SCHEMBL5406636

SCHEMBL5406636

CC(C)(C)OC(=O)N1C[C@H](SC(c2ccccc2)(c2ccccc2)c2ccccc2)C[C@H]1COS(C)(=O)=O

nearest known ligand 0.41

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
HCRTR2 O43614 1/20 0.41
NR1H2 P55055 7/20 0.40
NR1H3 Q13133 6/20 0.40
HSD11B1 P28845 1/20 0.38
CCR5 P51681 2/20 0.37
SRC P12931 4/20 0.36
JAK2 O60674 1/20 0.36
JAK1 P23458 1/20 0.36
STS P08842 1/20 0.35
GPR119 Q8TDV5 1/20 0.35
HDAC8 Q9BY41 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
SCHEMBL8782333 0.86 HCRTR2 (0.39) HCRTR2NR1H2NR1H3HSD11B1CCR5
SCHEMBL8789793 0.86 SRC (0.46) NR1H2NR1H3SRC
SCHEMBL5404919 0.86 SRC (0.46) NR1H2NR1H3SRC
SCHEMBL9754673 0.85 FAAH (0.36) HCRTR2
SCHEMBL7859632 0.85 FAAH (0.36) HCRTR2
SCHEMBL5409336 0.85 SRC (0.40) HCRTR2NR1H2NR1H3HSD11B1SRC
SCHEMBL8214261 0.84 SRC (0.39) HCRTR2NR1H2NR1H3HSD11B1SRC
SCHEMBL8214205 0.84 SRC (0.39) HCRTR2NR1H2NR1H3HSD11B1SRC
SCHEMBL7809176 0.82 HCRTR2 (0.41) HCRTR2
SCHEMBL8785177 0.82 ALDH1A1 (0.40) HCRTR2NR1H2NR1H3HSD11B1SRC

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 HCRTR2 2575/4885NR1H2 3255/4885NR1H3 3525/4885
US-20020040146-A1 Pyrrolidine derivatives PREP, PEPD, MMP3 HCRTR2 2575/4885NR1H2 3255/4885NR1H3 3525/4885
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 HCRTR2 2768/4885NR1H2 2699/4885NR1H3 3124/4885

“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.