SCHEMBL5420131

SCHEMBL5420131

O=C(OCc1ccccc1)[C@@H]1C[C@H](Br)CN1S(=O)(=O)c1ccc2ccccc2c1

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CCR4 P51679 5/20 0.45
MMP9 P14780 2/20 0.45
ELANE P08246 1/20 0.44
AKR1C3 P42330 3/20 0.43
AKR1C1 Q04828 1/20 0.43
MMP1 P03956 2/20 0.43
ADAM17 P78536 1/20 0.43
MME P08473 2/20 0.42
ACE P12821 2/20 0.42
ECE1 P42892 2/20 0.42
MMP3 P08254 1/20 0.42
MMP7 P09237 1/20 0.42
MMP13 P45452 1/20 0.42
CAPN1 P07384 1/20 0.42
MCL1 Q07820 1/20 0.41
KMT2A Q03164 1/20 0.41
F10 P00742 1/20 0.41
CTDSP1 Q9GZU7 1/20 0.40
TDP1 Q9NUW8 1/20 0.40
L3MBTL1 Q9Y468 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
SCHEMBL5722976 1.00 CCR4 (0.45) CCR4MMP9ELANEAKR1C3AKR1C1
SCHEMBL7138127 1.00 CCR4 (0.45) CCR4MMP9ELANEAKR1C3AKR1C1
SCHEMBL5406228 0.90 MMP1 (0.49) CCR4MMP9ELANEAKR1C3AKR1C1
SCHEMBL6979587 0.90 MMP1 (0.49) CCR4MMP9ELANEAKR1C3AKR1C1
SCHEMBL7145985 0.84 MMP9 (0.47) CCR4MMP9ELANEAKR1C3AKR1C1
SCHEMBL5415716 0.84 MMP9 (0.47) CCR4MMP9ELANEAKR1C3AKR1C1
SCHEMBL5415765 0.80 MMP1 (0.47) MMP9MMP1MMEACEECE1
SCHEMBL6968000 0.80 MMP1 (0.47) MMP9MMP1MMEACEECE1
SCHEMBL7143953 0.79 ECE1 (0.47) CCR4ELANEAKR1C3MMEACE
SCHEMBL7143957 0.79 ECE1 (0.47) CCR4ELANEAKR1C3MMEACE

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 12 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
EP-1317428-B1 PYRROLIDINE-2-CARBOXYLIC ACID HYDRAZIDE DERIVATIVES FOR USE AS METALLOPROTEASE INHIBITORS HOFFMANN LA ROCHE (CH) 2006-04-19 EP 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-1303485-A1 PYRROLIDINE DERIVATIVES AS INHIBITORS OF ENDOTHELIN-CONVERTING ENZYME F. HOFFMANN-LA ROCHE AG (CH) 2003-04-23 EP disclosed
US-6541638-B2 (2S,4S)-1-(4-Mercapto-1-(naphthalene-2-sulfonyl)-pyrrolidine-2 -carbonyl)-piperidine-4-carboxylic acid ethyl ester for example; zinc protease inhibitors; for treating diseases associated with vasoconstriction HOFFMAN-LA ROCHE INC. 2003-04-01 US disclosed
US-6444829-B1 (2S,4R)-4-MERCAPTO-1-(NAPHTHALENE-2-SULFONYL)-PYRROLIDINE-2 -CARBOXYLIC ACID N'-ISOBUTYL-N'-(4-METHYL-BENZENESULFONYL)-HYDRAZIDE, FOR EXAMPLE; INHIBITORS OF METALLOPROTEASES, E.G. ZINC PROTEASES; VASODILATORS HOFFMANN-LA ROCHE INC. 2002-09-03 US disclosed
US-20020049243-A1 Pyrrolidine derivatives HOFFMANN-LA ROCHE INC. 2002-04-25 US disclosed
US-20020040048-A1 PYRROLIDINE COMPOUNDS F. HOFFMANN-LA ROCHE AG (CH) 2002-04-04 US disclosed
US-20020040146-A1 Pyrrolidine derivatives F. HOFFMANN-LA ROCHE AG, A SWISS COMPANY (CH) 2002-04-04 US disclosed
WO-2002006222-A1 PYRROLIDINE DERIVATIVES AS INHIBITORS OF ENDOTHELIN-CONVERTING ENZYME F. HOFFMANN-LA ROCHE AG (CH) 2002-01-24 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 (5 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 CCR4 1718/4885MMP9 35/4885ELANE 129/4885
US-20020040146-A1 Pyrrolidine derivatives PREP, PEPD, MMP3 CCR4 1718/4885MMP9 35/4885ELANE 129/4885
US-20020040048-A1 PYRROLIDINE COMPOUNDS PREP, PEPD, MMP3 CCR4 1795/4885MMP9 21/4885ELANE 91/4885
US-20020049243-A1 Pyrrolidine derivatives PREP, PEPD, DNPEP CCR4 2784/4885MMP9 73/4885ELANE 122/4885
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 CCR4 4267/4885MMP9 7/4885ELANE 477/4885

“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.