Sugi Predict

Sugi Predict / Compounds / SCHEMBL3283283

SCHEMBL3283283

SCHEMBL3283283

CC(C)(C)C(=O)N(O)c1ccccc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KMT2A Q03164 3/20 0.60
▸ MEN1 O00255 2/20 0.60
▸ SMN1; SMN2 Q16637 2/20 0.60
▸ CYP3A4 P08684 1/20 0.60
▸ CYP2C9 P11712 1/20 0.60
▸ CYP2C19 P33261 1/20 0.60
▸ KDM4E B2RXH2 1/20 0.44
▸ HPGD P15428 1/20 0.44
▸ NPSR1 Q6W5P4 2/20 0.43
▸ ALDH1A1 P00352 2/20 0.41
▸ GLA P06280 1/20 0.41
▸ TSHR P16473 1/20 0.41
▸ RIPK1 Q13546 2/20 0.41
▸ POLB P06746 1/20 0.39
▸ RAB9A P51151 2/20 0.38
▸ MAPT P10636 2/20 0.38
▸ HSP90AA1 P07900 1/20 0.37
▸ NPC1 O15118 1/20 0.37
▸ ALOX15 P16050 1/20 0.37
▸ HSD17B10 Q99714 1/20 0.37

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
SCHEMBL12103685 0.82 TSHR (0.46) KMT2AMEN1SMN1; SMN2CYP3A4CYP2C9
SCHEMBL9611270 0.80 KMT2A (0.62) KMT2AMEN1SMN1; SMN2CYP3A4CYP2C9
SCHEMBL7609218 0.79 SMN1; SMN2 (0.47) KMT2AMEN1SMN1; SMN2CYP3A4CYP2C9
SCHEMBL8946139 0.78 KMT2A (0.60) KMT2AMEN1SMN1; SMN2CYP3A4CYP2C9
SCHEMBL9500913 0.77 KMT2A (0.58) KMT2AMEN1SMN1; SMN2CYP3A4CYP2C9
SCHEMBL9474692 0.77 KMT2A (0.58) KMT2AMEN1SMN1; SMN2CYP3A4CYP2C9
SCHEMBL11583122 0.77 KMT2A (0.58) KMT2AMEN1SMN1; SMN2CYP3A4CYP2C9
SCHEMBL7089700 0.77 KMT2A (0.58) KMT2AMEN1SMN1; SMN2CYP3A4CYP2C9
SCHEMBL11269635 0.77 CES1 (0.43) KMT2AMEN1SMN1; SMN2CYP3A4CYP2C9
SCHEMBL3786686 0.75 KMT2A (0.56) KMT2AMEN1SMN1; SMN2CYP3A4CYP2C9

