SCHEMBL4602806

SCHEMBL4602806

C=C(C)c1ccc(OCc2ccccc2)cc1

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAOB P27338 4/20 0.70
NR4A1 P22736 1/20 0.64
NR4A2 P43354 1/20 0.64
NR4A3 Q92570 1/20 0.64
PTGS1 P23219 2/20 0.61
PTGS2 P35354 2/20 0.61
LMNA P02545 1/20 0.61
CYP1A2 P05177 1/20 0.61
SLC6A2 P23975 1/20 0.61
CYP2C19 P33261 1/20 0.61
SLC6A3 Q01959 1/20 0.61
HIF1A Q16665 1/20 0.61
HDAC6 Q9UBN7 1/20 0.61
PARP10 Q53GL7 1/20 0.60
EGFR P00533 4/20 0.58
SRD5A2 P31213 1/20 0.58
SMN1; SMN2 Q16637 2/20 0.58
L3MBTL1 Q9Y468 2/20 0.58
ALDH1A1 P00352 1/20 0.58
HTT P42858 1/20 0.58

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
SCHEMBL2517329 0.93 MAOB (0.60) MAOBNR4A1NR4A2NR4A3PTGS1
SCHEMBL9551255 0.91 MAOB (0.64) MAOBNR4A2PARP10SMN1; SMN2L3MBTL1
SCHEMBL15596323 0.86 MAOB (0.66) MAOBNR4A1NR4A2NR4A3PTGS1
SCHEMBL5386288 0.85 NR4A1 (0.68) MAOBNR4A1NR4A2NR4A3PTGS1
SCHEMBL19157998 0.83 MAOB (0.61) MAOBNR4A1NR4A2NR4A3PTGS1
SCHEMBL13703984 0.82 MEN1 (0.54) MAOBNR4A1NR4A2NR4A3PTGS1
SCHEMBL5378418 0.82 NR4A1 (0.64) MAOBNR4A1NR4A2NR4A3PTGS1
SCHEMBL1229367 0.82 PTGS1 (0.61) MAOBNR4A1NR4A2NR4A3PTGS1
SCHEMBL42302 0.82 MAOB (1.00) MAOBNR4A1NR4A2NR4A3PARP10
SCHEMBL27604519 0.82 MAOB (0.70) MAOBNR4A1NR4A2NR4A3PTGS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102351655-A Synthesis method of 4-isopropylresorcinol HANGZHOU ALLSINO CHEMICAL CO LTD 2012-02-15 CN disclosed
EP-0979819-B1 Process for the production of substituted 3-hydroxypiperidines SPEEDEL PHARMA AG (CH) 2008-04-23 EP disclosed
EP-0979824-B1 Process for the preparation of substituted piperidine-epoxides HOFFMANN LA ROCHE (CH) 2004-10-06 EP disclosed
CN-1161335-C Method for preparing substituted piperidine - 2004-08-11 CN disclosed
US-6274735-B1 RENIN INHIBITORS HOFFMANN-LA ROCHE INC. 2001-08-14 US disclosed
US-6268499-B1 USEFUL AS RENIN INHIBITORS HOFFMAN-LA ROCHE INC. 2001-07-31 US disclosed
EP-0979824-A1 Process for the preparation of substituted piperidine-epoxides F. HOFFMANN-LA ROCHE AG (CH) 2000-02-16 EP disclosed
EP-0979819-A1 Process for the production of substituted 3-hydroxypiperidines F. HOFFMANN-LA ROCHE AG (CH) 2000-02-16 EP disclosed