SCHEMBL3615243

SCHEMBL3615243

CCS(=O)(=O)Nc1cccc2oc(C(=O)Nc3ccc(-c4ccc(S(=O)(=O)NC(C(=O)O)C(C)C)cc4)cc3)c(C)c12

nearest known ligand 0.84

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
MMP2 P08253 20/20 0.84
MMP13 P45452 20/20 0.84
MMP14 P50281 3/20 0.84
MMP9 P14780 2/20 0.84
ADAMTS4 O75173 2/20 0.84
MMP1 P03956 1/20 0.71
MMP3 P08254 1/20 0.71
MMP7 P09237 1/20 0.71
MMP8 P22894 1/20 0.71

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
SCHEMBL13314496 1.00 MMP2 (0.84) MMP2MMP13MMP14MMP9ADAMTS4
SCHEMBL13314499 0.92 MMP2 (0.89) MMP2MMP13MMP14MMP9ADAMTS4
SCHEMBL3610523 0.92 MMP2 (0.89) MMP2MMP13MMP14MMP9ADAMTS4
SCHEMBL3608983 0.92 MMP2 (0.71) MMP2MMP13MMP14MMP9ADAMTS4
SCHEMBL3610357 0.92 MMP2 (1.00) MMP2MMP13MMP14MMP9ADAMTS4
SCHEMBL13314471 0.92 MMP2 (1.00) MMP2MMP13MMP14MMP9ADAMTS4
SCHEMBL13314465 0.92 MMP2 (1.00) MMP2MMP13MMP14MMP9ADAMTS4
SCHEMBL3613470 0.91 MMP2 (0.86) MMP2MMP13MMP14MMP9ADAMTS4
SCHEMBL13314497 0.91 MMP2 (0.86) MMP2MMP13MMP14MMP9ADAMTS4
SCHEMBL3616707 0.90 MMP2 (0.83) MMP2MMP13MMP14MMP9ADAMTS4

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
EP-1692124-B1 BIARYL SULFONAMIDES AS MMP INHIBITORS WYETH CORP (US) 2008-10-15 EP claimed
US-7420001-B2 Biaryl sulfonamides and methods for using same WYETH (US) 2008-09-02 US claimed
US-20050143422-A1 Biaryl sulfonamides and methods for using same WYETH (US) 2005-06-30 US claimed
US-20100137298-A1 Biaryl Sulfonamides and Methods for Using Same WYETH (US) 2010-06-03 US disclosed
US-7645574-B2 Providing palladium ions, contacting ions and nucleic acids under conditions effective to bind palladium on one or more sites of the nucleic acid, contact with nickel or nickel alloy under conditions effective to deposit nickel or nickel alloy on nucleic acid, attach/immobilize to solid support; biochip INTEGRATED NANO-TECHNOLOGIES, LLC (US) 2010-01-12 US disclosed
EP-1692124-B1 BIARYL SULFONAMIDES AS MMP INHIBITORS WYETH CORP (US) 2008-10-15 EP disclosed
US-7420001-B2 Biaryl sulfonamides and methods for using same WYETH (US) 2008-09-02 US disclosed
WO-2006113457-A1 POLYMER-FLUOROSURFACTANT ASSOCIATIVE COMPLEXES THE CLOROX COMPANY (US) 2006-10-26 WO disclosed
EP-1692124-A1 BIARYL SULFONAMIDES AS MMP INHIBITORS Wyeth (US) 2006-08-23 EP disclosed
WO-2005061477-A1 BIARYL SULFONAMIDES AS MMP INHIBITORS WYETH (US) 2005-07-07 WO disclosed
US-20050143422-A1 Biaryl sulfonamides and methods for using same WYETH (US) 2005-06-30 US disclosed
US-20040229247-A1 Providing palladium ions, contacting ions and nucleic acids under conditions effective to bind palladium on one or more sites of the nucleic acid, contact with nickel or nickel alloy under conditions effective to deposit nickel or nickel alloy on nucleic acid, attach/immobilize to solid support; biochip ENPLAS AMERICA, INC. 2004-11-18 US disclosed
WO-2004096986-A2 METHOD FOR QUANTITATIVE DETECTION OF NUCLEIC ACID MOLECULES INTEGRATED NANO-TECHNOLOGIES, LLC (US) 2004-11-11 WO disclosed
WO-2004065570-A2 METHODS OF METALLIZING NUCLEIC ACID MOLECULES AND METHODS OF ATTACHING NUCLEIC ACID MOLECULES TO CONDUCTIVE SURFACES INTEGRATED NANO-TECHNOLOGIES, LLC (US) 2004-08-05 WO disclosed
US-3932610-A SURFACTANTS, SOLVENTS, HAIR GROOMING AGENTS LEVER BROTHERS COMPANY (US) 1976-01-13 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 (2 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-20100137298-A1 Biaryl Sulfonamides and Methods for Using Same STS, MMP3, AADAC MMP2 5/4885MMP13 13/4885MMP14 19/4885
US-20050143422-A1 Biaryl sulfonamides and methods for using same STS, MMP3, AADAC MMP2 5/4885MMP13 13/4885MMP14 19/4885

“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.