SCHEMBL15285331

SCHEMBL15285331

CC(C)(C)OC(=O)N(CCO)C1CC1

nearest known ligand 0.36

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA14 Q9ULX7 1/20 0.36
SSTR4 P31391 1/20 0.34
DPP4 P27487 1/20 0.33
ASGR1 P07306 1/20 0.33
NFKB1 P19838 1/20 0.33
NFKB2 Q00653 1/20 0.33
RELA Q04206 1/20 0.33
HDAC6 Q9UBN7 2/20 0.33
HDAC1 Q13547 1/20 0.33
HDAC2 Q92769 1/20 0.33
HSD11B1 P28845 2/20 0.32
CCR5 P51681 1/20 0.32
GPR119 Q8TDV5 1/20 0.32
ADORA2A P29274 1/20 0.32
ADORA1 P30542 1/20 0.32
NR1H2 P55055 1/20 0.32
REN P00797 1/20 0.32
TDP1 Q9NUW8 1/20 0.32
CHRM2 P08172 1/20 0.31
CHRM1 P11229 1/20 0.31

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
SCHEMBL10325232 0.94 ASGR1 (0.33) CA14SSTR4DPP4ASGR1NFKB1
SCHEMBL2660690 0.94 CA14 (0.33) CA14SSTR4DPP4ASGR1NFKB1
SCHEMBL1238808 0.94 CA14 (0.33) CA14SSTR4DPP4ASGR1NFKB1
SCHEMBL13641157 0.94 ASGR1 (0.33) CA14SSTR4DPP4ASGR1NFKB1
SCHEMBL10323856 0.93 CA14 (0.34) CA14SSTR4DPP4ASGR1NFKB1
SCHEMBL1067463 0.92 EPHX1 (0.36) CA14DPP4HSD11B1L3MBTL1
SCHEMBL4914499 0.90 CA14 (0.37) CA14SSTR4DPP4ASGR1NFKB1
SCHEMBL20674336 0.89 SLC6A4 (0.35) CA14RENCHRM3
SCHEMBL4711748 0.88 CA14 (0.39) CA14DPP4ASGR1NFKB1NFKB2
SCHEMBL8218482 0.88 NFKB1 (0.34) CA14SSTR4ASGR1NFKB1NFKB2

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240252506-A1 COMPOUNDS FOR TREATMENT OF BACTERIAL INFECTION HOFFMANN-LA ROCHE INC. (US) 2024-08-01 US disclosed
EP-4405353-A1 NEW COMPOUNDS AND THEIR USE IN THE TREATMENT OF BACTERIAL INFECTION F. Hoffmann-La Roche AG (CH) 2024-07-31 EP disclosed
EP-4126855-B1 COMPOUNDS AND THEIR USE IN THE TREATMENT OF BACTERIAL INFECTIONS HOFFMANN LA ROCHE (CH) 2024-04-24 EP disclosed
US-11873291-B2 Quinoline cGAS antagonist compounds IMMUNESENSOR THERAPEUTICS, INC. (US) 2024-01-16 US disclosed
US-20230167127-A1 COMPOUNDS AND THEIR USE IN THE TREATMENT OF BACTERIAL INFECTION HOFFMANN-LA ROCHE INC. (US) 2023-06-01 US disclosed
WO-2023041757-A1 NEW COMPOUNDS AND THEIR USE IN THE TREATMENT OF BACTERIAL INFECTION F. HOFFMANN-LA ROCHE AG (CH) 2023-03-23 WO disclosed
EP-4126855-A1 COMPOUNDS AND THEIR USE IN THE TREATMENT OF BACTERIAL INFECTION F. Hoffmann-La Roche AG (CH) 2023-02-08 EP disclosed
CN-115298176-A Compounds and their use in the treatment of bacterial infections 豪夫迈·罗氏有限公司 2022-11-04 CN disclosed
WO-2021190727-A1 COMPOUNDS AND THEIR USE IN THE TREATMENT OF BACTERIAL INFECTION F. HOFFMANN-LA ROCHE AG (CH) 2021-09-30 WO disclosed
EP-2831075-A1 1,3,4-OXADIAZOLE AND 1,3,4-THIADIAZOLE BETA-LACTAMASE INHIBITORS Cubist Pharmaceuticals, Inc. (US) 2015-02-04 EP disclosed
WO-2013149121-A1 1,3,4-OXADIAZOLE AND 1,3,4-THIADIAZOLE BETA-LACTAMASE INHIBITORS CUBIST PHARMACEUTICALS, INC. (US) 2013-10-03 WO disclosed
CN-100463908-C Substituted 8 '-pyridyl-dihydrospiro- [ cycloalkyl ] -pyrimido [1, 2-a ] pyrimidin-6-one and 8' -pyrimidinyl-dihydrospiro- [ cycloalkyl ] -pyrimido [1, 2-a ] pyrimidin-6-one derivatives SANOFI AVENTIS (FR) 2009-02-25 CN disclosed
CN-1777607-A Substituted 8 '-pyridyl-dihydrospiro- [ cycloalkyl ] -pyrimido [1, 2-a ] pyrimidin-6-one and 8' -pyrimidinyl-dihydrospiro- [ cycloalkyl ] -pyrimido [1, 2-a ] pyrimidin-6-one derivatives SANOFI AVENTIS (FR) 2006-05-24 CN 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 (3 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-11873291-B2 Quinoline cGAS antagonist compounds CGAS, GLS2, GLS CA14 3425/4885SSTR4 710/4885DPP4 332/4885
US-20230167127-A1 COMPOUNDS AND THEIR USE IN THE TREATMENT OF BACTERIAL INFECTION LTB4R, C5, C3AR1 CA14 2607/4885SSTR4 1973/4885DPP4 1404/4885
US-20240252506-A1 COMPOUNDS FOR TREATMENT OF BACTERIAL INFECTION C3AR1, LTB4R, C5 CA14 2865/4885SSTR4 2569/4885DPP4 2168/4885

“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.