SCHEMBL398795

SCHEMBL398795

Cc1ccc(NC(=O)Nc2cc(CN3CC[C@H](N(C)C(=O)C(C)C)C3)ccc2F)cn1

nearest known ligand 0.40

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CCR3 P51677 10/20 0.40
DRD2 P14416 1/20 0.39
ADRA1A P35348 1/20 0.39
THRB P10828 1/20 0.38
GALR3 O60755 1/20 0.38
RAB9A P51151 1/20 0.38
PDGFRB P09619 2/20 0.37
KDR P35968 2/20 0.37
MELK Q14680 1/20 0.37
S1PR1 P21453 1/20 0.37
MEN1 O00255 1/20 0.37
KMT2A Q03164 1/20 0.37
MAPK8 P45983 1/20 0.37
MAPK10 P53779 1/20 0.37

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
SCHEMBL399042 1.00 CCR3 (0.40) CCR3DRD2ADRA1ATHRBGALR3
SCHEMBL4011647 1.00 CCR3 (0.40) CCR3DRD2ADRA1ATHRBGALR3
SCHEMBL399032 0.95 KMT2A (0.41) CCR3RAB9AMEN1KMT2A
SCHEMBL544986 0.95 KMT2A (0.41) CCR3RAB9AMEN1KMT2A
SCHEMBL4012403 0.95 KMT2A (0.41) CCR3RAB9AMEN1KMT2A
SCHEMBL402485 0.95 CCR3 (0.43) CCR3DRD2ADRA1ATHRBGALR3
SCHEMBL4002497 0.91 JAK2 (0.43) CCR3THRBGALR3RAB9APDGFRB
SCHEMBL400960 0.91 JAK2 (0.43) CCR3THRBGALR3RAB9APDGFRB
SCHEMBL398992 0.91 JAK2 (0.43) CCR3THRBGALR3RAB9APDGFRB
SCHEMBL400464 0.90 CCR3 (0.39) CCR3DRD2ADRA1AGALR3RAB9A

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 40 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-8110595-B2 Ureas and their use in the treatment of heart failure CYTOKINETICS, INC. (US) 2012-02-07 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-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-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 (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 CCR3 4640/4885DRD2 4660/4885ADRA1A 1491/4885
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 CCR3 4670/4885DRD2 4395/4885ADRA1A 2135/4885
US-10385023-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 CCR3 4522/4885DRD2 4679/4885ADRA1A 1505/4885
US-20220185779-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 CCR3 4522/4885DRD2 4679/4885ADRA1A 1505/4885
US-12264133-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 CCR3 4522/4885DRD2 4679/4885ADRA1A 1505/4885
US-20090099198-A1 Compounds, Compositions and Methods TNNI3, TNNC1, TNNT2 CCR3 4522/4885DRD2 4679/4885ADRA1A 1505/4885
US-20190352267-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 CCR3 4522/4885DRD2 4679/4885ADRA1A 1505/4885
US-20070208000-A1 Certain chemical entities, compositions and methods TNNI3, TNNT2, MYLK2 CCR3 4640/4885DRD2 4660/4885ADRA1A 1491/4885
US-20150005296-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 CCR3 4522/4885DRD2 4679/4885ADRA1A 1505/4885
US-10975034-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 CCR3 4522/4885DRD2 4679/4885ADRA1A 1505/4885
US-20090036447-A1 Compounds, Compositions and Methods TNNI3, TNNC1, TNNT2 CCR3 4522/4885DRD2 4679/4885ADRA1A 1505/4885
US-20180305316-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 CCR3 4522/4885DRD2 4679/4885ADRA1A 1505/4885
US-20210198203-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 CCR3 4522/4885DRD2 4679/4885ADRA1A 1505/4885

“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.