SCHEMBL7180348

SCHEMBL7180348

O=C1CCc2ccc(-c3ccccc3)cc21

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.56
NPC1 O15118 2/20 0.56
MAPT P10636 2/20 0.56
KMT2A Q03164 2/20 0.56
SMN1; SMN2 Q16637 2/20 0.56
KDM4E B2RXH2 1/20 0.56
USP2 O75604 1/20 0.56
ALDH1A1 P00352 1/20 0.56
HPGD P15428 1/20 0.56
TYRO3 Q06418 1/20 0.54
NTRK2 Q16620 1/20 0.54
CLK4 Q9HAZ1 1/20 0.54
DYRK1B Q9Y463 1/20 0.54
PBRM1 Q86U86 1/20 0.53
HSD17B1 P14061 3/20 0.51
BRD4 O60885 1/20 0.49
CYP1A2 P05177 1/20 0.49
CYP11B1 P15538 1/20 0.49
CYP11B2 P19099 1/20 0.49
TDP2 O95551 1/20 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
SCHEMBL29395799 0.89 MAOA (0.58) MEN1NPC1MAPTKMT2ASMN1; SMN2
SCHEMBL5211178 0.89 MAOA (0.58) MEN1NPC1MAPTKMT2ASMN1; SMN2
SCHEMBL10045704 0.86 TYRO3 (0.56) MEN1NPC1MAPTKMT2ASMN1; SMN2
SCHEMBL10045703 0.86 TYRO3 (0.56) MEN1NPC1MAPTKMT2ASMN1; SMN2
SCHEMBL16802256 0.86 MEN1 (0.56) MEN1NPC1MAPTKMT2ASMN1; SMN2
SCHEMBL1745161 0.85 HSD17B1 (0.71) MEN1NPC1MAPTKMT2ASMN1; SMN2
SCHEMBL10045643 0.83 TYRO3 (0.53) MEN1NPC1MAPTKMT2ASMN1; SMN2
SCHEMBL10045664 0.83 CLK4 (0.53) MEN1NPC1MAPTKMT2ASMN1; SMN2
SCHEMBL5208267 0.83 BRD4 (0.55) MEN1NPC1MAPTKMT2ASMN1; SMN2
SCHEMBL16821228 0.82 PARP10 (0.52) MEN1NPC1MAPTKMT2ASMN1; 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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114127638-A Negative photosensitive resin composition, cured film, organic EL display, and method for producing cured film 东丽株式会社 2022-03-01 CN disclosed
EP-1059299-B1 Process for the polymerisation of olefins in the presence of indenyl compounds SABIC POLYPROPYLENES BV (NL) 2003-12-17 EP disclosed
US-6342622-B1 COMPOUNDS HAVING BRIDGING GROUP CONTAINING AT LEAST ONE SP2-HYBRIDISED CARBON ATOM BONDED TO INDENYL GROUP AT 2-POSITION ARE MORE ACTIVE AND/OR GIVE POLYMERS WITH HIGHER MOLECULAR WEIGHT DSM B.V. (NL) 2002-01-29 US disclosed
EP-1059299-A1 Indenyl compounds for the polymerisation of olefins DSM N.V. (NL) 2000-12-13 EP disclosed
EP-1059300-A1 Indenyl compounds for the polymerisation of olefins DSM N.V. (NL) 2000-12-13 EP disclosed
EP-0657426-B1 Tricyclic pyrrole derivatives HOFFMANN LA ROCHE (CH) 1998-07-22 EP disclosed
US-5646173-A ANTISEROTONINE AGENTS; CENTRAL NERVOUS SYSTEM DISORDERS; ANTIDEPRESSANTS HOFFMANN-LA ROCHE INC. (US) 1997-07-08 US disclosed
EP-0657426-A2 Tricyclic pyrrole derivatives F. HOFFMANN-LA ROCHE AG (CH) 1995-06-14 EP disclosed
EP-0240859-B1 LIPOXYGENASE INHIBITING COMPOUNDS ABBOTT LABORATORIES (US) 1993-04-28 EP disclosed