SCHEMBL5335243

SCHEMBL5335243

CN(C(=O)c1cccc(C(=O)Nc2ccc3c(c2)OCO3)c1)c1ccc2c(c1)OCO2

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 13/20 0.63
RAB9A P51151 13/20 0.63
SMN1; SMN2 Q16637 8/20 0.63
MAPT P10636 6/20 0.63
TP53 P04637 4/20 0.63
HPGD P15428 1/20 0.63
ALDH1A1 P00352 5/20 0.63
POLB P06746 3/20 0.63
TSHR P16473 2/20 0.63
LMNA P02545 1/20 0.63
HSD17B10 Q99714 1/20 0.63
PKM P14618 2/20 0.62
NFKB1 P19838 1/20 0.62
NFKB2 Q00653 1/20 0.62
RELA Q04206 1/20 0.62
KMT2A Q03164 2/20 0.61
MEN1 O00255 1/20 0.61
AGBL2 Q5U5Z8 1/20 0.58
GAA P10253 1/20 0.56
MAPK1 P28482 1/20 0.56

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
SCHEMBL21934954 0.82 RAB9A (0.53) NPC1RAB9ASMN1; SMN2MAPTTP53
SCHEMBL5337657 0.82 RAB9A (0.57) NPC1RAB9ASMN1; SMN2MAPTTP53
SCHEMBL30128152 0.81 HPGD (0.54) NPC1RAB9ASMN1; SMN2MAPTHPGD
SCHEMBL5338102 0.81 NPC1 (0.66) NPC1RAB9ASMN1; SMN2MAPTTP53
SCHEMBL5345438 0.81 MAPT (0.58) NPC1RAB9ASMN1; SMN2MAPTTP53
SCHEMBL6295679 0.78 NPC1 (1.00) NPC1RAB9ASMN1; SMN2MAPTTP53
SCHEMBL108116 0.78 NPC1 (1.00) NPC1RAB9ASMN1; SMN2MAPTTP53
SCHEMBL18941224 0.78 NPC1 (0.72) NPC1RAB9ASMN1; SMN2MAPTTP53
SCHEMBL6268222 0.77 KMT2A (0.50) NPC1RAB9ASMN1; SMN2MAPTTP53
SCHEMBL27179668 0.77 RAB9A (0.90) NPC1RAB9ASMN1; SMN2MAPTTP53

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 NPC1 1050/4885RAB9A 3620/4885SMN1; SMN2 2320/4885
US-20050004126-A1 Method of determining potential allosterically-binding matrix metalloproteinase inhibitors MMP13, MMP12, MMP25 NPC1 3219/4885RAB9A 3944/4885SMN1; SMN2 1854/4885
US-20020156061-A1 Isophthalic acid derivatives as matrix metalloproteinase inhibitors MMP13, MMP1, MMP11 NPC1 297/4885RAB9A 3450/4885SMN1; SMN2 1429/4885

“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.