SCHEMBL7862976

SCHEMBL7862976

CON=C(c1ccc(C)cc1)c1ccc(C)cc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 4/20 0.46
ESR2 Q92731 1/20 0.45
ALDH1A1 P00352 9/20 0.44
KMT2A Q03164 2/20 0.44
LMNA P02545 2/20 0.42
CES2 O00748 1/20 0.42
CES1 P23141 1/20 0.42
RXRA P19793 3/20 0.41
RXRB P28702 3/20 0.41
RXRG P48443 3/20 0.41
GAA P10253 2/20 0.41
SMN1; SMN2 Q16637 3/20 0.41
ACHE P22303 2/20 0.39
GSK3B P49841 1/20 0.38
PKM P14618 2/20 0.38
HTT P42858 2/20 0.38
ATM Q13315 2/20 0.38
NPSR1 Q6W5P4 2/20 0.38
HPGD P15428 1/20 0.38
NLRP1 Q9C000 1/20 0.38

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
SCHEMBL13606787 0.84 ALDH1A1 (0.39) TDP1ESR2ALDH1A1KMT2ALMNA
SCHEMBL13606854 0.81 ALDH1A1 (0.40) TDP1ESR2ALDH1A1KMT2ARXRA
SCHEMBL13606880 0.81 NNMT (0.49) ALDH1A1KMT2ALMNAGAASMN1; SMN2
SCHEMBL16440164 0.79 CYP1A2 (0.51) TDP1ALDH1A1KMT2ALMNACES2
SCHEMBL27944058 0.79 ALDH1A1 (0.59) ALDH1A1LMNACES2CES1SMN1; SMN2
SCHEMBL6449347 0.79 SMN1; SMN2 (0.47) ESR2KMT2ALMNACES2CES1
SCHEMBL6815200 0.79 CYP1A2 (0.51) TDP1ALDH1A1KMT2ALMNACES2
SCHEMBL9786513 0.79 CYP19A1 (0.41) TDP1ESR2ALDH1A1KMT2ALMNA
SCHEMBL12603677 0.79 CYP1A2 (0.51) TDP1ALDH1A1KMT2ALMNACES2
SCHEMBL13606831 0.78 NPC1 (0.54) ALDH1A1KMT2ALMNACES2CES1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0736509-B1 Processes for preparing optically active alcohols and optically active amines SUMITOMO CHEMICAL CO (JP) 2001-11-14 EP disclosed
US-6025531-A REACTING A PROCHIRAL KETONE WITH A MIXTURE BORON-CONTAINING COMPOUNDS HAVING A BORANE REACTION PRODUCT FROM OPTICALLY ACTIVE BETA-AMINOALCOHOL AND A BORON HYDRIDE OR A METAL BOROHYDRIDE, AND AN OPTICALLY ACTIVE OXAZABOROLIDINE SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2000-02-15 US disclosed
US-5801280-A Processes for preparing optically active alcohols and optically active amines SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1998-09-01 US disclosed
EP-0736509-A2 Processes for preparing optically active alcohols and optically active amines SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1996-10-09 EP disclosed