Ceritinib

Ceritinib

SCHEMBL1014329

Cc1cc(Nc2ncc(Cl)c(Nc3ccccc3S(=O)(=O)C(C)C)n2)c(OC(C)C)cc1C1CCNCC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ALKEML4NPM1

The experimentally established mechanism targets of Ceritinib. 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
ALK known ✓ Q9UM73 20/20 1.00
NPM1 known ✓ P06748 1/20 1.00
EML4 known ✓ Q9HC35 1/20 1.00
INSR P06213 9/20 1.00
KCNH2 Q12809 4/20 1.00
PLK4 O00444 1/20 1.00
BUB1B O60566 1/20 1.00
JAK2 O60674 1/20 1.00
ROCK2 O75116 1/20 1.00
ABL1 P00519 1/20 1.00
EGFR P00533 1/20 1.00
NTRK1 P04629 1/20 1.00
LCK P06239 1/20 1.00
FES P07332 1/20 1.00
LYN P07948 1/20 1.00
RET P07949 1/20 1.00
IGF1R P08069 1/20 1.00
ABCB1 P08183 1/20 1.00
MET P08581 1/20 1.00
ROS1 P08922 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
Ceritinib SCHEMBL29489147 1.00 ALK (1.00) ALKINSRKCNH2PLK4BUB1B
Ceritinib SCHEMBL29349781 1.00 ALK (1.00) ALKINSRKCNH2PLK4BUB1B
Ceritinib SCHEMBL29810752 0.99 ALK (0.98) ALKINSRKCNH2PLK4BUB1B
Ceritinib SCHEMBL30053881 0.99 ALK (0.98) ALKINSRKCNH2PLK4BUB1B
Ceritinib SCHEMBL9936675 0.99 ALK (0.98) ALKINSRKCNH2PLK4BUB1B
SCHEMBL1545837 0.97 ALK (0.94) ALKINSRKCNH2PLK4BUB1B
Ceritinib SCHEMBL17879538 0.95 ALK (0.90) ALKINSRKCNH2PLK4BUB1B
Ceritinib SCHEMBL17879536 0.95 ALK (0.93) ALKINSRKCNH2PLK4BUB1B
SCHEMBL24852882 0.95 ALK (1.00) ALKINSRKCNH2PLK4BUB1B
SCHEMBL1014579 0.94 ALK (0.89) ALKINSRKCNH2PLK4BUB1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3568204-B1 PHARMACEUTICAL COMBINATION COMPRISING AN ALK INHIBITOR AND AN SHP2 INHIBITOR NOVARTIS AG (CH) 2023-08-30 EP claimed
US-20220241277-A1 PHARMACEUTICAL COMBINATION COMPRISING AN ALK INHIBITOR AND A SHP2 INHIBITOR NOVARTIS AG (CH) 2022-08-04 US claimed
CN-110730678-B Pharmaceutical combination comprising an ALK inhibitor and an SHP2 inhibitor 诺华股份有限公司 2022-07-15 CN claimed
EP-3453708-B1 PROCESS FOR THE PREPARATION OF 5-CHLORO-N-(2-ISOPROPOXY-5-METHYL-4-PIPERIDIN-4-YL-PHENYL)-N-2-(ISOPROPYLSULFONYL)PHENYL)-2,4-DIAMINE DI-HYDROCHLORIDE NOVARTIS AG (CH) 2021-10-27 EP claimed
EP-3875078-A1 COMPOUNDS FOR THE TREATMENT OF COVID-19 Dompe' Farmaceutici S.P.A. (IT) 2021-09-08 EP claimed
CN-110730678-A Pharmaceutical combination comprising an ALK inhibitor and an SHP2 inhibitor 诺华股份有限公司 2020-01-24 CN claimed
US-20190343836-A1 PHARMACEUTICAL COMBINATION COMPRISING AN ALK INHIBITOR AND A SHP2 INHIBITOR NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH, INC. 2019-11-14 US claimed
US-20190134033-A1 PHARMACEUTICAL COMBINATIONS NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH, INC. 2019-05-09 US claimed
US-20180185365-A1 Pharmaceutical Combinations NOVARTIS AG (CH) 2018-07-05 US claimed
