SCHEMBL7219129

SCHEMBL7219129

CC(C)C1(C)NC(c2ccccc2Cl)OC1=O

nearest known ligand 0.35

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.35
ALOX15 P16050 1/20 0.35
PBRM1 Q86U86 2/20 0.35
ALDH1A1 P00352 4/20 0.34
KMT2A Q03164 2/20 0.34
TSHR P16473 2/20 0.34
POLB P06746 1/20 0.34
TP53 P04637 2/20 0.33
KDM4E B2RXH2 2/20 0.33
HPGD P15428 1/20 0.33
HSD17B10 Q99714 1/20 0.33
TNKS2 Q9H2K2 1/20 0.33
RECQL P46063 1/20 0.33
HSD11B1 P28845 1/20 0.33
LDHA P00338 1/20 0.33
CACNB4 O00305 1/20 0.33
CACNA1A O00555 1/20 0.33
CACNA1G O43497 1/20 0.33
CACNG3 O60359 1/20 0.33
CACNA1F O60840 1/20 0.33

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
SCHEMBL7214177 0.79 CA2 (0.41) SMN1; SMN2ALDH1A1HSD11B1
SCHEMBL11040615 0.64 CA2 (0.58) SMN1; SMN2PBRM1ALDH1A1KMT2ATSHR
SCHEMBL10448603 0.63 TP53 (0.42) SMN1; SMN2PBRM1ALDH1A1KMT2ATSHR
SCHEMBL8142165 0.59 TSHR (0.52) SMN1; SMN2ALOX15PBRM1ALDH1A1KMT2A
SCHEMBL15082804 0.58 HTT (0.36) SMN1; SMN2ALOX15ALDH1A1KMT2ATSHR
SCHEMBL20780483 0.58 HTR6 (0.49) SMN1; SMN2ALDH1A1POLBTP53RECQL
SCHEMBL10242244 0.57 SLC6A3 (0.46) SMN1; SMN2ALDH1A1KMT2ATSHRTP53
SCHEMBL10731027 0.57 MAPT (0.53) SMN1; SMN2ALDH1A1KMT2APOLBTP53
SCHEMBL16064832 0.57 SLC6A3 (0.46) SMN1; SMN2ALDH1A1KMT2ATSHRTP53
SCHEMBL8852665 0.57 GAA (0.39) SMN1; SMN2ALDH1A1KMT2ATSHRTP53

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
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