SCHEMBL650085

SCHEMBL650085

COc1ccc(S(=O)(=O)NC2Cc3cc(Cl)ccc3N(Cc3ccccc3)C2)cc1OC

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE4A P27815 4/20 0.50
PDE4B Q07343 4/20 0.50
PDE4C Q08493 4/20 0.50
PDE4D Q08499 4/20 0.50
FNTA P49354 1/20 0.46
FNTB P49356 1/20 0.46
ADRA1A P35348 4/20 0.46
ADRA1B P35368 4/20 0.46
DRD2 P14416 3/20 0.44
ADRA1D P25100 3/20 0.44
ALDH1A1 P00352 2/20 0.43
TP53 P04637 1/20 0.43
HTT P42858 1/20 0.43
HDAC8 Q9BY41 2/20 0.42
MAPK1 P28482 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
CYP1A2 P05177 1/20 0.42
CYP3A4 P08684 1/20 0.42
PKM P14618 1/20 0.42
TSHR P16473 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
SCHEMBL651258 0.86 FNTA (0.55) FNTAFNTBALDH1A1HTTHDAC8
SCHEMBL652931 0.85 FNTA (0.51) FNTAFNTBALDH1A1TP53HTT
SCHEMBL651390 0.85 FNTA (0.49) FNTAFNTBALDH1A1HTTHDAC8
SCHEMBL651621 0.84 FNTA (0.50) FNTAFNTBDRD2ALDH1A1HTT
SCHEMBL652980 0.84 FNTA (0.49) FNTAFNTBALDH1A1HTTHDAC8
SCHEMBL651334 0.84 FNTA (0.49) FNTAFNTBDRD2ALDH1A1HTT
SCHEMBL653026 0.83 FNTA (0.49) FNTAFNTBALDH1A1HTTHDAC8
SCHEMBL651205 0.83 FNTA (0.48) FNTAFNTBADRA1AADRA1BDRD2
SCHEMBL651292 0.82 FNTA (0.48) FNTAFNTBADRA1AADRA1BDRD2
SCHEMBL654001 0.82 FNTA (0.47) FNTAFNTBALDH1A1HTTHDAC8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7884113-B2 Tetrahydroquinoline derivatives as cannabinoid receptor modulators BRISTOL-MYERS SQUIBB COMPANY (US) 2011-02-08 US claimed
US-20080194625-A1 TETRAHYDROQUINOLINE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS BRISTOL-MYERS SQUIBB COMPANY 2008-08-14 US claimed
US-20050014786-A1 Tetrahydroquinoline derivatives as cannabinoid receptor modulators BRISTOL-MYERS SQUIBB COMPANY 2005-01-20 US claimed
EP-0876369-A1 2- 2- (2-HYDROXYETHYL)AMINO]ETHYL]-5- 2-METHYLAMINO)ETHYL]AMINO]INDAZOLO 4,3-gh]ISOQUINOLIN-6(2H)-ONE AS ANTITUMOR AGENT BOEHRINGER MANNHEIM ITALIA S.p.A. (IT) 1998-11-11 EP claimed
WO-1997010245-A1 2-[2-[(2-HYDROXYETHYL)AMINO]ETHYL]-5-[[2-METHYLAMINO)ETHYL]AMINO]INDAZOLO[4,3-gh]ISOQUINOLIN-6(2H)-ONE AS ANTITUMOR AGENT BOEHRINGER MANNHEIM ITALIA S.P.A. (IT) 1997-03-20 WO claimed
US-20230279312-A1 PROCESSES FOR MAKING CONCENTRATED SURFACTANT BLENDS THE PROCTER & GAMBLE COMPANY 2023-09-07 US disclosed
WO-2022117575-A1 PROCESS FOR THE CONVERSION OF ETHANE TO ETHYLENE GLYCOL STUDIENGESELLSCHAFT KOHLE MBH (DE) 2022-06-09 WO disclosed
EP-4008707-A1 PROCESS FOR THE CONVERSION OF ETHANE TO ETHYLENE GLYCOL Studiengesellschaft Kohle mbH (DE) 2022-06-08 EP disclosed
CN-105612142-B Esterification unit for producing crude methyl methacrylate, esterification method using the same 阿肯马法国公司 2021-09-07 CN disclosed
US-11084774-B2 Esterification unit for producing crude methyl methacrylate, esterification process using said unit and plant comprising said unit TRINSEO EUROPE GMBH 2021-08-10 US disclosed
WO-2021084330-A1 FUNCTIONALIZED OLEFIN OLIGOMERS CHEVRON ORONITE COMPANY LLC (US) 2021-05-06 WO disclosed
US-20200270195-A1 ESTERIFICATION UNIT FOR PRODUCING CRUDE METHYL METHACRYLATE, ESTERIFICATION PROCESS USING SAID UNIT AND PLANT COMPRISING SAID UNIT ALTER DOMUS (US) LLC 2020-08-27 US disclosed
US-5780421-A Sulfated/sulfonated surfactants HENKEL CORPORATION (US) 1998-07-14 US disclosed
WO-1997032953-A1 NOVEL SULFATED/SULFONATED SURFACTANTS HENKEL CORPORATION (US) 1997-09-12 WO disclosed
CN-1119866-A Enantioselective synthesis of 5,6-dihydro-(S)-4-(ethylamino)-(S)-6-methyl-4H-thieno[2,3-b]thiopyran-2-sulfonamide 7,7-dioxide and related compounds MERCK & CO INC (US) 1996-04-03 CN disclosed
US-5288908-A Process for the preparation of fluorine containing monomers HOECHST AKTIENGESELLSCHAFT (DE) 1994-02-22 US disclosed
CN-1023118-C Monomer containing fluorine, process for preparing them and use HOECHST AG (DE) 1993-12-15 CN disclosed
CN-1041358-A Fluorochemical monomer, their preparation method and application thereof HOECHST AG (DE) 1990-04-18 CN disclosed
US-4782150-A FIBER-REACTIVE DYES HOECHST AKTIENGESELLSCHAFT (DE) 1988-11-01 US disclosed
US-4140685-A BY NEUTRALIZATION WITH AMMONIA AND THEN EXTRACTION STAMICARBON, B.V. (NL) 1979-02-20 US 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 (4 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-11084774-B2 Esterification unit for producing crude methyl methacrylate, esterification process using said unit and plant comprising said unit MMAB, SAMM50, MRM1 PDE4A 2672/4885PDE4B 2449/4885PDE4C 1969/4885
US-20050014786-A1 Tetrahydroquinoline derivatives as cannabinoid receptor modulators CNR2, CNR1, OPRL1 PDE4A 1688/4885PDE4B 1524/4885PDE4C 1727/4885
US-20200270195-A1 ESTERIFICATION UNIT FOR PRODUCING CRUDE METHYL METHACRYLATE, ESTERIFICATION PROCESS USING SAID UNIT AND PLANT COMPRISING SAID UNIT MMAB, SAMM50, MRM1 PDE4A 2672/4885PDE4B 2449/4885PDE4C 1969/4885
US-20080194625-A1 TETRAHYDROQUINOLINE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS CNR2, CNR1, OPRL1 PDE4A 1688/4885PDE4B 1524/4885PDE4C 1727/4885

“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.