SCHEMBL5994700

SCHEMBL5994700

CS(=O)(=O)NCCc1ccc(OBOc2ccc(CCNS(C)(=O)=O)cc2)cc1

nearest known ligand 0.51

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ CA12 O43570 2/20 0.51
▸ CA1 P00915 2/20 0.51
▸ CA2 P00918 2/20 0.51
▸ CA9 Q16790 2/20 0.51
▸ CA5A P35218 1/20 0.51
▸ CA14 Q9ULX7 1/20 0.51
▸ ALDH1A1 P00352 6/20 0.50
▸ SMN1; SMN2 Q16637 1/20 0.50
▸ POLB P06746 2/20 0.47
▸ GRIA4 P48058 2/20 0.45
▸ MEN1 O00255 1/20 0.42
▸ KMT2A Q03164 1/20 0.42
▸ MTNR1A P48039 1/20 0.41
▸ ALOX15 P16050 1/20 0.41
▸ TBXA2R P21731 1/20 0.40
▸ TBXAS1 P24557 1/20 0.40
▸ NQO2 P16083 1/20 0.40
▸ RECQL P46063 1/20 0.40

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
SCHEMBL2093102 0.83 CA12 (0.73) CA12CA1CA2CA9CA5A
SCHEMBL3321085 0.83 KMT2A (0.53) ALDH1A1SMN1; SMN2POLBMEN1KMT2A
SCHEMBL5991959 0.78 GRIA4 (0.63) CA12CA1CA2CA9CA5A
SCHEMBL660035 0.77 ALDH1A1 (0.68) CA12CA1CA2CA9CA5A
SCHEMBL1265707 0.76 GRIA4 (0.69) CA1CA2ALDH1A1SMN1; SMN2POLB
SCHEMBL6788476 0.75 TAAR1 (0.57) CA12CA1CA2CA9CA5A
SCHEMBL4887431 0.75 CA1 (0.58) CA12CA1CA2CA9CA5A
SCHEMBL1267234 0.75 MEN1 (0.57) CA12CA1CA2CA9ALDH1A1
SCHEMBL5993697 0.75 POLB (0.53) CA12CA1CA2CA9CA5A
SCHEMBL11340894 0.75 TBXA2R (0.69) CA12CA1CA2CA9CA5A

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 CA12 3830/4885CA1 624/4885CA2 1437/4885
US-20030225163-A1 Sulfonamide derivatives GRIN1, SLC1A2, GRIN2A CA12 1290/4885CA1 277/4885CA2 751/4885
US-20030092947-A1 Process for preparing biphenyl compounds CYP1B1, CYP4B1, CYP2B6 CA12 2855/4885CA1 4001/4885CA2 3522/4885
US-20040235957-A1 Use of sulfonamide derivatives as pharmaceuticals compounds GABRE, SCN2A, SCN1A CA12 1034/4885CA1 1076/4885CA2 416/4885

“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.

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