SCHEMBL987578

SCHEMBL987578

Cc1ccc(S(=O)(=O)N[C@@H]2CCCC[C@H]2N)cc1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.62
TSHR P16473 2/20 0.62
CYP3A4 P08684 1/20 0.62
SMN1; SMN2 Q16637 2/20 0.50
KDM4E B2RXH2 1/20 0.50
RECQL P46063 1/20 0.50
NPSR1 Q6W5P4 2/20 0.48
LMNA P02545 2/20 0.48
USP2 O75604 1/20 0.48
HTT P42858 1/20 0.48
MCOLN2 Q8IZK6 2/20 0.47
MCOLN3 Q8TDD5 2/20 0.47
MCOLN1 Q9GZU1 2/20 0.47
PSEN1 P49768 2/20 0.47
PSEN2 P49810 2/20 0.47
APH1B Q8WW43 2/20 0.47
NCSTN Q92542 2/20 0.47
APH1A Q96BI3 2/20 0.47
PSENEN Q9NZ42 2/20 0.47
TP53 P04637 1/20 0.47

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
SCHEMBL419813 1.00 ALDH1A1 (0.62) ALDH1A1TSHRCYP3A4SMN1; SMN2KDM4E
SCHEMBL6816353 1.00 ALDH1A1 (0.62) ALDH1A1TSHRCYP3A4SMN1; SMN2KDM4E
SCHEMBL810319 1.00 ALDH1A1 (0.62) ALDH1A1TSHRCYP3A4SMN1; SMN2KDM4E
P-Xylene SCHEMBL5422459 0.98 ALDH1A1 (0.60) ALDH1A1TSHRCYP3A4SMN1; SMN2KDM4E
P-Xylene SCHEMBL5421280 0.98 ALDH1A1 (0.60) ALDH1A1TSHRCYP3A4SMN1; SMN2KDM4E
SCHEMBL6055077 0.98 ALDH1A1 (0.60) ALDH1A1TSHRCYP3A4SMN1; SMN2KDM4E
SCHEMBL3499611 0.97 ALDH1A1 (0.58) ALDH1A1TSHRCYP3A4SMN1; SMN2KDM4E
Benzene SCHEMBL5180862 0.96 ALDH1A1 (0.57) ALDH1A1TSHRCYP3A4SMN1; SMN2KDM4E
Hexamethylbenzene SCHEMBL5424696 0.96 ALDH1A1 (0.57) ALDH1A1TSHRCYP3A4SMN1; SMN2KDM4E
Benzene SCHEMBL5181252 0.96 ALDH1A1 (0.57) ALDH1A1TSHRCYP3A4SMN1; SMN2KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3318260-A1 METHODS OF PREPARING 4-PHENYL-6-(2,2,2- TRIFLUORO-1-PHENYLETHOXY) PYRIMIDINE-BASED COMPOUNDS Lexicon Pharmaceuticals, Inc. (US) 2018-05-09 EP claimed
EP-2187887-B1 METHODS OF PREPARING 4-PHENYL-6-(2,2,2-TRIFLUORO-1-PHENYLETHOXY)PYRIMIDINE-BASED COMPOUNDS LEXICON PHARMACEUTICALS INC (US) 2017-11-15 EP claimed
US-8575362-B2 Methods of preparing 4-phenyl-6-(2,2,2-trifluoro-1-phenylethoxy)pyrimidine-based compounds LEXICON PHARMACEUTICALS, INC. (US) 2013-11-05 US claimed
EP-2529740-A1 Methods of preparing 4-Phenyl-6(2,2,2-Trifluoro-1-Phenylethoxy) Pyrimidine-based compounds. Lexicon Pharmaceuticals, Inc. (US) 2012-12-05 EP claimed
US-20110301349-A1 METHODS OF PREPARING 4-PHENYL-6-(2,2,2-TRIFLUORO-1-PHENYLETHOXY)PYRIMIDINE-BASED COMPOUNDS TERSERA THERAPEUTICS LLC 2011-12-08 US claimed
EP-2187887-A1 METHODS OF PREPARING 4-PHENYL-6-(2,2,2-TRIFLUORO-1-PHENYLETHOXY)PYRIMIDINE-BASED COMPOUNDS Lexicon Pharmaceuticals, Inc. (US) 2010-05-26 EP claimed
WO-2009029499-A1 METHODS OF PREPARING 4-PHENYL-6-(2,2,2-TRIFLUORO-1-PHENYLETHOXY)PYRIMIDINE-BASED COMPOUNDS LEXICON PHARMACEUTICALS, INC. (US) 2009-03-05 WO claimed
EP-0915076-B1 Process for the preparation of trans-(R,R)-actinol HOFFMANN LA ROCHE (CH) 2002-01-16 EP claimed
