Azathioprine
An immunosuppressant prodrug that is converted in the body to 6-mercaptopurine, which interferes with DNA synthesis in rapidly dividing immune cells, reducing the immune response. It is used to prevent organ transplant rejection and to treat autoimmune conditions.
分子量
277.2700 g/mol
LogP
0.10
TPSA
143.00 Ų
Lipinski 五规则
符合
治疗领域
作用机制
Suppresses the immune system by inhibiting T-cell activation, lymphocyte proliferation, or cytokine production. This prevents immune-mediated tissue damage and graft rejection.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Suppresses the immune system by inhibiting T-cell activation, lymphocyte proliferation, or cytokine production. This prevents immune-mediated tissue damage and graft rejection.
二维结构
Cite this structure
Embed this structure
SMILES
Cn1cnc([N+](=O)[O-])c1Sc1ncnc2[nH]cnc12
InChI
InChI=1S/C9H7N7O2S/c1-15-4-14-7(16(17)18)9(15)19-8-5-6(11-2-10-5)12-3-13-8/h2-4H,1H3,(H,10,11,12,13)
Molecular Formula
C9H7N7O2S
HBD / HBA
1 / 7
可旋转键数
2
重原子数
19
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
An immunosuppressant prodrug that is converted in the body to 6-mercaptopurine, which interferes with DNA synthesis in rapidly dividing immune cells, reducing the immune response. It is used to prevent organ transplant rejection and to treat autoimmune conditions.
Suppresses the immune system by inhibiting T-cell activation, lymphocyte proliferation, or cytokine production. This prevents immune-mediated tissue damage and graft rejection.
Yes, Azathioprine 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). CHEMBL1542. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 2265. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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