SCHEMBL3223877

SCHEMBL3223877

Cc1ccc(C(=O)Nc2ccc(F)cc2)cc1

nearest known ligand 0.81

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 6/20 0.81
NPC1 O15118 5/20 0.81
PTPN1 P18031 1/20 0.73
MEN1 O00255 5/20 0.73
KMT2A Q03164 5/20 0.73
MITF O75030 1/20 0.71
ATM Q13315 1/20 0.70
MAPT P10636 1/20 0.68
SMN1; SMN2 Q16637 1/20 0.68
POLB P06746 2/20 0.65
TDP1 Q9NUW8 1/20 0.65
SNCA P37840 1/20 0.63
NOS1 P29475 1/20 0.60
NOS2 P35228 1/20 0.60
KDM4E B2RXH2 1/20 0.59

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
SCHEMBL10192214 1.00 RAB9A (0.81) RAB9ANPC1PTPN1MEN1KMT2A
Hydrochloric Acid SCHEMBL5794257 0.98 RAB9A (0.79) RAB9ANPC1PTPN1MEN1KMT2A
SCHEMBL15164871 0.91 NPC1 (0.68) RAB9ANPC1PTPN1MEN1KMT2A
SCHEMBL14580374 0.90 RAB9A (1.00) RAB9ANPC1MEN1KMT2AMAPT
SCHEMBL12310125 0.90 RAB9A (1.00) RAB9ANPC1MEN1KMT2AMAPT
SCHEMBL27181403 0.90 RAB9A (1.00) RAB9ANPC1MEN1KMT2AMAPT
SCHEMBL10684470 0.90 PTPN1 (0.88) RAB9ANPC1PTPN1MEN1KMT2A
SCHEMBL822378 0.90 RAB9A (1.00) RAB9ANPC1MEN1KMT2AMAPT
SCHEMBL15214321 0.90 RAB9A (1.00) RAB9ANPC1MEN1KMT2AMAPT
SCHEMBL14433920 0.86 PTPN1 (0.69) RAB9ANPC1PTPN1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101495475-A Process for preparing pyrido[2,3-d]pyrimidin-7-one and 3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one derivatives GLAXO GROUP LTD (GB) 2009-07-29 CN claimed
EP-2034838-A2 NOVEL COMPOUNDS Glaxo Group Limited (GB) 2009-03-18 EP claimed
EP-2032142-A2 NOVEL COMPOUNDS GLAXO GROUP LIMITED (GB) 2009-03-11 EP claimed
US-20080096905-A1 Process For Preparing Pyrido[2,3-D]Pyrimidin-7-One And 3,4-Dihydropyrimido{4,5-D}Pyrimidin-2(1H)-One Derivatives GLAXO GROUP LIMITED (GB) 2008-04-24 US claimed
WO-2007147103-A2 NOVEL COMPOUNDS GLAXO GROUP LIMITED (GB) 2007-12-21 WO claimed
WO-2007147109-A2 NOVEL COMPOUNDS GLAXO GROUP LIMITED (GB) 2007-12-21 WO claimed
EP-1865959-A2 PROCESS FOR PREPARING PYRIDOÝ2,3-D¨PYRIMIDIN-7-ONE AND 3,4-DIHYDROPYRIMIDOÝ4,5-D¨PYRIMIDIN-2(1H)-ONE DERIVATIVES GLAXO GROUP LIMITED (GB) 2007-12-19 EP claimed
US-20060258687-A1 Process for preparing pyrido[2,3-d]pyrimidin-7-one and 3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one derivatives GLAXO GROUP LIMITED (GB) 2006-11-16 US claimed
WO-2006104917-A2 PROCESS FOR PREPARING PYRIDO[2,3-D]PYRIMIDIN-7-ONE AND 3,4-DIHYDROPYRIMIDO[4,5-D]PYRIMIDIN-2(1H)-ONE DERIVATIVES GLAXO GROUP LIMITED (GB) 2006-10-05 WO claimed
CN-115304506-B Preparation method of secondary amide compound by activating primary amide through boron salt catalysis 中国人民解放军国防科技大学 2023-11-14 CN disclosed
US-20230157996-A1 SMALL-MOLECULE INHIBITOR TARGETING EB VIRUS NUCLEAR ANTIGEN PROTEIN, PREPARATION METHOD AND USE THEREOF Shenzhen Bay Laboratory (CN) 2023-05-25 US disclosed
CN-115974711-A Preparation method of aryl amide compound by using aromatic ester catalytically activated by boron salt 湖南农业大学 2023-04-18 CN disclosed
CN-115304506-A Preparation method of secondary amide compound by activating primary amide under catalysis of boron salt 中国人民解放军国防科技大学 2022-11-08 CN disclosed
CN-107628964-B A kind of synthetic method of N- aryl Zhong Fang amide 陕西科技大学 2019-06-21 CN disclosed
CN-101184758-A Novel compounds GLAXO GROUP LTD (GB) 2008-05-21 CN disclosed
US-20080096905-A1 Process For Preparing Pyrido[2,3-D]Pyrimidin-7-One And 3,4-Dihydropyrimido{4,5-D}Pyrimidin-2(1H)-One Derivatives GLAXO GROUP LIMITED (GB) 2008-04-24 US disclosed
WO-2006104915-A9 8-PHENYL-7,8-DIHYDROPYRIDO[2,3-d]PYRIMIDIN-7-ONES AND THEIR USE AS PHARMACEUTICALS GLAXO GROUP LTD (GB) 2008-01-03 WO disclosed
EP-1865959-A2 PROCESS FOR PREPARING PYRIDOÝ2,3-D¨PYRIMIDIN-7-ONE AND 3,4-DIHYDROPYRIMIDOÝ4,5-D¨PYRIMIDIN-2(1H)-ONE DERIVATIVES GLAXO GROUP LIMITED (GB) 2007-12-19 EP disclosed
US-20060258687-A1 Process for preparing pyrido[2,3-d]pyrimidin-7-one and 3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one derivatives GLAXO GROUP LIMITED (GB) 2006-11-16 US disclosed
WO-2006104917-A2 PROCESS FOR PREPARING PYRIDO[2,3-D]PYRIMIDIN-7-ONE AND 3,4-DIHYDROPYRIMIDO[4,5-D]PYRIMIDIN-2(1H)-ONE DERIVATIVES GLAXO GROUP LIMITED (GB) 2006-10-05 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-20230157996-A1 SMALL-MOLECULE INHIBITOR TARGETING EB VIRUS NUCLEAR ANTIGEN PROTEIN, PREPARATION METHOD AND USE THEREOF SSB, EBNA1BP2, PML RAB9A 1810/4885NPC1 1422/4885PTPN1 2596/4885
US-20060258687-A1 Process for preparing pyrido[2,3-d]pyrimidin-7-one and 3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one derivatives CBR3, CBR1, CYP2S1 RAB9A 1737/4885NPC1 4045/4885PTPN1 2282/4885
US-20080096905-A1 Process For Preparing Pyrido[2,3-D]Pyrimidin-7-One And 3,4-Dihydropyrimido{4,5-D}Pyrimidin-2(1H)-One Derivatives CYP2S1, CYP2F1, CBR3 RAB9A 1800/4885NPC1 3552/4885PTPN1 2339/4885

“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.