SCHEMBL5409722

SCHEMBL5409722

CS(=O)(=O)N1CC(SC(c2ccccc2)(c2ccccc2)c2ccccc2)CC1CCO

nearest known ligand 0.36

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
HCRTR2 O43614 1/20 0.36
KIF11 P52732 2/20 0.34
SLC6A1 P30531 1/20 0.33
SLC6A11 P48066 1/20 0.33
MEN1 O00255 1/20 0.32
KMT2A Q03164 1/20 0.32
SIGMAR1 Q99720 3/20 0.32
LMNA P02545 1/20 0.32
CA1 P00915 6/20 0.31
CA2 P00918 6/20 0.31
CA4 P22748 6/20 0.31
CA9 Q16790 6/20 0.31
CYP2D6 P10635 1/20 0.31
MAPK1 P28482 1/20 0.31
L3MBTL1 Q9Y468 1/20 0.31

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
SCHEMBL5409731 1.00 HCRTR2 (0.36) HCRTR2KIF11SLC6A1SLC6A11MEN1
SCHEMBL5415717 0.90 KIF11 (0.36) KIF11SLC6A1SLC6A11CA1CA2
SCHEMBL5415722 0.90 KIF11 (0.36) KIF11SLC6A1SLC6A11CA1CA2
SCHEMBL7150563 0.85 KIF11 (0.34) KIF11SLC6A1SLC6A11CA1CA2
SCHEMBL7138136 0.85 KIF11 (0.34) KIF11SLC6A1SLC6A11CA1CA2
SCHEMBL5416668 0.82 AKR1C3 (0.42) LMNA
SCHEMBL5416660 0.82 AKR1C3 (0.42) LMNA
SCHEMBL5409750 0.81 ALDH1A1 (0.35) KIF11LMNA
SCHEMBL5415447 0.81 ALDH1A1 (0.35) KIF11LMNA
SCHEMBL5410585 0.81 PTGIR (0.33) HCRTR2KIF11CA1CA2CA4

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 2575/4885KIF11 3206/4885SLC6A1 1590/4885
US-20020040146-A1 Pyrrolidine derivatives PREP, PEPD, MMP3 HCRTR2 2575/4885KIF11 3206/4885SLC6A1 1590/4885
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 2768/4885KIF11 4047/4885SLC6A1 1703/4885

“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.