SCHEMBL179913

SCHEMBL179913

O=C1CCc2cc3c(cc21)CCC3

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.64
MAPK1 P28482 1/20 0.64
KMT2A Q03164 1/20 0.64
NPSR1 Q6W5P4 1/20 0.64
MAOA P21397 4/20 0.48
MAOB P27338 4/20 0.48
PRKCI P41743 1/20 0.48
CDC25B P30305 1/20 0.48
PBRM1 Q86U86 1/20 0.47
CASP1 P29466 1/20 0.47
CASP7 P55210 1/20 0.47
HSD17B10 Q99714 1/20 0.47
CYP2A6 P11509 1/20 0.45
HSD17B1 P14061 3/20 0.43
GRIN2D O15399 1/20 0.41
GRIN3B O60391 1/20 0.41
GRIN1 Q05586 1/20 0.41
GRIN2A Q12879 1/20 0.41
GRIN2B Q13224 1/20 0.41
GRIN2C Q14957 1/20 0.41

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
SCHEMBL11111147 0.95 MEN1 (0.59) MEN1MAPK1KMT2ANPSR1MAOA
SCHEMBL3454654 0.93 MEN1 (0.73) MEN1MAPK1KMT2ANPSR1MAOA
SCHEMBL20681358 0.93 MEN1 (0.54) MEN1MAPK1KMT2ANPSR1MAOA
SCHEMBL25945154 0.91 MEN1 (0.70) MEN1MAPK1KMT2ANPSR1MAOA
SCHEMBL4878423 0.88 MEN1 (0.67) MEN1MAPK1KMT2ANPSR1MAOA
SCHEMBL21810615 0.86 MEN1 (0.50) MEN1MAPK1KMT2ANPSR1MAOA
SCHEMBL8284440 0.85 MEN1 (0.69) MEN1MAPK1KMT2ANPSR1MAOA
SCHEMBL15549968 0.79 MEN1 (1.00) MEN1MAPK1KMT2ANPSR1MAOA
SCHEMBL20681295 0.76 GRIN2D (0.46) MEN1MAPK1KMT2ANPSR1MAOA
SCHEMBL28655417 0.76 HSD17B1 (0.65) MEN1MAPK1KMT2ANPSR1MAOA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3867231-B1 NOVEL PROCESSES INFLAZOME LTD (IE) 2024-05-01 EP claimed
US-11724988-B2 Processes INFLAZOME LIMITED (IE) 2023-08-15 US claimed
US-20220064125-A1 NOVEL PROCESSES INFLAZOME LIMITED (IE) 2022-03-03 US claimed
US-12617802-B2 Sulfonimidamide compounds as NLRP3 modulators GENENTECH, INC. (US) 2026-05-05 US disclosed
US-12577228-B2 Dihydrocyclopenta-isoquinoline-sulfonamide derivatives compounds UCB Biopharma SRL (BE) 2026-03-17 US disclosed
EP-4081296-B1 DIHYDROCYCLOPENTA-ISOQUINOLINE-SULFONAMIDE DERIVATIVES COMPOUNDS UCB Biopharma SRL (BE) 2026-02-11 EP disclosed
EP-4034579-B1 CATALYSTS BOREALIS AG (AT) 2025-07-23 EP disclosed
US-12319772-B2 Catalysts BOREALIS AG (AT) 2025-06-03 US disclosed
CN-119823022-A NLRP3 small-molecule protein degradation agent and preparation method and application thereof 复旦大学 2025-04-15 CN disclosed
US-20240391884-A1 COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH NLRP ACTIVITY NOVARTIS AG (CH) 2024-11-28 US disclosed
US-12084424-B2 Compounds and compositions for treating conditions associated with NLRP activity NOVARTIS AG (CH) 2024-09-10 US disclosed
WO-2001019390-A1 COMBINATION TREATMENT WITH IL-1RA AND DIARYL SULPHONYL UREA COMPOUNDS PFIZER PRODUCTS INC. (US) 2001-03-22 WO disclosed
US-6166064-A Sulfonyl urea derivatives and their use in the control of interleukin-1 activity PFIZER INC (US) 2000-12-26 US disclosed
EP-0964849-A1 SULFONYL UREA DERIVATIVES AND THEIR USE IN THE CONTROL OF INTERLEUKIN-1 ACTIVITY PFIZER INC. (US) 1999-12-22 EP disclosed
EP-0923589-A1 3-HETEROATOM SUBSTITUTED CYCLOPENTADIENYL-CONTAINING METAL COMPLEXES AND OLEFIN POLYMERIZATION PROCESS THE DOW CHEMICAL COMPANY (US) 1999-06-23 EP 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-1998006727-A1 3-HETEROATOM SUBSTITUTED CYCLOPENTADIENYL-CONTAINING METAL COMPLEXES AND OLEFIN POLYMERIZATION PROCESS THE DOW CHEMICAL COMPANY (US) 1998-02-19 WO disclosed
EP-0039025-B1 DERIVATIVES OF ARYL KETONES AS SENSITIZERS OF PHOTOPOLYMERIZABLE COMPOUNDS FOR THE VISIBLE SPECTRAL RANGE, AND PHOTOPOLYMERIZABLE COMPOSITIONS COMPRISING THE SAID SENSITIZERS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1984-03-14 EP disclosed
US-4351893-A TRIARYLIMIDAZOLE DIMER INITIATORS E. I. DU PONT DE NEMOURS AND COMPANY (US) 1982-09-28 US disclosed
EP-0039025-A1 Derivatives of aryl ketones as sensitizers of photopolymerizable compounds for the visible spectral range, and photopolymerizable compositions comprising the said sensitizers E.I. DU PONT DE NEMOURS AND COMPANY (US) 1981-11-04 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 (7 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-12319772-B2 Catalysts SIGMAR1, C1S, CYCS MEN1 1417/4885MAPK1 2399/4885KMT2A 1180/4885
US-12617802-B2 Sulfonimidamide compounds as NLRP3 modulators NLRP3, NLRP1, PYCARD MEN1 4299/4885MAPK1 1095/4885KMT2A 3993/4885
US-12577228-B2 Dihydrocyclopenta-isoquinoline-sulfonamide derivatives compounds FCGR2A, FCER2, FCGR1A MEN1 3166/4885MAPK1 2556/4885KMT2A 1500/4885
US-20220064125-A1 NOVEL PROCESSES NLRP3, NOD1, NLRP1 MEN1 4329/4885MAPK1 1614/4885KMT2A 4832/4885
US-12084424-B2 Compounds and compositions for treating conditions associated with NLRP activity NLRP1, NLRP3, NOD1 MEN1 3390/4885MAPK1 1647/4885KMT2A 4441/4885
US-20240391884-A1 COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH NLRP ACTIVITY NLRP1, NLRP3, NOD1 MEN1 3390/4885MAPK1 1647/4885KMT2A 4441/4885
US-11724988-B2 Processes NLRP3, NOD1, NLRP1 MEN1 3749/4885MAPK1 1548/4885KMT2A 4604/4885

“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.