SCHEMBL1412816

SCHEMBL1412816

O=C(NO)c1ccccn1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CES2 O00748 1/20 0.61
▸ CES1 P23141 1/20 0.61
▸ LMNA P02545 2/20 0.59
▸ L3MBTL1 Q9Y468 2/20 0.59
▸ NAPRT Q6XQN6 1/20 0.59
▸ P4HTM Q9NXG6 1/20 0.59
▸ TLR7 Q9NYK1 2/20 0.59
▸ HDAC6 Q9UBN7 3/20 0.58
▸ HDAC3 O15379 2/20 0.58
▸ HDAC4 P56524 2/20 0.58
▸ HDAC1 Q13547 2/20 0.58
▸ HDAC7 Q8WUI4 2/20 0.58
▸ HDAC2 Q92769 2/20 0.58
▸ HDAC10 Q969S8 2/20 0.58
▸ HDAC11 Q96DB2 2/20 0.58
▸ HDAC8 Q9BY41 2/20 0.58
▸ HDAC9 Q9UKV0 2/20 0.58
▸ HDAC5 Q9UQL6 2/20 0.58
▸ ALDH1A1 P00352 3/20 0.57
▸ KMT2A Q03164 3/20 0.56

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
Iodomethane SCHEMBL17005795 0.94 ALDH1A1 (0.57) CES2CES1LMNAL3MBTL1NAPRT
SCHEMBL1147702 0.84 KDM4E (0.73) CES2CES1LMNAL3MBTL1NAPRT
SCHEMBL4508472 0.84 CES2 (0.64) CES2CES1LMNAL3MBTL1NAPRT
SCHEMBL1422257 0.83 CES2 (0.61) CES2CES1LMNAL3MBTL1NAPRT
SCHEMBL11223392 0.83 CES2 (0.61) CES2CES1LMNAL3MBTL1NAPRT
SCHEMBL28727383 0.83 CES2 (0.61) CES2CES1LMNAL3MBTL1NAPRT
SCHEMBL674215 0.82 HDAC2 (0.62) TLR7HDAC6HDAC2HDAC8SMN1; SMN2
SCHEMBL23723198 0.81 CES2 (0.59) CES2CES1LMNAL3MBTL1NAPRT
SCHEMBL162189 0.81 ALDH1A1 (0.61) CES2CES1LMNAL3MBTL1NAPRT
SCHEMBL4754862 0.81 CES2 (0.59) CES2CES1LMNAL3MBTL1NAPRT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025011632-A1 HYDROXIMIC ACID COMPOUNDS CONTAINING TETRAHYDROBENZO[4,5]FURANO[2,3-C]PYRIDINE, PREPARATION METHOD THEREFOR, AND USES THEREOF 浙江大学 2025-01-16 — — WO claimed
CN-117088891-A Tetrahydrobenzo [4,5] furan [2,3-C ] pyridine hydroxamic acid compound and preparation method and application thereof 浙江大学 2023-11-21 — — CN claimed
WO-2023097386-A1 SELECTIVE HDAC6-INHIBITING N-ACYLHYDRAZONE COMPOUNDS, METHODS FOR PRODUCING SAME, COMPOSITIONS, USES, TREATMENT METHODS AND KITS EUROFARMA LABORATÓRIOS S.A (BR) 2023-06-08 — — WO claimed
US-7754730-B2 Arylindenopyridines and arylindenopyrimidines and related therapeutic and prophylactic methods ORTHO-MCNEIL PHARMACEUTICAL, INC. (US) 2010-07-13 — — US claimed
EP-1003751-A1 HYDROXAMIC ACID SUBSTITUTED FUSED HETEROCYCLIC METALLOPROTEINASE INHIBITORS AMGEN INC. (US) 2000-05-31 — — EP claimed
WO-1999006410-A1 HYDROXAMIC ACID SUBSTITUTED FUSED HETEROCYCLIC METALLOPROTEINASE INHIBITORS AMGEN INC. (US) 1999-02-11 — — WO claimed
EP-0060144-A2 Cephalosporin antibiotics ELI LILLY AND COMPANY (US) 1982-09-15 — — EP claimed
JP-57120597-A — — None — — JP disclosed
JP-5201964-A — — None — — JP disclosed
US-20260098032-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION PMV PHARMACEUTICALS INC (US) 2026-04-09 — — US disclosed
US-12570645-B2 Uses of p53 x-ray co-crystal structures PMV PHARMACEUTICALS, INC. (US) 2026-03-10 — — US disclosed
US-20260027097-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION PMV PHARMACEUTICALS INC (US) 2026-01-29 — — US disclosed
US-20250319063-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT P53 FUNCTION PMV PHARMACEUTICALS, INC. 2025-10-16 — — US disclosed
WO-1993015044-A1 N-BENZYLOXAMIC ACID, OXAMATE, AND OXAMIDE DERIVATIVES AND THEIR USE AS TNF AND PDE IV INHIBITORS SMITHKLINE BEECHAM CORPORATION (US) 1993-08-05 — — WO disclosed
EP-0065039-B1 AN O-(N-ALKOXY-PYRIDINECARBOXIMIDOYL)PHOSPHATE, A PROCESS FOR PRODUCING THE SAME, AND AN INSECTICIDAL OR ACARICIDAL COMPOSITION CONTAINING THE SAME ISHIHARA SANGYO KAISHA LTD. (JP) 1984-08-22 — — EP disclosed
EP-0065039-A1 An O-(N-alkoxy-pyridinecarboximidoyl)phosphate, a process for producing the same, and an insecticidal or acaricidal composition containing the same ISHIHARA SANGYO KAISHA LTD. (JP) 1982-11-24 — — EP disclosed
EP-0060144-A2 Cephalosporin antibiotics ELI LILLY AND COMPANY (US) 1982-09-15 — — EP disclosed
JP-S57120597-A ORGANOPHOSPHORUS COMPOUND AND INSECTICIDE CONTAINING THE SAME ISHIHARA SANGYO KAISHA LTD 1982-07-27 — — JP disclosed
US-4336253-A Cephalosporin antibiotics ELI LILLY AND COMPANY (US) 1982-06-22 — — US disclosed
US-4327089-A O-(N-Alkoxy-pyridinecarboximidoyl) phosphates, process for producing the same, and insecticidal or acaridical compositions containing the same ISHIHARA SANGYO KAISHA LTD. (JP) 1982-04-27 — — 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 (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-20250319063-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT P53 FUNCTION TP53, TP53BP1, KRAS CES2 3852/4885CES1 3063/4885LMNA 2868/4885
US-20260027097-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION TP53, TP53BP1, BRCA1 CES2 4582/4885CES1 3502/4885LMNA 3630/4885
US-12570645-B2 Uses of p53 x-ray co-crystal structures TP53, TP53BP1, ERCC2 CES2 4627/4885CES1 3155/4885LMNA 2092/4885
US-20260098032-A1 METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION TP53, TP53BP1, MDM2 CES2 4735/4885CES1 4448/4885LMNA 662/4885

“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.

Send feedback