SCHEMBL2744206

SCHEMBL2744206

CNc1cccc(Cl)c1C(=O)O

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PBRM1 Q86U86 1/20 0.60
FABP4 P15090 5/20 0.57
FABP3 P05413 4/20 0.57
PLK1 P53350 1/20 0.47
ALDH1A1 P00352 3/20 0.47
MEN1 O00255 3/20 0.46
KMT2A Q03164 3/20 0.46
MAPT P10636 2/20 0.46
HPGD P15428 2/20 0.46
USP2 O75604 1/20 0.46
MT-CO2 P00403 1/20 0.46
LMNA P02545 1/20 0.46
TTR P02766 1/20 0.46
PLA2G1B P04054 1/20 0.46
CYP1A2 P05177 1/20 0.46
PGR P06401 1/20 0.46
CYP3A4 P08684 1/20 0.46
HTR1A P08908 1/20 0.46
ADRA2A P08913 1/20 0.46
ADORA3 P0DMS8 1/20 0.46

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
Hydrochloric Acid SCHEMBL8512694 0.98 PBRM1 (0.58) PBRM1FABP4FABP3PLK1ALDH1A1
SCHEMBL9840008 0.85 ALDH1A1 (0.47) PBRM1FABP4FABP3ALDH1A1MEN1
SCHEMBL7748934 0.83 ALDH1A1 (0.46) PBRM1ALDH1A1MEN1KMT2AMAPT
SCHEMBL31488086 0.81 PBRM1 (0.57) PBRM1FABP4FABP3PLK1ALDH1A1
SCHEMBL9609179 0.81 POLB (0.53) ALDH1A1MEN1KMT2AMAPTLMNA
SCHEMBL6801278 0.81 PBRM1 (0.57) PBRM1FABP4FABP3PLK1ALDH1A1
SCHEMBL2137697 0.81 PBRM1 (0.60) PBRM1FABP4FABP3PLK1ALDH1A1
SCHEMBL22237905 0.81 PBRM1 (0.60) PBRM1FABP4FABP3PLK1ALDH1A1
SCHEMBL3816160 0.80 ALDH1A1 (0.42) PBRM1FABP4FABP3ALDH1A1MEN1
Hydrochloric Acid SCHEMBL28022291 0.79 PBRM1 (0.58) PBRM1FABP4FABP3PLK1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2682120-B1 Stable laquinimod preparations TEVA PHARMA (IL) 2016-08-03 EP disclosed
US-9340307-B2 Stable laquinimod preparations TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 2016-05-17 US disclosed
EP-2977049-A1 STABLE LAQUINIMOD PREPARATIONS TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 2016-01-27 EP disclosed
US-9102592-B2 Intermediate compounds and processes for the preparation of quinoline derivatives such as laquinimod sodium MAPI PHARMA LTD. (IL) 2015-08-11 US disclosed
US-9102592-B2 Intermediate compounds and processes for the preparation of quinoline derivatives such as laquinimod sodium MAPI PHARMA LTD. (IL) 2015-08-11 US disclosed
US-9102592-B2 Intermediate compounds and processes for the preparation of quinoline derivatives such as laquinimod sodium MAPI PHARMA LTD. (IL) 2015-08-11 US disclosed
US-20150051419-A1 INTERMEDIATE COMPOUNDS AND PROCESSES FOR THE PREPARATION OF QUINOLINE DERIVATIVES SUCH AS LAQUINIMOD SODIUM MAPI PHARMA LTD. (IL) 2015-02-19 US disclosed
US-20150051419-A1 INTERMEDIATE COMPOUNDS AND PROCESSES FOR THE PREPARATION OF QUINOLINE DERIVATIVES SUCH AS LAQUINIMOD SODIUM MAPI PHARMA LTD. (IL) 2015-02-19 US disclosed
US-20150051419-A1 INTERMEDIATE COMPOUNDS AND PROCESSES FOR THE PREPARATION OF QUINOLINE DERIVATIVES SUCH AS LAQUINIMOD SODIUM MAPI PHARMA LTD. (IL) 2015-02-19 US disclosed
US-8865742-B2 Intermediate compounds and processes for the preparation of quinoline derivatives such as Laquinimod sodium MAPI PHARMA LTD. (IL) 2014-10-21 US disclosed
CN-101087779-A Selected benzofuran derivatives ARPIDA AG (CH) 2007-12-12 CN disclosed
EP-1838704-A1 SELECTED BENZOFURAN DERIVATIVES Arpida AG (CH) 2007-10-03 EP disclosed
WO-2006072370-A1 SELECTED BENZOFURAN DERIVATIVES ARPIDA AG (CH) 2006-07-13 WO disclosed
US-6844435-B2 Heterocyclic compounds useful as inhibitors of tyrosine kinases BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) 2005-01-18 US disclosed
US-20030207902-A1 Heterocyclic compounds useful as inhibitors of tyrosine kinases BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. 2003-11-06 US disclosed
EP-1309596-A2 HETEROCYCLIC COMPOUNDS USEFUL AS INHIBITORS OF TYROSINE KINASES BOEHRINGER INGELHEIM PHARMACEUTICALS INC. (US) 2003-05-14 EP disclosed
US-6489328-B2 AUTOIMMUNE DISEASE; ANTIINFLAMMATORY AGENTS; ANTIALLERGENS; ANTIPROLIFERATIVE AGENTS; ANTICANCER AGENTS BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. 2002-12-03 US disclosed
US-20020119975-A1 Heterocyclic compounds useful as inhibitors of tyrosine kinases BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. 2002-08-29 US disclosed
WO-2002014319-A2 HETEROCYCLIC COMPOUNDS USEFUL AS INHIBITORS OF TYROSINE KINASES BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) 2002-02-21 WO disclosed
EP-0542372-A1 2-Substituted saccharin derivative proteolytic enzyme inhibitors STERLING WINTHROP INC. (US) 1993-05-19 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 (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-20020119975-A1 Heterocyclic compounds useful as inhibitors of tyrosine kinases LTK, JAK1, LCK PBRM1 2285/4885FABP4 4518/4885FABP3 3427/4885
US-20150051419-A1 INTERMEDIATE COMPOUNDS AND PROCESSES FOR THE PREPARATION OF QUINOLINE DERIVATIVES SUCH AS LAQUINIMOD SODIUM TLR7, NQO1, NQO2 PBRM1 612/4885FABP4 4025/4885FABP3 4695/4885
US-20030207902-A1 Heterocyclic compounds useful as inhibitors of tyrosine kinases LTK, JAK1, LCK PBRM1 2285/4885FABP4 4518/4885FABP3 3427/4885

“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.