SCHEMBL6927904

SCHEMBL6927904

O=C(O)C(Cc1cccc2ccccc12)c1ccccc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CTNNB1 P35222 1/20 0.58
ALDH1A1 P00352 1/20 0.55
TDP1 Q9NUW8 1/20 0.54
MMP9 P14780 1/20 0.48
MMP8 P22894 1/20 0.48
MMP14 P50281 1/20 0.48
HRH4 Q9H3N8 1/20 0.48
SLC1A3 P43003 1/20 0.48
SLC1A2 P43004 1/20 0.48
SLC1A1 P43005 1/20 0.48
CYP1A2 P05177 1/20 0.47
MME P08473 2/20 0.47
ACE P12821 2/20 0.47
CMA1 P23946 1/20 0.47
CPA1 P15085 1/20 0.47
ACE2 Q9BYF1 1/20 0.47
SLC6A4 P31645 1/20 0.47
ACP3 P15309 1/20 0.45
CYP2C19 P33261 1/20 0.45
MEN1 O00255 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
SCHEMBL28107952 0.87 EPHX1 (0.58) CTNNB1ALDH1A1TDP1MMP9MMP8
SCHEMBL7272663 0.82 CTNNB1 (0.75) CTNNB1TDP1HRH4SLC1A3SLC1A2
SCHEMBL9518880 0.81 ALDH1A1 (0.50) CTNNB1ALDH1A1TDP1SLC1A3SLC1A2
SCHEMBL6677809 0.81 CTNNB1 (0.63) CTNNB1TDP1HRH4SLC1A3SLC1A2
SCHEMBL8871925 0.81 CTNNB1 (0.59) CTNNB1ALDH1A1TDP1MMP9MMP8
SCHEMBL5831545 0.80 TDP1 (0.50) CTNNB1TDP1MMP9MMP8MMP14
SCHEMBL599243 0.80 ALDH1A1 (0.51) CTNNB1ALDH1A1TDP1CYP2C19
SCHEMBL2684738 0.79 CTNNB1 (0.61) CTNNB1TDP1HRH4SLC1A3SLC1A2
SCHEMBL1826710 0.79 CTNNB1 (0.61) CTNNB1TDP1HRH4SLC1A3SLC1A2
SCHEMBL10170673 0.79 CTNNB1 (0.61) CTNNB1TDP1HRH4SLC1A3SLC1A2

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4709082-A 2-phenylpropionic acid esters, method for optical resolution thereof and optically active substance thereof NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 1987-11-24 US claimed
CN-1241913-C Method of preparing 2-phenyl-3-naphthyl propionic acid derivative DAIICHI SEIYAKU CO (JP) 2006-02-15 CN disclosed
CN-1535955-A Method of preparing 2-phenyl-3-naphthyl propionic acid derivative 第一制药株式会社 2004-10-13 CN disclosed
CN-1535954-A Method of preparing 2-phenyl-3-naphthyl propionic acid derivative 第一制药株式会社 2004-10-13 CN disclosed
CN-1104415-C Process for preparing 2-phenyl-3-naphthylpropionic acid derivatives DAIICHI SEIYAKU CO (JP) 2003-04-02 CN disclosed
US-6515142-B2 Intermediates of aromatic amidine derivatives which have anticoagulation action DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2003-02-04 US disclosed
US-6515142-B2 Intermediates of aromatic amidine derivatives which have anticoagulation action DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2003-02-04 US disclosed
US-20020062033-A1 Process for preparing 2-phenyl-3-naphthylpropionic acid derivatives DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2002-05-23 US disclosed
US-20020062033-A1 Process for preparing 2-phenyl-3-naphthylpropionic acid derivatives DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2002-05-23 US disclosed
US-6337405-B1 MULTISTAGE REACTION OF PYRROLE SUBSTITUTED WITH SULFONATE GROUPS AND HYDROXYPHENYLACETIC ACID DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2002-01-08 US disclosed
US-6337405-B1 MULTISTAGE REACTION OF PYRROLE SUBSTITUTED WITH SULFONATE GROUPS AND HYDROXYPHENYLACETIC ACID DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2002-01-08 US disclosed
US-6252088-B1 COUPLING A NITRILE CONTAININ NAPHTHALENE COMPOUND WITH A COMPOUND CONTAINING PROPIONIC ACID GROUP DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2001-06-26 US disclosed
US-6252088-B1 COUPLING A NITRILE CONTAININ NAPHTHALENE COMPOUND WITH A COMPOUND CONTAINING PROPIONIC ACID GROUP DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2001-06-26 US disclosed
CN-1232449-A Process for preparing 2-phenyl-3-naphthylpropionic acid derivatives DAIICHI SEIYAKU CO (JP) 1999-10-20 CN disclosed
EP-0936215-A1 PROCESS FOR PREPARING 2-PHENYL-3-NAPHTHYLPROPIONIC ACID DERIVATIVES DAIICHI PHARMACEUTICAL CO., LTD. (JP) 1999-08-18 EP disclosed
EP-0179487-B1 2-PHENYLPROPIONIC ACID ESTERS, METHOD FOR OPTICAL RESOLUTION THEREOF AND OPTICALLY ACTIVE SUBSTANCE THEREOF NISSAN CHEMICAL INDUSTRIES LTD. (JP) 1988-08-10 EP disclosed
US-4709082-A 2-phenylpropionic acid esters, method for optical resolution thereof and optically active substance thereof NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 1987-11-24 US disclosed
EP-0179487-A1 2-Phenylpropionic acid esters, method for optical resolution thereof and optically active substance thereof NISSAN CHEMICAL INDUSTRIES LTD. (JP) 1986-04-30 EP 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 (1 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-20020062033-A1 Process for preparing 2-phenyl-3-naphthylpropionic acid derivatives PROC, F12, F2 CTNNB1 3567/4885ALDH1A1 2372/4885TDP1 3124/4885

“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.