SCHEMBL7220673

SCHEMBL7220673

CCOC(=O)CC(=O)C(C)(NC(=O)c1ccccc1)C(C)C

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 4/20 0.46
NPC1 O15118 2/20 0.46
GAA P10253 1/20 0.46
RAB9A P51151 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.44
POLB P06746 1/20 0.44
MAPK1 P28482 2/20 0.42
NPSR1 Q6W5P4 1/20 0.42
ALDH1A1 P00352 4/20 0.41
LMNA P02545 2/20 0.41
PRSS1 P07477 1/20 0.41
CTSG P08311 1/20 0.41
CTRB1 P17538 1/20 0.41
CMA1 P23946 1/20 0.41
TSHR P16473 1/20 0.41
KMT2A Q03164 3/20 0.41
MEN1 O00255 2/20 0.41
CYP2C9 P11712 1/20 0.40
KDM4E B2RXH2 1/20 0.40
PPID Q08752 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
SCHEMBL7213700 0.77 GAA (0.45) GAAL3MBTL1ALDH1A1LMNATSHR
SCHEMBL7221377 0.76 CXCL8 (0.44) RAB9AALDH1A1TSHRKMT2AMEN1
SCHEMBL10683565 0.75 POLB (0.46) SMN1; SMN2NPC1GAARAB9APOLB
SCHEMBL11186243 0.74 MAPK1 (0.47) SMN1; SMN2NPC1GAARAB9APOLB
SCHEMBL27574236 0.73 NPSR1 (0.50) SMN1; SMN2NPC1GAARAB9AL3MBTL1
SCHEMBL7220546 0.73 CYP3A4 (0.39) SMN1; SMN2GAAL3MBTL1ALDH1A1LMNA
SCHEMBL820885 0.72 SMN1; SMN2 (0.49) SMN1; SMN2NPC1GAARAB9AL3MBTL1
SCHEMBL1221369 0.72 RAB9A (0.66) SMN1; SMN2NPC1GAARAB9APOLB
SCHEMBL7890971 0.72 L3MBTL1 (0.48) SMN1; SMN2NPC1GAARAB9AL3MBTL1
SCHEMBL27553077 0.72 PRSS1 (0.48) SMN1; SMN2NPC1GAARAB9AL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6504046-B1 Cyclization of nitriles using acids, to form oxazolinone chemical intermediates such as 2-phenyl-4-isopropyl-4-methyl-1,3-oxazol-5-one, used as fungicides IHARA CHEMICAL INDUSTRY CO., LTD. (JP) 2003-01-07 US disclosed
CN-1304399-A Process for preparation of amides IHARA CHEMICAL IND CO (JP) 2001-07-18 CN disclosed
EP-1092705-A1 PROCESS FOR THE PREPARATION OF AMIDES IHARA CHEMICAL INDUSTRY Co., Ltd. (JP) 2001-04-18 EP disclosed