SCHEMBL4470491

SCHEMBL4470491

COc1cccc(CNS(=O)(=O)c2ccc3cc(NC(C)=O)ccc3c2)c1OC

nearest known ligand 0.66

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 4/20 0.53
KMT2A Q03164 4/20 0.53
HTT P42858 2/20 0.52
LMNA P02545 2/20 0.51
SMN1; SMN2 Q16637 1/20 0.51
NPSR1 Q6W5P4 1/20 0.51
KAT6A Q92794 1/20 0.49
ALOX12 P18054 1/20 0.48
HIF1A Q16665 1/20 0.47
NAMPT P43490 1/20 0.46
MAPK1 P28482 2/20 0.46
MAPT P10636 1/20 0.46
ALOX15 P16050 1/20 0.46
TSHR P16473 1/20 0.46
GAA P10253 1/20 0.46

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL4482015 0.85 MEN1 (0.47) MEN1KMT2AHTTLMNASMN1; SMN2
SCHEMBL4479011 0.85 CASP6 (0.55) MEN1KMT2AHTTLMNASMN1; SMN2
SCHEMBL4478841 0.83 LMNA (0.52) MEN1KMT2ALMNASMN1; SMN2NPSR1
SCHEMBL4485797 0.80 POLB (0.48) MEN1KMT2AHTTLMNASMN1; SMN2
SCHEMBL4471169 0.79 LMNA (0.50) MEN1KMT2ALMNASMN1; SMN2NPSR1
SCHEMBL4492170 0.77 LMNA (0.50) MEN1KMT2ALMNASMN1; SMN2NPSR1
SCHEMBL4489812 0.76 LMNA (0.61) MEN1KMT2AHTTLMNASMN1; SMN2
SCHEMBL2855464 0.76 F2 (0.51) MEN1KMT2AHTTLMNASMN1; SMN2
SCHEMBL2855466 0.75 CYP19A1 (0.56) MEN1KMT2ALMNASMN1; SMN2NPSR1
SCHEMBL4449293 0.74 MEN1 (0.45) MEN1KMT2ALMNASMN1; SMN2NPSR1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7598418-B2 Naphthalene-1-(sulfonamide or carboxamide) derivatives; e.g. N-Benzyl-5-{[(4-methylphenyl)sulfonyl]oxy}naphthalene-1-sulfonamide; protein kinase inhibitors sensitize cancer cells to radiotherapy or anticancer agents; side effect reduction INSTITUTE OF MEDICINAL MOLECULAR DESIGN, INC. (JP) 2009-10-06 US claimed
US-20050215645-A1 Amide derivatives INSTITUTE OF MEDICINAL MOLECULAR DESIGN. INC. (JP) 2005-09-29 US claimed
US-7598418-B2 Naphthalene-1-(sulfonamide or carboxamide) derivatives; e.g. N-Benzyl-5-{[(4-methylphenyl)sulfonyl]oxy}naphthalene-1-sulfonamide; protein kinase inhibitors sensitize cancer cells to radiotherapy or anticancer agents; side effect reduction INSTITUTE OF MEDICINAL MOLECULAR DESIGN, INC. (JP) 2009-10-06 US disclosed
US-20050215645-A1 Amide derivatives INSTITUTE OF MEDICINAL MOLECULAR DESIGN. INC. (JP) 2005-09-29 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050215645-A1 Amide derivatives OGG1, HDAC1, BCL2A1 MEN1 4507/4885KMT2A 1012/4885HTT 4096/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.