SCHEMBL541965

SCHEMBL541965

Cc1ccc(O[C@H](C(=O)O)[C@H](Oc2ccc(C)cc2)C(=O)O)cc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PPARG P37231 4/20 0.51
PPARA Q07869 4/20 0.51
LMNA P02545 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.47
KMT2A Q03164 3/20 0.46
MEN1 O00255 1/20 0.46
CYP1A2 P05177 1/20 0.46
GAA P10253 1/20 0.46
CYP2C9 P11712 1/20 0.46
PKM P14618 1/20 0.46
CYP2C19 P33261 1/20 0.46
TDP1 Q9NUW8 1/20 0.46
LDHA P00338 1/20 0.45
ALDH1A1 P00352 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
MAPT P10636 1/20 0.44
NLRP1 Q9C000 1/20 0.44
ACHE P22303 1/20 0.42
CYP3A4 P08684 1/20 0.41
TSHR P16473 1/20 0.41

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
SCHEMBL375933 1.00 PPARG (0.51) PPARGPPARALMNAL3MBTL1KMT2A
SCHEMBL338001 1.00 PPARG (0.51) PPARGPPARALMNAL3MBTL1KMT2A
SCHEMBL1714102 1.00 PPARG (0.51) PPARGPPARALMNAL3MBTL1KMT2A
SCHEMBL1714197 1.00 PPARG (0.51) PPARGPPARALMNAL3MBTL1KMT2A
Water SCHEMBL3347709 0.98 PPARG (0.50) PPARGPPARALMNAL3MBTL1KMT2A
Water SCHEMBL2789432 0.98 PPARG (0.50) PPARGPPARALMNAL3MBTL1KMT2A
SCHEMBL27510640 0.90 PPARG (0.45) PPARGPPARALMNAL3MBTL1KMT2A
SCHEMBL11708010 0.90 PPARG (0.53) PPARGPPARALMNAL3MBTL1KMT2A
SCHEMBL1974348 0.88 PPARG (0.54) PPARGPPARALMNAL3MBTL1KMT2A
SCHEMBL2952466 0.88 PPARG (0.54) PPARGPPARALMNAL3MBTL1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024110862-A9 PROCESS FOR PREPARING ZANUBRUTINIB OLON S.P.A. (IT) 2024-11-28 WO claimed
CN-114698375-B Process for preparing 2-cyanoethyl (4S) -4- (4-cyano-2-methoxyphenyl) -5-ethoxy-2, 8-dimethyl-1, 4-dihydro-1, 6-naphthyridine-3-carboxylate 拜耳公司 2024-08-02 CN claimed
US-20240199599-A1 PROCESS FOR THE PREPARATION OF 2-CYANOETHYL (4S)-4-(4-CYANO-2-METHOXY-PHENYL)-5-ETHOXY-2,8-DIMETHYL-1,4-DIHYDRO-1,6-NAPHTHYRIDINE-3-CARBOXYLATE BY RESOLUTION OF RACEMATES BY MEANS OF DIASTEREOMERIC TARTARIC ACID ESTERS BAYER AKTIENGESELLSCHAFT (DE) 2024-06-20 US claimed
WO-2024110862-A1 PROCESS FOR PREPARING ZANUBRUTINIB OLON S.P.A. (IT) 2024-05-30 WO claimed
CN-114698375-A Method for preparing 2-cyanoethyl (4S) -4- (4-cyano-2-methoxyphenyl) -5-ethoxy-2, 8-dimethyl-1, 4-dihydro-1, 6-naphthyridine-3-carboxylic ester by splitting racemic modification from diastereomeric tartrate 拜耳公司 2022-07-01 CN claimed
CN-113527202-A Hydroxychloroquine sulfate crystal 健亚生物科技股份有限公司 2021-10-22 CN claimed
WO-2021074078-A1 PROCESS FOR THE PREPARATION OF 2-CYANOETHYL (4S)-4-(4-CYANO-2-METHOXY-PHENYL)-5-ETHOXY-2,8-DIMETHYL-1,4-DIHYDRO-1,6-NAPHTHYRIDINE-3-CARBOXYLATE BY RESOLUTION OF RACEMATES BY MEANS OF DIASTEREOMERIC TARTARIC ACID ESTERS BAYER AKTIENGESELLSCHAFT (DE) 2021-04-22 WO claimed
EP-2831036-B1 PROCESS FOR PREPARING FLUOROLEUCINE ALKYL ESTERS INTERVET INT BV (NL) 2018-09-12 EP claimed
