Cenisertib

Cenisertib

SCHEMBL10086258

Cc1cc(Nc2ncc(F)c(NC3C(C(N)=O)[C@@H]4C=C[C@H]3C4)n2)ccc1N1CCN(C)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AURKAAURKBAURKC

The experimentally established mechanism targets of Cenisertib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AURKB known ✓ Q96GD4 7/20 1.00
AURKA known ✓ O14965 2/20 1.00
IRAK4 Q9NWZ3 11/20 1.00
KDR P35968 8/20 1.00
ALK Q9UM73 3/20 1.00
INSR P06213 2/20 1.00
MET P08581 2/20 1.00
LCK P06239 2/20 1.00
PDGFRA P16234 2/20 1.00
FLT3 P36888 2/20 1.00
SYK P43405 2/20 1.00
CDC7 O00311 1/20 1.00
PLK4 O00444 1/20 1.00
CHEK1 O14757 1/20 1.00
DCLK1 O15075 1/20 1.00
PDPK1 O15530 1/20 1.00
DAPK3 O43293 1/20 1.00
JAK2 O60674 1/20 1.00
ROCK2 O75116 1/20 1.00
PRKD3 O94806 1/20 1.00

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
Cenisertib SCHEMBL1079632 1.00 IRAK4 (1.00) IRAK4KDRAURKBALKINSR
Cenisertib SCHEMBL15169719 1.00 IRAK4 (1.00) IRAK4KDRAURKBALKINSR
Cenisertib SCHEMBL400147 1.00 IRAK4 (1.00) IRAK4KDRAURKBALKINSR
Cenisertib SCHEMBL1000933 1.00 IRAK4 (1.00) IRAK4KDRAURKBALKINSR
Cenisertib SCHEMBL30097376 1.00 IRAK4 (1.00) IRAK4KDRAURKBALKINSR
Cenisertib SCHEMBL15290367 1.00 IRAK4 (1.00) IRAK4KDRAURKBALKINSR
Cenisertib SCHEMBL1066287 1.00 IRAK4 (1.00) IRAK4KDRAURKBALKINSR
Cenisertib SCHEMBL352432 1.00 IRAK4 (1.00) IRAK4KDRAURKBALKINSR
Cenisertib SCHEMBL1001874 1.00 IRAK4 (1.00) IRAK4KDRAURKBALKINSR
Cenisertib SCHEMBL12972652 1.00 IRAK4 (1.00) IRAK4KDRAURKBALKINSR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9725419-B2 Cycloalkyl substituted pyrimidinediamine compounds and their uses RIGEL PHARMACEUTICALS, INC. (US) 2017-08-08 US disclosed
US-9725419-B2 Cycloalkyl substituted pyrimidinediamine compounds and their uses RIGEL PHARMACEUTICALS, INC. (US) 2017-08-08 US disclosed
US-20130210814-A1 Cycloalkyl Substituted Pyrimidinediamine Compounds And Their Uses RIGEL PHARMACEUTICALS, INC. (US) 2013-08-15 US disclosed
US-20130210814-A1 Cycloalkyl Substituted Pyrimidinediamine Compounds And Their Uses RIGEL PHARMACEUTICALS, INC. (US) 2013-08-15 US disclosed
US-8410093-B2 Cycloalkyl substituted pyrimidinediamine compounds and their uses RIGEL PHARMACEUTICALS, INC. (US) 2013-04-02 US disclosed
US-8101627-B2 Stereoisomerically enriched 3-aminocarbonyl bicycloheptene pyrimidinediamine compounds and their uses RIGEL PHARMACEUTICALS, INC. (US) 2012-01-24 US disclosed
US-8044054-B2 Stereoisomerically enriched 3-aminocarbonyl bicycloheptene pyrimidinediamine compounds and their uses RIGEL PHARMACEUTICALS, INC. (US) 2011-10-25 US disclosed
US-8030483-B2 Stereoisomerically enriched 3-aminocarbonyl bicycloheptene pyrimidinediamine compounds and their uses RIGEL PHARMACEUTICALS, INC. (US) 2011-10-04 US disclosed
US-20110152518-A1 Cycloalkyl Substituted Pyrimidinediamine Compounds And Their Uses RIGEL PHARMACEUTICALS, INC. (US) 2011-06-23 US disclosed
US-7868013-B2 Cycloalkyl substituted pyrimidinediamine compounds and their uses RIGEL PHARMACEUTICALS, INC. (US) 2011-01-11 US disclosed
US-7858633-B2 Cycloalkyl substituted pyrimidinediamine compounds and their uses RIGEL PHARMACEUTICALS, INC. (US) 2010-12-28 US disclosed
