SCHEMBL6839679

SCHEMBL6839679

CC(OCCCl)Oc1ccc(C=CC(C=Cc2ccccc2)=Cc2ccc(O)cc2)cc1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LTB4R Q15722 1/20 0.37
LTB4R2 Q9NPC1 1/20 0.37
ABCG2 Q9UNQ0 4/20 0.37
AKR1B10 O60218 4/20 0.36
AKR1B1 P15121 4/20 0.36
MAOB P27338 1/20 0.36
GSK3B P49841 1/20 0.36
BACE1 P56817 1/20 0.36
CA12 O43570 2/20 0.36
CA7 P43166 2/20 0.36
CA9 Q16790 2/20 0.36
CA14 Q9ULX7 2/20 0.36
CA4 P22748 1/20 0.36
CA6 P23280 1/20 0.36
CA5A P35218 1/20 0.36
CA5B Q9Y2D0 1/20 0.36
CYP19A1 P11511 2/20 0.36
ESR1 P03372 1/20 0.36
ESR2 Q92731 1/20 0.36
CA1 P00915 1/20 0.35

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
SCHEMBL3842067 0.87 LTB4R (0.41) LTB4RLTB4R2ABCG2AKR1B10AKR1B1
SCHEMBL7199294 0.87 LTB4R (0.41) LTB4RLTB4R2ABCG2AKR1B10AKR1B1
SCHEMBL7172181 0.86 ABCG2 (0.46) ABCG2AKR1B10AKR1B1MAOBGSK3B
SCHEMBL6866016 0.86 CA12 (0.41) LTB4RLTB4R2ABCG2AKR1B10AKR1B1
SCHEMBL6551714 0.85 MMP1 (0.41) AKR1B10AKR1B1MAOBMMP1MMP2
SCHEMBL6276080 0.85 ABCG2 (0.42) LTB4RLTB4R2ABCG2AKR1B10AKR1B1
SCHEMBL8735872 0.83 AKR1B10 (0.42) LTB4RLTB4R2ABCG2AKR1B10AKR1B1
SCHEMBL6833601 0.82 APP (0.43) ABCG2AKR1B10AKR1B1MAOBCA12
SCHEMBL7138148 0.80 MAOB (0.42) ABCG2AKR1B10AKR1B1MAOBCA12
SCHEMBL6280782 0.78 ABCG2 (0.46) ABCG2AKR1B10AKR1B1MAOBCA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6686121-B2 WITHOUT PURIFYING RESIST MATERIALS FORMED BY REACTION, BY REACTING AN ALKALI-SOLUBLE POLYMER HAVING PHENOLIC HYDROXYL GROUPS OR CARBOXYL GROUP WITH A VINYL ETHER AND/OR DIALKYL CARBONATE IN CATALYST, APROTIC SOLVENT, ADDING ACID GENERATOR CLARIANT FINANCE (BVI) LIMITED (VG) 2004-02-03 US disclosed
EP-0942329-B1 NOVEL PROCESS FOR PREPARING RESISTS CLARIANT FINANCE BVI LTD (VG) 2002-11-13 EP disclosed
US-20010024765-A1 Novel process for preparing resists MERCK PATENT GMBH (DE) 2001-09-27 US disclosed
US-6284427-B1 Process for preparing resists CLARIANT FINANCE (BVI) LIMITED (VG) 2001-09-04 US disclosed
EP-0942329-A1 NOVEL PROCESS FOR PREPARING RESISTS Clariant International Ltd. (CH) 1999-09-15 EP disclosed