Uracil Mustard
Uracil mustard is an alkylating antineoplastic agent that combines a uracil base with a nitrogen mustard moiety, enabling it to cross-link DNA strands and inhibit DNA replication in rapidly proliferating cancer cells. It was used orally for treatment of chronic lymphocytic leukemia, non-Hodgkin lymphoma, and other hematologic malignancies, as well as certain solid tumors including breast cancer. It has largely been replaced by more targeted therapies but served as an important early oral alkylating agent.
分子量
252.0900 g/mol
LogP
0.50
TPSA
61.40 Ų
Lipinski 五规则
符合
治疗领域
Pharmacokinetics (PK)
Pharmacodynamics (PD)
二维结构
Cite this structure
Embed this structure
SMILES
Oc1ncc(N(CCCl)CCCl)c(O)n1
InChI
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)
Molecular Formula
C8H11Cl2N3O2
HBD / HBA
2 / 3
可旋转键数
5
重原子数
15
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
常见问题
Uracil mustard is an alkylating antineoplastic agent that combines a uracil base with a nitrogen mustard moiety, enabling it to cross-link DNA strands and inhibit DNA replication in rapidly proliferating cancer cells. It was used orally for treatment of chronic lymphocytic leukemia, non-Hodgkin lymphoma, and other hematologic malignancies, as well as certain solid tumors including breast cancer. It has largely been replaced by more targeted therapies but served as an important early oral alkylating agent.
Yes, Uracil Mustard is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1488. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 6194. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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