SCHEMBL8437

SCHEMBL8437

COc1cccnc1[N+](=O)[O-]

nearest known ligand 0.56

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
HTT P42858 2/20 0.55
KMT2A Q03164 4/20 0.55
MEN1 O00255 3/20 0.54
ATM Q13315 1/20 0.53
L3MBTL1 Q9Y468 2/20 0.52
ALDH1A1 P00352 4/20 0.52
TDP1 Q9NUW8 1/20 0.52
NPC1 O15118 2/20 0.51
S1PR4 O95977 1/20 0.51
RAB9A P51151 1/20 0.51
POLB P06746 2/20 0.51
MAPT P10636 2/20 0.51
ESR2 Q92731 1/20 0.51
KDM4E B2RXH2 1/20 0.47
RECQL P46063 1/20 0.47
MCL1 Q07820 1/20 0.47

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
SCHEMBL15767908 0.88 KMT2A (0.50) HTTKMT2AMEN1ATML3MBTL1
SCHEMBL27867259 0.83 KMT2A (0.56) HTTKMT2AMEN1ATML3MBTL1
SCHEMBL5143899 0.82 NPC1 (0.63) HTTKMT2AMEN1ATML3MBTL1
SCHEMBL3142475 0.82 S1PR4 (0.63) HTTKMT2AMEN1ATML3MBTL1
SCHEMBL8159969 0.81 KMT2A (0.54) HTTKMT2AMEN1L3MBTL1ALDH1A1
SCHEMBL8789338 0.81 KMT2A (0.54) HTTKMT2AMEN1L3MBTL1ALDH1A1
SCHEMBL31040108 0.81 HTT (0.53) HTTKMT2AMEN1ATML3MBTL1
SCHEMBL26481653 0.81 NPC1 (0.51) HTTKMT2AMEN1L3MBTL1ALDH1A1
SCHEMBL17066377 0.80 S1PR4 (0.60) HTTKMT2AMEN1ATML3MBTL1
SCHEMBL4555887 0.79 NPC1 (0.59) HTTKMT2AMEN1L3MBTL1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116589399-A Preparation method of 3-methoxy-2-nitropyridine 济南大学 2023-08-15 CN claimed
CN-103483247-B Preparation method of 2-bromo-3-methoxypyridine BEIJING GREENCHEM TECHNOLOGY CO LTD 2015-05-13 CN claimed
CN-103483247-A Preparation method of 2-bromo-3-methoxypyridine BEIJING GREENCHEM TECHNOLOGY CO LTD 2014-01-01 CN claimed
EP-4262788-B1 UREA OREXIN RECEPTOR AGONISTS MERCK SHARP & DOHME LLC (US) 2026-01-21 EP disclosed
US-12528834-B2 Method for producing peptide compound NISSAN CHEMICAL CORPORATION (JP) 2026-01-20 US disclosed
EP-4425181-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTE Bertis Inc (KR) 2024-09-04 EP disclosed
CN-117794529-A POLO-like kinase 4 inhibitors 欧瑞克制药公司 2024-03-29 CN disclosed
US-20240101555-A1 UREA OREXIN RECEPTOR AGONISTS MERCK SHARP & DOHME LLC (US) 2024-03-28 US disclosed
US-20240011979-A1 COMPOSITION FOR DETECTING OR MEASURING ANALYTES BERTIS INC. (KR) 2024-01-11 US disclosed
US-11858915-B2 Polo like kinase 4 inhibitors ORIC PHARMACEUTICALS, INC. (US) 2024-01-02 US disclosed
EP-4262788-A1 UREA OREXIN RECEPTOR AGONISTS Merck Sharp & Dohme LLC (US) 2023-10-25 EP disclosed
US-RE38073-E1 Biosynthesis; using dehydration agent RESEARCH CORPORATIONS TECHNOLOGIES, INC. 2003-04-08 US disclosed
US-RE37686-E1 Azahydroxybenzotriazoles and derivatives thereof for peptide coupling reactions RESEARCH CORPORATION TECHNOLOGIES, INC. 2002-04-30 US disclosed
US-5698675-A AMIDATION; ESTERIFICATION RESEARCH CORPORATION TECH., INC. (US) 1997-12-16 US disclosed
US-5644029-A TRIAZOLO-PYRIDINE HETEROCYCLIC COMPOUNDS RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1997-07-01 US disclosed
US-5580981-A YELLOW INDICATORS FADING TO COLORLESS UPON COMPLETION OF THE ACYLATION STEP IN AMIDE FORMATION; REACTION ACCELERATORS; LOWERS RACEMIZATION RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1996-12-03 US disclosed
EP-0662078-A1 NEW REAGENTS FOR PEPTIDE COUPLINGS RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1995-07-12 EP disclosed
WO-1994007910-A1 NEW REAGENTS FOR PEPTIDE COUPLINGS RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1994-04-14 WO disclosed
US-4264599-A HYPOTENSIVE AGENTS, ADRENERGIC BLOCKING AGENTS CIBA-GEIGY CORPORATION (US) 1981-04-28 US disclosed
EP-0000485-A1 Piperidino-propanols, their preparation and pharmaceutical compounds containing them CIBA-GEIGY AG (CH) 1979-02-07 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 (3 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-11858915-B2 Polo like kinase 4 inhibitors PLK4, PLK2, PLK3 HTT 4049/4885KMT2A 1756/4885MEN1 4192/4885
US-12528834-B2 Method for producing peptide compound VIP, IAPP, NPPA HTT 162/4885KMT2A 3946/4885MEN1 355/4885
US-20240101555-A1 UREA OREXIN RECEPTOR AGONISTS HCRTR1, HCRTR2, UTS2R HTT 135/4885KMT2A 2161/4885MEN1 2168/4885

“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.