SCHEMBL995085

SCHEMBL995085

O=C(Nc1ccccc1)c1ccccc1[N+](=O)[O-]

nearest known ligand 0.77

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 3/20 0.77
SMN1; SMN2 Q16637 2/20 0.77
HTT P42858 2/20 0.77
NCOA1 Q15788 1/20 0.77
NCOA3 Q9Y6Q9 1/20 0.77
MEN1 O00255 4/20 0.69
KMT2A Q03164 4/20 0.69
ALDH1A1 P00352 4/20 0.69
P2RX1 P51575 1/20 0.65
CYP1A2 P05177 1/20 0.65
CYP3A4 P08684 1/20 0.65
CYP2D6 P10635 1/20 0.65
CYP2C9 P11712 1/20 0.65
CYP2C19 P33261 1/20 0.65
CTSD P07339 1/20 0.65
LMNA P02545 2/20 0.64
MAPT P10636 2/20 0.64
SLC12A2 P55011 1/20 0.64
SLC12A5 Q9H2X9 1/20 0.64
RAB9A P51151 2/20 0.62

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
Methyl Alcohol SCHEMBL4957272 0.97 GAA (0.73) GAASMN1; SMN2HTTNCOA1NCOA3
SCHEMBL4958310 0.92 GAA (0.71) GAASMN1; SMN2HTTNCOA1NCOA3
SCHEMBL4958300 0.92 GAA (0.71) GAASMN1; SMN2HTTNCOA1NCOA3
SCHEMBL94829 0.89 GAA (0.71) GAASMN1; SMN2HTTNCOA1NCOA3
SCHEMBL27657640 0.89 GAA (0.71) GAASMN1; SMN2HTTNCOA1NCOA3
SCHEMBL6814805 0.87 GAA (0.69) GAASMN1; SMN2HTTNCOA1NCOA3
SCHEMBL5226448 0.87 MAPT (0.78) GAASMN1; SMN2HTTNCOA1NCOA3
SCHEMBL1010241 0.87 GAA (0.69) GAASMN1; SMN2HTTNCOA1NCOA3
SCHEMBL8114708 0.87 SMN1; SMN2 (1.00) GAASMN1; SMN2HTTNCOA1NCOA3
SCHEMBL394290 0.87 MEN1 (0.65) GAASMN1; SMN2HTTNCOA1NCOA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115108930-A Synthetic method and application of aminophenyl benzamide compound 合肥工业大学 2022-09-27 CN claimed
CN-108409674-A A kind of preparation method of Ai Dailalisi intermediates 南京法恩化学有限公司 2018-08-17 CN claimed
US-7539006-B2 Electrolytic solution for driving electrolytic capacitor and electrolytic capacitor RUBYCON CORPORATION (JP) 2009-05-26 US claimed
US-20070029529-A1 Electrolytic solution for driving electrolytic capacitor and electrolytic capacitor KOMATSU AKIHIKO 2007-02-08 US claimed
US-20040245105-A1 Electrolyte solution for driving electrolytic capacitor and electrolytic capacitor RUBYCON CORPORATION (JP) 2004-12-09 US claimed
EP-1437749-A1 ELECTROLYTE SOLUTION FOR DRIVING ELECTROLYTIC CAPACITOR AND ELECTROLYTIC CAPACITOR Rubycon Corporation (JP) 2004-07-14 EP claimed
EP-0670855-A1 NITRO OR NITROSO GROUP TERMINATED MESOGENIC EPOXY RESIN ADDUCTS THE DOW CHEMICAL COMPANY (US) 1995-09-13 EP claimed
WO-1994012555-A1 NITRO OR NITROSO GROUP TERMINATED MESOGENIC EPOXY RESIN ADDUCTS THE DOW CHEMICAL COMPANY (US) 1994-06-09 WO claimed
US-3969510-A BENZAMIDE BADISCHE ANILIN- & SODA-FABRIK AKTIENGESELLSCHAFT (DT) 1976-07-13 US claimed
EP-4622964-A1 QUINAZOLINONE DERIVATIVES FOR HDAC INHIBITION Gilva Therapeutics Co., Ltd. (TW) 2025-10-01 EP disclosed
WO-2025085669-A1 QUINAZOLINONE DERIVATIVES FOR HDAC INHIBITION GILVA THERAPEUTICS CO., LTD. (CN) 2025-04-24 WO disclosed
US-12065421-B2 Inhibitors of oplophorus luciferase-derived bioluminescent complexes PROMEGA CORPORATION (US) 2024-08-20 US disclosed
EP-4140991-B1 INHIBITORS OF OPLOPHORUS LUCIFERASE-DERIVED BIOLUMINESCENT COMPLEXES PROMEGA CORP (US) 2024-05-15 EP disclosed
EP-4140991-A1 INHIBITORS OF OPLOPHORUS LUCIFERASE-DERIVED BIOLUMINESCENT COMPLEXES Promega Corporation (US) 2023-03-01 EP disclosed
US-5047573-A Process for the production of peptides using diacylamines BRADACZEK HANS (DE) 1991-09-10 US disclosed
EP-0259396-B1 PROCESS FOR PEPTIDE PRODUCTION BRADACZEK, Hans (DE) 1991-07-24 EP disclosed
EP-0259396-A1 PROCESS FOR PEPTIDE PRODUCTION. BRADACZEK HANS (DE) 1988-03-16 EP disclosed
WO-1987005292-A1 PROCESS FOR PEPTIDE PRODUCTION BRADACZEK HANS (DE) 1987-09-11 WO disclosed
US-4123554-A Fungicidal and germicidal benzanilides KUMIAI CHEMICAL INDUSTRY CO., LTD. (JP) 1978-10-31 US disclosed
US-4004029-A BENZAMIDES THE UPJOHN COMPANY (US) 1977-01-18 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 (1 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-12065421-B2 Inhibitors of oplophorus luciferase-derived bioluminescent complexes LUC7L2, LYPLAL1, GUSB GAA 937/4885SMN1; SMN2 2491/4885HTT 3910/4885

“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.