SCHEMBL118496

SCHEMBL118496

COC(=O)c1cc(=O)[nH]c(=O)[nH]1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 1.00
LMNA P02545 2/20 0.59
ALDH1A1 P00352 1/20 0.59
GPR84 Q9NQS5 4/20 0.55
MEN1 O00255 2/20 0.49
KMT2A Q03164 2/20 0.49
MAPK1 P28482 1/20 0.47
GAA P10253 3/20 0.46
GLA P06280 2/20 0.46
KDM4E B2RXH2 2/20 0.46
CA1 P00915 1/20 0.43
XDH P47989 1/20 0.42
MAPT P10636 3/20 0.42
SMN1; SMN2 Q16637 1/20 0.41
ALPL P05186 1/20 0.39
POLB P06746 1/20 0.39
RAB9A P51151 1/20 0.39

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
SCHEMBL11841644 0.83 CYP1A2 (0.71) CYP1A2LMNAALDH1A1GPR84MEN1
SCHEMBL28078211 0.82 CYP1A2 (0.69) CYP1A2LMNAALDH1A1GPR84MEN1
Ammonia Solution, Strong SCHEMBL28111982 0.82 CYP1A2 (0.69) CYP1A2LMNAALDH1A1GPR84MEN1
SCHEMBL27735725 0.82 CYP1A2 (0.69) CYP1A2LMNAALDH1A1GPR84MEN1
SCHEMBL11042365 0.81 CYP1A2 (0.68) CYP1A2LMNAALDH1A1GPR84MEN1
SCHEMBL12872719 0.81 CYP1A2 (0.68) CYP1A2LMNAALDH1A1GPR84KMT2A
SCHEMBL29216003 0.80 CYP1A2 (0.67) CYP1A2LMNAALDH1A1GPR84MEN1
SCHEMBL1050338 0.80 CYP1A2 (0.67) CYP1A2LMNAALDH1A1GPR84MEN1
SCHEMBL917082 0.79 GPR84 (0.68) CYP1A2LMNAALDH1A1GPR84MEN1
SCHEMBL4283121 0.78 CYP1A2 (0.64) CYP1A2LMNAALDH1A1GPR84MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119855815-A KRAS mutant protein inhibitor, and preparation method and application thereof 甘李药业股份有限公司 2025-04-18 CN claimed
CN-118325313-A Polylactic acid composition and application thereof in degradable food packaging 山东铭达包装制品股份有限公司 2024-07-12 CN claimed
WO-2024061333-A1 KRAS MUTANT PROTEIN INHIBITOR, PREPARATION METHOD THEREFOR, AND USE THEREOF 甘李药业股份有限公司 2024-03-28 WO claimed
CN-107298656-A For pyrimidine intermediate and for pyrimidine intermediate, for pyrimidine, for the preparation method of pyrimidine hydrochloride 四川同晟生物医药有限公司 2017-10-27 CN claimed
CN-106831607-A A kind of synthetic method of 6 chloromethyluracil 山东创新药物研发有限公司 2017-06-13 CN claimed
EP-3881848-B1 METHOD FOR PRODUCING OROTIC ACID DERIVATIVE RESONAC CORP (JP) 2025-07-23 EP disclosed
WO-2025136936-A1 AGONISTS OF TREM2 ACTIVITY MERCK SHARP & DOHME LLC (US) 2025-06-26 WO disclosed
EP-4551575-A2 TREM2 MODULATORS Muna Therapeutics ApS (DK) 2025-05-14 EP disclosed
US-20250136587-A1 N3-SUBSTITUTED URACIL COMPOUNDS AS TRPA1 INHIBITORS D. E. SHAW RESEARCH, LLC 2025-05-01 US disclosed
CN-119855815-A KRAS mutant protein inhibitor, and preparation method and application thereof 甘李药业股份有限公司 2025-04-18 CN disclosed
CN-119403806-A TREM2 modulators 穆纳治疗有限公司 2025-02-07 CN disclosed
EP-4472627-A2 N3-SUBSTITUTED URACIL COMPOUNDS AS TRPA1 INHIBITORS D.E. Shaw Research, LLC (US) 2024-12-11 EP disclosed
US-5659348-A APPLYING TO A SUBSTRATE XEROX CORPORATION (US) 1997-08-19 US disclosed
EP-0743573-A2 Method for obtaining image contrast migration imaging members XEROX CORPORATION (US) 1996-11-20 EP disclosed
EP-0743574-A2 Migration imaging members XEROX CORPORATION (US) 1996-11-20 EP disclosed
US-5563014-A SOFTENABLE LAYER CONTAINIG PHOTOSENSITIVE MARKING MATERIAL; TRANSPARENTIZING AGENT XEROX CORPORATION (US) 1996-10-08 US disclosed
US-5514505-A SELECTIVE TRANSPARENTIZATION OF PHOTOSENSITIVE MIGRATION MARKING PARTICLES EMBEDDED NEAR THE SURFACE OF A SOFTENABLE LAYER SUPPORTED BY AN ELECTROCONDUCTIVE SUBSTRATE XEROX CORPORATION (US) 1996-05-07 US disclosed
EP-0673783-A2 Recording sheets containing purine, pyrimidine, benzimidazole, imidazolidine, urazole, pyrazole, triazole, benzotriazole, tetrazole, and pyrazine compounds XEROX CORPORATION (US) 1995-09-27 EP disclosed
US-4419351-A ANTITUMOR AGENTS RESEARCH CORPORATION (US) 1983-12-06 US disclosed
US-4045556-A ANTIDEPRESSANTS, PYSCHOSTIMULANTS; SILYLATION SCHWERTNER EBERHARD 1977-08-30 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-20250136587-A1 N3-SUBSTITUTED URACIL COMPOUNDS AS TRPA1 INHIBITORS TRPA1, TRPV1, SLC28A1 CYP1A2 2013/4885LMNA 3418/4885ALDH1A1 268/4885

“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.