SCHEMBL8697389

SCHEMBL8697389

O=C(O)Cc1cccc2c1C(S(=O)(=O)O)c1ccccc1-2

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AKR1B1 P15121 1/20 0.41
TDP1 Q9NUW8 1/20 0.41
PTGER1 P34995 1/20 0.38
PTGER4 P35408 1/20 0.38
PTGER3 P43115 1/20 0.38
PTGER2 P43116 1/20 0.38
MMP2 P08253 3/20 0.38
MMP12 P39900 3/20 0.38
MMP13 P45452 3/20 0.38
MMP14 P50281 3/20 0.38
MMP1 P03956 2/20 0.38
MMP3 P08254 2/20 0.38
MMP9 P14780 2/20 0.38
MMP8 P22894 2/20 0.38
MMP16 P51512 2/20 0.38
CYP1A2 P05177 1/20 0.37
TSHR P16473 1/20 0.37
MAPT P10636 1/20 0.36
PPIA P62937 1/20 0.36
PTGS2 P35354 2/20 0.35

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
SCHEMBL5818114 0.82 CA1 (0.33) CYP1A2PPIA
SCHEMBL2587914 0.82 PPIA (0.40) CYP1A2TSHRMAPTPPIACYP2C9
SCHEMBL5917355 0.80 CA1 (0.32) CYP1A2PPIACYP2C9HPGDCYP2C19
SCHEMBL1934600 0.80 ALDH1A1 (0.40) MMP2MMP12MMP1MMP9CYP1A2
SCHEMBL114462 0.80 CA1 (0.35) CYP1A2MAPTPPIA
SCHEMBL5488253 0.79 CA1 (0.37) PPIA
SCHEMBL11570150 0.78 AKR1B1 (0.44) AKR1B1TDP1PTGER1PTGER4PTGER3
SCHEMBL1456494 0.77 CA1 (0.33)
SCHEMBL8084163 0.77 AKR1B1 (0.43) AKR1B1TDP1PTGER1PTGER4PTGER3
SCHEMBL3165966 0.74 TTR (0.35) CYP1A2TSHRPPIATTR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9359333-B2 Efficient process for the preparation of Lapatinib and salts thereof by means of new intermediates F.I.S.—Fabbrica Italiana Sintetiei (IT) 2016-06-07 US claimed
US-20150322050-A1 Efficient Process for the Preparation of Lapatinib and Salts Thereof by Means of New Intermediates F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2015-11-12 US claimed
US-9169236-B2 Efficient process for the preparation of lapatinib and salts thereof by means of new intermediates F.I.S.-Fabbrica Italiana Sintetiei S.p.A. (IT) 2015-10-27 US claimed
EP-2921490-A2 PROCESS FOR THE PREPARATION OF LAPATINIB AND SALTS THEREOF BY MEANS OF NEW INTERMEDIATES F.I.S.- Fabbrica Italiana Sintetici S.p.A. (IT) 2015-09-23 EP claimed
US-20150225376-A1 Efficient Process for the Preparation of Lapatinib and Salts thereof by Means of New Intermediates F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2015-08-13 US claimed
US-9024023-B2 Efficient process for the preparation of lapatinib and salts thereof by means of new intermediates F.I.S.—Fabbrica Italiana Sintetici S.p.A. (IT) 2015-05-05 US claimed
US-20150065710-A1 EFFICIENT PROCESS FOR THE PREPARATION OF LAPATINIB AND SALTS THEREOF BY MEANS OF NEW INTERMEDIATES F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2015-03-05 US claimed
US-9359333-B2 Efficient process for the preparation of Lapatinib and salts thereof by means of new intermediates F.I.S.—Fabbrica Italiana Sintetiei (IT) 2016-06-07 US disclosed
US-20150322050-A1 Efficient Process for the Preparation of Lapatinib and Salts Thereof by Means of New Intermediates F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2015-11-12 US disclosed
US-9169236-B2 Efficient process for the preparation of lapatinib and salts thereof by means of new intermediates F.I.S.-Fabbrica Italiana Sintetiei S.p.A. (IT) 2015-10-27 US disclosed
EP-2921490-A2 PROCESS FOR THE PREPARATION OF LAPATINIB AND SALTS THEREOF BY MEANS OF NEW INTERMEDIATES F.I.S.- Fabbrica Italiana Sintetici S.p.A. (IT) 2015-09-23 EP disclosed
US-20150225376-A1 Efficient Process for the Preparation of Lapatinib and Salts thereof by Means of New Intermediates F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2015-08-13 US disclosed
US-9024023-B2 Efficient process for the preparation of lapatinib and salts thereof by means of new intermediates F.I.S.—Fabbrica Italiana Sintetici S.p.A. (IT) 2015-05-05 US disclosed
US-20150065710-A1 EFFICIENT PROCESS FOR THE PREPARATION OF LAPATINIB AND SALTS THEREOF BY MEANS OF NEW INTERMEDIATES F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2015-03-05 US disclosed
US-5712418-A FLUOROFORMAMIDINIUM SALTS AS FLUORINATION AGENTS TO FORM PEPTIDES RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1998-01-27 US disclosed
WO-1996004297-A1 SYNTHESIS AND USE OF AMINO ACID FLUORIDES AS PEPTIDE COUPLING REAGENTS RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1996-02-15 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-20150225376-A1 Efficient Process for the Preparation of Lapatinib and Salts thereof by Means of New Intermediates ERBB2, EGFR, ERBB4 AKR1B1 2246/4885TDP1 2149/4885PTGER1 3342/4885
US-20150065710-A1 EFFICIENT PROCESS FOR THE PREPARATION OF LAPATINIB AND SALTS THEREOF BY MEANS OF NEW INTERMEDIATES ERBB2, EGFR, ERBB4 AKR1B1 2246/4885TDP1 2149/4885PTGER1 3342/4885
US-20150322050-A1 Efficient Process for the Preparation of Lapatinib and Salts Thereof by Means of New Intermediates ERBB2, EGFR, ERBB4 AKR1B1 2246/4885TDP1 2149/4885PTGER1 3342/4885

“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.