SCHEMBL56571

SCHEMBL56571

CN(C)CCOc1ccc(N)cc1

nearest known ligand 0.67

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
KEAP1 Q14145 1/20 0.67
NFE2L2 Q16236 1/20 0.67
HRH3 Q9Y5N1 4/20 0.63
LTA4H P09960 2/20 0.61
TDP1 Q9NUW8 2/20 0.55
KDM4E B2RXH2 2/20 0.55
ALDH1A1 P00352 2/20 0.55
SMN1; SMN2 Q16637 1/20 0.55
TSHR P16473 1/20 0.54
PHLPP2 Q6ZVD8 1/20 0.51
LSS P48449 1/20 0.50
MAPT P10636 1/20 0.50

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
Hydrochloric Acid SCHEMBL3570082 0.98 KEAP1 (0.65) KEAP1NFE2L2HRH3LTA4HTDP1
Hydrochloric Acid SCHEMBL56159 0.98 KEAP1 (0.65) KEAP1NFE2L2HRH3LTA4HTDP1
SCHEMBL188971 0.90 KDM4E (0.69) KEAP1NFE2L2HRH3LTA4HTDP1
SCHEMBL14547108 0.89 KEAP1 (0.54) KEAP1NFE2L2HRH3LTA4HTDP1
SCHEMBL3367452 0.88 KDM4E (0.70) KEAP1NFE2L2HRH3LTA4HTDP1
Hydrochloric Acid SCHEMBL3657036 0.88 KDM4E (0.67) KEAP1NFE2L2HRH3LTA4HTDP1
SCHEMBL2022333 0.88 KCNH2 (0.56) KEAP1NFE2L2HRH3LTA4HTDP1
SCHEMBL27750471 0.86 KEAP1 (0.51) KEAP1NFE2L2HRH3LTA4HTDP1
SCHEMBL12156398 0.86 TDP1 (0.53) KEAP1NFE2L2HRH3LTA4HTDP1
Hydrochloric Acid SCHEMBL5159771 0.86 KCNH2 (0.54) KEAP1NFE2L2HRH3LTA4HTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2282995-B1 DERIVATIVES OF QUINOLINES AND QUINOXALINES AS PROTEIN TYROSINE KINASE INHIBITORS NOVARTIS AG (CH) 2015-08-26 EP claimed
US-8536175-B2 Quinoxaline carboxamide derivatives as protein tyrosine kinase inhibitors NOVARTIS AG (CH) 2013-09-17 US claimed
US-20080032975-A1 Substituted Fused Pyrroleoximes and Fused Pyrazoleoximes NEUROGEN CORPORATION, A CORPORATION OF THE STATE OF DELAWARE (US) 2008-02-07 US claimed
US-7297693-B2 Nitrogen-containing heterocyclic compounds and their use as Raf inhibitors SMITHKLINE BEECHAM P.L.C. (GB) 2007-11-20 US claimed
US-7282498-B2 Substituted fused pyrroleoximes and fused pyrazoleoximes NEUROGEN CORPORATION (US) 2007-10-16 US claimed
EP-1432702-B1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS AND THEIR USE AS RAF INHIBITORS SMITHKLINE BEECHAM PLC (GB) 2006-08-16 EP claimed
US-20050059826-A1 Substituted fused pyrroleoximes and fused pyrazoleoximes NEUROGEN CORPORATION 2005-03-17 US claimed
US-20040209883-A1 Nitrogen-containing heterocyclic compounds and their use as raf inhibitors SMITHKLINE BEECHAM P.L.C. (GB) 2004-10-21 US claimed
EP-1326831-A1 SUBSTITUTED FUSED PYRROLEIMINES AND PYRAZOLEIMINES NEUROGEN CORPORATION (US) 2003-07-16 EP claimed
US-20020128236-A1 Substituted fused pyrroleoximes and fused pyrazoleoximes NEUROGEN CORPORATION 2002-09-12 US claimed
