SCHEMBL8437540

SCHEMBL8437540

CC(C)C[C@@H](O)COc1ccccc1

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.66
CYP2D6 P10635 3/20 0.62
ADRB2 P07550 1/20 0.62
ADRB1 P08588 1/20 0.62
ADRB3 P13945 1/20 0.62
L3MBTL1 Q9Y468 1/20 0.53
KDM4E B2RXH2 1/20 0.51
MEN1 O00255 1/20 0.51
ALDH1A1 P00352 1/20 0.51
KMT2A Q03164 1/20 0.51
MAPT P10636 2/20 0.50
TSHR P16473 1/20 0.50
HIF1A Q16665 1/20 0.50
MAOA P21397 1/20 0.50
PTGS1 P23219 1/20 0.50
HTT P42858 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
RECQL P46063 1/20 0.50
POLB P06746 1/20 0.49
MTNR1A P48039 2/20 0.49

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
SCHEMBL8437536 1.00 LMNA (0.66) LMNACYP2D6ADRB2ADRB1ADRB3
SCHEMBL8437532 1.00 LMNA (0.66) LMNACYP2D6ADRB2ADRB1ADRB3
SCHEMBL19865603 0.87 MAPK1 (0.60) LMNACYP2D6ADRB2ADRB1ADRB3
SCHEMBL267463 0.83 LMNA (0.68) LMNACYP2D6ADRB2ADRB1ADRB3
SCHEMBL13263721 0.83 USP2 (0.58) LMNACYP2D6KDM4EMEN1ALDH1A1
SCHEMBL16885283 0.83 POLB (0.54) ADRB2ADRB1ADRB3KDM4EMEN1
SCHEMBL19865604 0.81 MAPK1 (0.54) LMNACYP2D6ADRB2ADRB1ADRB3
SCHEMBL18568523 0.80 LMNA (0.59) LMNACYP2D6ADRB2ADRB1ADRB3
SCHEMBL166337 0.80 LMNA (0.64) LMNACYP2D6ADRB2ADRB1ADRB3
SCHEMBL16448411 0.80 LMNA (0.54) LMNACYP2D6ADRB2ADRB1ADRB3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2022047375-A1 NOVEL FUNGAL MODULATORS TRUSTEES OF BOSTON UNIVERSITY (US) 2022-03-03 WO disclosed
US-5977409-A Method of using α-substituted benzylamine chiral auxiliary synthetic reagents UNIVERSITY OF TOLEDO (US) 1999-11-02 US disclosed