Drug Details
General Information of the Drug (ID: DR1960) | ||||
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Name |
3'-azido-3'-deoxythymidine
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Synonyms |
NSC602670; Azidothymidine (AZT); BW-A 509U; Aztec; 3'-Deoxy-3'-azidothymidine; Azitidin; Timazid; Zidovudine, AZT; NSC 602670; NSC-602670; Thymidine, 8CI,; Trizivir (Salt/Mix); ACMC-209hgl; 3-Azido-3-deoxythymidine; 1-[4-azido-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione; CHEMBL178240; SCHEMBL13609910; 3'-epi-Azido-3'-deoxythymidine; component of Combivir (Salt/Mix); HMS3369K15; HMS3656A20; BCP03622; STL451000; STL454167; ZINC04164448; AKOS015949577; AKOS037482514; CCG-229922; MCULE-3669241621; NCGC00015044-03; NCGC00015044-04; NCGC00015044-05; NCGC00094963-01; NCGC00094963-02; NCI60_004566; FT-0601543; 1-(3-azido-2,3-dideoxypentofuranosyl)-2-hydroxy-5-methylpyrimidin-4(1H)-one; 1-(3-azido-2,3-dideoxypentofuranosyl)-4-hydroxy-5-methylpyrimidin-2(1H)-one; ZVD
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Molecular Type |
Small molecule
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Disease | Human immunodeficiency virus disease [ICD-11: 1C62] | Approved | [1] | |
Structure |
Click to Download Mol2D MOL |
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Click to Show/Hide the Molecular Information and External Link(s) of This Natural Product | ||||
Formula |
C10H13N5O4
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PubChem CID | ||||
Canonical SMILES |
CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)N=[N+]=[N-]
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InChI |
1S/C10H13N5O4/c1-5-3-15(10(18)12-9(5)17)8-2-6(13-14-11)7(4-16)19-8/h3,6-8,16H,2,4H2,1H3,(H,12,17,18)
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InChIKey |
HBOMLICNUCNMMY-UHFFFAOYSA-N
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CAS Number |
CAS 30516-87-1
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DrugBank ID |
Combinatorial Therapeutic Effect(s) Validated Clinically or Experimentally | ||||||
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α. A List of Natural Product(s) Able to Enhance the Efficacy of This Drug | ||||||
Paclitaxel | Taxus brevifolia | Click to Show/Hide the Molecular Data of This NP | ||||
Achieving Therapeutic Synergy | Click to Show/Hide | |||||
Representative Experiment Reporting the Effect of This Combination | [2] | |||||
Detail(s) | Combination Info click to show the detail info of this combination | |||||
In-vitro Model | FaDu | CVCL_1218 | Squamous cell carcinoma | Homo sapiens | ||
Experimental
Result(s) |
Paclitaxel combinated with low and nontoxic AZT dose was a novel cancer therapeutic approach to human pharynx faDu cells. |
Target and Pathway | ||||
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Target(s) | Histone deacetylase (HDAC) | Molecule Info | [3] |