US-7754714-B2 (1S, 2R)-N4-(2-Aminocarbonylcyclopent-1-yl)-5-fluoro-N2-[4-(4-methylpiperazin-1-yl)-3-methylphenyl]-2,4-pyrimidinediamine, having antiproliferative activity, used to inhibit cellular proliferation and to treat proliferate diseases such as cancers RIGEL PHARMACEUTICALS, INC. (US) 2010-07-13 US disclosed
US-7754714-B2 (1S, 2R)-N4-(2-Aminocarbonylcyclopent-1-yl)-5-fluoro-N2-[4-(4-methylpiperazin-1-yl)-3-methylphenyl]-2,4-pyrimidinediamine, having antiproliferative activity, used to inhibit cellular proliferation and to treat proliferate diseases such as cancers RIGEL PHARMACEUTICALS, INC. (US) 2010-07-13 US disclosed
US-20090176981-A1 Stereoisomerically Enriched 3-Aminocarbonyl Bicycloheptene Pyrimidinediamine Compounds And Their Uses RIGEL PHARMACEUTICALS, INC. (US) 2009-07-09 US disclosed
US-20090137589-A1 Stereoisomerically Enriched 3-Aminocarbonyl Bicycloheptene Pyrimidinediamine Compounds And Their Uses RIGEL PHARMACEUTICALS, INC. (US) 2009-05-28 US disclosed
US-20080051412-A1 Stereoisomerically Enriched 3-Aminocarbonyl Bicycloheptene Pyrimidinediamine Compounds and their Uses RIGEL PHARMACEUTICALS, INC. (US) 2008-02-28 US disclosed
US-20080009494-A1 Cycloalkyl Substituted Pyrimidinediamine Compounds And Their Uses RIGEL PHARMACEUTICALS, INC. (US) 2008-01-10 US disclosed
US-20080009494-A1 Cycloalkyl Substituted Pyrimidinediamine Compounds And Their Uses RIGEL PHARMACEUTICALS, INC. (US) 2008-01-10 US disclosed
US-20070299060-A1 Cycloalkyl Substituted Pyrimidinediamine Compounds And Their Uses RIGEL PHARMACEUTICALS, INC. (US) 2007-12-27 US disclosed
US-20070179140-A1 Stereoisomerically Enriched 3-Aminocarbonyl Bicycloheptene Pyrimidinediamine Compounds And Their Uses RIGEL PHARMACEUTICALS, INC. (US) 2007-08-02 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 (8 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-20110152518-A1 Cycloalkyl Substituted Pyrimidinediamine Compounds And Their Uses MKI67, PCNA, TK1 AURKB 145/4885AURKA 422/4885IRAK4 4592/4885
US-20080051412-A1 Stereoisomerically Enriched 3-Aminocarbonyl Bicycloheptene Pyrimidinediamine Compounds and their Uses MKI67, PCNA, CCNI AURKB 135/4885AURKA 256/4885IRAK4 4671/4885
US-20070299060-A1 Cycloalkyl Substituted Pyrimidinediamine Compounds And Their Uses MKI67, PCNA, TK1 AURKB 145/4885AURKA 422/4885IRAK4 4592/4885
US-20070179140-A1 Stereoisomerically Enriched 3-Aminocarbonyl Bicycloheptene Pyrimidinediamine Compounds And Their Uses MKI67, PCNA, CCNI AURKB 135/4885AURKA 256/4885IRAK4 4671/4885
US-20080009494-A1 Cycloalkyl Substituted Pyrimidinediamine Compounds And Their Uses MKI67, PCNA, TK1 AURKB 145/4885AURKA 422/4885IRAK4 4592/4885
US-20130210814-A1 Cycloalkyl Substituted Pyrimidinediamine Compounds And Their Uses MKI67, PCNA, TK1 AURKB 145/4885AURKA 422/4885IRAK4 4592/4885
US-20090176981-A1 Stereoisomerically Enriched 3-Aminocarbonyl Bicycloheptene Pyrimidinediamine Compounds And Their Uses MKI67, PCNA, CCNI AURKB 125/4885AURKA 216/4885IRAK4 4622/4885
US-20090137589-A1 Stereoisomerically Enriched 3-Aminocarbonyl Bicycloheptene Pyrimidinediamine Compounds And Their Uses MKI67, PCNA, CCNI AURKB 135/4885AURKA 256/4885IRAK4 4671/4885

“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.