EP-1884514-B1 METHOD FOR THE RESOLUTION OF 2-AMINO-6-PROPYLAMINO-4,5,6,7-TETRAHYDROBENZOTHIAZOL AND INTERMEDIATE COMPOUNDS CRYSTAL PHARMA SAU (ES) 2017-04-12 EP claimed
US-9493400-B2 Process for preparing fluoroleucine alkyl esters MERCK SHARP & DOHME CORP. (US) 2016-11-15 US claimed
WO-2008068569-A2 PROCESSES FOR THE PREPARATION OF CLOPIDOGREL HYDROCHLORIDE WOCKHARDT RESEARCH CENTRE (IN) 2008-06-12 WO claimed
EP-1884514-A1 METHOD FOR THE RESOLUTION OF 2-AMINO-6-PROPYLAMINO-4,5,6,7-TETRAHYDROBENZOTHIAZOL AND INTERMEDIATE COMPOUNDS Ragactives, S.L. (ES) 2008-02-06 EP claimed
EP-1841774-A1 PROCESS FOR PREPARING 5,6-DIHYDRO-4-(S)-(ETHYLAMINO)-6-(S) METHYL-4H-THIENOÝ2,3b¨THIOPYRAN-2-SULPHONAMIDE-7,7-DIOXIDE HCI USV LIMITED (IN) 2007-10-10 EP claimed
WO-2007083188-A2 IMPROVED PROCESS FOR THE PREPARATION OF AN OPTICALLY ACTIVE 5H-PYRROLO [3,4-B] PYRAZINE DERIVATIVE GLENMARK PHARMACEUTICALS LIMITED (US) 2007-07-26 WO claimed
US-7109353-B2 Process for preparing 5,6-dihydro-4-(S)-(ethylamino)-6-(S) methyl-4H-thieno[2,3b]thiopyran-2-sulphonamide-7,7-dioxide HCl COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2006-09-19 US claimed
WO-2006070387-A1 PROCESS FOR PREPARING 5,6-DIHYDRO-4-(S)-(ETHYLAMINO)-6-(S) METHYL-4H-THIENO[2,3b]THIOPYRAN-2-SULPHONAMIDE-7,7-DIOXIDE HCI COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2006-07-06 WO claimed
US-20060142595-A1 Process for preparing 5,6-dihydro-4-(S)-(ethylamino)-6-(S) methyl-4H-thieno[2,3b]thiopyran-2-sulphonamide-7,7-dioxide HCI COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH 2006-06-29 US claimed
EP-1024137-B1 RESOLUTION OF AMINES ESTEVE LABOR DR (ES) 2003-09-24 EP claimed
US-6187930-B1 REACTING SELECTED AMINE WITH OPTICALLY ACTIVE ACID SELECTED FROM (+)-DITOLUYL-L-TARTARIC ACID AND/OR (-)-DITOLUYL-L-TARTARIC ACID IN SOLVENT TO FORM DIASTEROISOMERIC SALT, SEPARATING, ISOLATING ENANTIOMER LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2001-02-13 US claimed
EP-1024137-A1 RESOLUTION OF AMINES LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2000-08-02 EP claimed

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-20060142595-A1 Process for preparing 5,6-dihydro-4-(S)-(ethylamino)-6-(S) methyl-4H-thieno[2,3b]thiopyran-2-sulphonamide-7,7-dioxide HCI CA7, CYP3A7, CA2 PPARG 3620/4885PPARA 3665/4885LMNA 2340/4885
US-20240199599-A1 PROCESS FOR THE PREPARATION OF 2-CYANOETHYL (4S)-4-(4-CYANO-2-METHOXY-PHENYL)-5-ETHOXY-2,8-DIMETHYL-1,4-DIHYDRO-1,6-NAPHTHYRIDINE-3-CARBOXYLATE BY RESOLUTION OF RACEMATES BY MEANS OF DIASTEREOMERIC TARTARIC ACID ESTERS MVD, VARS1, CYP4B1 PPARG 854/4885PPARA 548/4885LMNA 1222/4885

“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.