SCHEMBL5409551

SCHEMBL5409551

CC(=S)O[C@H]1C[C@@H](COc2ccccc2)N(S(=O)(=O)c2ccc3ccccc3c2)C1

nearest known ligand 0.43

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CASP3 P42574 11/20 0.43
CASP7 P55210 9/20 0.43
CASP1 P29466 2/20 0.40
CASP6 P55212 2/20 0.40
CASP2 P42575 2/20 0.40
CASP9 P55211 2/20 0.40
ALDH1A1 P00352 1/20 0.40
LMNA P02545 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
CASP4 P49662 1/20 0.40
CASP8 Q14790 1/20 0.40
ECE1 P42892 2/20 0.40
MME P08473 1/20 0.40
ACE P12821 1/20 0.40
PTGDR2 Q9Y5Y4 1/20 0.40
AKR1C3 P42330 2/20 0.39
AKR1C1 Q04828 1/20 0.39
PKM P14618 2/20 0.39

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
SCHEMBL5405153 1.00 CASP3 (0.43) CASP3CASP7CASP1CASP6CASP2
SCHEMBL5405158 0.91 CASP3 (0.44) CASP3CASP7CASP1CASP6CASP2
SCHEMBL5421525 0.88 MMP9 (0.41) ALDH1A1LMNASMN1; SMN2ECE1MME
SCHEMBL5401021 0.88 MMP9 (0.41) ALDH1A1LMNASMN1; SMN2ECE1MME
SCHEMBL5405172 0.85 CASP3 (0.45) CASP3CASP7CASP1CASP6CASP2
SCHEMBL5405167 0.85 CASP3 (0.45) CASP3CASP7CASP1CASP6CASP2
SCHEMBL5403951 0.84 CASP3 (0.44) CASP3CASP7CASP1CASP6CASP2
SCHEMBL5403947 0.82 CASP3 (0.46) CASP3CASP7CASP1CASP6CASP2
SCHEMBL7139591 0.82 CASP3 (0.46) CASP3CASP7CASP1CASP6CASP2
SCHEMBL5407330 0.81 ECE1 (0.49) CASP3CASP7CASP1CASP6CASP2

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 4 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
EP-1303486-A1 PYRROLIDINE DERIVATIVES AS METALLOPROTEASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2003-04-23 EP 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 (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-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 3004/4885CASP1 1757/4885

“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.