SCHEMBL6844679

SCHEMBL6844679

O=C(O)C(Br)COc1ccccc1

nearest known ligand 0.52

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.52
MTNR1A P48039 3/20 0.50
MTNR1B P49286 3/20 0.50
PPARG P37231 1/20 0.50
PPARA Q07869 1/20 0.50
ALOX15 P16050 1/20 0.50
CYP2D6 P10635 2/20 0.46
ADRB2 P07550 1/20 0.46
ADRB1 P08588 1/20 0.46
ADRB3 P13945 1/20 0.46
SCN4A P35499 2/20 0.46
PKM P14618 1/20 0.44
MAPT P10636 3/20 0.43
HTT P42858 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
RAB9A P51151 1/20 0.43
CYP1A2 P05177 1/20 0.43

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
SCHEMBL6844672 1.00 LMNA (0.52) LMNAMTNR1AMTNR1BPPARGPPARA
SCHEMBL10829632 0.83 PPARG (0.58) PPARGPPARASCN4ARAB9ACYP1A2
SCHEMBL5512521 0.81 LMNA (0.57) LMNAMTNR1AMTNR1BPPARGPPARA
SCHEMBL7122514 0.81 PPARG (0.53) MTNR1AMTNR1BPPARGPPARAALOX15
SCHEMBL4093444 0.79 LMNA (0.54) LMNAMTNR1AMTNR1BPPARGPPARA
SCHEMBL8468149 0.78 LMNA (0.59) LMNAMTNR1AMTNR1BPPARGPPARA
SCHEMBL2731803 0.78 LMNA (0.59) LMNAMTNR1AMTNR1BPPARGPPARA
SCHEMBL5421055 0.78 LMNA (0.59) LMNAMTNR1AMTNR1BPPARGPPARA
SCHEMBL9283760 0.78 LMNA (0.59) LMNAMTNR1AMTNR1BPPARGPPARA
SCHEMBL17386434 0.77 LMNA (0.63) LMNAMTNR1AMTNR1BCYP2D6ADRB2

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-6770775-B2 REACTING ACID HALIDES WITH A CINCHONA ALKALOID CATALYST AND A BASE TO FORM INTERMEDIATE KETENES, WHICH ARE THEN REACTED WITH ELECTROPHILIC HALOGENATING REAGENTS TO PRODUCE ALPHA-HALO-ESTERS WITH HIGH ENANTIOMERIC EXCESS WACK HARALD (DE) 2004-08-03 US claimed
US-6770775-B2 REACTING ACID HALIDES WITH A CINCHONA ALKALOID CATALYST AND A BASE TO FORM INTERMEDIATE KETENES, WHICH ARE THEN REACTED WITH ELECTROPHILIC HALOGENATING REAGENTS TO PRODUCE ALPHA-HALO-ESTERS WITH HIGH ENANTIOMERIC EXCESS WACK HARALD (DE) 2004-08-03 US disclosed
US-20030050501-A1 Method of synthesizing optically enriched alpha-halo-esters, and product and composition therefrom WACK HARALD (DE) 2003-03-13 US disclosed