SCHEMBL202880

SCHEMBL202880

Nc1c([N+](=O)[O-])cnc2ccccc12

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 1/20 0.51
CTSB P07858 1/20 0.46
MEN1 O00255 3/20 0.45
KMT2A Q03164 3/20 0.45
NCOA1 Q15788 1/20 0.44
NCOA3 Q9Y6Q9 1/20 0.44
ALDH1A1 P00352 3/20 0.44
HTT P42858 1/20 0.43
CYP1A2 P05177 1/20 0.43
TSHR P16473 1/20 0.43
TDP1 Q9NUW8 2/20 0.42
SMN1; SMN2 Q16637 2/20 0.42
KDM4E B2RXH2 1/20 0.42
GLA P06280 1/20 0.42
CHRM2 P08172 1/20 0.42
ADRA2A P08913 1/20 0.42
ADORA3 P0DMS8 1/20 0.42
CHRM1 P11229 1/20 0.42
HPGD P15428 1/20 0.42
NQO2 P16083 1/20 0.42

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
SCHEMBL8561101 0.81 POLB (0.53) POLBMEN1KMT2ANCOA1NCOA3
SCHEMBL28058588 0.79 POLB (0.51) POLBMEN1KMT2ANCOA1NCOA3
SCHEMBL15824026 0.79 POLB (0.51) POLBCTSBMEN1KMT2ANCOA1
SCHEMBL4727431 0.79 POLB (0.51) POLBMEN1KMT2ANCOA1NCOA3
SCHEMBL1033969 0.79 POLB (0.51) POLBCTSBMEN1KMT2ANCOA1
SCHEMBL202663 0.79 POLB (0.51) POLBMEN1KMT2ANCOA1NCOA3
SCHEMBL8570782 0.79 POLB (0.51) POLBCTSBMEN1KMT2ANCOA1
SCHEMBL29381779 0.79 POLB (0.51) POLBMEN1KMT2ANCOA1NCOA3
Hydrochloric Acid SCHEMBL3867195 0.78 POLB (0.50) POLBMEN1KMT2ANCOA1NCOA3
SCHEMBL31197366 0.78 POLB (0.50) POLBMEN1KMT2ANCOA1NCOA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108003153-A Nitrogenous five-ring heterocycles and quinolines and its salt, preparation method, pharmaceutical composition and purposes 中国医学科学院肿瘤医院 2018-05-08 CN claimed
EP-4178676-B1 N-1 BRANCHED IMIDAZOQUINOLINES, CONJUGATES THEREOF, AND METHODS SOLVENTUM INTELLECTUAL PROPERTIES COMPANY (US) 2026-04-15 EP disclosed
US-12540137-B2 N-1 branched alkyl ether substituted imidazo[4,5-c]quinoline compounds, compositions, and methods SOLVENTUM INTELLECTUAL PROPERTIES COMPANY (US) 2026-02-03 US disclosed
US-12398134-B2 N-1 branched cycloalkyl substituted imidazo[4,5-c]quinoline compounds, compositions, and methods SOLVENTUM INTELLECTUAL PROPERTIES COMPANY (US) 2025-08-26 US disclosed
US-20250129082-A1 N-1 Triazole Substituted Imidazoquinolines, Conjugates Thereof, and Methods SOLVENTUM INTELLECTUAL PROPERTIES COMPANY 2025-04-24 US disclosed
EP-4522615-A1 LRRK2 INHIBITORS Interline Therapeutics, Inc. (US) 2025-03-19 EP disclosed
EP-3759107-B1 SUBSTITUTED IMIDAZO[4,5-C]QUINOLINE COMPOUNDS WITH AN N-1 BRANCHED GROUP SOLVENTUM INTELLECTUAL PROPERTIES COMPANY (US) 2024-12-04 EP disclosed
EP-4448519-A1 N-1 TRIAZOLE SUBSTITUTED IMIDAZOQUINOLINES, CONJUGATES THEREOF, AND METHODS Solventum Intellectual Properties Company (US) 2024-10-23 EP disclosed
US-20240300947-A1 N-1 Branched Alkyl Ether Substituted Imidazo[4,5-c]Quinoline Compounds, Compositions, and Methods SOLVENTUM INTELLECTUAL PROPERTIES COMPANY (US) 2024-09-12 US disclosed
CN-118401523-A N-1 triazole substituted imidazoquinolines, conjugates thereof and methods 舒万诺知识产权公司 2024-07-26 CN disclosed
EP-1198233-A1 SULFONAMIDE AND SULFAMIDE SUBSTITUTED IMIDAZOQUINOLINES 3M Innovative Properties Company (US) 2002-04-24 EP disclosed
EP-1198232-A1 UREA SUBSTITUTED IMIDAZOQUINOLINES 3M Innovative Properties Company (US) 2002-04-24 EP disclosed
EP-1187613-A1 AMIDE SUBSTITUTED IMIDAZOQUINOLINES 3M Innovative Properties Company (US) 2002-03-20 EP disclosed
US-6331539-B1 INDUCE BIOSYNTHESIS OF INTERFERON ALPHA IN ANIMALS 3M INNOVATIVE PROPERTIES COMPANY 2001-12-18 US disclosed
WO-2000076505-A1 AMIDE SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES COMPANY (US) 2000-12-21 WO disclosed
WO-2000076518-A1 UREA SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES COMPANY (US) 2000-12-21 WO disclosed
WO-2000076519-A1 SULFONAMIDE AND SULFAMIDE SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES COMPANY (US) 2000-12-21 WO disclosed
EP-0735025-B1 Process for producing aminonitropyridines SUMITOMO CHEMICAL CO (JP) 1998-07-01 EP disclosed
US-5648496-A AMINATION SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1997-07-15 US disclosed
EP-0735025-A1 Process for producing aminonitropyridines SUMITOMO CHEMICAL COMPANY LIMITED (JP) 1996-10-02 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 (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-12540137-B2 N-1 branched alkyl ether substituted imidazo[4,5-c]quinoline compounds, compositions, and methods IRF3, IFNAR1, IFNG POLB 1249/4885CTSB 3036/4885MEN1 2108/4885
US-20240300947-A1 N-1 Branched Alkyl Ether Substituted Imidazo[4,5-c]Quinoline Compounds, Compositions, and Methods IFNG, IFNAR1, IRF3 POLB 1634/4885CTSB 3011/4885MEN1 1417/4885
US-12398134-B2 N-1 branched cycloalkyl substituted imidazo[4,5-c]quinoline compounds, compositions, and methods IFNG, IFNAR1, CCL5 POLB 877/4885CTSB 1770/4885MEN1 1490/4885
US-20250129082-A1 N-1 Triazole Substituted Imidazoquinolines, Conjugates Thereof, and Methods IFNG, IFNAR1, IL2 POLB 2893/4885CTSB 2240/4885MEN1 707/4885

“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.