SCHEMBL9957133

SCHEMBL9957133

COC(=O)c1c(-c2ccccc2C)noc1C1CC1

nearest known ligand 0.47

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ GPBAR1 Q8TDU6 3/20 0.47
▸ PTGS1 P23219 1/20 0.44
▸ ALDH1A1 P00352 6/20 0.42
▸ KDM4E B2RXH2 3/20 0.42
▸ KMT2A Q03164 2/20 0.42
▸ MEN1 O00255 1/20 0.42
▸ MAPT P10636 1/20 0.42
▸ L3MBTL1 Q9Y468 1/20 0.42
▸ HPGD P15428 4/20 0.42
▸ NR1H4 Q96RI1 3/20 0.41
▸ TSHR P16473 1/20 0.40
▸ POLB P06746 2/20 0.39
▸ LMNA P02545 2/20 0.39
▸ SMN1; SMN2 Q16637 2/20 0.39
▸ TP53 P04637 1/20 0.38
▸ PTBP1 P26599 1/20 0.38

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
SCHEMBL26485417 0.88 GPBAR1 (0.48) GPBAR1ALDH1A1KDM4EKMT2AMEN1
SCHEMBL28608757 0.88 GPBAR1 (0.47) GPBAR1PTGS1ALDH1A1KDM4EKMT2A
SCHEMBL22790165 0.86 GPBAR1 (0.47) GPBAR1PTGS1ALDH1A1KDM4EKMT2A
SCHEMBL17358926 0.86 GPBAR1 (0.50) GPBAR1ALDH1A1KMT2AMEN1NR1H4
SCHEMBL25942183 0.85 GPBAR1 (0.52) GPBAR1ALDH1A1KMT2ANR1H4TSHR
SCHEMBL17358925 0.85 GPBAR1 (0.49) GPBAR1ALDH1A1KMT2AMEN1NR1H4
SCHEMBL20031247 0.83 NR1H4 (0.52) GPBAR1KDM4ENR1H4
SCHEMBL28587444 0.83 GPBAR1 (0.44) GPBAR1PTGS1ALDH1A1KDM4EKMT2A
SCHEMBL29556452 0.82 NR1H4 (0.55) NR1H4
SCHEMBL22570925 0.82 EPAS1 (0.47) GPBAR1PTGS1ALDH1A1KDM4EKMT2A

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-20230357244-A1 FXR SMALL-MOLECULE AGONIST, AND PREPARATION METHOD THEREFOR AND USE THEREOF SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES (CN) 2023-11-09 — — US disclosed
US-20230295141-A1 FXR SMALL MOLECULE AGONIST, THE PREPARATION AND USE THEREOF CASCADE PHARMACEUTICALS, INC. (CN) 2023-09-21 — — US disclosed
US-20220213083-A1 FXR SMALL MOLECULE AGONIST AND PREPARATION METHOD THEREFOR AND USE THEREOF VAN ANDEL RESEARCH INSTITUTE 2022-07-07 — — US disclosed
WO-2022068815-A1 FXR SMALL-MOLECULE AGONIST, AND PREPARATION METHOD THEREFOR AND USE THEREOF 中国科学院上海药物研究所 2022-04-07 — — WO disclosed
WO-2020211872-A1 FXR SMALL MOLECULE AGONIST AND PREPARATION METHOD THEREFOR AND USE THEREOF 中国科学院上海药物研究所 2020-10-22 — — WO disclosed
EP-2655370-B1 COMPOSITIONS AND METHODS FOR MODULATING FXR NOVARTIS AG (CH) 2017-08-02 — — EP disclosed
EP-2655370-B1 COMPOSITIONS AND METHODS FOR MODULATING FXR NOVARTIS AG (CH) 2017-08-02 — — EP disclosed
US-20150366856-A1 COMPOUNDS AND METHODS FOR MODULATING FXR NOVARTIS AG (CH) 2015-12-24 — — US disclosed
US-20150366856-A1 COMPOUNDS AND METHODS FOR MODULATING FXR NOVARTIS AG (CH) 2015-12-24 — — US disclosed
US-20150366856-A1 COMPOUNDS AND METHODS FOR MODULATING FXR NOVARTIS AG (CH) 2015-12-24 — — US disclosed
US-9150568-B2 Compositions and methods for modulating FXR NOVARTIS AG (CH) 2015-10-06 — — US disclosed
US-9150568-B2 Compositions and methods for modulating FXR NOVARTIS AG (CH) 2015-10-06 — — US disclosed
US-9150568-B2 Compositions and methods for modulating FXR NOVARTIS AG (CH) 2015-10-06 — — US disclosed
US-20140039007-A1 COMPOSITIONS AND METHODS FOR MODULATING FARNESOID X RECEPTORS TULLY DAVID C (US) 2014-02-06 — — US disclosed
US-20130331349-A1 COMPOSITIONS AND METHODS FOR MODULATING FXR IRM LLC (BM) 2013-12-12 — — US disclosed
EP-2655370-A1 COMPOSITIONS AND METHODS FOR MODULATING FXR IRM LLC (BM) 2013-10-30 — — EP disclosed
WO-2012087519-A1 COMPOSITIONS AND METHODS FOR MODULATING FXR IRM LLC (BM) 2012-06-28 — — WO disclosed
WO-2012087519-A1 COMPOSITIONS AND METHODS FOR MODULATING FXR IRM LLC (BM) 2012-06-28 — — 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 (6 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-20230295141-A1 FXR SMALL MOLECULE AGONIST, THE PREPARATION AND USE THEREOF FXR1, NR1H4, FXR2 GPBAR1 4/4885PTGS1 1197/4885ALDH1A1 2240/4885
US-20150366856-A1 COMPOUNDS AND METHODS FOR MODULATING FXR NR1H4, SLC10A1, FXR1 GPBAR1 6/4885PTGS1 1202/4885ALDH1A1 2611/4885
US-20140039007-A1 COMPOSITIONS AND METHODS FOR MODULATING FARNESOID X RECEPTORS NR1H4, GPBAR1, SLC10A1 GPBAR1 2/4885PTGS1 1267/4885ALDH1A1 2875/4885
US-20220213083-A1 FXR SMALL MOLECULE AGONIST AND PREPARATION METHOD THEREFOR AND USE THEREOF FXR1, NR1H4, FXR2 GPBAR1 4/4885PTGS1 840/4885ALDH1A1 2516/4885
US-20230357244-A1 FXR SMALL-MOLECULE AGONIST, AND PREPARATION METHOD THEREFOR AND USE THEREOF FXR1, NR1H4, FXR2 GPBAR1 6/4885PTGS1 951/4885ALDH1A1 2161/4885
US-20130331349-A1 COMPOSITIONS AND METHODS FOR MODULATING FXR NR1H4, SLC10A1, FXR1 GPBAR1 5/4885PTGS1 1210/4885ALDH1A1 2951/4885

“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.

Send feedback