SCHEMBL1305402

SCHEMBL1305402

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

nearest known ligand 0.34

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
KIF11 P52732 5/20 0.34
PKM P14618 1/20 0.34
GRN P28799 1/20 0.32
SORT1 Q99523 1/20 0.32
LTA4H P09960 3/20 0.32
POLB P06746 1/20 0.31
NPC1 O15118 1/20 0.31
RAB9A P51151 1/20 0.31
L3MBTL1 Q9Y468 1/20 0.31
SLC1A5 Q15758 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
SCHEMBL1304464 0.83 KIF11 (0.35) KIF11LTA4HNPC1RAB9AL3MBTL1
SCHEMBL12099900 0.81 PKM (0.39) PKMNPC1RAB9AL3MBTL1
SCHEMBL1078041 0.65 ALDH1A1 (0.43) NPC1RAB9AL3MBTL1
SCHEMBL1304403 0.65 MAPT (0.36) POLBNPC1RAB9A
SCHEMBL5309684 0.63 ALPL (0.44) POLBNPC1RAB9AL3MBTL1
SCHEMBL12468595 0.63 PARP10 (0.39) NPC1RAB9AL3MBTL1
SCHEMBL5367643 0.60 SSTR4 (0.51) POLBNPC1RAB9AL3MBTL1
SCHEMBL3249158 0.59 RECQL (0.40) L3MBTL1
SCHEMBL6544667 0.59 ALDH1A1 (0.41) PKMNPC1RAB9A
SCHEMBL1835145 0.59 ALPI (0.55) KIF11PKM

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