SCHEMBL29975832

SCHEMBL29975832

O=C(O)CC=CC=Cc1cccc2ccccc12

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMPD2 O60906 2/20 0.51
HDAC8 Q9BY41 1/20 0.50
HDAC6 Q9UBN7 1/20 0.50
GRIK1 P39086 1/20 0.49
GRIK2 Q13002 1/20 0.49
MTNR1A P48039 1/20 0.49
MTNR1B P49286 1/20 0.49
PAM P19021 1/20 0.47
ALDH1A1 P00352 1/20 0.46
CYP1A1 P04798 1/20 0.46
CYP1A2 P05177 1/20 0.46
CYP2D6 P10635 1/20 0.46
MAPT P10636 1/20 0.46
HPGD P15428 1/20 0.46
NPY1R P25929 1/20 0.46
MAPK1 P28482 1/20 0.46
NPY2R P49146 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
CYP1B1 Q16678 1/20 0.46
RXRA P19793 1/20 0.45

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
SCHEMBL8844798 0.88 SMPD2 (0.58) SMPD2HDAC8HDAC6GRIK1GRIK2
SCHEMBL10741168 0.81 CHAT (0.48) SMPD2HDAC8HDAC6GRIK1GRIK2
SCHEMBL10741170 0.81 CHAT (0.48) SMPD2HDAC8HDAC6GRIK1GRIK2
SCHEMBL4626591 0.80 RXRA (0.57) HDAC8HDAC6MTNR1AMTNR1BALDH1A1
SCHEMBL4626594 0.80 RXRA (0.57) HDAC8HDAC6MTNR1AMTNR1BALDH1A1
SCHEMBL29399914 0.80 RXRA (0.57) HDAC8HDAC6MTNR1AMTNR1BALDH1A1
SCHEMBL3979958 0.80 HDAC8 (0.57) SMPD2HDAC8HDAC6GRIK1GRIK2
SCHEMBL1233027 0.80 HDAC8 (0.57) SMPD2HDAC8HDAC6GRIK1GRIK2
SCHEMBL27525379 0.78 RXRA (0.55) HDAC8HDAC6MTNR1AMTNR1BALDH1A1
SCHEMBL27495890 0.78 RXRA (0.55) HDAC8HDAC6MTNR1AMTNR1BALDH1A1

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