SCHEMBL4736323

SCHEMBL4736323

Nc1ncnc(Nc2ccc(OCc3ccccc3)c(Cl)c2)c1C=NOCCN1CCOCC1

nearest known ligand 0.71

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
EGFR P00533 18/20 0.71
ERBB2 P04626 16/20 0.71
AURKA O14965 1/20 0.55

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
SCHEMBL1105316 1.00 EGFR (0.71) EGFRERBB2AURKA
SCHEMBL30362981 1.00 EGFR (0.71) EGFRERBB2AURKA
SCHEMBL31466883 1.00 EGFR (0.71) EGFRERBB2AURKA
Hydrochloric Acid SCHEMBL29409572 0.99 EGFR (0.70) EGFRERBB2AURKA
Hydrochloric Acid SCHEMBL30363008 0.99 EGFR (0.70) EGFRERBB2AURKA
Hydrochloric Acid SCHEMBL4997757 0.99 EGFR (0.70) EGFRERBB2AURKA
Hydrochloric Acid SCHEMBL5007769 0.99 EGFR (0.70) EGFRERBB2AURKA
Hydrochloric Acid SCHEMBL5007744 0.99 EGFR (0.70) EGFRERBB2AURKA
Hydrochloric Acid SCHEMBL20214611 0.99 EGFR (0.70) EGFRERBB2AURKA
SCHEMBL5005197 0.96 EGFR (0.72) EGFRERBB2AURKA

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250262213-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. (US) 2025-08-21 US disclosed
US-20220054491-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. 2022-02-24 US disclosed
EP-3849538-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. (US) 2021-07-21 EP disclosed
WO-2020055756-A1 COMBINATION THERAPIES Mirati Therapeutics, Inc. (US) 2020-03-19 WO disclosed
US-8367825-B2 Substituted pyrimidinyl oxime kinase inhibitors JANSSEN PHARMACEUTICA N.V. (BE) 2013-02-05 US disclosed
US-8278446-B2 reacting 4-amino-6-chloro-pyrimidine-5-carbaldehyde with 4-benzyloxy-3-chloro-phenylamine in an aqueous solvent and a catalytic amount of hydrochloric acid, to providw 4-amino-6-(4-benzyloxy-3-chloro-phenylamino)-pyrimidine-5-carbaldehyde, then oximination with (2-morpholin-4-yl-ethyl)-hydroxylamine JANSSEN PHARMACEUTICA N.V. (BE) 2012-10-02 US disclosed
US-20120157412-A1 Substituted Pyrimidinyl Oxime Kinase Inhibitors BATTISTA KATHLEEN A (US) 2012-06-21 US disclosed
US-20080249304-A1 PROCESS FOR PREPARING SUBSTITUTED DIAMINOPYRIMIDINE OXIMES JANSSEN PHARMACEUTICA N.V. (BE) 2008-10-09 US disclosed
WO-2008073519-A1 PROCESS FOR PREPARING SUBSTITUTED DIAMINOPYRIMIDINE OXIMES JANSSEN PHARMACEUTICA, N.V. (BE) 2008-06-19 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 (4 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-20120157412-A1 Substituted Pyrimidinyl Oxime Kinase Inhibitors MAP3K2, MAP3K1, MAP3K20 EGFR 1201/4885ERBB2 124/4885AURKA 766/4885
US-20250262213-A1 COMBINATION THERAPIES KRAS, NRAS, HRAS EGFR 4/4885ERBB2 5/4885AURKA 852/4885
US-20220054491-A1 COMBINATION THERAPIES KRAS, NRAS, HRAS EGFR 4/4885ERBB2 5/4885AURKA 932/4885
US-20080249304-A1 PROCESS FOR PREPARING SUBSTITUTED DIAMINOPYRIMIDINE OXIMES DHPS, DPYD, DCPS EGFR 1036/4885ERBB2 301/4885AURKA 530/4885

“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.