US-6187961-B1 HYDROGENATING (R)-LEVODIONE IN PRESENCE OF HYDROGEN DONAR AND A SOLVENT OR IN PRESENCE OF HYDROGEN DONOR WHICH SIMULTANEOUSLY USED AS THE SOLVENT, AND AN AMINO-AMIDE-RUTHENIUM COMPLEX ROCHE VITAMINS INC. 2001-02-13 US claimed
CN-1223998-A Process for producing trans- (R, R) -actinol HOFFMANN LA ROCHE (CH) 1999-07-28 CN claimed
EP-0915076-A1 Process for the preparation of trans-(R,R)-actinol F. HOFFMANN-LA ROCHE AG (CH) 1999-05-12 EP claimed
US-20230285945-A1 CATALYST CONTAINING ACTIVATED CARBON ADSORBED WITH RUTHENIUM COMPLEX, AND METHOD FOR PRODUCING REDUCTION PRODUCT USING SAME TAKASAGO INTERNATIONAL CORPORATION (JP) 2023-09-14 US disclosed
EP-4115975-A1 CATALYST CONTAINING ACTIVATED CARBON ON WHICH RUTHENIUM COMPLEX IS ADSORBED, AND METHOD FOR PRODUCING REDUCTION PRODUCT USING SAME Takasago International Corporation (JP) 2023-01-11 EP disclosed
EP-3318260-A1 METHODS OF PREPARING 4-PHENYL-6-(2,2,2- TRIFLUORO-1-PHENYLETHOXY) PYRIMIDINE-BASED COMPOUNDS Lexicon Pharmaceuticals, Inc. (US) 2018-05-09 EP disclosed
US-20180093943-A1 Processes and Intermediates for Preparing a Macrocyclic Protease Inhibitor of HCV Janssen Pharmaceuticals, Inc. (US) 2018-04-05 US disclosed
WO-1997033588-A1 IRON COMPLEXES OF NITROGEN-CONTAINING MACROCYCLIC LIGANDS EFFECTIVE AS CATALYSTS FOR DISMUTATING SUPEROXIDE MONSANTO COMPANY (US) 1997-09-18 WO disclosed
WO-1997006830-A1 METHODS OF DIAGNOSTIC IMAGE ANALYSIS USING BIOCONJUGATES OF METAL COMPLEXES OF NITROGEN-CONTAINING MACROCYCLIC LIGANDS MONSANTO COMPANY (US) 1997-02-27 WO disclosed
WO-1997006824-A2 BIOCONJUGATES OF MANGANESE COMPLEXES AND THEIR APPLICATION AS CATALYSTS MONSANTO COMPANY (US) 1997-02-27 WO disclosed
EP-0756495-A1 DIAGNOSTIC IMAGE ANALYSIS WITH METAL COMPLEXES MONSANTO COMPANY (US) 1997-02-05 EP disclosed
WO-1995028968-A1 DIAGNOSTIC IMAGE ANALYSIS WITH METAL COMPLEXES MONSANTO COMPANY (US) 1995-11-02 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 (3 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-20230285945-A1 CATALYST CONTAINING ACTIVATED CARBON ADSORBED WITH RUTHENIUM COMPLEX, AND METHOD FOR PRODUCING REDUCTION PRODUCT USING SAME RRS1, POR, SCO2 ALDH1A1 492/4885TSHR 4343/4885CYP3A4 59/4885
US-20180093943-A1 Processes and Intermediates for Preparing a Macrocyclic Protease Inhibitor of HCV CTRC, HAVCR2, HGFAC ALDH1A1 4165/4885TSHR 3530/4885CYP3A4 52/4885
US-20110301349-A1 METHODS OF PREPARING 4-PHENYL-6-(2,2,2-TRIFLUORO-1-PHENYLETHOXY)PYRIMIDINE-BASED COMPOUNDS DPYD, TYMP, NUDT1 ALDH1A1 490/4885TSHR 3411/4885CYP3A4 69/4885

“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.