Thymidine
Zalmoxis (thymidine) is a small molecule pharmaceutical. Thymidine was first approved as Zalmoxis on 2016-08-18. It has been approved in Europe to treat graft vs host disease and hematopoietic stem cell transplantation.
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New Drug Application (NDA)
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Abbreviated New Drug Application (ANDA)
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Indications
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Clinical
Clinical Trials
13 clinical trials
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Indications Phases 4
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Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Breast neoplasms | D001943 | EFO_0003869 | C50 | — | — | 1 | — | 1 | 2 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Non-small-cell lung carcinoma | D002289 | — | 1 | — | — | 2 | 3 | ||
Liver neoplasms | D008113 | EFO_1001513 | C22.0 | 1 | 1 | — | — | — | 2 |
Ovarian neoplasms | D010051 | EFO_0003893 | C56 | — | 1 | — | — | — | 1 |
Fallopian tube neoplasms | D005185 | — | 1 | — | — | — | 1 | ||
Mitochondrial diseases | D028361 | EFO_0000591 | — | 1 | — | — | — | 1 | |
Mitochondrial encephalomyopathies | D017237 | — | 1 | — | — | — | 1 | ||
Liver transplantation | D016031 | EFO_0010682 | — | 1 | — | — | — | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | THYMIDINE |
INN | doxribtimine |
Description | Thymidine is a pyrimidine 2'-deoxyribonucleoside having thymine as the nucleobase. It has a role as a metabolite, a human metabolite, an Escherichia coli metabolite and a mouse metabolite. It is functionally related to a thymine. It is an enantiomer of a telbivudine. |
Classification | Small molecule |
Drug class | — |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | Cc1cn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]c1=O |
Identifiers
PDB | — |
CAS-ID | 50-89-5 |
RxCUI | 1372538 |
ChEMBL ID | CHEMBL52609 |
ChEBI ID | 17748 |
PubChem CID | 5789 |
DrugBank | DB04485 |
UNII ID | VC2W18DGKR (ChemIDplus, GSRS) |
Target
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Safety
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0 adverse events reported
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