SCHEMBL400383

SCHEMBL400383

CCS(=O)(=O)N1CCN(CCCc2cc(F)cc(NC(=O)Nc3ccc(OC)nc3)c2)CC1

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 7/20 0.45
MEN1 O00255 6/20 0.45
PABPC1 P11940 4/20 0.45
NPC1 O15118 5/20 0.41
MAPT P10636 5/20 0.41
FPR3 P25089 1/20 0.41
FPR2 P25090 1/20 0.41
ALDH1A1 P00352 5/20 0.40
LMNA P02545 5/20 0.40
S1PR2 O95136 3/20 0.40
S1PR4 O95977 3/20 0.40
S1PR1 P21453 3/20 0.40
NPSR1 Q6W5P4 3/20 0.40
RAB9A P51151 3/20 0.40
SMN1; SMN2 Q16637 3/20 0.40
HTT P42858 2/20 0.40
TLR9 Q9NR96 1/20 0.40
XBP1 P17861 1/20 0.40
EPHX2 P34913 1/20 0.40
USP2 O75604 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
SCHEMBL402430 0.89 HTR1A (0.42) KMT2AMEN1MAPTFPR3FPR2
SCHEMBL3204846 0.88 MEN1 (0.47) KMT2AMEN1PABPC1NPC1MAPT
SCHEMBL400040 0.88 MEN1 (0.47) KMT2AMEN1PABPC1NPC1MAPT
SCHEMBL400961 0.88 MEN1 (0.47) KMT2AMEN1PABPC1NPC1MAPT
SCHEMBL4299685 0.84 UBE2M (0.40) KMT2AMEN1NPC1MAPTALDH1A1
SCHEMBL399090 0.83 HTR1A (0.50) KMT2AMEN1NPC1MAPTALDH1A1
SCHEMBL402096 0.80 CYP1A2 (0.46) FPR3FPR2ALDH1A1LMNAEPHX2
SCHEMBL23573834 0.79 PIK3CA (0.45) MAPTFPR3FPR2ALDH1A1RAB9A
SCHEMBL401663 0.78 HTR1A (0.42) MAPTFPR3FPR2EPHX2ADRA2A
SCHEMBL402023 0.78 KDM4E (0.43) NPC1MAPTLMNANPSR1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210198203-A1 COMPOUNDS, COMPOSITIONS AND METHODS CYTOKINETICS, INCORPORATED 2021-07-01 US claimed
US-20190352267-A1 COMPOUNDS, COMPOSITIONS AND METHODS CYTOKINETICS, INCORPORATED 2019-11-21 US claimed
US-20180305316-A1 COMPOUNDS, COMPOSITIONS AND METHODS CYTOKINETICS, INCORPORATED 2018-10-25 US claimed
EP-2862859-A2 Compounds, compositions and methods Cytokinetics, Inc. (US) 2015-04-22 EP claimed
US-20150005296-A1 COMPOUNDS, COMPOSITIONS AND METHODS CYTOKINETICS, INCORPORATED 2015-01-01 US claimed
US-20090036447-A1 Compounds, Compositions and Methods CYTOKINETICS, INC. (US) 2009-02-05 US claimed
US-20060014761-A1 Substituted urea derivatives activate the cardiac sarcomere by potentiating cardiac myosin; systolic heart failure including congestive heart failure; 4-[(3-fluoro-5-{[(6-methyl(3-pyridyl))amino]carbonylamino}-phenyl)methyl]piperazinecarboxylate CYTOKINETICS, INCORPORATED 2006-01-19 US claimed
US-12264133-B2 Compounds, compositions and methods CYTOKINETICS, INCORPORATED (US) 2025-04-01 US disclosed
US-20220185779-A1 COMPOUNDS, COMPOSITIONS AND METHODS CYTOKINETICS, INCORPORATED 2022-06-16 US disclosed
US-20210198203-A1 COMPOUNDS, COMPOSITIONS AND METHODS CYTOKINETICS, INCORPORATED 2021-07-01 US disclosed
US-10975034-B2 Compounds, compositions and methods CYTOKINETICS, INC. (US) 2021-04-13 US disclosed
US-20190352267-A1 COMPOUNDS, COMPOSITIONS AND METHODS CYTOKINETICS, INCORPORATED 2019-11-21 US disclosed
US-10385023-B2 Compounds, compositions and methods CYTOKINETICS, INC. (US) 2019-08-20 US disclosed
US-20090036447-A1 Compounds, Compositions and Methods CYTOKINETICS, INC. (US) 2009-02-05 US disclosed
