SCHEMBL5711166

SCHEMBL5711166

O=Cc1ccc2cccc-2cc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2A6 P11509 4/20 0.55
ALDH1A1 P00352 4/20 0.55
DRD1 P21728 4/20 0.55
TRIM24 O15164 1/20 0.50
TRIM33 Q9UPN9 1/20 0.50
HSD17B10 Q99714 1/20 0.50
ALDH5A1 P51649 1/20 0.50
ABAT P80404 1/20 0.50
CA12 O43570 1/20 0.48
CA1 P00915 1/20 0.48
CA2 P00918 1/20 0.48
CA9 Q16790 1/20 0.48
KIF11 P52732 1/20 0.45
TYR P14679 1/20 0.44
KDM4E B2RXH2 1/20 0.44
CYP2A13 Q16696 1/20 0.44
ELANE P08246 1/20 0.44
TP53 P04637 1/20 0.43
DRD2 P14416 1/20 0.42
DRD4 P21917 1/20 0.42

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
Hydrochloric Acid SCHEMBL27796624 0.97 DRD1 (0.53) CYP2A6ALDH1A1DRD1TRIM24TRIM33
SCHEMBL1669178 0.92 DRD1 (0.59) CYP2A6ALDH1A1DRD1TRIM24TRIM33
SCHEMBL6032 0.92 ALDH1A1 (0.68) CYP2A6ALDH1A1DRD1TRIM24TRIM33
Benzene SCHEMBL28288569 0.92 ALDH1A1 (0.68) CYP2A6ALDH1A1DRD1TRIM24TRIM33
SCHEMBL10969109 0.92 ALDH1A1 (0.68) CYP2A6ALDH1A1DRD1TRIM24TRIM33
SCHEMBL5733969 0.92 ALDH1A1 (0.68) CYP2A6ALDH1A1DRD1TRIM24TRIM33
SCHEMBL25288128 0.91 CYP2A6 (0.58) CYP2A6ALDH1A1DRD1TRIM24TRIM33
SCHEMBL1666706 0.91 CYP2A6 (0.58) CYP2A6ALDH1A1DRD1TRIM24TRIM33
SCHEMBL976904 0.91 CYP2A6 (0.58) CYP2A6ALDH1A1DRD1TRIM24TRIM33
SCHEMBL27335985 0.91 CYP2A6 (0.58) CYP2A6ALDH1A1DRD1TRIM24TRIM33

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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107011213-B Multi-channel luminous fluorescent probe and preparation method and application thereof 复旦大学 2020-05-12 CN claimed
CN-101268077-A Tricyclic benzimidazoles and their use as metabotropic glutamate receptor modulators ASTRAZENECA AB (SE) 2008-09-17 CN claimed
CN-107011213-B Multi-channel luminous fluorescent probe and preparation method and application thereof 复旦大学 2020-05-12 CN disclosed
CN-105246866-B The method of synthesis ingenol and its intermediate 利奥实验室有限公司 2017-06-16 CN disclosed
CN-105246866-A Methods of synthesis of ingenol and intermediates thereof LEO LAB LTD 2016-01-13 CN disclosed
CN-101535276-B 2, 4-diaminopyrimidine fused bicyclic derivatives as ALK and c-MET inhibitors CEPHALON INC 2013-08-28 CN disclosed
CN-101679447-A pyrimidodiazepinone derivative KYOWA HAKKO KIRIN CO LTD 2010-03-24 CN disclosed
CN-101535276-A 2, 4-diaminopyrimidine fused bicyclic derivatives as ALK and c-MET inhibitors CEPHALON INC (US) 2009-09-16 CN disclosed
CN-101268077-A Tricyclic benzimidazoles and their use as metabotropic glutamate receptor modulators ASTRAZENECA AB (SE) 2008-09-17 CN disclosed
EP-0888290-B1 AZULENYL NITRONE SPIN TRAPPING AGENTS, METHODS OF MAKING AND USING SAME FLORIDA INTERNAT UNIVERSITY (US) 2006-12-27 EP disclosed
CN-1751047-A Triazole compounds useful in therapy PFIZER (US) 2006-03-22 CN disclosed
CN-1474820-A Benzodiazepine derivatives as GABA A receptor modulators - 2004-02-11 CN disclosed
CN-1446218-A Benzimidazole derivatives, their preparation and their therapeutic use SANOFI SYNTHELABO (FR) 2003-10-01 CN disclosed
CN-1384835-A Tricycle inhibitors of poly(ADP-ribose) polymerases AGOURON PHARMA (US) 2002-12-11 CN disclosed
US-6291702-B1 AS AGENTS FOR TRAPPING AND IDENTIFYING FREE RADICAL SPECIES AND FIND USE AS EFFICIENT ANTIOXIDANTS IN PHYSICOCHEMICAL AND BIOLOGICAL SYSTEMS. FLORIDA INTERNATIONAL UNIVERSITY 2001-09-18 US disclosed
US-6197825-B1 EFFECTIVE AGENTS FOR TRAPPING AND IDENTIFYING FREE RADICAL SPECIES AND FIND USE AS EFFICIENT ANTIOXIDANTS IN PHYSICOCHEMICAL AND BIOLOGICAL SYSTEMS. DIAMAGNETIC NITRONE COMPOUND (THE ?SPIN TRAP?) REACTS WITH A TRANSIENT FREE FLORIDA INTERNATIONAL UNIVERSITY 2001-03-06 US disclosed
US-6083988-A AZULENYL NITRONES ARE EFFECTIVE AGENTS FOR TRAPPING AND IDENTIFYING FREE RADICALS AND FIND USE AS EFFICIENT ANTIOXIDANT IN PHYSICOCHEMICAL AND BIOLOGICAL SYSTEMS FLORIDA INTERNATIONAL UNIVERSITY 2000-07-04 US disclosed
EP-0888290-A1 AZULENYL NITRONE SPIN TRAPPING AGENTS, METHODS OF MAKING AND USING SAME Florida International University (US) 1999-01-07 EP disclosed
WO-1997019054-A9 AZULENYL NITRONE SPIN TRAPPING AGENTS, METHODS OF MAKING AND USING SAME 1997-08-07 WO disclosed
WO-1997019054-A1 AZULENYL NITRONE SPIN TRAPPING AGENTS, METHODS OF MAKING AND USING SAME FLORIDA INTERNATIONAL UNIVERSITY (US) 1997-05-29 WO disclosed