SCHEMBL5994696

SCHEMBL5994696

CS(=O)(=O)NCCc1ccccc1.OBO

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 2/20 0.69
CA12 O43570 1/20 0.53
CA7 P43166 1/20 0.53
CA9 Q16790 1/20 0.53
CA14 Q9ULX7 1/20 0.53
ALDH1A1 P00352 5/20 0.51
MAPT P10636 2/20 0.51
KDM4E B2RXH2 1/20 0.51
LMNA P02545 1/20 0.51
CYP3A4 P08684 1/20 0.51
GAA P10253 1/20 0.51
BLM P54132 1/20 0.51
GFER P55789 1/20 0.51
PMP22 Q01453 1/20 0.51
L3MBTL1 Q9Y468 2/20 0.50
MEN1 O00255 1/20 0.49
KMT2A Q03164 1/20 0.49
NPSR1 Q6W5P4 1/20 0.49
TAAR1 Q96RJ0 1/20 0.49
HSD17B10 Q99714 1/20 0.49

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
SCHEMBL4520702 0.93 POLB (0.79) POLBCA12CA7CA9CA14
SCHEMBL27426082 0.87 POLB (0.71) POLBCA12CA7CA9CA14
SCHEMBL10312250 0.82 POLB (0.64) POLBCA12CA7CA9CA14
SCHEMBL4513715 0.81 POLB (1.00) POLBALDH1A1GAAL3MBTL1MEN1
SCHEMBL3322671 0.81 POLB (0.64) POLBCA12CA7CA9CA14
SCHEMBL15218452 0.80 POLB (0.89) POLBALDH1A1KDM4ECYP3A4GAA
SCHEMBL5349769 0.77 KMT2A (0.70) POLBCA9ALDH1A1KDM4EKMT2A
SCHEMBL11109419 0.77 TBXA2R (0.60) POLBCA12CA7CA9CA14
SCHEMBL15672851 0.77 MEN1 (0.58) POLBALDH1A1MAPTKDM4ELMNA
SCHEMBL5991959 0.77 GRIA4 (0.63) POLBCA12CA9CA14ALDH1A1

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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6984756-B2 Process for preparing biphenyl compounds ELI LILLY AND COMPANY (US) 2006-01-10 US disclosed
EP-1294683-B1 A PROCESS FOR PREPARING BIPHENYL COMPOUNDS LILLY CO ELI (US) 2005-11-30 EP disclosed
US-6900353-B2 Cyclopentyl sulfonamide derivatives ELI LILLY AND COMPANY (US) 2005-05-31 US disclosed
US-20040235957-A1 Use of sulfonamide derivatives as pharmaceuticals compounds BLEAKMAN DAVID (US) 2004-11-25 US disclosed
EP-1438036-A2 USE OF SULFONAMIDE DERIVATIVES AS PHARMACEUTICALS COMPOUNDS ELI LILLY AND COMPANY (US) 2004-07-21 EP disclosed
US-20040067984-A1 Cyclopentyl sulfonamide derivatives CANTRELL BUDDY EUGENE (US) 2004-04-08 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-20030225163-A1 Sulfonamide derivatives ELI LILLY AND COMPANY 2003-12-04 US disclosed
EP-1334087-A1 CYCLOALKYLFLUOROSULFONAMIDE DERIVATIVES ELI LILLY AND COMPANY (US) 2003-08-13 EP disclosed
EP-1311474-A1 SULFONAMIDE DERIVATIVES ELI LILLY AND COMPANY (US) 2003-05-21 EP disclosed
US-20030092947-A1 Process for preparing biphenyl compounds GARDNER JOHN PAUL (US) 2003-05-15 US disclosed
WO-2003032974-A2 USE OF SULFONAMIDE DERIVATIVES AS PHARMACEUTICALS COMPOUNDS ELI LILLY AND COMPANY (US) 2003-04-24 WO disclosed
EP-1294683-A2 A PROCESS FOR PREPARING BIPHENYL COMPOUNDS ELI LILLY AND COMPANY (US) 2003-03-26 EP disclosed
EP-1292311-A2 COMBINATION THERAPY FOR THE TREATMENT OF DEPRESSION COMPRISING AN ANTIDEPRESSANT AND AN AMPA RECEPTOR POTENTIATOR ELI LILLY AND COMPANY (US) 2003-03-19 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-2002032858-A1 CYCLOALKYLFLUOROSULFONAMIDE DERIVATIVES ELI LILLY AND COMPANY (US) 2002-04-25 WO disclosed
WO-2001089530-A2 COMBINATION THERAPY FOR TREATMENT OF DEPRESSION COMPRISING AN ANTIDEPRESSANT AND AN AMPA RECEPTOR POTENTIATOR ELI LILLY AND COMPANY (US) 2001-11-29 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-2001090055-A2 A PROCESS FOR PREPARING BIPHENYL COMPOUNDS ELI LILLY AND COMPANY (US) 2001-11-29 WO disclosed
WO-2001090057-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-20040067984-A1 Cyclopentyl sulfonamide derivatives GRIN2A, GRIN1, GRIK5 POLB 4431/4885CA12 3830/4885CA7 4217/4885
US-20030225163-A1 Sulfonamide derivatives GRIN1, SLC1A2, GRIN2A POLB 4447/4885CA12 1290/4885CA7 2453/4885
US-20030092947-A1 Process for preparing biphenyl compounds CYP1B1, CYP4B1, CYP2B6 POLB 191/4885CA12 2855/4885CA7 1577/4885
US-20040235957-A1 Use of sulfonamide derivatives as pharmaceuticals compounds GABRE, SCN2A, SCN1A POLB 4315/4885CA12 1034/4885CA7 2104/4885

“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.