WO-2017175111-A1 STRN-ALK FUSION AS A THERAPEUTIC TARGET IN COLORECTAL CANCER NOVARTIS AG (CH) 2017-10-12 WO claimed
US-20130296357-A1 METHODS OF USING ALK INHIBITORS IRM LLC (BM) 2013-11-07 US claimed
EP-2651918-A1 CRYSTALLINE FORMS OF 5-CHLORO-N2-(2-ISOPROPOXY-5-METHYL-4-PIPERIDIN-4-YL-PHENYL)-N4[2-(PROPANE-2-SULFONYL)-PHENYL]-PYRIMIDINE-2,4-DIAMINE Novartis AG (CH) 2013-10-23 EP claimed
US-20130274279-A1 CRYSTALLINE FORMS OF 5-CHLORO-N2-(2-ISOPROPOXY-5-METHYL-4-PIPERIDIN-4-YL-PHENYL)-N4-[2-(PROPANE-2-SULFONYL)-PHENYL]-PYRIMIDINE-2, 4-DIAMINE NOVARTIS AG (CH) 2013-10-17 US claimed
US-8377921-B2 Compounds and compositions as protein kinase inhibitors IRM LLC (BM) 2013-02-19 US claimed
WO-2012106540-A1 METHODS OF USING ALK INHIBITORS IRM LLC (BM) 2012-08-09 WO claimed
WO-2012082972-A1 CRYSTALLINE FORMS OF 5-CHLORO-N2-(2-ISOPROPOXY-5-METHYL-4-PIPERIDIN-4-YL-PHENYL)-N4[2-(PROPANE-2-SULFONYL)-PHENYL]-PYRIMIDINE-2,4-DIAMINE NOVARTIS AG (CH) 2012-06-21 WO claimed
US-20110257155-A1 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS IRM LLC (BM) 2011-10-20 US claimed
US-8039479-B2 Such as 6-{5-Chloro-4-[2-(propane-2-sulfonyl)-phenylamino]-pyrimidin-2-ylamino}-5-isopropoxy-2-piperidin-4-yl-2,3-dihydro-isoindol-1-one; tumors, cancer; inhibition of anaplastic lymphoma, focal adhesion, zeta chain associated protein 70 and/or insulin like growth factor IRM LLC (BM) 2011-10-18 US claimed
EP-2091918-A2 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS IRM LLC (BM) 2009-08-26 EP claimed
WO-2008073687-A2 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS IRM LLC (BM) 2008-06-19 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (7 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-20190343836-A1 PHARMACEUTICAL COMBINATION COMPRISING AN ALK INHIBITOR AND A SHP2 INHIBITOR ALK, PTPRJ, PTPN1 ALK 1/4885NPM1 673/4885EML4 2163/4885
US-20180185365-A1 Pharmaceutical Combinations TP53, HRAS, KRAS ALK 6/4885NPM1 274/4885EML4 1673/4885
US-20190134033-A1 PHARMACEUTICAL COMBINATIONS TP53, HRAS, KRAS ALK 6/4885NPM1 274/4885EML4 1673/4885
US-20110257155-A1 COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS ZAP70, IGF1R, PTK2 ALK 23/4885NPM1 2242/4885EML4 3931/4885
US-20220241277-A1 PHARMACEUTICAL COMBINATION COMPRISING AN ALK INHIBITOR AND A SHP2 INHIBITOR ALK, PTPRJ, PTPN1 ALK 1/4885NPM1 673/4885EML4 2163/4885
US-20130296357-A1 METHODS OF USING ALK INHIBITORS ALK, EML4, EGFR ALK 1/4885NPM1 489/4885EML4 2/4885
US-20130274279-A1 CRYSTALLINE FORMS OF 5-CHLORO-N2-(2-ISOPROPOXY-5-METHYL-4-PIPERIDIN-4-YL-PHENYL)-N4-[2-(PROPANE-2-SULFONYL)-PHENYL]-PYRIMIDINE-2, 4-DIAMINE PKD2, NT5C, PKD1 ALK 500/4885NPM1 206/4885EML4 626/4885

“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.