SCHEMBL1305520

SCHEMBL1305520

CC(C)(Oc1ccc(NC(=O)Nc2ccccn2)cc1)C(=O)O

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ NPC1 O15118 10/20 0.63
▸ RAB9A P51151 10/20 0.63
▸ SMN1; SMN2 Q16637 3/20 0.63
▸ FLT3 P36888 2/20 0.63
▸ ADORA3 P0DMS8 1/20 0.63
▸ PIM1 P11309 1/20 0.63
▸ ADORA2A P29274 1/20 0.63
▸ ADORA2B P29275 1/20 0.63
▸ ADORA1 P30542 1/20 0.63
▸ PIM3 Q86V86 1/20 0.63
▸ AURKB Q96GD4 1/20 0.63
▸ LMNA P02545 2/20 0.57
▸ KMT2A Q03164 4/20 0.51
▸ MEN1 O00255 3/20 0.51
▸ PPARA Q07869 2/20 0.51
▸ TSHR P16473 1/20 0.50
▸ PKM P14618 1/20 0.49
▸ CYP1A2 P05177 1/20 0.48
▸ CYP2C9 P11712 1/20 0.48
▸ CYP2C19 P33261 1/20 0.48

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
SCHEMBL1304683 0.85 PPARA (0.61) NPC1RAB9ASMN1; SMN2KMT2AMEN1
SCHEMBL16303954 0.84 PPARA (0.61) NPC1RAB9ASMN1; SMN2LMNAKMT2A
SCHEMBL805971 0.84 PPARA (0.61) NPC1RAB9ASMN1; SMN2LMNAKMT2A
SCHEMBL1304620 0.81 CYP1A2 (0.60) NPC1RAB9AKMT2AMEN1PPARA
SCHEMBL9317689 0.79 RAB9A (1.00) NPC1RAB9ASMN1; SMN2FLT3ADORA3
SCHEMBL1305523 0.79 RAB9A (0.70) NPC1RAB9ASMN1; SMN2LMNAKMT2A
SCHEMBL1305108 0.78 PPARA (0.54) NPC1RAB9ASMN1; SMN2KMT2AMEN1
SCHEMBL1304254 0.78 RAB9A (0.69) NPC1RAB9ASMN1; SMN2KMT2AMEN1
SCHEMBL5335446 0.78 PPARA (0.50) NPC1RAB9ASMN1; SMN2LMNAKMT2A
SCHEMBL1305198 0.77 PPARA (0.53) NPC1RAB9ASMN1; SMN2LMNAKMT2A

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 14 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
EP-1165064-B1 NOVEL INHIBITORS OF FORMATION OF ADVANCED GLYCATION ENDPRODUCTS (AGE'S) HOPE CITY (US) 2004-02-25 — — EP 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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