SCHEMBL1149066

SCHEMBL1149066

Cc1cccc(C(C)C)c1N=C=O

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GABRA1 P14867 4/20 0.44
GABRB2 P47870 3/20 0.44
CYP3A4 P08684 3/20 0.42
LMNA P02545 3/20 0.38
GABRG2 P18507 2/20 0.38
GABRB3 P28472 2/20 0.38
TSHR P16473 2/20 0.38
FAAH O00519 1/20 0.38
CA1 P00915 1/20 0.38
CA2 P00918 1/20 0.38
CYP1A2 P05177 1/20 0.38
HPGD P15428 1/20 0.38
GABRB1 P18505 1/20 0.38
PTGS1 P23219 1/20 0.38
SLC6A2 P23975 1/20 0.38
HTR2C P28335 1/20 0.38
GABRA5 P31644 1/20 0.38
GABRA3 P34903 1/20 0.38
HTR2B P41595 1/20 0.38
GABRA2 P47869 1/20 0.38

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
SCHEMBL191769 0.88 GABRA1 (0.50) GABRA1GABRB2CYP3A4LMNAGABRG2
SCHEMBL11416327 0.85 GABRA1 (0.40) GABRA1GABRB2CYP3A4LMNAGABRG2
Carbimide SCHEMBL29047475 0.83 GABRA1 (0.46) GABRA1GABRB2CYP3A4LMNAGABRG2
SCHEMBL24228574 0.83 GABRA1 (0.39) GABRA1GABRB2CYP3A4LMNAGABRG2
SCHEMBL374209 0.82 GABRA1 (0.56) GABRA1GABRB2CYP3A4TSHRCA1
SCHEMBL112144 0.81 CYP3A4 (0.52) GABRA1GABRB2CYP3A4LMNAGABRG2
SCHEMBL1019702 0.81 GABRA1 (0.43) GABRA1GABRB2CYP3A4LMNAGABRG2
SCHEMBL9623520 0.80 GABRA1 (0.47) GABRA1GABRB2CYP3A4LMNAGABRG2
SCHEMBL3440189 0.80 CYP3A4 (0.50) GABRA1GABRB2CYP3A4TRPA1
SCHEMBL1456958 0.79 GABRA1 (0.70) GABRA1GABRB2CYP3A4LMNAGABRG2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103304446-B Derivatization method of optically active phenylacetylene compound UNIV HARBIN ENG 2015-02-25 CN claimed
EP-1377589-B1 OXAZOLYL-PYRAZOLE DERIVATIVES AS KINASE INHIBITORS PHARMACIA ITALIA SPA (IT) 2005-09-07 EP claimed
US-20250223263-A1 SELECTIVE INHIBITORS OF NLRP3 INFLAMMASOME NodThera Limited (GB) 2025-07-10 US disclosed
US-12247011-B2 Selective inhibitors of NLRP3 inflammasome NodThera Limited (GB) 2025-03-11 US disclosed
CN-118930990-A Preparation process of flexible plastic sports ground material 道一高分子聚合物(宁波)有限公司 2024-11-12 CN disclosed
CN-111356680-B Selective inhibitors of NLRP3 inflammasome 诺瑟拉有限公司 2023-11-28 CN disclosed
EP-3661921-B1 SELECTIVE INHIBITORS OF NLRP3 INFLAMMASOME NODTHERA LTD (GB) 2023-10-18 EP disclosed
EP-3661921-B1 SELECTIVE INHIBITORS OF NLRP3 INFLAMMASOME NODTHERA LTD (GB) 2023-10-18 EP disclosed
US-11773312-B2 Breaker additives for extended delay in removal of oil-based filter cakes HALLIBURTON ENERGY SERVICES, INC. (US) 2023-10-03 US disclosed
US-20220220358-A1 Breaker Additives For Extended Delay In Removal Of Oil-Based Filter Cakes HALLIBURTON ENERGY SERVICES, INC. (US) 2022-07-14 US disclosed
CN-114231163-A Polyurethane organic-inorganic composite material and preparation method and application thereof 武汉工程大学 2022-03-25 CN disclosed
WO-1998046786-A1 COMBINATORIAL LIBRARIES OF PEPTIDOMIMETIC AMINOTHIOETHER ACIDS ELI LILLY AND COMPANY (US) 1998-10-22 WO disclosed
WO-1998032733-A1 SULFONYL UREA DERIVATIVES AND THEIR USE IN THE CONTROL OF INTERLEUKIN-1 ACTIVITY PFIZER INC. (US) 1998-07-30 WO disclosed
WO-1998008839-A1 COMBINATORIAL PROCESS FOR PREPARING SUBSTITUTED THIOPHENE LIBRARIES ELI LILLY AND COMPANY (US) 1998-03-05 WO disclosed
EP-0816309-A1 Scavenger assisted combinatorial process for preparing libraries of urea and thiourea compounds ELI LILLY AND COMPANY (US) 1998-01-07 EP disclosed
WO-1997026300-A1 COMBINATORIAL PROCESS FOR PREPARING SUBSTITUTED INDANE LIBRARIES ELI LILLY AND COMPANY (US) 1997-07-24 WO disclosed
CN-1047859-A Benzo cycloalkane derivatives and preparation method thereof TAKEDA CHEMICAL INDUSTRIES LTD (JP) 1990-12-19 CN disclosed
EP-0217787-A4 AMIDINOUREA PROCESS AND PHARMACEUTICAL COMPOSITION. RORER INTERNAT OVERSEAS INC (US) 1988-07-21 EP disclosed
EP-0217787-A1 AMIDINOUREA PROCESS AND PHARMACEUTICAL COMPOSITION RORER INTERNATIONAL (OVERSEAS) INC. (a Delaware corporation) (US) 1987-04-15 EP disclosed
WO-1986004935-A1 AMIDINOUREA PROCESS AND PHARMACEUTICAL COMPOSITION RORER INTERNATIONAL (OVERSEAS) INC. (US) 1986-08-28 WO 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 (2 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-12247011-B2 Selective inhibitors of NLRP3 inflammasome NLRP3, NOD1, NLRP1 GABRA1 2922/4885GABRB2 2882/4885CYP3A4 2832/4885
US-20250223263-A1 SELECTIVE INHIBITORS OF NLRP3 INFLAMMASOME NLRP3, NOD1, NLRP1 GABRA1 2922/4885GABRB2 2882/4885CYP3A4 2832/4885

“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.