SCHEMBL7224903

SCHEMBL7224903

COc1ccc(C(=O)Nc2ccc3c(c2)oc2ccc(S(=O)(=O)N4CCSC(C)(C)C4C(=O)NO)cc23)cc1OC

nearest known ligand 0.53

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ MMP13 P45452 17/20 0.53
▸ MMP1 P03956 16/20 0.53
▸ MMP2 P08253 13/20 0.53
▸ MMP3 P08254 9/20 0.53
▸ MMP9 P14780 8/20 0.53
▸ MMP7 P09237 8/20 0.53
▸ MMP8 P22894 6/20 0.53
▸ ADAM17 P78536 9/20 0.52
▸ MMP14 P50281 2/20 0.47
▸ CYP2D6 P10635 1/20 0.45
▸ CYP2C9 P11712 1/20 0.45
▸ CYP2C19 P33261 1/20 0.45
▸ USP2 O75604 1/20 0.44
▸ POLB P06746 1/20 0.44
▸ GAA P10253 1/20 0.44
▸ MAPT P10636 1/20 0.44

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
SCHEMBL7226342 1.00 MMP13 (0.53) MMP13MMP1MMP2MMP3MMP9
SCHEMBL7219692 0.90 MMP1 (0.57) MMP13MMP1MMP2MMP3MMP9
SCHEMBL7225017 0.90 MMP1 (0.57) MMP13MMP1MMP2MMP3MMP9
SCHEMBL7221063 0.89 MMP1 (0.53) MMP13MMP1MMP2MMP3MMP9
SCHEMBL7219971 0.89 MMP1 (0.55) MMP13MMP1MMP2MMP3MMP9
SCHEMBL7220023 0.87 MMP13 (0.48) MMP13MMP1MMP2MMP3MMP9
SCHEMBL7225630 0.86 MMP1 (0.54) MMP13MMP1MMP2MMP3MMP9
SCHEMBL7220199 0.86 MMP13 (0.48) MMP13MMP1MMP2MMP3MMP9
SCHEMBL7225363 0.86 MMP13 (0.46) MMP13MMP1MMP2MMP3MMP9
SCHEMBL7219120 0.85 MEN1 (0.62) MMP13MMP1MMP2MMP3MMP9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6559142-B2 Tricyclic substituted cyclic sulfonamides compound is useful for treating heart disease, multiple sclerosis, arthritis, atherosclerosis, and osteoporosis WARNER-LAMBERT COMPANY 2003-05-06 — — US claimed
US-20020169160-A1 Sulfonamide matrix metalloproteinase inhibitors O'BRIEN PATRICK MICHAEL (US) 2002-11-14 — — US claimed
EP-1233017-A1 Tricyclic sulfonamides useful as matrix metalloproteinase inhibitors WARNER-LAMBERT COMPANY (US) 2002-08-21 — — EP claimed
US-6559142-B2 Tricyclic substituted cyclic sulfonamides compound is useful for treating heart disease, multiple sclerosis, arthritis, atherosclerosis, and osteoporosis WARNER-LAMBERT COMPANY 2003-05-06 — — US disclosed
US-20020169160-A1 Sulfonamide matrix metalloproteinase inhibitors O'BRIEN PATRICK MICHAEL (US) 2002-11-14 — — US disclosed
EP-1233017-A1 Tricyclic sulfonamides useful as matrix metalloproteinase inhibitors WARNER-LAMBERT COMPANY (US) 2002-08-21 — — EP 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 (1 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-20020169160-A1 Sulfonamide matrix metalloproteinase inhibitors MMP9, MMP10, MMP3 MMP13 8/4885MMP1 4/4885MMP2 12/4885

“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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