SCHEMBL30253993

SCHEMBL30253993

N=C(Cc1cc(Br)ccc1Br)c1ccc(Br)cc1O

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALOX15 P16050 4/20 0.38
LMNA P02545 3/20 0.36
RAB9A P51151 3/20 0.36
MAPT P10636 2/20 0.36
ALOX12 P18054 2/20 0.36
NPC1 O15118 2/20 0.36
GAA P10253 1/20 0.36
KDM4E B2RXH2 2/20 0.35
HPGD P15428 3/20 0.34
CYP1A2 P05177 2/20 0.34
CYP2C9 P11712 2/20 0.34
CES2 O00748 1/20 0.34
GALR3 O60755 1/20 0.34
CASP1 P29466 1/20 0.34
CYP2C19 P33261 1/20 0.34
TSHR P16473 1/20 0.34
GFER P55789 1/20 0.34
CA12 O43570 1/20 0.33
CA1 P00915 1/20 0.33
CA2 P00918 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
SCHEMBL17740977 1.00 ALOX15 (0.38) ALOX15LMNARAB9AMAPTALOX12
SCHEMBL17429524 0.84 MAPT (0.35) ALOX15LMNARAB9AMAPTALOX12
SCHEMBL17429601 0.84 ALDH1A1 (0.37) ALOX15LMNARAB9AMAPTALOX12
SCHEMBL17429591 0.81 HTT (0.41) ALOX15LMNAMAPTALOX12HPGD
SCHEMBL17740976 0.80 LMNA (0.54) ALOX15LMNARAB9AMAPTALOX12
SCHEMBL28227556 0.73 AKR1C4 (0.39) RAB9AMAPTNPC1KDM4ECA12
SCHEMBL24314179 0.69 C1S (0.45) ALOX15LMNARAB9AMAPTALOX12
SCHEMBL17204756 0.69 ALOX15 (0.43) ALOX15LMNARAB9AMAPTALOX12
SCHEMBL29661155 0.67 PTGDR2 (0.46) LMNAMAPTKDM4EHPGDALDH1A1
SCHEMBL1758414 0.67 PTGDR2 (0.46) LMNAMAPTKDM4EHPGDALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115806493-B Method for synthesizing epstein chiral intermediate by asymmetric hydrogenation 南京工业大学 2024-03-22 CN claimed
CN-115806493-A Method for synthesizing chiral ebavir intermediate by asymmetric hydrogenation 南京工业大学 2023-03-17 CN claimed
CN-115806493-B Method for synthesizing epstein chiral intermediate by asymmetric hydrogenation 南京工业大学 2024-03-22 CN disclosed
CN-115806493-B Method for synthesizing epstein chiral intermediate by asymmetric hydrogenation 南京工业大学 2024-03-22 CN disclosed
CN-115806493-A Method for synthesizing chiral ebavir intermediate by asymmetric hydrogenation 南京工业大学 2023-03-17 CN disclosed
CN-115806493-A Method for synthesizing chiral ebavir intermediate by asymmetric hydrogenation 南京工业大学 2023-03-17 CN disclosed