SCHEMBL29975428

SCHEMBL29975428

COc1cccc(C=CC=CC(=O)O)c1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ FOS P01100 1/20 0.62
▸ JUN P05412 1/20 0.62
▸ BCHE P06276 1/20 0.62
▸ MAOB P27338 4/20 0.58
▸ SMN1; SMN2 Q16637 2/20 0.56
▸ KDM4E B2RXH2 1/20 0.56
▸ ALDH1A1 P00352 1/20 0.56
▸ CYP1A2 P05177 3/20 0.55
▸ CYP2D6 P10635 3/20 0.55
▸ ABCG2 Q9UNQ0 2/20 0.55
▸ MAOA P21397 2/20 0.55
▸ CYP1A1 P04798 2/20 0.55
▸ CYP1B1 Q16678 2/20 0.55
▸ RELA Q04206 2/20 0.54
▸ NR1H4 Q96RI1 2/20 0.53
▸ NPC1 O15118 1/20 0.53
▸ LMNA P02545 1/20 0.53
▸ MAPT P10636 1/20 0.53
▸ HPGD P15428 1/20 0.53
▸ NFKB1 P19838 1/20 0.53

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
SCHEMBL3452240 1.00 FOS (0.62) FOSJUNBCHEMAOBSMN1; SMN2
SCHEMBL3452239 1.00 FOS (0.62) FOSJUNBCHEMAOBSMN1; SMN2
SCHEMBL80786 0.89 FOS (0.72) FOSJUNBCHEMAOBSMN1; SMN2
SCHEMBL30584119 0.89 FOS (0.72) FOSJUNBCHEMAOBSMN1; SMN2
SCHEMBL80787 0.89 FOS (0.72) FOSJUNBCHEMAOBSMN1; SMN2
SCHEMBL15932965 0.88 MAOB (0.58) FOSJUNBCHEMAOBSMN1; SMN2
Hydrochloric Acid SCHEMBL8098406 0.87 FOS (0.70) FOSJUNBCHEMAOBSMN1; SMN2
SCHEMBL16410054 0.86 MAOB (0.57) FOSJUNBCHEMAOBSMN1; SMN2
SCHEMBL12698272 0.86 MAOB (0.57) FOSJUNBCHEMAOBSMN1; SMN2
SCHEMBL15929625 0.84 MAOB (0.55) FOSJUNBCHEMAOBSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115073294-A Method for synthesizing axial chiral aryl conjugated diene through asymmetric alfa-C-H olefination reaction and product thereof 杭州师范大学 2022-09-20 — — CN disclosed
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