SCHEMBL6556147

SCHEMBL6556147

CC(C)S(=O)(=O)NC[C@H](C)c1cccc([N+](=O)[O-])c1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GRIA4 P48058 10/20 0.52
KMT2A Q03164 4/20 0.50
MEN1 O00255 2/20 0.50
HPGD P15428 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.50
CYP3A4 P08684 2/20 0.46
CYP1A2 P05177 1/20 0.46
CYP2C19 P33261 1/20 0.46
CYP19A1 P11511 1/20 0.46
GRIA2 P42262 2/20 0.45
GRIA1 P42261 1/20 0.45
GRIA3 P42263 1/20 0.45
CA1 P00915 1/20 0.44
CA2 P00918 1/20 0.44
MMP1 P03956 1/20 0.44
MMP2 P08253 1/20 0.44
MMP9 P14780 1/20 0.44
MMP8 P22894 1/20 0.44
MMP13 P45452 1/20 0.44
LMNA P02545 1/20 0.43

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
SCHEMBL5877971 0.87 GRIA4 (0.66) GRIA4KMT2AMEN1GRIA2GRIA1
SCHEMBL6556293 0.84 GRIA4 (0.60) GRIA4GRIA2GRIA1GRIA3CA1
SCHEMBL5878346 0.84 GRIA4 (0.60) GRIA4GRIA2GRIA1GRIA3CA1
SCHEMBL6556154 0.83 GRIA4 (0.49) GRIA4KMT2AMEN1HPGDL3MBTL1
SCHEMBL18896279 0.77 KMT2A (0.58) KMT2AMEN1HPGDL3MBTL1CA1
SCHEMBL338391 0.77 GRIA4 (0.81) GRIA4GRIA2GRIA1GRIA3
SCHEMBL3704221 0.77 GRIA4 (0.81) GRIA4GRIA2GRIA1GRIA3
SCHEMBL6554405 0.77 GRIA4 (0.81) GRIA4GRIA2GRIA1GRIA3
SCHEMBL6562896 0.77 GRIA4 (0.57) GRIA4GRIA2GRIA1GRIA3CA1
SCHEMBL3069746 0.76 KMT2A (0.57) KMT2AMEN1HPGDL3MBTL1CA2

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040235957-A1 Use of sulfonamide derivatives as pharmaceuticals compounds BLEAKMAN DAVID (US) 2004-11-25 US disclosed
US-6803484-B2 Sulfonamide derivatives ELI LILLY AND COMPANY 2004-10-12 US disclosed
US-20040143020-A1 Sulfonamide derivatives AIKINS JAMES ABRAHAM (US) 2004-07-22 US disclosed
EP-1438036-A2 USE OF SULFONAMIDE DERIVATIVES AS PHARMACEUTICALS COMPOUNDS ELI LILLY AND COMPANY (US) 2004-07-21 EP disclosed
US-6720357-B2 TREATMENT OF CONDITIONS ASSOCIATED WITH GLUTAMATE HYPOFUNCTION, SUCH AS PSYCHIATRIC AND NEUROLOGICAL DISORDERS; N-2-(4-N-(3,5-DIFLUOROBENZAMIDO)PHENYL)PROPYL-2-PROPANESULFONAMIDE ELI LILLY AND COMPANY 2004-04-13 US disclosed
EP-1390072-A2 USE OF AN AMPA RECEPTOR POTENTIATOR FOR THE MANUFACTURE OF A MEDICAMENT FOR THE TREATMENT OF TYPE 2 DIABETES ELI LILLY AND COMPANY (US) 2004-02-25 EP disclosed
US-20030233015-A1 Sulfonamide derivatives ELI LILLY AND COMPANY 2003-12-18 US disclosed
US-20030225127-A1 Heterocyclic sulfonamide derivatives BENDER DAVID MICHAEL (US) 2003-12-04 US disclosed
EP-1309577-A2 HETEROCYCLIC SULFONAMIDE DERIVATIVES AND THEIR USE FOR POTENTIATING GLUTAMATE RECEPTOR FUNCTION ELI LILLY AND COMPANY (US) 2003-05-14 EP disclosed
WO-2003032974-A2 USE OF SULFONAMIDE DERIVATIVES AS PHARMACEUTICALS COMPOUNDS ELI LILLY AND COMPANY (US) 2003-04-24 WO disclosed
EP-1296944-A1 SULFONAMIDE DERIVATIVES ELI LILLY AND COMPANY (US) 2003-04-02 EP disclosed
WO-2002089848-A2 USE OF AN AMPA RECEPTOR POTENTIATOR FOR THE MANUFACTURE OF A MEDICAMENT FOR THE TREATMENT OF TYPE 2 DIABETES ELI LILLY AND COMPANY (US) 2002-11-14 WO disclosed
WO-2002014294-A2 HETEROCYCLIC SULFONAMIDE DERIVATIVES AND THEIR USE FOR POTENTIATING GLUTAMATE RECEPTOR FUNCTION ELI LILLY AND COMPANY (US) 2002-02-21 WO disclosed
WO-2001089510-A2 USE OF AN AMPA RECEPTOR POTENTIATOR FOR THE TREATMENT OF OBESITY ELI LILLY AND COMPANY (US) 2001-11-29 WO disclosed
WO-2001090056-A1 SULFONAMIDE DERIVATIVES ELI LILLY AND COMPANY (US) 2001-11-29 WO 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 (4 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-20030233015-A1 Sulfonamide derivatives GRIN2A, GRIN1, SLC1A2 GRIA4 14/4885KMT2A 597/4885MEN1 4032/4885
US-20040143020-A1 Sulfonamide derivatives GRIN2A, GRIN2B, SLC1A2 GRIA4 13/4885KMT2A 515/4885MEN1 4306/4885
US-20040235957-A1 Use of sulfonamide derivatives as pharmaceuticals compounds GABRE, SCN2A, SCN1A GRIA4 212/4885KMT2A 664/4885MEN1 1630/4885
US-20030225127-A1 Heterocyclic sulfonamide derivatives GRIN2A, GRIN2B, GRIN1 GRIA4 12/4885KMT2A 915/4885MEN1 4088/4885

“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.