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
EP-1483795-B1 MANUFACTURING METHODS FOR RESISTANCE VARIABLE MATERIAL CELLS MICRON TECHNOLOGY INC (US) 2010-06-30 — — EP claimed
EP-0825294-B2 Multicomponent system for modifying, decomposing or bleaching lignin, or lignin-containing materials and method of using this system CONSORTIUM ELEKTROCHEM IND (DE) 2005-02-09 — — EP claimed
US-20010018956-A1 Multi-component system for modifying, degrading or bleaching lignin, lignin-containing materials or similar substances and processes for its use CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH 2001-09-06 — — US claimed
EP-0825294-B1 Multicomponent system for modifying, decomposing or bleaching lignin, or lignin-containing materials and method of using this system CONSORTIUM ELEKTROCHEM IND (DE) 1999-09-15 — — EP claimed
CN-113416139-B 4-fluorine substituted aryl amine compound and synthetic method thereof 江苏笃行致远新材料科技有限公司 2022-06-03 — — CN disclosed
US-20110266945-A1 DISPLAY ELEMENT KONICA MINOLTA HOLDINGS, INC. (JP) 2011-11-03 — — US disclosed
US-20110266945-A1 DISPLAY ELEMENT KONICA MINOLTA HOLDINGS, INC. (JP) 2011-11-03 — — US disclosed
US-20110019265-A1 DISPLAY ELEMENT AND METHOD OF FORMING POROUS LAYER IN DISPLAY ELEMENT KONICA MINOLTA HOLDINGS, INC. (JP) 2011-01-27 — — US disclosed
US-20110019265-A1 DISPLAY ELEMENT AND METHOD OF FORMING POROUS LAYER IN DISPLAY ELEMENT KONICA MINOLTA HOLDINGS, INC. (JP) 2011-01-27 — — US disclosed
US-7700196-B2 Method for producing carbonyl group-containing organosilicon compounds WACKER CHEMIE AG (DE) 2010-04-20 — — US disclosed
US-20070129520-A1 High yield of 2-formylethyldimethylsilanol-modified polydimethylsiloxane obtained by the continuous process of oxidizing 3-hydroxypropyldimethylsilanol-modified corresponding polymer using Tempoas an oxidation catalyst and air or oxygen as oxidizer in an aqueous dispersion; industrial scale; low cost WACKER CHEMIE AG (DE) 2007-06-07 — — US disclosed
US-20060217281-A1 Oxidation system containing a macrocyclic metal complex, the production thereof and its use LANXESS B.V. (NL) 2006-09-28 — — US disclosed
US-20010018956-A1 Multi-component system for modifying, degrading or bleaching lignin, lignin-containing materials or similar substances and processes for its use CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH 2001-09-06 — — US disclosed
US-6258209-B1 DELIGNIFICATION; POLLUTION CONTROL Consortium für elektrochemische Industrie GmbH (DE) 2001-07-10 — — US disclosed
US-6242245-B1 DELIGNIFICATION BY ADDING SUSPENSION OF LACCASE, OXIDANT, MEDIATOR SUCH AS VIOLURIC ACID, AND XYLANASE TO AQUEOUS SUSPENSION OF LIGNIN MATERIAL AND MIXING; MEDIATOR DOES NOT DEACTIVATE ENZYME Consortium für elektrochemische Industrie GmbH (DE) 2001-06-05 — — US disclosed
US-6187170-B1 SYSTEM FOR THE ELECTROCHEMICAL CLEAVAGE OF COMPOUNDS WHICH INCLUDES A MEDIATOR AND AT LEAST TWO ELECTRODES FOR THE ELECTROCHEMICAL ACTIVATION OF THE MEDIATOR Consortium für elektrochemische Industrie GmbH (DE) 2001-02-13 — — US disclosed
US-6169213-B1 REACTING A HETEROARYL METHANOL WITH AN OXIDANT AND A MEDIATOR CONTAINING AMINO OXIDE GROUP TO FORM HETEROARYL ALDEHYDE OR A HETEROARYL KETONE Consortium f{umlaut over (u)}r elektrochemische Industrie GmbH (DE) 2001-01-02 — — US disclosed
US-6069282-A REACTION OF VINYL-, ALKYNYL- OR ARYL-METHANOLS WITH THE AID OF A MEDIATOR AND AN OXIDANT, WHEREIN THE MEDIATOR IS SELECTED FROM THE GROUP OF THE ALIPHATIC, CYCLOALIPHATIC, HETEROCYCLIC OR AROMATIC NO OR NOH CONTAINING COMPOUNDS CONSORTIUM FUR ELEKTROCHEMISCHE INDUSTRIE GMBH (DE) 2000-05-30 — — US disclosed
US-6023000-A Process for the preparation of aldehydes and ketones Consortium fur elektrochemisch Industrie GmbH (DE) 2000-02-08 — — US disclosed
CN-1189556-A Multi-component system for modifying, degrading or bleaching lignin, lignin-containing materials or similar substances and processes for its use CONSORTIUM ELEKTROCHEM IND (DE) 1998-08-05 — — CN disclosed