SCHEMBL7219783

SCHEMBL7219783

CC1(C)[C@H](C(=O)NO)N(S(=O)(=O)c2ccc3oc4ccccc4c3c2)CCS1(=O)=O

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MMP3 P08254 12/20 0.61
▸ MMP1 P03956 10/20 0.61
▸ MMP13 P45452 9/20 0.61
▸ MMP2 P08253 8/20 0.61
▸ MMP7 P09237 8/20 0.57
▸ MMP8 P22894 6/20 0.56
▸ MMP9 P14780 3/20 0.55
▸ SMN1; SMN2 Q16637 2/20 0.47
▸ HSD11B1 P28845 1/20 0.47
▸ KDM4E B2RXH2 2/20 0.45
▸ CYP3A4 P08684 1/20 0.45
▸ TSHR P16473 1/20 0.45
▸ CYP2C19 P33261 1/20 0.45
▸ HTT P42858 1/20 0.45
▸ MMP14 P50281 1/20 0.42
▸ HDAC1 Q13547 1/20 0.41
▸ MEN1 O00255 1/20 0.40
▸ ALDH1A1 P00352 1/20 0.40
▸ KMT2A Q03164 1/20 0.40
▸ NPSR1 Q6W5P4 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
SCHEMBL7219546 0.82 MMP1 (0.63) MMP3MMP1MMP13MMP2MMP7
SCHEMBL7163700 0.79 MMP1 (0.58) MMP3MMP1MMP13MMP2MMP7
SCHEMBL7166258 0.79 MMP1 (0.58) MMP3MMP1MMP13MMP2MMP7
SCHEMBL7163665 0.79 MMP1 (0.58) MMP3MMP1MMP13MMP2MMP7
SCHEMBL7163437 0.79 MMP1 (0.58) MMP3MMP1MMP13MMP2MMP7
SCHEMBL6666886 0.77 MMP1 (0.56) MMP3MMP1MMP13MMP2MMP7
SCHEMBL7219734 0.77 MMP1 (0.63) MMP3MMP1MMP13MMP2MMP7
SCHEMBL6765824 0.76 MMP1 (0.82) MMP3MMP1MMP13MMP2MMP7
SCHEMBL7219446 0.74 MMP3 (0.52) MMP3MMP1MMP13MMP2MMP7
SCHEMBL6162727 0.73 MMP1 (0.51) MMP3MMP1MMP13MMP2MMP7

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 MMP3 3/4885MMP1 4/4885MMP13 8/4885

“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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