SCHEMBL2749671

SCHEMBL2749671

Oc1ccc(Cc2ccccn2)cc1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 1/20 0.65
ESR1 P03372 1/20 0.50
ESR2 Q92731 1/20 0.50
KEAP1 Q14145 1/20 0.47
HRH3 Q9Y5N1 2/20 0.44
HRH1 P35367 1/20 0.44
MET P08581 1/20 0.43
HRH4 Q9H3N8 1/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
LMNA P02545 1/20 0.43
TAAR1 Q96RJ0 1/20 0.43
ALDH1A1 P00352 1/20 0.43
ALOX15 P16050 1/20 0.43
CD74 P04233 1/20 0.42
MIF P14174 1/20 0.42
MAPT P10636 1/20 0.42
LIN28A Q9H9Z2 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
PGR P06401 1/20 0.42
ADORA3 P0DMS8 1/20 0.42

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
SCHEMBL29373231 0.83 L3MBTL1 (0.68) L3MBTL1HRH3HRH1HRH4SMN1; SMN2
SCHEMBL64435 0.83 L3MBTL1 (0.68) L3MBTL1HRH3HRH1HRH4SMN1; SMN2
SCHEMBL5807622 0.83 ALDH1A1 (0.60) L3MBTL1ESR1ESR2SMN1; SMN2LMNA
SCHEMBL1772721 0.82 CYP1A2 (0.56) L3MBTL1ESR1ESR2HRH3HRH1
SCHEMBL31236458 0.81 L3MBTL1 (0.66) L3MBTL1HRH3HRH1HRH4SMN1; SMN2
SCHEMBL31276017 0.81 L3MBTL1 (0.66) L3MBTL1HRH3HRH1HRH4LMNA
SCHEMBL29985764 0.81 L3MBTL1 (0.66) L3MBTL1HRH3HRH1HRH4SMN1; SMN2
Hydrochloric Acid SCHEMBL31087535 0.81 L3MBTL1 (0.71) L3MBTL1HRH3HRH1HRH4LMNA
Bromide SCHEMBL10759788 0.81 L3MBTL1 (0.66) L3MBTL1HRH3HRH1HRH4SMN1; SMN2
SCHEMBL30021715 0.81 L3MBTL1 (0.66) L3MBTL1HRH3HRH1HRH4SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106750191-B Sulfonated polyether ketone copolymers of the main chain containing pyridine groups, preparation method and application 中国工程物理研究院化工材料研究所 2018-10-26 CN claimed
CN-106750191-A Sulfonated polyether ketone copolymers, preparation method and application of the main chain containing pyridine groups 中国工程物理研究院化工材料研究所 2017-05-31 CN claimed
CN-106750191-B Sulfonated polyether ketone copolymers of the main chain containing pyridine groups, preparation method and application 中国工程物理研究院化工材料研究所 2018-10-26 CN disclosed
CN-106750191-A Sulfonated polyether ketone copolymers, preparation method and application of the main chain containing pyridine groups 中国工程物理研究院化工材料研究所 2017-05-31 CN disclosed
CN-104854150-B Activator compositions, their preparation, and their use in catalysts 阿尔比马尔公司 2017-05-24 CN disclosed
CN-103380154-B Activator composition, its preparation and the purposes in catalysis thereof 阿尔比马尔公司 2016-08-24 CN disclosed
CN-104854150-A Activator compositions, their preparation, and their use in catalysts ALBEMARLE CORP 2015-08-19 CN disclosed
US-20140186872-A1 BISACODYL AND ITS ANALOGUES AS DRUGS FOR USE IN THE TREATMENT OF CANCER CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE- CNRS (FR) 2014-07-03 US disclosed
US-20140186872-A1 BISACODYL AND ITS ANALOGUES AS DRUGS FOR USE IN THE TREATMENT OF CANCER CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE- CNRS (FR) 2014-07-03 US disclosed
US-8586755-B2 Substituted nicotinamides as KCNQ2/3 modulators Grünenthal GmbH (DE) 2013-11-19 US disclosed
WO-2012168885-A2 BISACODYL AND ANALOGUES AS DRUGS FOR TREATING CANCER UNIVERSITÉ DE STRASBOURG (FR) 2012-12-13 WO disclosed
EP-1636207-A1 SUBSTITUTED PIPERIDINE CARBAMATES FOR USE AS INHIBITORS OF HORMONE SENSITIVE LIPASE NOVO NORDISK A/S (DK) 2006-03-22 EP disclosed
CN-1602191-A Compounds and uses thereof for decreasing activity of hormone-sensitive lipase NOVO NORDISK AS (DK) 2005-03-30 CN disclosed
WO-2004111032-A1 SUBSTITUTED PIPERIDINE CARBAMATES FOR USE AS INHIBITORS OF HORMONE SENSITIVE LIPASE NOVO NORDISK A/S (DK) 2004-12-23 WO disclosed
EP-1458374-A2 COMPOUNDS AND USES THEREOF FOR DECREASING ACTIVITY OF HORMONE-SENSITIVE LIPASE NOVO NORDISK A/S (DK) 2004-09-22 EP disclosed
EP-1458375-A2 COMPOSITIONS FOR DECREASING ACTIVITY OF HORMONE-SENSITIVE LIPASE NOVO NORDISK A/S (DK) 2004-09-22 EP disclosed
US-20030166644-A1 Compounds and uses thereof for decreasing activity of hormone-sensitive lipase NOVO NORDISK A/S (DK) 2003-09-04 US disclosed
US-20030166690-A1 Use of compounds for decreasing activity of hormone-sensitive NOVO NORDISK A/S (DK) 2003-09-04 US disclosed
WO-2003051842-A2 COMPOSITIONS DECREASING ACTIVITY OF HORMONE-SENSITIVE LIPASE NOVO NORDISK A/S (DK) 2003-06-26 WO disclosed
WO-2003051841-A2 COMPOUNDS AND USES THEREOF FOR DECREASING ACTIVITY OF HORMONE-SENSITIVE LIPASE NOVO NORDISK A/S (DK) 2003-06-26 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-20140186872-A1 BISACODYL AND ITS ANALOGUES AS DRUGS FOR USE IN THE TREATMENT OF CANCER CCND1, DEGS1, MCL1 L3MBTL1 499/4885ESR1 1880/4885ESR2 1851/4885
US-20030166644-A1 Compounds and uses thereof for decreasing activity of hormone-sensitive lipase LIPE, PNLIP, LPL L3MBTL1 1427/4885ESR1 1412/4885ESR2 683/4885
US-20030166690-A1 Use of compounds for decreasing activity of hormone-sensitive LIPE, PNLIP, LPL L3MBTL1 2654/4885ESR1 890/4885ESR2 326/4885

“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.