SCHEMBL9863678

SCHEMBL9863678

COC(=O)c1cc(C(=O)CN(Cc2ccccc2)C(C)(C)C)ccc1O

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 6/20 0.45
▸ MEN1 O00255 4/20 0.45
▸ KMT2A Q03164 4/20 0.45
▸ HPGD P15428 3/20 0.44
▸ TSHR P16473 2/20 0.44
▸ HSD17B10 Q99714 2/20 0.44
▸ CA12 O43570 1/20 0.42
▸ CA1 P00915 1/20 0.42
▸ CA2 P00918 1/20 0.42
▸ CA7 P43166 1/20 0.42
▸ CA9 Q16790 1/20 0.42
▸ CA14 Q9ULX7 1/20 0.42
▸ EGFR P00533 2/20 0.41
▸ ALDH1A1 P00352 6/20 0.41
▸ KDM4E B2RXH2 5/20 0.41
▸ NOX4 Q9NPH5 1/20 0.40
▸ MAPT P10636 3/20 0.39
▸ SMN1; SMN2 Q16637 2/20 0.39
▸ NPC1 O15118 1/20 0.39
▸ TP53 P04637 1/20 0.39

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
SCHEMBL11099488 0.86 LMNA (0.40) LMNAMEN1KMT2AHPGDTSHR
SCHEMBL11594746 0.81 HTT (0.47) MEN1KMT2AHPGDALDH1A1KDM4E
SCHEMBL32668832 0.80 PKM (0.47) LMNAMEN1KMT2AHPGDTSHR
SCHEMBL14445127 0.80 PKM (0.47) LMNAMEN1KMT2AHPGDTSHR
Hydrochloric Acid SCHEMBL11671567 0.80 APP (0.47) LMNAMEN1KMT2AHPGDTSHR
Hydrochloric Acid SCHEMBL31199080 0.79 PKM (0.46) LMNAMEN1KMT2AHPGDTSHR
Bromide SCHEMBL29484430 0.75 LMNA (0.42) LMNAMEN1KMT2ATSHREGFR
SCHEMBL9863679 0.74 LMNA (0.45) LMNAMEN1KMT2AHPGDTSHR
SCHEMBL9574173 0.74 MAOB (0.43) LMNAMEN1KMT2AEGFR
SCHEMBL10076826 0.74 MAOB (0.43) LMNAMEN1KMT2AEGFR

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-5011993-A Method for the preparation of α1 [[(1,1-dimethylethyl)amino]methyl]-4-hydroxy-1,3-benzenedimethanol SCHERING CORPORATION (US) 1991-04-30 — — US disclosed
US-4952729-A Intermediates in the preparation of alpha1(((1,1-dimethylethyl) amino) methyl)-4-hydroxy-1,3-benzenedimethanol SCHERING-PLOUGH CORP. (US) 1990-08-28 — — US disclosed
EP-0259159-A2 Method for the preparation of alpha1- [[(1,1-Dimethylethyl) amino] methyl]-4-hydroxy-1,3-benzenedimethanol, and intermediates used in its preparation SCHERING CORPORATION (US) 1988-03-09 — — EP disclosed
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