SCHEMBL1304060

SCHEMBL1304060

CC(COc1ccc(NC(=O)Cc2ccc(Cl)c(Cl)c2)cc1)C(=O)O

nearest known ligand 0.55

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ SMN1; SMN2 Q16637 3/20 0.55
▸ MEN1 O00255 2/20 0.54
▸ KMT2A Q03164 2/20 0.54
▸ LMNA P02545 2/20 0.54
▸ MAPT P10636 2/20 0.54
▸ HTT P42858 2/20 0.54
▸ L3MBTL1 Q9Y468 1/20 0.54
▸ DGAT1 O75907 1/20 0.51
▸ POLB P06746 1/20 0.48
▸ NPC1 O15118 1/20 0.48
▸ HPGD P15428 1/20 0.48
▸ RAB9A P51151 1/20 0.48
▸ MAOB P27338 1/20 0.47
▸ ALDH1A1 P00352 1/20 0.47
▸ ANO1 Q5XXA6 1/20 0.46
▸ ADRB1 P08588 1/20 0.46
▸ ADRB3 P13945 1/20 0.46
▸ PTGDR2 Q9Y5Y4 1/20 0.46

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
SCHEMBL8411677 0.87 ADRB1 (0.57) SMN1; SMN2MEN1KMT2ALMNAMAPT
SCHEMBL8411344 0.85 RORC (0.48) SMN1; SMN2MEN1KMT2ALMNAMAPT
SCHEMBL8410207 0.85 RAB9A (0.56) SMN1; SMN2MEN1KMT2ALMNAMAPT
SCHEMBL8412730 0.84 SMN1; SMN2 (0.47) SMN1; SMN2MEN1KMT2ALMNAMAPT
SCHEMBL2517202 0.84 FFAR1 (0.55) MAOB
SCHEMBL8695260 0.83 SMN1; SMN2 (0.56) SMN1; SMN2MEN1KMT2ALMNAMAPT
SCHEMBL8411536 0.83 RAB9A (0.61) SMN1; SMN2MEN1KMT2ALMNAMAPT
SCHEMBL8412806 0.82 GAA (0.61) SMN1; SMN2MEN1KMT2ALMNAMAPT
SCHEMBL8409841 0.80 SMN1; SMN2 (0.48) SMN1; SMN2MEN1KMT2ALMNAMAPT
SCHEMBL8700685 0.80 EPHX2 (0.54) SMN1; SMN2MEN1KMT2ALMNAMAPT

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 13 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
EP-1165064-B1 NOVEL INHIBITORS OF FORMATION OF ADVANCED GLYCATION ENDPRODUCTS (AGE'S) HOPE CITY (US) 2004-02-25 — — EP claimed
US-6337350-B1 CROSSLINKING INHIBITION OF PROTEINS CITY OF HOPE 2002-01-08 — — US claimed
EP-1165064-A2 NOVEL INHIBITORS OF FORMATION OF ADVANCED GLYCATION ENDPRODUCTS (AGE'S) City of Hope (US) 2002-01-02 — — EP claimed
WO-2000059875-A2 NOVEL INHIBITORS OF FORMATION OF ADVANCED GLYCATION ENDPRODUCTS (AGE'S) CITY OF HOPE (US) 2000-10-12 — — WO 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
US-6337350-B1 CROSSLINKING INHIBITION OF PROTEINS CITY OF HOPE 2002-01-08 — — US disclosed
EP-1165064-A2 NOVEL INHIBITORS OF FORMATION OF ADVANCED GLYCATION ENDPRODUCTS (AGE'S) City of Hope (US) 2002-01-02 — — EP disclosed
WO-2000059875-A2 NOVEL INHIBITORS OF FORMATION OF ADVANCED GLYCATION ENDPRODUCTS (AGE'S) CITY OF HOPE (US) 2000-10-12 — — WO disclosed
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