Uramustine |
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| ATC code | |
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| Protein binding | 5% |
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| Excretion | Renal |
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5-[bis(2-Chloroethyl)amino]-1H-pyrimidine-2,4-dione
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| CAS Number | |
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| DrugBank | |
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| CompTox Dashboard (EPA) | |
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| ECHA InfoCard | 100.000.574 |
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| Formula | C8H11Cl2N3O2 |
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| Molar mass | 252.10 g·mol−1 |
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| 3D model (JSmol) | |
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O=C1C(\N(CCCl)CCCl)=C/NC(=O)N1
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InChI=1S/C8H11Cl2N3O2/c9-1-3-13(4-2-10)6-5-11-8(15)12-7(6)14/h5H,1-4H2,(H2,11,12,14,15) NKey:IDPUKCWIGUEADI-UHFFFAOYSA-N N
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N Y (what is this?) (verify) |
Uramustine (INN) or uracil mustard is a chemotherapy drug which belongs to the class of alkylating agents.[1] It is used in lymphatic malignancies such as non-Hodgkin's lymphoma. It works by damaging DNA, primarily in cancer cells that preferentially take up the uracil due to their need to make nucleic acids during their rapid cycles of cell division. The DNA damage leads to apoptosis of the affected cells. Bone marrow suppression and nausea are the main side effects.
Chemically it is a derivative of nitrogen mustard and uracil.
References
Intracellular chemotherapeutic agents / antineoplastic agents (L01) |
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SPs/MIs (M phase) | | Block microtubule assembly | |
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| Block microtubule disassembly |
- Taxanes (Cabazitaxel
- Docetaxel#
- Larotaxel
- Ortataxel†
- Paclitaxel#
- Tesetaxel)
- Epothilones (Ixabepilone)
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DNA replication inhibitor | DNA precursors/ antimetabolites (S phase) | | Folic acid | |
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| Purine | |
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| Pyrimidine |
- DNA polymerase inhibitor (Cytarabine# +daunorubicin)
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| Deoxyribonucleotide | |
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Topoisomerase inhibitors (S phase) | | I |
- Camptotheca (Belotecan
- Camptothecin
- Cositecan†
- Etirinotecan pegol†
- Exatecan
- Gimatecan
- Irinotecan#
- Lurtotecan‡
- Rubitecan‡
- Silatecan§
- Topotecan)
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| II | |
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| II+Intercalation | |
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Crosslinking of DNA (CCNS) | | Alkylating | |
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| Platinum-based | |
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| Nonclassical | |
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| Intercalation | |
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| Photosensitizers/PDT | |
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| Other | | Enzyme inhibitors |
- FI (Tipifarnib§)
- CDK inhibitors (Abemaciclib
- Alvocidib†
- Palbociclib
- Ribociclib
- Seliciclib†)
- PrI
- PhI (Anagrelide)
- IMPDI (Tiazofurin§)
- LI (Masoprocol)
- PARP inhibitor (Fuzuloparib
- Niraparib +abiraterone acetate
- Olaparib
- Rucaparib)
- HDAC (Belinostat
- Entinostat
- Panobinostat
- Romidepsin
- Vorinostat)
- PIKI (Pi3K) (Alpelisib
- Copanlisib‡
- Duvelisib
- Idelalisib
- Inavolisib
- Umbralisib‡)
- IDH (Enasidenib
- Ivosidenib
- Olutasidenib
- Vorasidenib)
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| Receptor antagonists | |
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| Other/ungrouped |
- Adagrasib
- Aflibercept
- Arsenic trioxide# (Realgar/Indigo naturalis#)
- Asparagine depleters (Asparaginase#/Pegaspargase)
- Axicabtagene ciloleucel
- Belzutifan
- Bexarotene
- Brexucabtagene autoleucel
- Calaspargase pegol
- Celecoxib
- Ciltacabtagene autoleucel
- Darinaparsin
- Demecolcine
- Denileukin diftitox
- Eflornithine
- Elesclomol§
- Elsamitrucin
- Epacadostat
- Eribulin
- Estramustine
- Glasdegib
- Idecabtagene vicleucel
- Idroxioleic acid
- Imetelstat
- Lifileucel
- Lisocabtagene maraleucel
- Lonidamine
- Lucanthone
- Lurbinectedin
- Mitoguazone
- Mitotane
- Nadofaragene firadenovec
- Navitoclax
- Nirogacestat
- Obecabtagene autoleucel
- Oblimersen†
- Omacetaxine mepesuccinate
- Para-toluenesulfonamide
- Pelabresib
- Plitidepsin
- Retinoids (Alitretinoin
- Tretinoin#)
- Selinexor
- Sitimagene ceradenovec
- Sotorasib
- Tabelecleucel
- Tagraxofusp
- Talimogene laherparepvec
- Tazemetostat
- Tebentafusp
- Tiazofurine
- Tigilanol tiglate
- Tisagenlecleucel
- Trabectedin
- Veliparib
- Venetoclax
- Verdinexor
- Vosaroxin
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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