SCHEMBL20162222

SCHEMBL20162222

COc1cc(F)c([N+](=O)[O-])cc1Nc1nccc(-n2c(=O)[nH]c3cc(C)ccc32)n1.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.36

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
KDR known ✓ P35968 6/20 0.36
EGFR known ✓ P00533 5/20 0.35
IGF1R known ✓ P08069 1/20 0.32
MKNK1 Q9BUB5 1/20 0.35
SCN9A Q15858 2/20 0.34
MET P08581 4/20 0.33
CDK4 P11802 1/20 0.33
CDK2 P24941 1/20 0.33
JAK2 O60674 1/20 0.33
JAK1 P23458 1/20 0.33
TYK2 P29597 1/20 0.33
PRMT7 Q9NVM4 1/20 0.33
FGFR4 P22455 1/20 0.33
TNK2 Q07912 1/20 0.33
ALK Q9UM73 3/20 0.32

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
SCHEMBL30010761 1.00 KDR (0.36) KDRMKNK1EGFRSCN9AMET
SCHEMBL30011346 0.96 EGFR (0.38) KDRMKNK1EGFRMETJAK2
SCHEMBL20162200 0.96 EGFR (0.38) KDRMKNK1EGFRMETJAK2
SCHEMBL30011674 0.94 OPRK1 (0.36) KDRMKNK1EGFRMETJAK2
SCHEMBL20162198 0.94 OPRK1 (0.36) KDRMKNK1EGFRMETJAK2
SCHEMBL18386897 0.93 KDR (0.40) KDRMKNK1EGFRSCN9ATNK2
SCHEMBL18386904 0.87 KDR (0.40) KDREGFR
SCHEMBL18386752 0.84 EGFR (0.39) KDRMKNK1EGFR
SCHEMBL20162213 0.84 EGFR (0.38) KDRMKNK1EGFRSCN9ACDK2
SCHEMBL30012138 0.84 EGFR (0.38) KDRMKNK1EGFRSCN9ACDK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10329277-B2 N-(2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxy-5-((4-(3-methyl-2-OXO-2,3-dihydro-1h-benzo[d]imidazol-1-yl)pyrimidin-2-yl)amino)phenyl)acrylamide hydrochloride as an inhibitor of epidermal growth factor receptor activity CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. (CN) 2019-06-25 US disclosed
US-20180208581-A1 ANILINE PYRIMIDINE DERIVATIVES AND USES THEREOF CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. (CN) 2018-07-26 US disclosed
EP-3323817-A1 ANILINE PYRIMIDINE DERIVATIVES AND USES THEREOF Chia Tai Tianqing Pharmaceutical Group Co.,Ltd (CN) 2018-05-23 EP 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 (2 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-20180208581-A1 ANILINE PYRIMIDINE DERIVATIVES AND USES THEREOF EGFR, ERBB2, ERBB3 KDR 44/4885EGFR 1/4885IGF1R 172/4885
US-10329277-B2 N-(2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxy-5-((4-(3-methyl-2-OXO-2,3-dihydro-1h-benzo[d]imidazol-1-yl)pyrimidin-2-yl)amino)phenyl)acrylamide hydrochloride as an inhibitor of epidermal growth factor receptor activity EGFR, ERBB2, ERBB3 KDR 12/4885EGFR 1/4885IGF1R 19/4885

“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.