SCHEMBL523295

SCHEMBL523295

[O]c1cccc(Oc2ccccc2)c1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 3/20 0.57
TSHR P16473 1/20 0.57
MAOB P27338 2/20 0.56
AKR1C3 P42330 1/20 0.55
HDAC8 Q9BY41 1/20 0.48
PTGS1 P23219 1/20 0.47
GSTP1 P09211 1/20 0.47
MEN1 O00255 1/20 0.46
MITF O75030 1/20 0.46
ALDH1A1 P00352 1/20 0.46
GAA P10253 1/20 0.46
MAPT P10636 1/20 0.46
GFER P55789 1/20 0.46
KMT2A Q03164 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
NLRP1 Q9C000 1/20 0.46
NOD2 Q9HC29 1/20 0.46
MAOA P21397 2/20 0.46
ERCC5 P28715 1/20 0.44
FEN1 P39748 1/20 0.44

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
SCHEMBL1174126 0.98 LTA4H (0.55) LTA4HTSHRMAOBAKR1C3HDAC8
SCHEMBL6842201 0.83 MAPT (0.45) TSHRAKR1C3MEN1MITFALDH1A1
SCHEMBL3759340 0.83 MAOA (0.47) MAOBAKR1C3MEN1MITFALDH1A1
SCHEMBL22559 0.82 LTA4H (0.75) LTA4HTSHRMAOBAKR1C3HDAC8
SCHEMBL30211827 0.82 LTA4H (0.75) LTA4HTSHRMAOBAKR1C3HDAC8
SCHEMBL380685 0.82 LTA4H (0.75) LTA4HTSHRMAOBAKR1C3HDAC8
SCHEMBL4025817 0.82 LTA4H (0.75) LTA4HTSHRMAOBAKR1C3HDAC8
SCHEMBL30018242 0.82 LTA4H (0.75) LTA4HTSHRMAOBAKR1C3HDAC8
SCHEMBL1173711 0.82 LTA4H (0.75) LTA4HTSHRMAOBAKR1C3HDAC8
SCHEMBL1173869 0.82 LTA4H (0.75) LTA4HTSHRMAOBAKR1C3HDAC8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230257408-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2023-08-17 US disclosed
EP-4186882-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2023-05-31 EP disclosed
CN-115836041-A Process for producing optically active compound 住友化学株式会社 2023-03-21 CN disclosed
CN-105189524-B The synthetic method of optical activity alpha-amino acid 浜理药品工业株式会社 2019-07-19 CN disclosed
US-10059700-B2 Supported catalyst for aldehyde coupling reaction , method for performing aldehyde coupling reaction, and method for regenerating supported catalyst for aldehyde coupling reaction SEKISUI CHEMICAL CO., LTD. (JP) 2018-08-28 US disclosed
EP-3006449-B1 METHOD FOR SYNTHESIZING OPTICALLY ACTIVE ALPHA-AMINO ACID USING CHIRAL METAL COMPLEX COMPRISING AXIALLY CHIRAL N-(2-ACYLARYL)-2-[5,7-DIHYDRO-6H-DIBENZO[C,E]AZEPIN-6-YL]ACETAMIDE COMPOUND AND AMINO ACID HAMARI CHEMICALS LTD (JP) 2018-01-31 EP disclosed
US-9695112-B2 Method for synthesizing optically active α-amino acid using chiral metal complex comprising axially chiral N-(2-acylaryl)-2-[5,7-dihydro-6H-dibenzo[c,e]azepin-6-yl] acetamide compound and amino acid HAMARI CHEMICALS, LTD. (JP) 2017-07-04 US disclosed
CN-104109150-B COMPOUND CONTAINING PYRIDINE RING AND METHOD FOR PRODUCING HALOGENATED PICOLINE DERIVATIVE AND TETRAZOLYLOXIME DERIVATIVE 日本曹达株式会社 2017-04-12 CN disclosed
WO-2016195115-A1 SUPPORTED CATALYST FOR ALDEHYDE COUPLING REACTION, METHOD FOR PERFORMING ALDEHYDE COUPLING REACTION, AND METHOD FOR REGENERATING SUPPORTED CATALYST FOR ALDEHYDE COUPLING REACTION SEKISUI CHEMICAL CO., LTD. (JP) 2016-12-08 WO disclosed
