Details
Stereochemistry | ACHIRAL |
Molecular Formula | C16H15ClN2O3S |
Molecular Weight | 350.82 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC=C(NC(=O)NS(=O)(=O)C2=CC3=C(CCC3)C=C2)C=C1
InChI
InChIKey=JQJSFAJISYZPER-UHFFFAOYSA-N
InChI=1S/C16H15ClN2O3S/c17-13-5-7-14(8-6-13)18-16(20)19-23(21,22)15-9-4-11-2-1-3-12(11)10-15/h4-10H,1-3H2,(H2,18,19,20)
Sulofenur is an orally active diarylsulfonylurea derivative patented by American pharmaceutical company Eli Lilly and Co. as an antitumor agent. In preclinical studies, Sulofenur exhibits significant activity against advanced colon adenocarcinoma xenografts intrinsically resistant to virtually all standard chemotherapeutic agents and also had very significant activity against several pediatric tumors grown as xenografts. Clinically, Sulofenur was disappointing, and although some responses were reported in phase I trials this was not confirmed for ovarian cancer in the phase II setting. Toxicity in man was due mainly to methemoglobinemia and anemia, which limited the concentrations of drug that could be achieved to levels well below those shown to elicit a therapeutic response in the xenograft models.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL3301398 Sources: https://adisinsight.springer.com/drugs/800000891 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1421428
700 mg/m2 for 14 days every 3 weeks
Route of Administration:
Oral
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NCI_THESAURUS |
C2186
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DTXSID20149208
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60417
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Z45N070N3S
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AA-11
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110311-27-8
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CHEMBL7643
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100000082975
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C058179
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6607
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C1432
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SUB10753MIG
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ACTIVE MOIETY
METABOLITE (PARENT)
METABOLITE (PARENT)