Sugi Predict

Sugi Predict / Compounds / SCHEMBL3199702

SCHEMBL3199702

SCHEMBL3199702

Cc1ccc(NC(=O)Nc2cccc(CCCN3CCN(C(=O)O)CC3)c2F)cn1

nearest known ligand 0.43

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ DDX3X O00571 3/20 0.43
▸ MAPK10 P53779 8/20 0.42
▸ MAPK8 P45983 7/20 0.42
▸ RORC P51449 1/20 0.41
▸ DHODH Q02127 1/20 0.41
▸ NPSR1 Q6W5P4 1/20 0.41
▸ HTR1A P08908 2/20 0.41
▸ HTR1D P28221 2/20 0.41
▸ HTR1B P28222 2/20 0.41
▸ CCR3 P51677 2/20 0.41
▸ FPR3 P25089 1/20 0.39
▸ FPR2 P25090 1/20 0.39
▸ NPC1 O15118 1/20 0.39
▸ RAB9A P51151 1/20 0.39
▸ SMN1; SMN2 Q16637 1/20 0.39
▸ MAPK9 P45984 1/20 0.39
▸ EPHX2 P34913 1/20 0.38

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
SCHEMBL5653128 0.95 CCR3 (0.46) DDX3XMAPK10MAPK8RORCDHODH
SCHEMBL460041 0.94 DDX3X (0.43) DDX3XMAPK10MAPK8RORCDHODH
SCHEMBL401118 0.92 DDX3X (0.42) DDX3XMAPK10MAPK8RORCDHODH
SCHEMBL401741 0.91 ALDH1A1 (0.43) DDX3XMAPK10MAPK8SMN1; SMN2
SCHEMBL10315559 0.90 HRH3 (0.46) DDX3XMAPK10MAPK8NPSR1CCR3
SCHEMBL3196731 0.89 RORC (0.50) MAPK10MAPK8RORCDHODHNPSR1
SCHEMBL401388 0.88 MAPK10 (0.43) DDX3XMAPK10MAPK8NPSR1CCR3
SCHEMBL402606 0.88 EPHX2 (0.46) DDX3XMAPK10MAPK8SMN1; SMN2EPHX2
SCHEMBL545121 0.88 DDX3X (0.42) DDX3XMAPK10MAPK8NPSR1HTR1A
SCHEMBL8239429 0.86 DDX3X (0.41) DDX3XMAPK10MAPK8NPSR1HTR1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220185779-A1 COMPOUNDS, COMPOSITIONS AND METHODS CYTOKINETICS, INCORPORATED 2022-06-16 — — 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-10035770-B2 Compounds, compositions and methods CYTOKINETICS, INCORPORATED (US) 2018-07-31 — — US disclosed
US-20170267638-A1 COMPOUNDS, COMPOSITIONS AND METHODS CYTOKINETICS, INCORPORATED 2017-09-21 — — US disclosed
US-9643925-B2 Compounds, compositions and methods CYTOKINETICS, INCORPORATED 2017-05-09 — — US disclosed
US-20160115133-A1 COMPOUNDS, COMPOSITIONS AND METHODS CYTOKINETICS, INCORPORATED 2016-04-28 — — US disclosed
US-9150564-B2 Compounds, compositions and methods CYTOKINETICS, INC. (US) 2015-10-06 — — US disclosed
US-20120172372-A1 Ureas and Their Use in the Treatment of Heart Failure CYTOKINETICS, INC. 2012-07-05 — — US disclosed
US-20100029680-A1 Certain Chemical Entities, Compositions and Methods CYTOKINETICS, INC. 2010-02-04 — — US disclosed
US-20090247544-A1 Certain Chemical Entities, Compositions and Methods CYTOKINETICS, INC. 2009-10-01 — — 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 (17 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-20120172372-A1 Ureas and Their Use in the Treatment of Heart Failure TNNI3, TNNT2, MYLK2 DDX3X 2715/4885MAPK10 2342/4885MAPK8 3165/4885
US-20070161617-A1 Certain chemical entities, compositions and methods TNNI3, TNNT2, MYLK2 DDX3X 1211/4885MAPK10 2458/4885MAPK8 3317/4885
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 DDX3X 2903/4885MAPK10 1989/4885MAPK8 2821/4885
US-20170267638-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 DDX3X 1478/4885MAPK10 2521/4885MAPK8 3460/4885
US-10385023-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 DDX3X 1478/4885MAPK10 2521/4885MAPK8 3460/4885
US-20220185779-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 DDX3X 1478/4885MAPK10 2521/4885MAPK8 3460/4885
US-20090099198-A1 Compounds, Compositions and Methods TNNI3, TNNC1, TNNT2 DDX3X 1478/4885MAPK10 2521/4885MAPK8 3460/4885
US-20190352267-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 DDX3X 1478/4885MAPK10 2521/4885MAPK8 3460/4885
US-20070208000-A1 Certain chemical entities, compositions and methods TNNI3, TNNT2, MYLK2 DDX3X 1211/4885MAPK10 2458/4885MAPK8 3317/4885
US-20070197505-A1 Certain chemical entities, compositions and methods TNNC1, TNNI3, TNNT2 DDX3X 1494/4885MAPK10 2706/4885MAPK8 3594/4885
US-20160115133-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 DDX3X 1478/4885MAPK10 2521/4885MAPK8 3460/4885
US-10975034-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 DDX3X 1478/4885MAPK10 2521/4885MAPK8 3460/4885
US-10035770-B2 Compounds, compositions and methods TNNI3, TNNC1, TNNT2 DDX3X 1478/4885MAPK10 2521/4885MAPK8 3460/4885
US-20100029680-A1 Certain Chemical Entities, Compositions and Methods TNNI3, TNNT2, MYLK2 DDX3X 1211/4885MAPK10 2458/4885MAPK8 3317/4885
US-20090036447-A1 Compounds, Compositions and Methods TNNI3, TNNC1, TNNT2 DDX3X 1478/4885MAPK10 2521/4885MAPK8 3460/4885
US-20180305316-A1 COMPOUNDS, COMPOSITIONS AND METHODS TNNI3, TNNC1, TNNT2 DDX3X 1478/4885MAPK10 2521/4885MAPK8 3460/4885
US-20090247544-A1 Certain Chemical Entities, Compositions and Methods TNNC1, TNNI3, TNNT2 DDX3X 1494/4885MAPK10 2706/4885MAPK8 3594/4885

“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.