SCHEMBL3385155

SCHEMBL3385155

CS(=O)(=O)O.Cc1cc(-c2ccn3c(-c4ccc(NC(=O)Nc5cc(C(C)(C)C)on5)c(F)c4)cnc3c2)ccn1

nearest known ligand 0.49

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 1/20 0.49
RAB9A P51151 1/20 0.49
MAPK14 Q16539 4/20 0.46
MAPK13 O15264 1/20 0.46
FLT3 P36888 10/20 0.46
RET P07949 3/20 0.43
MAPT P10636 2/20 0.40
HTT P42858 2/20 0.40
KDM4E B2RXH2 1/20 0.40
POLB P06746 1/20 0.40
CSF1R P07333 1/20 0.40
ATM Q13315 1/20 0.40

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
SCHEMBL3381118 0.89 NPC1 (0.54) NPC1RAB9AMAPK14MAPK13FLT3
SCHEMBL3381854 0.89 NPC1 (0.49) NPC1RAB9AMAPK14MAPK13FLT3
SCHEMBL3383303 0.89 NPC1 (0.52) NPC1RAB9AMAPK14MAPK13FLT3
SCHEMBL3385839 0.88 NPC1 (0.51) NPC1RAB9AMAPK14MAPK13FLT3
SCHEMBL3383068 0.87 NPC1 (0.50) NPC1RAB9AMAPK14MAPK13FLT3
SCHEMBL3198885 0.85 NPC1 (0.53) NPC1RAB9AMAPK14MAPK13FLT3
SCHEMBL3381837 0.85 NPC1 (0.48) NPC1RAB9AMAPK14MAPK13FLT3
SCHEMBL13002517 0.85 FLT3 (0.48) NPC1RAB9AMAPK14MAPK13FLT3
Hydrochloric Acid SCHEMBL3189282 0.84 FLT3 (0.47) NPC1RAB9AMAPK14MAPK13FLT3
Hydrochloric Acid SCHEMBL3185922 0.84 MAPK14 (0.48) NPC1RAB9AMAPK14MAPK13FLT3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1904494-B1 IMIDAZO[1,2-A]PYRIDINE COMPOUNDS AS VEGF-R2 INHIBITORS LILLY CO ELI (US) 2010-12-01 EP disclosed