SCHEMBL402765

SCHEMBL402765

Cc1ccc(NC(=O)Nc2cc(F)cc(CN3CCN4C(=O)OC[C@H]4C3)c2)cn1

nearest known ligand 0.41

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 2/20 0.41
PARP1 P09874 4/20 0.40
GRIN2B Q13224 2/20 0.36
ADRB2 P07550 2/20 0.36
RORC P51449 1/20 0.36
MTOR P42345 3/20 0.36
PIK3R1 P27986 2/20 0.36
MAPK10 P53779 3/20 0.36
MAPK8 P45983 2/20 0.36
KCNQ3 O43525 1/20 0.36
KCNQ2 O43526 1/20 0.36
BRAF P15056 1/20 0.35
KDR P35968 1/20 0.35
NPY5R Q15761 1/20 0.35

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
SCHEMBL402476 1.00 LTA4H (0.41) LTA4HPARP1GRIN2BADRB2RORC
SCHEMBL4238184 1.00 LTA4H (0.41) LTA4HPARP1GRIN2BADRB2RORC
SCHEMBL23573826 0.90 LTA4H (0.43) LTA4HPARP1GRIN2BADRB2RORC
SCHEMBL23573800 0.90 LTA4H (0.43) LTA4HPARP1GRIN2BADRB2RORC
SCHEMBL397586 0.88 LTA4H (0.42) LTA4HPARP1MTORPIK3R1MAPK10
SCHEMBL401672 0.88 LTA4H (0.42) LTA4HPARP1MTORPIK3R1MAPK10
SCHEMBL3198756 0.82 SIRT2 (0.40) LTA4HPARP1RORCMTORPIK3R1
SCHEMBL3198667 0.82 SIRT2 (0.40) LTA4HPARP1RORCMTORPIK3R1
SCHEMBL400317 0.81 PLK4 (0.38) GRIN2BADRB2RORCMAPK10MAPK8
SCHEMBL401842 0.81 PLK4 (0.38) GRIN2BADRB2RORCMAPK10MAPK8

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 39 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
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-20180305316-A1 COMPOUNDS, COMPOSITIONS AND METHODS CYTOKINETICS, INCORPORATED 2018-10-25 US disclosed
US-20090099198-A1 Compounds, Compositions and Methods CYTOKINETICS, INC. 2009-04-16 US disclosed
US-7507735-B2 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, INC. (US) 2009-03-24 US disclosed
US-20090036447-A1 Compounds, Compositions and Methods CYTOKINETICS, INC. (US) 2009-02-05 US 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
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 (14 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 LTA4H 3839/4885PARP1 4871/4885GRIN2B 4683/4885
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 LTA4H 4548/4885PARP1 4712/4885GRIN2B 4732/4885
US-10385023-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 LTA4H 4058/4885PARP1 4835/4885GRIN2B 4653/4885
US-20220185779-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 LTA4H 4058/4885PARP1 4835/4885GRIN2B 4653/4885
US-12264133-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 LTA4H 4058/4885PARP1 4835/4885GRIN2B 4653/4885
US-20090099198-A1 Compounds, Compositions and Methods TNNI3, TNNC1, TNNT2 LTA4H 4058/4885PARP1 4835/4885GRIN2B 4653/4885
US-20190352267-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 LTA4H 4058/4885PARP1 4835/4885GRIN2B 4653/4885
US-20070208000-A1 Certain chemical entities, compositions and methods TNNI3, TNNT2, MYLK2 LTA4H 3839/4885PARP1 4871/4885GRIN2B 4683/4885
US-20070197505-A1 Certain chemical entities, compositions and methods TNNC1, TNNI3, TNNT2 LTA4H 3020/4885PARP1 3956/4885GRIN2B 4268/4885
US-20150005296-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 LTA4H 4058/4885PARP1 4835/4885GRIN2B 4653/4885
US-10975034-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 LTA4H 4058/4885PARP1 4835/4885GRIN2B 4653/4885
US-20090036447-A1 Compounds, Compositions and Methods TNNI3, TNNC1, TNNT2 LTA4H 4058/4885PARP1 4835/4885GRIN2B 4653/4885
US-20180305316-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 LTA4H 4058/4885PARP1 4835/4885GRIN2B 4653/4885
US-20210198203-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 LTA4H 4058/4885PARP1 4835/4885GRIN2B 4653/4885

“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.