Lisdexamfetamine
A prodrug of dextroamphetamine for ADHD and binge eating disorder.
Khối lượng phân tử
263,3800 g/mol
LogP
1,20
TPSA
81,10 Ų
Lipinski RO5
Đạt
Lĩnh vực điều trị
Cơ chế tác dụng
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
Cấu trúc 2D
Cite this structure
Embed this structure
SMILES
C[C@@H](Cc1ccccc1)NC(=O)[C@@H](N)CCCCN
InChI
InChI=1S/C15H25N3O/c1-12(11-13-7-3-2-4-8-13)18-15(19)14(17)9-5-6-10-16/h2-4,7-8,12,14H,5-6,9-11,16-17H2,1H3,(H,18,19)/t12-,14-/m0/s1
Molecular Formula
C15H25N3O
HBD / HBA
3 / 3
Liên kết có thể quay
8
Nguyên tử nặng
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.
Câu hỏi thường gặp
A prodrug of dextroamphetamine for ADHD and binge eating disorder.
Administered as an inactive precursor that is metabolically converted to its active form in the body. This prodrug design improves bioavailability, absorption, or targeted delivery compared to the active compound.
Yes, Lisdexamfetamine 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). CHEMBL1201222. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 11597698. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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