SCHEMBL2294891

SCHEMBL2294891

O=C(CCl)N(Cc1ccccc1)C[C@@H](O)c1ccc(F)cc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 3/20 0.46
NPC1 O15118 2/20 0.46
RAB9A P51151 2/20 0.46
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
YAP1 P46937 1/20 0.45
TEAD4 Q15561 1/20 0.45
TEAD2 Q15562 1/20 0.45
ALDH1A1 P00352 5/20 0.44
HTT P42858 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
GLA P06280 1/20 0.44
PAX8 Q06710 1/20 0.44
KDM4E B2RXH2 3/20 0.43
AOC3 Q16853 1/20 0.42
CNR2 P34972 1/20 0.41
LMNA P02545 2/20 0.41
NPSR1 Q6W5P4 2/20 0.41
EGFR P00533 1/20 0.39
ERBB2 P04626 1/20 0.39

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
SCHEMBL25181454 1.00 TDP1 (0.46) TDP1NPC1RAB9AMEN1KMT2A
SCHEMBL2296124 1.00 TDP1 (0.46) TDP1NPC1RAB9AMEN1KMT2A
SCHEMBL2294032 0.87 MEN1 (0.46) TDP1NPC1RAB9AMEN1KMT2A
SCHEMBL27711319 0.87 MEN1 (0.46) TDP1NPC1RAB9AMEN1KMT2A
SCHEMBL2291932 0.87 MEN1 (0.46) TDP1NPC1RAB9AMEN1KMT2A
SCHEMBL2296266 0.87 KDM4E (0.42) TDP1MEN1KMT2AALDH1A1HTT
SCHEMBL2294819 0.87 KDM4E (0.42) TDP1MEN1KMT2AALDH1A1HTT
SCHEMBL2293196 0.83 CRHBP (0.55) TDP1NPC1RAB9AMEN1KMT2A
SCHEMBL2295641 0.83 CRHBP (0.55) TDP1NPC1RAB9AMEN1KMT2A
SCHEMBL2295326 0.83 ALOX5 (0.49) NPC1RAB9AMEN1KMT2ASMN1; 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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090156804-A1 INTERMEDIATE COMPOUND FOR SYNTHESIZING PHARMACEUTICAL AGENT AND PRODUCTION METHOD THEREOF MITSUBISHI TANABE PHARMA CORPORATION (JP) 2009-06-18 US claimed
EP-2809661-B1 NOVEL MORPHOLINYL DERIVATIVES USEFUL AS MOGAT-2 INHIBITORS LILLY CO ELI (US) 2016-04-06 EP disclosed
EP-2809661-B1 NOVEL MORPHOLINYL DERIVATIVES USEFUL AS MOGAT-2 INHIBITORS LILLY CO ELI (US) 2016-04-06 EP disclosed
US-8993568-B2 Morpholinyl derivatives useful as MOGAT-2 inhibitors ELI LILLY AND COMPANY (US) 2015-03-31 US disclosed
US-8993568-B2 Morpholinyl derivatives useful as MOGAT-2 inhibitors ELI LILLY AND COMPANY (US) 2015-03-31 US disclosed
US-8993568-B2 Morpholinyl derivatives useful as MOGAT-2 inhibitors ELI LILLY AND COMPANY (US) 2015-03-31 US disclosed
US-20150005305-A1 NOVEL MORPHOLINYL DERIVATIVES USEFUL AS MOGAT-2 INHIBITORS ELI LILLY AND COMPANY (US) 2015-01-01 US disclosed
US-20150005305-A1 NOVEL MORPHOLINYL DERIVATIVES USEFUL AS MOGAT-2 INHIBITORS ELI LILLY AND COMPANY (US) 2015-01-01 US disclosed
US-20150005305-A1 NOVEL MORPHOLINYL DERIVATIVES USEFUL AS MOGAT-2 INHIBITORS ELI LILLY AND COMPANY (US) 2015-01-01 US disclosed
EP-2809661-A1 NOVEL MORPHOLINYL DERIVATIVES USEFUL AS MOGAT-2 INHIBITORS Eli Lilly and Company (US) 2014-12-10 EP disclosed
CN-104080777-A Morpholinyl derivatives as MOGAT-2 inhibitors LILLY CO ELI 2014-10-01 CN disclosed
WO-2013116075-A1 BENZYL SULFONAMIDE DERIVATIVES USEFUL AS MOGAT - 2 INHIBITORS ELI LILLY AND COMPANY (US) 2013-08-08 WO disclosed
WO-2013116065-A1 NOVEL MORPHOLINYL DERIVATIVES USEFUL AS MOGAT-2 INHIBITORS ELI LILLY AND COMPANY (US) 2013-08-08 WO disclosed
WO-2013116065-A1 NOVEL MORPHOLINYL DERIVATIVES USEFUL AS MOGAT-2 INHIBITORS ELI LILLY AND COMPANY (US) 2013-08-08 WO disclosed
US-20110257392-A1 INTERMEDIATE COMPOUND FOR SYNTHESIZING PHARMACEUTICAL AGENT AND PRODUCTION METHOD THEREOF SANOFI-AVENTIS (FR) 2011-10-20 US disclosed
US-20110251385-A1 INTERMEDIATE COMPOUND FOR SYNTHESIZING PHARMACEUTICAL AGENT AND PRODUCTION METHOD THEREOF SANOFI-AVENTIS (FR) 2011-10-13 US disclosed
US-7994315-B2 Intermediate compound for synthesizing pharmaceutical agent and production method thereof MITSUBISHI TANABE PHARMA CORPORATION (JP) 2011-08-09 US disclosed
EP-2221305-A1 Method for synthesizing intermediate compound for synthesizing a pharmaceutical agent Mitsubishi Tanabe Pharma Corporation (JP) 2010-08-25 EP disclosed
EP-2221304-A1 Method for synthesizing intermediate compound for synthesizing a pharmaceutical agent Mitsubishi Tanabe Pharma Corporation (JP) 2010-08-25 EP disclosed
US-20090156804-A1 INTERMEDIATE COMPOUND FOR SYNTHESIZING PHARMACEUTICAL AGENT AND PRODUCTION METHOD THEREOF MITSUBISHI TANABE PHARMA CORPORATION (JP) 2009-06-18 US 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 (4 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-20110257392-A1 INTERMEDIATE COMPOUND FOR SYNTHESIZING PHARMACEUTICAL AGENT AND PRODUCTION METHOD THEREOF MAPT, PSEN1, PSEN2 TDP1 659/4885NPC1 1685/4885RAB9A 3397/4885
US-20110251385-A1 INTERMEDIATE COMPOUND FOR SYNTHESIZING PHARMACEUTICAL AGENT AND PRODUCTION METHOD THEREOF MAPT, PSEN1, PSEN2 TDP1 659/4885NPC1 1685/4885RAB9A 3397/4885
US-20090156804-A1 INTERMEDIATE COMPOUND FOR SYNTHESIZING PHARMACEUTICAL AGENT AND PRODUCTION METHOD THEREOF MAPT, PSEN1, PSEN2 TDP1 659/4885NPC1 1685/4885RAB9A 3397/4885
US-20150005305-A1 NOVEL MORPHOLINYL DERIVATIVES USEFUL AS MOGAT-2 INHIBITORS MOGAT2, SOAT2, SOAT1 TDP1 2511/4885NPC1 29/4885RAB9A 3424/4885

“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.