US-20160346774-A1 SUPPORTED CATALYST FOR ALDEHYDE COUPLING REACTION , METHOD FOR PERFORMING ALDEHYDE COUPLING REACTION, AND METHOD FOR REGENERATING SUPPORTED CATALYST FOR ALDEHYDE COUPLING REACTION SEKISUI CHEMICAL CO., LTD. (JP) 2016-12-01 US disclosed
US-5104559-A Lubricants or oil additives THE DOW CHEMICAL COMPANY (US) 1992-04-14 US disclosed
EP-0163895-B1 PROCESS FOR THE DIASTEREOSELECTIVE REDUCTION OF ALPHA-TRIAZOLYL KETONES TO BETA-TRIAZOLYL CARBINOLS BASF Aktiengesellschaft (DE) 1989-04-12 EP disclosed
US-4748250-A Diastereoselective reduction of alpha-triazolylketones to betatriazolylcarbinols BASF AKTIENGESELLSCHAFT (DE) 1988-05-31 US disclosed
EP-0090312-B1 3-ACYL SUBSTITUTED DERIVATIVES OF 2- OR 4-THIAZOLIDINE-CARBOXYLIC ACID HAVING A PHYTO GROWTH REGULATING AND BIOSTIMULATING ACTION Montedison S.p.A. (IT) 1987-09-09 EP disclosed
US-4685954-A 3-acyl substituted of 2- or 4-thiazolidine-carboxylic acid having a phyto growth regulating and biostimulating action MONTEDISON S.P.A (IT) 1987-08-11 US disclosed
US-4655818-A 3-acyl substituted derivatives of 2- or 4-thiazolidine-carboxylic acid having a phyto growth regulating and biostimulating action MONTEDISON S.P.A. (IT) 1987-04-07 US disclosed
EP-0163895-A1 Process for the diastereoselective reduction of alpha-triazolyl ketones to beta-triazolyl carbinols BASF Aktiengesellschaft (DE) 1985-12-11 EP disclosed
EP-0090312-A2 3-Acyl substituted derivatives of 2- or 4-thiazolidine-carboxylic acid having a phyto growth regulating and biostimulating action Montedison S.p.A. (IT) 1983-10-05 EP disclosed
EP-0018324-A1 Herbicidal, substituted diphenyl-ether derivatives, process for their preparation, as well as herbicidal compositions and their use CIBA-GEIGY AG (CH) 1980-10-29 EP disclosed
US-3939084-A Functional fluid compositions containing substituted pyrimidines MONSANTO COMPANY (US) 1976-02-17 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 (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-20230257408-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND SIRT1, SIRT3, HCCS LTA4H 3612/4885TSHR 688/4885MAOB 1073/4885
US-20160346774-A1 SUPPORTED CATALYST FOR ALDEHYDE COUPLING REACTION , METHOD FOR PERFORMING ALDEHYDE COUPLING REACTION, AND METHOD FOR REGENERATING SUPPORTED CATALYST FOR ALDEHYDE COUPLING REACTION ALDH2, ALDH7A1, ALDH3A1 LTA4H 1051/4885TSHR 1261/4885MAOB 785/4885
US-10059700-B2 Supported catalyst for aldehyde coupling reaction , method for performing aldehyde coupling reaction, and method for regenerating supported catalyst for aldehyde coupling reaction ALDH2, ALDH7A1, ALDH3A1 LTA4H 1051/4885TSHR 1261/4885MAOB 785/4885

“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.