SCHEMBL212265

SCHEMBL212265

CN1CCN(C)C1=NOCc1ccccc1

nearest known ligand 0.51

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ NPC1 O15118 3/20 0.51
▸ RAB9A P51151 3/20 0.51
▸ TSHR P16473 1/20 0.39
▸ HRH3 Q9Y5N1 3/20 0.39
▸ TP53 P04637 1/20 0.39
▸ GRM5 P41594 2/20 0.38
▸ MC4R P32245 1/20 0.38
▸ ALDH1A1 P00352 1/20 0.38
▸ MAPT P10636 1/20 0.38
▸ LTA4H P09960 2/20 0.37
▸ HSD11B1 P28845 1/20 0.37
▸ TMEM97 Q5BJF2 1/20 0.37
▸ CARM1 Q86X55 1/20 0.37
▸ PRMT6 Q96LA8 1/20 0.37
▸ SIGMAR1 Q99720 1/20 0.37
▸ PRMT8 Q9NR22 1/20 0.37
▸ IDO1 P14902 1/20 0.36

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
SCHEMBL212459 0.75 MC4R (0.35) NPC1RAB9AGRM5MC4RMAPT
SCHEMBL17257082 0.74 NPC1 (0.41) NPC1RAB9AHSD11B1
SCHEMBL17257078 0.74 NPC1 (0.41) NPC1RAB9AHSD11B1
SCHEMBL2045918 0.71 NPC1 (0.59) NPC1RAB9ATSHRALDH1A1HSD11B1
SCHEMBL2045062 0.71 NPC1 (0.59) NPC1RAB9ATSHRALDH1A1MAPT
SCHEMBL19100010 0.69 NPC1 (0.42) NPC1RAB9ATSHRHRH3TP53
SCHEMBL2044477 0.69 TSHR (0.48) NPC1RAB9ATSHRALDH1A1MAPT
SCHEMBL2050061 0.68 RAB9A (0.47) NPC1RAB9ATSHRHRH3ALDH1A1
SCHEMBL7373187 0.68 RAB9A (0.56) NPC1RAB9ATSHRALDH1A1MAPT
SCHEMBL2050063 0.68 RAB9A (0.47) NPC1RAB9ATSHRHRH3ALDH1A1

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120077941-A1 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS BRIDGESTONE CORPORATION (JP) 2012-03-29 — — US claimed
US-8088868-B2 oximation of cojugated homopolymers formed by addtion polymerization of conjugated diene monomer in the presence lanthanide copmpounds as polymerization catalysts; polymers used in the manufacture of tires having reduced hysteresis BRIDGESTONE CORPORATION (JP) 2012-01-03 — — US claimed
US-20080146745-A1 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS BRIDGESTONE CORPORATION (JP) 2008-06-19 — — US claimed
US-8541509-B2 Polymers functionalized with protected oxime compounds BRIDGESTONE CORPORATION (JP) 2013-09-24 — — US disclosed
EP-1913036-B1 AMINE FUNCTIONALIZED POLYMERS BRIDGESTONE CORP (JP) 2013-03-06 — — EP disclosed
US-20120077941-A1 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS BRIDGESTONE CORPORATION (JP) 2012-03-29 — — US disclosed
US-8088868-B2 oximation of cojugated homopolymers formed by addtion polymerization of conjugated diene monomer in the presence lanthanide copmpounds as polymerization catalysts; polymers used in the manufacture of tires having reduced hysteresis BRIDGESTONE CORPORATION (JP) 2012-01-03 — — US disclosed
US-7820765-B2 Amine functionalized polymers BRIDGESTONE CORPORATION (JP) 2010-10-26 — — US disclosed
US-20100120976-A1 AMINE FUNCTIONALIZED POLYMERS BRIDGESTONE CORPORATION (JP) 2010-05-13 — — US disclosed
US-20080146745-A1 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS BRIDGESTONE CORPORATION (JP) 2008-06-19 — — US disclosed
EP-1913036-A1 AMINE FUNCTIONALIZED POLYMERS Bridgestone Corporation (JP) 2008-04-23 — — EP disclosed
WO-2007015872-A1 AMINE FUNCTIONALIZED POLYMERS BRIDGESTONE CORPORATION (JP) 2007-02-08 — — WO disclosed
Send feedback