Drug Details
| General Information of the Drug (ID: DR5996) | ||||
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| Name |
Sulindac sulfone
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| Synonyms |
Aposulind; Aptosyn; FGN-1; Prevatac (former Brand Name); Exisulind; (Z)-5-Fluoro-2-methyl-1-[4-(methylsulfonyl)benzylidene]-1H-indene-3-acetic acid
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| Molecular Type |
Small molecule
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| Disease | Colorectal cancer [ICD-11: 2B91] | Phase 3 | [1] | |
| Structure |
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Click to Download Mol2D MOL |
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| Click to Show/Hide the Molecular Information and External Link(s) of This Natural Product | ||||
| Formula |
C20H17FO4S
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| PubChem CID | ||||
| Canonical SMILES |
CC1=C(C2=C(C1=CC3=CC=C(C=C3)S(=O)(=O)C)C=CC(=C2)F)CC(=O)O
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| InChI |
1S/C20H17FO4S/c1-12-17(9-13-3-6-15(7-4-13)26(2,24)25)16-8-5-14(21)10-19(16)18(12)11-20(22)23/h3-10H,11H2,1-2H3,(H,22,23)/b17-9-
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| InChIKey |
MVGSNCBCUWPVDA-MFOYZWKCSA-N
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| CAS Number |
CAS 59973-80-7
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| TTD Drug ID | ||||
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| Combinatorial Therapeutic Effect(s) Validated Clinically or Experimentally | ||||||
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| α. A List of Natural Product(s) Able to Enhance the Efficacy of This Drug | ||||||
| Curcumin | Hellenia speciosa | Click to Show/Hide the Molecular Data of This NP | ||||
| Achieving Therapeutic Synergy | Click to Show/Hide | |||||
| Representative Experiment Reporting the Effect of This Combination | [2] | |||||
| Detail(s) |
Combination Info
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| Biological
Regulation |
Induction | Cell cycle arrest in G2/M phase | ||||
| In-vitro Model | HT-29 | CVCL_0320 | Colon adenocarcinoma | Homo sapiens | ||
| In-vivo Model | Aberrant crypt foci (ACF) were induced male Wistar rats (6-week old) with DMH. | |||||
| Experimental
Result(s) |
Curcumin potentiates the pro-apoptotic effects of sulindac sulfone in colorectal cancer. | |||||
| Target and Pathway | ||||
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| Target(s) | Phosphodiesterase 5A (PDE5A) | Molecule Info | [3] | |
| KEGG Pathway | Purine metabolism | Click to Show/Hide | ||
| 2 | cGMP-PKG signaling pathway | |||
| NetPath Pathway | TGF_beta_Receptor Signaling Pathway | Click to Show/Hide | ||
| Reactome | cGMP effects | Click to Show/Hide | ||