SCHEMBL4869134

SCHEMBL4869134

O=[N+]([O-])c1cccc(S(=O)(=O)NOC2CCCC2)c1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 3/20 0.56
MMP2 P08253 2/20 0.56
CA1 P00915 1/20 0.56
MMP1 P03956 1/20 0.56
MMP9 P14780 1/20 0.56
MMP8 P22894 1/20 0.56
MMP13 P45452 1/20 0.56
KMT2A Q03164 2/20 0.55
MEN1 O00255 1/20 0.55
GAA P10253 1/20 0.51
HTT P42858 1/20 0.51
CYP19A1 P11511 1/20 0.50
ACHE P22303 1/20 0.50
ALDH1A1 P00352 2/20 0.49
F2 P00734 2/20 0.49
PRSS1 P07477 2/20 0.49
PRSS2 P07478 2/20 0.49
PRSS3 P35030 2/20 0.49
LMNA P02545 1/20 0.49
CA5A P35218 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
SCHEMBL1725394 0.82 CA2 (0.60) CA2MMP2CA1MMP1MMP9
SCHEMBL4873352 0.81 KMT2A (0.47) KMT2AMEN1HTTCYP19A1ALDH1A1
SCHEMBL17526212 0.79 CA2 (0.63) CA2MMP2CA1MMP1MMP9
SCHEMBL9099702 0.78 PRMT5 (0.55) CA2MMP2CA1MMP1MMP9
SCHEMBL4863860 0.78 POLB (0.48) CA2CA1KMT2ACYP19A1ALDH1A1
SCHEMBL18770212 0.78 ALDH1A1 (0.43) KMT2AMEN1GAAHTTALDH1A1
SCHEMBL5188248 0.77 CA2 (0.65) CA2MMP2CA1MMP1MMP9
SCHEMBL4867769 0.76 KDM4E (0.44) CA2MMP2CA1MMP1MMP9
SCHEMBL4733977 0.76 KMT2A (0.54) CA2MMP2CA1MMP1MMP9
SCHEMBL13590904 0.75 CA2 (0.75) CA2MMP2CA1MMP1MMP9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7419967-B2 Sulfonamide inhibitors of aspartyl protease VERTEX PHARMACEUTICALS INCORPORATED (US) 2008-09-02 US disclosed
US-7419967-B2 Sulfonamide inhibitors of aspartyl protease VERTEX PHARMACEUTICALS INCORPORATED (US) 2008-09-02 US disclosed
US-20060172936-A1 Sulfonamide inhibitors of aspartyl protease VERTEX PHARMACEUTICALS INCORPORATED 2006-08-03 US disclosed
EP-1086076-B1 SULFONAMIDE INHIBITORS OF ASPARTYL PROTEASE VERTEX PHARMA (US) 2004-12-22 EP disclosed
US-20040097594-A1 Sulfonamide inhibitors of aspartyl protease HALE MICHAEL ROBIN (US) 2004-05-20 US disclosed
US-6613743-B2 Administering to a patient suffering from viral infections a sulfonamides antiviral agents which are aspartyl protease inhibitors VERTEX PHARMACEUTICALS INCORPORATED 2003-09-02 US disclosed
US-20020049201-A1 Sulfonamide inhibitors of aspartyl protease VERTEX PHARMACEUTICALS INCORPORATED 2002-04-25 US disclosed
EP-1086076-A1 SULFONAMIDE INHIBITORS OF ASPARTYL PROTEASE Vertex Pharmaceuticals Incorporated (US) 2001-03-28 EP disclosed
WO-1999065870-A2 SULFONAMIDE INHIBITORS OF ASPARTYL PROTEASE VERTEX PHARMACEUTICALS INCORPORATED (US) 1999-12-23 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 (3 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-20040097594-A1 Sulfonamide inhibitors of aspartyl protease SPINT2, PRSS1, DNPEP CA2 409/4885MMP2 465/4885CA1 394/4885
US-20060172936-A1 Sulfonamide inhibitors of aspartyl protease SPINT2, PRSS1, DNPEP CA2 409/4885MMP2 465/4885CA1 394/4885
US-20020049201-A1 Sulfonamide inhibitors of aspartyl protease SPINT2, PRSS1, DNPEP CA2 409/4885MMP2 465/4885CA1 394/4885

“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.