Cysteamine Bitartrate
The bitartrate salt of cysteamine, used orally to treat nephropathic cystinosis by reducing intracellular cystine accumulation. The delayed-release bitartrate formulation improves tolerability compared to the immediate-release form.
Khối lượng phân tử
227,2400 g/mol
TPSA
142,00 Ų
Lĩnh vực điều trị
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Cấu trúc 2D
Cite this structure
Embed this structure
SMILES
NCCS.O=C(O)[C@H](O)[C@@H](O)C(=O)O
InChI
InChI=1S/C4H6O6.C2H7NS/c5-1(3(7)8)2(6)4(9)10;3-1-2-4/h1-2,5-6H,(H,7,8)(H,9,10);4H,1-3H2/t1-,2-;/m1./s1
Molecular Formula
C6H13NO6S
HBD / HBA
6 / 8
Liên kết có thể quay
4
Nguyên tử nặng
14
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.
Câu hỏi thường gặp
The bitartrate salt of cysteamine, used orally to treat nephropathic cystinosis by reducing intracellular cystine accumulation. The delayed-release bitartrate formulation improves tolerability compared to the immediate-release form.
Yes, Cysteamine Bitartrate 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). CHEMBL1200577. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 11958147. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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