SCHEMBL5401128

SCHEMBL5401128

COc1ccc(CS[C@@H]2C[C@@H](COc3ccccc3)N(S(C)(=O)=O)C2)cc1

nearest known ligand 0.41

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CASP3 P42574 2/20 0.41
CASP7 P55210 2/20 0.41
DRD4 P21917 1/20 0.41
GRM2 Q14416 1/20 0.38
LMNA P02545 1/20 0.37
MAPT P10636 1/20 0.37
RECQL P46063 1/20 0.37
NPSR1 Q6W5P4 1/20 0.37
MMP1 P03956 1/20 0.35
MMP3 P08254 1/20 0.35
MMP7 P09237 1/20 0.35
MMP9 P14780 1/20 0.35
MMP13 P45452 1/20 0.35
HTT P42858 1/20 0.35
PKM P14618 1/20 0.35

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
SCHEMBL5401130 1.00 CASP3 (0.41) CASP3CASP7DRD4GRM2LMNA
SCHEMBL5409836 0.87 APLNR (0.37) LMNAMAPTRECQLNPSR1MMP1
SCHEMBL5409843 0.87 APLNR (0.37) LMNAMAPTRECQLNPSR1MMP1
SCHEMBL5406275 0.85 MMP1 (0.43) LMNAMAPTRECQLNPSR1MMP1
SCHEMBL5405049 0.84 SIGMAR1 (0.38) MMP1MMP3MMP9MMP13
SCHEMBL5405046 0.84 SIGMAR1 (0.38) MMP1MMP3MMP9MMP13
SCHEMBL5407550 0.83 HTT (0.43) LMNAMAPTRECQLNPSR1MMP1
SCHEMBL5407554 0.83 HTT (0.43) LMNAMAPTRECQLNPSR1MMP1
SCHEMBL7140147 0.82 HTT (0.38) LMNAMAPTNPSR1MMP1MMP3
SCHEMBL7140145 0.82 HTT (0.38) LMNAMAPTNPSR1MMP1MMP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7189756-B2 Pyrrolidine derivatives HOFFMAN-LA ROCHE INC. (US) 2007-03-13 US disclosed
US-20040242672-A1 Useful as inhibitors of metalloproteases, e.g. zinc proteases; effective in treating disease states associated with vasoconstriction such as high blood pressure, coronary disorders, cardiac insufficiency, renal and myocardial ischaemia, renal insufficiency, dialysis, cerebral ischaemia AEBI JOHANNES (CH) 2004-12-02 US disclosed
US-6790860-B2 USEFUL AS INHIBITORS OF METALLOPROTEASES, E.G. ZINC PROTEASES; EFFECTIVE IN TREATING DISEASE STATES ASSOCIATED WITH VASOCONSTRICTION HOFFMANN-LA ROCHE INC. 2004-09-14 US disclosed
US-20030199569-A1 Pyrrolidine derivatives AEBI JOHANNES (CH) 2003-10-23 US disclosed
EP-1303486-A1 PYRROLIDINE DERIVATIVES AS METALLOPROTEASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2003-04-23 EP disclosed
US-20020040146-A1 Pyrrolidine derivatives F. HOFFMANN-LA ROCHE AG, A SWISS COMPANY (CH) 2002-04-04 US disclosed
WO-2002008185-A1 PYRROLIDINE DERIVATIVES AS METALLOPROTEASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2002-01-31 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-20030199569-A1 Pyrrolidine derivatives PREP, PEPD, MMP3 CASP3 818/4885CASP7 1467/4885DRD4 2277/4885
US-20020040146-A1 Pyrrolidine derivatives PREP, PEPD, MMP3 CASP3 818/4885CASP7 1467/4885DRD4 2277/4885
US-20040242672-A1 Useful as inhibitors of metalloproteases, e.g. zinc proteases; effective in treating disease states associated with vasoconstriction such as high blood pressure, coronary disorders, cardiac insufficiency, renal and myocardial ischaemia, renal insufficiency, dialysis, cerebral ischaemia MMP1, PEPD, MMP25 CASP3 1917/4885CASP7 3004/4885DRD4 1829/4885

“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.