SCHEMBL652096

SCHEMBL652096

CC(=O)Nc1ncc(/C=C2\S/C(=N\c3ccc(O)c(F)c3)NC2=O)s1

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTPN11 Q06124 1/20 0.45
KMT2A Q03164 10/20 0.45
MEN1 O00255 9/20 0.45
APOBEC3A P31941 1/20 0.45
APOBEC3G Q9HC16 1/20 0.45
MAPT P10636 10/20 0.42
LMNA P02545 3/20 0.42
POLB P06746 5/20 0.42
PKM P14618 1/20 0.42
CDC25A P30304 3/20 0.41
CDC25B P30305 3/20 0.41
PSMD14 O00487 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
MAPK1 P28482 3/20 0.41
HPGD P15428 1/20 0.41
PTPN7 P35236 1/20 0.41
DUSP3 P51452 1/20 0.41
PTPN12 Q05209 1/20 0.41
PTPN22 Q9Y2R2 1/20 0.41
NPSR1 Q6W5P4 1/20 0.40

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
SCHEMBL649799 1.00 PTPN11 (0.45) PTPN11KMT2AMEN1APOBEC3AAPOBEC3G
SCHEMBL651590 0.84 NPC1 (0.54) KMT2AMEN1APOBEC3AAPOBEC3GMAPT
SCHEMBL649125 0.84 NPC1 (0.54) KMT2AMEN1APOBEC3AAPOBEC3GMAPT
SCHEMBL650783 0.83 CSNK2A2 (0.49) PTPN11KMT2AMEN1APOBEC3AAPOBEC3G
SCHEMBL652094 0.83 OGA (0.42) PTPN11KMT2AMEN1APOBEC3AAPOBEC3G
SCHEMBL652095 0.83 OGA (0.42) PTPN11KMT2AMEN1APOBEC3AAPOBEC3G
SCHEMBL651291 0.82 OGA (0.47) PTPN11KMT2AMEN1APOBEC3AAPOBEC3G
SCHEMBL650970 0.82 MAPT (0.41) PTPN11KMT2AMEN1APOBEC3AAPOBEC3G
SCHEMBL651290 0.82 OGA (0.47) PTPN11KMT2AMEN1APOBEC3AAPOBEC3G
SCHEMBL651253 0.82 MAPT (0.41) PTPN11KMT2AMEN1APOBEC3AAPOBEC3G

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2013240-B1 PROCESS FOR THE PREPARATION OF CROSSLINKED NITROXIDE POLYMERS PIOTREK CO LTD (JP) 2017-05-31 EP disclosed
US-8492511-B2 Process for the preparation of crosslinked nitroxide polymers PIOTREK CO., LTD. (JP) 2013-07-23 US disclosed
US-8252862-B2 Silane coupling agents for filled rubbers BASF SE (DE) 2012-08-28 US disclosed
US-8119812-B2 Thiazolidinone derivative SBI BIOTECH CO., LTD. (JP) 2012-02-21 US disclosed
US-8119710-B2 Filled rubber compounds with improved processability BASF SE (DE) 2012-02-21 US disclosed
EP-2190912-B1 SILANE COUPLING AGENTS FOR FILLED RUBBERS BASF SE (DE) 2011-11-23 EP disclosed
EP-1945705-B1 PHOTOLATENT SYSTEMS BASF SE (DE) 2011-10-19 EP disclosed
US-20110190299-A1 THIAZOLIDINONE DERIVATIVE SBI BIOTECH CO., LTD. (JP) 2011-08-04 US disclosed
US-7902368-B2 Cationic substituted 2,2,6,6-tetraalkylpiperidinyl alkoxyamines BASF SE (DE) 2011-03-08 US disclosed
US-7868171-B2 N-alkoxy-4, 4-dioxy-polyalkyl-piperidines as radical polymerization initiators CIBA SPECIALTY CHEMICALS CORP. (US) 2011-01-11 US disclosed
WO-2004022617-A1 METHOD OF PRODUCING COMB OR STAR COPOLYMERS USING EPOXY-FUNCTIONALIZED NITROXYLETHERS CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2004-03-18 WO disclosed
EP-1397349-A1 4-IMINO-N-ALKOXY OR OXY-POLYALKYL-PIPERIDINE COMPOUNDS AND THEIR USE AS POLYMERIZATION REGULATORS Ciba SC Holding AG (CH) 2004-03-17 EP disclosed
US-20040049043-A1 N-alkoxy-4,4-dioxy-polyalkyl-piperidine compounds, with glycidyl or alkylcarbonyl groups as functional initiators for controlled radical polymerization CIBA SPECIALTY CHEMICALS CORP. 2004-03-11 US disclosed
WO-2004000809-A1 CATIONIC ALKOXYAMINES AND THEIR USE IN PRODUCING NANO PARTICLES FROM NATURAL OR SYNTHETIC CLAYS CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2003-12-31 WO disclosed
EP-1343827-A1 N-ALKOXY-4,4-DIOXY-POLYALKYL-PIPERIDINE COMPOUNDS, THEIR CORRESPONDING N-OXIDES AND CONTROLLED RADICAL POLYMERIZATION THEREWITH Ciba SC Holding AG (CH) 2003-09-17 EP disclosed
WO-2003075091-A1 COLOUR PHOTOGRAPHIC RECORDING MATERIAL CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2003-09-12 WO disclosed
EP-1341763-A2 N-ALKOXY-4,4-DIOXY-POLYALKYL-PIPERIDINE COMPOUNDS, WITH GLYCIDYL OR ALKYLCARBONYL GROUPS AS FUNCTIONAL INITIATORS FOR CONTROLLED RADICAL POLYMERIZATION Ciba SC Holding AG (CH) 2003-09-10 EP disclosed
WO-2002100831-A1 4-IMINO-N-ALKOXY OR OXY-POLYALKYL-PIPERIDINE COMPOUNDS AND THEIR USE AS POLYMERIZATION REGULATORS CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2002-12-19 WO disclosed
WO-2002048109-A2 N-ALKOXY-4,4-DIOXY-POLYALKYL-PIPERIDINES AS RADICAL POLYMERIZATION INITIATORS CIBA SPECIALTY CHEMICLAS HOLDING INC. (CH) 2002-06-20 WO disclosed
WO-2002048205-A1 N-ALKOXY-4,4-DIOXY-POLYALKYL-PIPERIDINE COMPOUNDS, THEIR CORRESPONDING N-OXIDES AND CONTROLLED RADICAL POLYMERIZATION THEREWITH CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2002-06-20 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20110190299-A1 THIAZOLIDINONE DERIVATIVE CDC7, CDK17, CDCA2 PTPN11 1970/4885KMT2A 3437/4885MEN1 1406/4885
US-20040049043-A1 N-alkoxy-4,4-dioxy-polyalkyl-piperidine compounds, with glycidyl or alkylcarbonyl groups as functional initiators for controlled radical polymerization PAOX, ALKBH3, PTGER4 PTPN11 4189/4885KMT2A 1176/4885MEN1 4857/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.