Triacetyldiphenolisatin

CHEMBL1909288 Phase 4 معتمد Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
443.4 g/mol
LogP
3.4
Phase
4

Triacetyldiphenolisatin is a triacetate prodrug of diphenolisatin, a stimulant laxative that upon hydrolysis releases isatin compounds that stimulate colonic motility by irritating the colonic mucosa and increasing intestinal peristalsis. It was used for treatment of constipation but has largely been replaced by safer laxative agents. Its mechanism involves direct irritant stimulation of the colon similar to other anthraquinone-based laxatives.

الوزن الجزيئي

443,4000 g/mol

LogP

3,40

TPSA

90,00 Ų

قاعدة ليبينسكي للخمسة

ناجح

آلية العمل

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)

الآلية

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.

البنية ثنائية الأبعاد

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SMILES

CC(=O)Oc1ccc(C2(c3ccc(OC(C)=O)cc3)C(=O)N(C(C)=O)c3ccccc32)cc1

InChI

InChI=1S/C26H21NO6/c1-16(28)27-24-7-5-4-6-23(24)26(25(27)31,19-8-12-21(13-9-19)32-17(2)29)20-10-14-22(15-11-20)33-18(3)30/h4-15H,1-3H3

Molecular Formula

C26H21NO6

HBD / HBA

- / 6

الروابط القابلة للدوران

6

الذرات الثقيلة

33

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.

الأسئلة الشائعة

Triacetyldiphenolisatin is a triacetate prodrug of diphenolisatin, a stimulant laxative that upon hydrolysis releases isatin compounds that stimulate colonic motility by irritating the colonic mucosa and increasing intestinal peristalsis. It was used for treatment of constipation but has largely been replaced by safer laxative agents. Its mechanism involves direct irritant stimulation of the colon similar to other anthraquinone-based laxatives.

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, Triacetyldiphenolisatin is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1909288. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 29321. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

إخلاء المسؤولية الطبية

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.