SCHEMBL1304464

SCHEMBL1304464

NC(=O)NC(COc1ccccc1)(Cc1cc(Cl)cc(Cl)c1)C(=O)C(C[C@H](N)C(=O)O)C(=O)O

nearest known ligand 0.35

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
KIF11 P52732 6/20 0.35
LTA4H P09960 3/20 0.35
L3MBTL1 Q9Y468 2/20 0.32
NPC1 O15118 1/20 0.32
RAB9A P51151 1/20 0.32
PLAU P00749 1/20 0.32
SLC1A3 P43003 1/20 0.32
SLC1A2 P43004 1/20 0.32
SLC1A1 P43005 1/20 0.32
SLC1A5 Q15758 1/20 0.32
PPARG P37231 1/20 0.32
PPARA Q07869 1/20 0.32

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
SCHEMBL12099900 0.83 PKM (0.39) L3MBTL1NPC1RAB9APPARGPPARA
SCHEMBL1305402 0.83 KIF11 (0.34) KIF11LTA4HL3MBTL1NPC1RAB9A
SCHEMBL1078041 0.66 ALDH1A1 (0.43) L3MBTL1NPC1RAB9APPARGPPARA
SCHEMBL1304403 0.66 MAPT (0.36) NPC1RAB9A
SCHEMBL12468595 0.64 PARP10 (0.39) L3MBTL1NPC1RAB9A
SCHEMBL6544667 0.60 ALDH1A1 (0.41) NPC1RAB9A
SCHEMBL5309684 0.59 ALPL (0.44) L3MBTL1NPC1RAB9APPARGPPARA
SCHEMBL5082950 0.59 LTA4H (0.53) KIF11LTA4HPPARGPPARA
SCHEMBL5082944 0.59 LTA4H (0.53) KIF11LTA4HPPARGPPARA
SCHEMBL9090603 0.59 LTA4H (0.53) KIF11LTA4HPPARGPPARA

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-8048896-B2 Inhibit nonenzymatic formation of advanced glycation end-products (AGE) using e.g. aminoguanidine, OPB-9195 [(+/-)-2-isopropylidenehydrazono-4-oxo-thiazolidin-5-yla cetanilide], pyridoxamine, antioxidants, alagebrium, antihypertensives, angiotensin-converting enzyme inhibitors Cell Viable Corporation (US) 2011-11-01 US claimed
US-6605642-B2 Administering specified compounds which are derivatives of phenoxyisobutyric acids and of benzoic acid including aryl and heterocyclic ureido derivatives and aryl and heterocyclic carboxamido derivatives; treating aging, arthritis, diabetes CITY OF HOPE 2003-08-12 US claimed
US-8053449-B2 Method for inhibiting AGE complex formation Cell Viable Corporation (US) 2011-11-08 US disclosed
US-8048896-B2 Inhibit nonenzymatic formation of advanced glycation end-products (AGE) using e.g. aminoguanidine, OPB-9195 [(+/-)-2-isopropylidenehydrazono-4-oxo-thiazolidin-5-yla cetanilide], pyridoxamine, antioxidants, alagebrium, antihypertensives, angiotensin-converting enzyme inhibitors Cell Viable Corporation (US) 2011-11-01 US disclosed
US-20080076804-A1 METHODS FOR INHIBITING AND BREAKING AGE COMPLEX FORMATION Cell Viable Corporation 2008-03-27 US disclosed
US-20070099966-A1 Device and Method for Inhibiting AGE Complex Formation Cell Viable Corporation 2007-05-03 US disclosed
WO-2007044309-A2 DEVICE AND METHOD FOR INHIBITING AGE COMPLEX FORMATION VASIX CORPORATION (US) 2007-04-19 WO disclosed