SCHEMBL5331977

SCHEMBL5331977

COc1ccc(CNC(=O)c2cccc(C(=O)NCc3ccc(OC)cc3)c2)cc1

nearest known ligand 0.76

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MMP13 P45452 2/20 0.76
NPC1 O15118 3/20 0.68
RAB9A P51151 3/20 0.68
MEN1 O00255 1/20 0.65
EPHX2 P34913 1/20 0.65
KMT2A Q03164 1/20 0.65
NR1H4 Q96RI1 1/20 0.65
L3MBTL1 Q9Y468 1/20 0.65
ALDH1A1 P00352 2/20 0.63
SMN1; SMN2 Q16637 2/20 0.63
HPGD P15428 3/20 0.63
LMNA P02545 1/20 0.63
ERN1 O75460 1/20 0.60
HDAC2 Q92769 2/20 0.59
HDAC8 Q9BY41 2/20 0.59
HDAC6 Q9UBN7 2/20 0.59
HDAC1 Q13547 2/20 0.59
KDM1A O60341 1/20 0.59
HDAC5 Q9UQL6 1/20 0.59
STAMBP O95630 1/20 0.58

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
SCHEMBL5331526 0.96 MMP13 (0.74) MMP13NPC1RAB9AMEN1EPHX2
SCHEMBL9416562 0.94 MMP13 (0.76) MMP13NPC1RAB9AMEN1EPHX2
SCHEMBL5332456 0.93 MMP13 (0.89) MMP13NPC1RAB9AMEN1KMT2A
SCHEMBL20804653 0.92 NPC1 (0.70) MMP13NPC1RAB9AMEN1EPHX2
SCHEMBL18773965 0.91 NPC1 (0.64) MMP13NPC1RAB9AMEN1EPHX2
SCHEMBL26625669 0.91 MMP13 (0.64) MMP13NPC1RAB9AMEN1EPHX2
SCHEMBL31324978 0.90 HPGD (0.79) MMP13NPC1RAB9AMEN1EPHX2
SCHEMBL12674158 0.90 MMP13 (0.63) MMP13NPC1RAB9AMEN1EPHX2
SCHEMBL1197501 0.90 MMP13 (0.63) MMP13NPC1RAB9AMEN1EPHX2
SCHEMBL15676735 0.90 MMP13 (0.67) MMP13NPC1RAB9AMEN1EPHX2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7214712-B2 Isophthalic acid derivatives as matrix metalloproteinase inhibitors WARNER-LAMBERT COMPANY (US) 2007-05-08 US disclosed
US-6995151-B2 Isophthalic acid derivatives as matrix metalloproteinase inhibitors WARNER-LAMBERT COMPANY (US) 2006-02-07 US disclosed
US-20060025396-A1 Isophthalic acid derivatives as matrix metalloproteinase inhibitors BARVIAN NICOLE C 2006-02-02 US disclosed
EP-1536786-A1 COMBINATION OF AN ALLOSTERIC INHIBITOR OF MATRIX METALLOPROTEINASE-13 WITH CELECOXIB OR VALDECOXIB WARNER-LAMBERT COMPANY LLC (US) 2005-06-08 EP disclosed
EP-1531904-A1 COMBINATION OF AN ALLOSTERIC INHIBITOR OF MATRIX METALLOPROTEINASE-13 WITH A SELECTIVE INHIBITOR OF CYCLOOXYGENASE-2 THAT IS NOT CELECOXIB OR VALDECOXIB Warner-Lambert Company LLC (US) 2005-05-25 EP disclosed
US-20050004126-A1 Method of determining potential allosterically-binding matrix metalloproteinase inhibitors ANDRIANJARA CHARLES (FR) 2005-01-06 US disclosed
WO-2004007024-A1 COMBINATION OF AN ALLOSTERIC INHIBITOR OF MATRIX METALLOPROTEINASE-13 WITH A SELECTIVE INHIBITOR OF CYCLOOXYGENASE-2 THAT IS NOT CELECOXIB OR VALDECOXIB WARNER-LAMBERT COMPANY LLC (US) 2004-01-22 WO disclosed
WO-2004006913-A1 COMBINATION OF AN ALLOSTERIC INHIBITOR OF MATRIX METALLOPROTEINASE-13 WITH CELECOXIB OR VALDECOXIB WARNER-LAMBERT COMPANY LLC (US) 2004-01-22 WO disclosed
EP-1362028-A2 ISOPHTHALIC ACID DERIVATIVES AS MATRIX METALLOPROTEINASE INHIBITORS Warner-Lambert Company LLC (US) 2003-11-19 EP disclosed
US-20020156061-A1 Isophthalic acid derivatives as matrix metalloproteinase inhibitors BARVIAN NICOLE CHANTEL (US) 2002-10-24 US disclosed
WO-2002064547-A2 ISOPHTHALIC ACID DERIVATIVES AS MATRIX METALLOPROTEINASE INHIBITORS WARNER-LAMBERT COMPANY LLC (US) 2002-08-22 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-20060025396-A1 Isophthalic acid derivatives as matrix metalloproteinase inhibitors MMP13, MMP11, MMP3 MMP13 1/4885NPC1 1050/4885RAB9A 3620/4885
US-20050004126-A1 Method of determining potential allosterically-binding matrix metalloproteinase inhibitors MMP13, MMP12, MMP25 MMP13 1/4885NPC1 3219/4885RAB9A 3944/4885
US-20020156061-A1 Isophthalic acid derivatives as matrix metalloproteinase inhibitors MMP13, MMP1, MMP11 MMP13 1/4885NPC1 297/4885RAB9A 3450/4885

“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.