Descriptor English: | Zidovudine | ||||||
Descriptor Spanish: |
Zidovudina
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Descriptor Portuguese: | Zidovudina | ||||||
Descriptor French: | Zidovudine | ||||||
Entry term(s): |
3' Azido 2',3' Dideoxythymidine 3' Azido 3' deoxythymidine 3'-Azido-2',3'-Dideoxythymidine 3'-Azido-3'-deoxythymidine AZT (Antiviral) AZT Antiviral AZT, Antiviral Antiviral AZT Azidothymidine BW A509U BWA 509U BWA-509U BWA509U Retrovir |
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Tree number(s): |
D03.383.742.680.705.950 D13.570.230.500.950 D13.570.230.855.950 D13.570.685.705.950 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D015215 | ||||||
Scope note: | A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is a potent inhibitor of HIV replication, acting as a chain-terminator of viral DNA during reverse transcription. It improves immunologic function, partially reverses the HIV-induced neurological dysfunction, and improves certain other clinical abnormalities associated with AIDS. Its principal toxic effect is dose-dependent suppression of bone marrow, resulting in anemia and leukopenia. |
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Allowable Qualifiers: |
AA analogs & derivatives AD administration & dosage AE adverse effects AG agonists AI antagonists & inhibitors AN analysis BL blood CF cerebrospinal fluid CH chemistry CL classification CS chemical synthesis EC economics HI history IM immunology IP isolation & purification ME metabolism PD pharmacology PK pharmacokinetics PO poisoning RE radiation effects SD supply & distribution ST standards TO toxicity TU therapeutic use UR urine |
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Pharm Action: |
Antimetabolites Reverse Transcriptase Inhibitors Anti-HIV Agents |
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Registry Number: | 4B9XT59T7S | ||||||
CAS Type 1 Name: | Thymidine, 3'-azido-3'-deoxy- | ||||||
Previous Indexing: |
Thymidine/analogs & derivatives (1975-1988) |
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Public MeSH Note: | 89 |
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History Note: | 89 |
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DeCS ID: | 23867 | ||||||
Unique ID: | D015215 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1989/01/01 | ||||||
Date of Entry: | 1988/05/09 | ||||||
Revision Date: | 2016/06/01 |
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CHEMICALS AND DRUGS
Heterocyclic Compounds [D03]Heterocyclic Compounds
|
Zidovudine
- Preferred
Retrovir
- Related but not broader or narrower
BW A509U
- Narrower
Concept UI |
M0023377 |
Scope note | A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is a potent inhibitor of HIV replication, acting as a chain-terminator of viral DNA during reverse transcription. It improves immunologic function, partially reverses the HIV-induced neurological dysfunction, and improves certain other clinical abnormalities associated with AIDS. Its principal toxic effect is dose-dependent suppression of bone marrow, resulting in anemia and leukopenia. |
Preferred term | Zidovudine |
Entry term(s) |
3' Azido 2',3' Dideoxythymidine 3' Azido 3' deoxythymidine 3'-Azido-2',3'-Dideoxythymidine 3'-Azido-3'-deoxythymidine AZT (Antiviral) AZT Antiviral AZT, Antiviral Antiviral AZT Azidothymidine |
Concept UI |
M0023378 |
Preferred term | Retrovir |
Concept UI |
M0373894 |
Preferred term | BW A509U |
Entry term(s) |
BWA 509U BWA-509U BWA509U |
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