SCHEMBL12964728

SCHEMBL12964728

CN1CCN(Cc2ccc(Nc3ncc(Cl)c(Nc4ccccc4C(=O)N4CCCC4)n3)cc2)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
▸ AXL P30530 13/20 1.00
▸ AURKB Q96GD4 2/20 0.65
▸ AURKA O14965 1/20 0.65
▸ EGFR P00533 4/20 0.63
▸ ALK Q9UM73 2/20 0.62
▸ JAK2 O60674 1/20 0.62
▸ IGF1R P08069 1/20 0.62
▸ MAP3K7 O43318 2/20 0.57

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
SCHEMBL12813313 0.87 AXL (1.00) AXLAURKBAURKAEGFRALK
SCHEMBL12964725 0.85 AXL (1.00) AXLAURKBAURKAEGFRALK
SCHEMBL12964722 0.82 AXL (1.00) AXLAURKBAURKAALKJAK2
SCHEMBL30184335 0.82 EGFR (0.74) AXLAURKBAURKAEGFRIGF1R
SCHEMBL28917519 0.82 EGFR (0.74) AXLAURKBAURKAEGFRIGF1R
SCHEMBL24072926 0.82 AXL (0.69) AXLAURKAEGFRALK
SCHEMBL30184441 0.81 EGFR (0.72) AXLAURKBAURKAEGFRIGF1R
SCHEMBL28916674 0.81 EGFR (0.72) AXLAURKBAURKAEGFRIGF1R
SCHEMBL21446892 0.79 AXL (0.80) AXLAURKBAURKAALKJAK2
SCHEMBL22872058 0.79 AXL (0.71) AXLAURKBAURKAALKJAK2

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-20230165857-A1 AXL KINASE INHIBITORS AND USE OF THE SAME SUMITOMO PHARMA ONCOLOGY, INC. 2023-06-01 — — US disclosed
US-20230165857-A1 AXL KINASE INHIBITORS AND USE OF THE SAME SUMITOMO PHARMA ONCOLOGY, INC. 2023-06-01 — — US disclosed
US-20210205304-A1 AXL KINASE INHIBITORS AND USE OF THE SAME SUMITOMO DAINIPPON PHARMA ONCOLOGY, INC. (US) 2021-07-08 — — US disclosed
US-11013741-B1 AXL kinase inhibitors and use of the same SUMITOMO DAINIPPON PHARMA ONCOLOGY, INC. (US) 2021-05-25 — — US disclosed
US-10888562-B1 — — 2021-01-12 — — US disclosed
EP-3628665-A1 SUBSTITUTED N-PHENYLPYRIMIDIN-2-AMINE ANALOGS AS INHIBITORS OF THE AXL KINASE University of Utah Research Foundation (US) 2020-04-01 — — EP disclosed
WO-2019195753-A1 AXL KINASE INHIBITORS AND USE OF THE SAME TOLERO PHARMACEUTICALS, INC. (US) 2019-10-10 — — WO disclosed
EP-2693881-B1 SUBSTITUTED N-PHENYLPYRIMIDIN-2-AMINE ANALOGS AS INHIBITORS OF THE AXL KINASE UNIV UTAH RES FOUND (US) 2019-09-04 — — EP disclosed
EP-2693881-B1 SUBSTITUTED N-PHENYLPYRIMIDIN-2-AMINE ANALOGS AS INHIBITORS OF THE AXL KINASE UNIV UTAH RES FOUND (US) 2019-09-04 — — EP disclosed
US-20170298058-A1 HETEROCYCLIC RING AND CARBOCYCLIC DERIVATIVE SHIONOGI & CO (JP) 2017-10-19 — — US disclosed
US-20160024072-A1 Heterocyclic Ring and Carbocyclic Derivative SHIONOGI & CO., LTD. (JP) 2016-01-28 — — US disclosed
US-20160024072-A1 Heterocyclic Ring and Carbocyclic Derivative SHIONOGI & CO., LTD. (JP) 2016-01-28 — — US disclosed
US-8901120-B2 Substituted N-phenylpyrimidin-2-amine analogs as inhibitors of the Axl kinase UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2014-12-02 — — US disclosed
US-8901120-B2 Substituted N-phenylpyrimidin-2-amine analogs as inhibitors of the Axl kinase UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2014-12-02 — — US disclosed
US-8901120-B2 Substituted N-phenylpyrimidin-2-amine analogs as inhibitors of the Axl kinase UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2014-12-02 — — US disclosed
WO-2013118855-A1 HETEROCYCLIC RING AND CARBOCYCLIC DERIVATIVE 塩野義製薬株式会社 (JP) 2013-08-15 — — WO disclosed
US-20120283261-A1 SUBSTITUTED N-PHENYLPYRIMIDIN-2-AMINE ANALOGS AS INHIBITORS OF THE AXL KINASE SUMITOMO PHARMA ONCOLOGY, INC. 2012-11-08 — — US disclosed
US-20120283261-A1 SUBSTITUTED N-PHENYLPYRIMIDIN-2-AMINE ANALOGS AS INHIBITORS OF THE AXL KINASE SUMITOMO PHARMA ONCOLOGY, INC. 2012-11-08 — — US disclosed
US-20120283261-A1 SUBSTITUTED N-PHENYLPYRIMIDIN-2-AMINE ANALOGS AS INHIBITORS OF THE AXL KINASE SUMITOMO PHARMA ONCOLOGY, INC. 2012-11-08 — — US disclosed
WO-2012135800-A1 SUBSTITUTED N-PHENYLPYRIMIDIN-2-AMINE ANALOGS AS INHIBITORS OF THE AXL KINASE UNIVERSITY OF UTAH RESEARCH FOUNDATION (US) 2012-10-04 — — WO 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 (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-20170298058-A1 HETEROCYCLIC RING AND CARBOCYCLIC DERIVATIVE P2RX3, P2RX7, P2RX2 AXL 1822/4885AURKB 3023/4885AURKA 4009/4885
US-20160024072-A1 Heterocyclic Ring and Carbocyclic Derivative P2RX3, P2RX7, P2RX2 AXL 1822/4885AURKB 3023/4885AURKA 4009/4885
US-20120283261-A1 SUBSTITUTED N-PHENYLPYRIMIDIN-2-AMINE ANALOGS AS INHIBITORS OF THE AXL KINASE AXL, TYRO3, MERTK AXL 1/4885AURKB 198/4885AURKA 159/4885
US-11013741-B1 AXL kinase inhibitors and use of the same AXL, FLT3, TEC AXL 1/4885AURKB 167/4885AURKA 100/4885
US-20210205304-A1 AXL KINASE INHIBITORS AND USE OF THE SAME AXL, FLT3, TEC AXL 1/4885AURKB 146/4885AURKA 81/4885
US-20230165857-A1 AXL KINASE INHIBITORS AND USE OF THE SAME AXL, FLT3, TEC AXL 1/4885AURKB 164/4885AURKA 94/4885
US-10888562-B1 — TP53, TARBP2, FLT3 AXL 927/4885AURKB 1490/4885AURKA 590/4885

“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.

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