RXNORM |
| 22372 | MMSL |
| d05912 | MMSL |
| 011809 | NDDF |
| 424071004 | SNOMEDCT_US |
| 425347005 | SNOMEDCT_US |
None