EP-1959960-A2 CERTAIN CHEMICAL ENTITIES, COMPOSITIONS AND METHODS Cytokinetics, Inc. (US) 2008-08-27 EP disclosed
US-20070208000-A1 Certain chemical entities, compositions and methods CYTOKINETICS, INC. 2007-09-06 US disclosed
US-20070197505-A1 Certain chemical entities, compositions and methods CYTOKINETICS, INC. 2007-08-23 US disclosed
US-20070161617-A1 Certain chemical entities, compositions and methods CYTOKINETICS, INC. 2007-07-12 US disclosed
WO-2007070683-A2 CERTAIN CHEMICAL ENTITIES, COMPOSITIONS AND METHODS CYTOKINETICS, INC. (US) 2007-06-21 WO disclosed
US-20060014761-A1 Substituted urea derivatives activate the cardiac sarcomere by potentiating cardiac myosin; systolic heart failure including congestive heart failure; 4-[(3-fluoro-5-{[(6-methyl(3-pyridyl))amino]carbonylamino}-phenyl)methyl]piperazinecarboxylate CYTOKINETICS, INCORPORATED 2006-01-19 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 (13 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-20070161617-A1 Certain chemical entities, compositions and methods TNNI3, TNNT2, MYLK2 KMT2A 4052/4885MEN1 4319/4885PABPC1 2199/4885
US-20060014761-A1 Substituted urea derivatives activate the cardiac sarcomere by potentiating cardiac myosin; systolic heart failure including congestive heart failure; 4-[(3-fluoro-5-{[(6-methyl(3-pyridyl))amino]carbonylamino}-phenyl)methyl]piperazinecarboxylate TNNI3, MYLK2, TNNT2 KMT2A 2999/4885MEN1 4745/4885PABPC1 1282/4885
US-10385023-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 KMT2A 4396/4885MEN1 4344/4885PABPC1 2166/4885
US-20220185779-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 KMT2A 4396/4885MEN1 4344/4885PABPC1 2166/4885
US-12264133-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 KMT2A 4396/4885MEN1 4344/4885PABPC1 2166/4885
US-20190352267-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 KMT2A 4396/4885MEN1 4344/4885PABPC1 2166/4885
US-20070208000-A1 Certain chemical entities, compositions and methods TNNI3, TNNT2, MYLK2 KMT2A 4052/4885MEN1 4319/4885PABPC1 2199/4885
US-20070197505-A1 Certain chemical entities, compositions and methods TNNC1, TNNI3, TNNT2 KMT2A 4149/4885MEN1 4493/4885PABPC1 1234/4885
US-20150005296-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 KMT2A 4396/4885MEN1 4344/4885PABPC1 2166/4885
US-10975034-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 KMT2A 4396/4885MEN1 4344/4885PABPC1 2166/4885
US-20090036447-A1 Compounds, Compositions and Methods TNNI3, TNNC1, TNNT2 KMT2A 4396/4885MEN1 4344/4885PABPC1 2166/4885
US-20180305316-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 KMT2A 4396/4885MEN1 4344/4885PABPC1 2166/4885
US-20210198203-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 KMT2A 4396/4885MEN1 4344/4885PABPC1 2166/4885

“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.