WO-2002020480-A1 SUBSTITUTED FUSED PYRROLEIMINES AND PYRAZOLEIMINES NEUROGEN CORPORATION (US) 2002-03-14 WO claimed
US-20260137703-A1 2-AMINO-PYRIDO[2,3-D]PYRIMIDIN-7(8H)-ONE AND 7-AMINO-1-PYRIMIDO[4,5-D]PYRIMIDIN-2(1 H)-ONE DERIVATIVES AS EGFR INHIBITORS FOR THE TREATMENT OF CANCER CANCER RESEARCH TECH LIMITED (GB) 2026-05-21 US disclosed
EP-4716593-A2 MIXED MODE SUBTRACTIVE ANION EXCHANGE CHROMATOGRAPHY LIGANDS BASED ON 4-(2-(DIMETHYLAMINO)ETHOXY)ANILINE STRUCTURES Bio-Rad Laboratories, Inc. (US) 2026-04-01 EP disclosed
EP-4716593-A2 MIXED MODE SUBTRACTIVE ANION EXCHANGE CHROMATOGRAPHY LIGANDS BASED ON 4-(2-(DIMETHYLAMINO)ETHOXY)ANILINE STRUCTURES Bio-Rad Laboratories, Inc. (US) 2026-04-01 EP disclosed
CN-121263398-A Mixed mode subtractive anion exchange chromatography ligands based on 4- (2- (dimethylamino) ethoxy) aniline structures 生物辐射实验室股份有限公司 2026-01-02 CN disclosed
US-4344879-A Quaternary and basic azamethine compounds and their use as colorants HOECHST AKTIENGESELLSCHAFT (DE) 1982-08-17 US disclosed
EP-0029136-A2 Quaternary and basic azomethine compounds, process for their preparation and their use as dyestuffs HOECHST AKTIENGESELLSCHAFT (DE) 1981-05-27 EP disclosed
US-4247337-A STABILIZED AGAINST FLOCCULATION BY ADDITION OF A PHENYLAMINOSULFONYL DERIVATIVE OF PHTHALOCYANINE CIBA-GEIGY CORPORATION (US) 1981-01-27 US disclosed
US-3994900-A 6-(Or 8)-[[(substituted amino)alkyl]oxy(or thio)]-3,4-dihydro-4-phenyl-2(1H)-quinolinones E. R. SQUIBB & SONS, INC. (US) 1976-11-30 US disclosed
US-3875215-A Substituted phenoxyalkyl quaternary ammonium compounds DOW CHEMICAL CO 1975-04-01 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 (5 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-20260137703-A1 2-AMINO-PYRIDO[2,3-D]PYRIMIDIN-7(8H)-ONE AND 7-AMINO-1-PYRIMIDO[4,5-D]PYRIMIDIN-2(1 H)-ONE DERIVATIVES AS EGFR INHIBITORS FOR THE TREATMENT OF CANCER EGFR, KRAS, O60361 KEAP1 2073/4885NFE2L2 3808/4885HRH3 1940/4885
US-20050059826-A1 Substituted fused pyrroleoximes and fused pyrazoleoximes NPSR1, GABRE, CHRNE KEAP1 4109/4885NFE2L2 3357/4885HRH3 235/4885
US-20040209883-A1 Nitrogen-containing heterocyclic compounds and their use as raf inhibitors BRAF, RAF1, NPR1 KEAP1 355/4885NFE2L2 1418/4885HRH3 1027/4885
US-20020128236-A1 Substituted fused pyrroleoximes and fused pyrazoleoximes HTR1A, GABRA1, GABRE KEAP1 4263/4885NFE2L2 3283/4885HRH3 269/4885
US-20080032975-A1 Substituted Fused Pyrroleoximes and Fused Pyrazoleoximes NPSR1, GABRE, CHRNE KEAP1 4109/4885NFE2L2 3357/4885HRH3 235/4885

“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.