SCHEMBL1028205

SCHEMBL1028205

CCCCCO[C@H]1CCC[C@@H]1N1C(=O)C=CC1=O

nearest known ligand 0.40

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
PTGS1 P23219 3/20 0.37
PTGS2 P35354 3/20 0.37
MGLL Q99685 3/20 0.37
FAAH O00519 1/20 0.37
PPARG P37231 2/20 0.34
PPARD Q03181 1/20 0.34
PPARA Q07869 1/20 0.34
GBA1 P04062 2/20 0.33
LMNA P02545 1/20 0.33
CHRM1 P11229 3/20 0.32
CHRM2 P08172 1/20 0.32
TP53 P04637 1/20 0.32
MAPT P10636 1/20 0.32
KCNA5 P22460 1/20 0.32
SCN5A Q14524 1/20 0.32

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
SCHEMBL1027864 0.95 USP2 (0.34) PTGS1PTGS2MGLLFAAHLMNA
SCHEMBL1026590 0.89 KCNA5 (0.33) MGLLLMNACHRM1CHRM2MAPT
SCHEMBL1024748 0.83 MAPK1 (0.34) MGLLLMNAMAPT
SCHEMBL1028081 0.79 USP2 (0.34) PTGS1PTGS2MGLLFAAHGBA1
SCHEMBL1025836 0.79 USP2 (0.34) PTGS1PTGS2MGLLFAAHGBA1
SCHEMBL1027234 0.77 USP2 (0.34) PTGS1PTGS2MGLLFAAHGBA1
SCHEMBL1027625 0.77 USP2 (0.34) PTGS1PTGS2MGLLFAAHGBA1
SCHEMBL1028203 0.76 SLC18A3 (0.44) CHRM1CHRM2
SCHEMBL1027575 0.76 CTSV (0.40)
SCHEMBL1026428 0.74 KCNA5 (0.42) MGLLFAAHKCNA5SCN5A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1479669-B1 Optically active maleimide derivatives and polymaleimides for use as chiral adsorbent in chromatography TOSOH CORP (JP) 2011-01-19 EP disclosed
US-7645889-B2 Optically active polymaleimide derivatives and process for their production TOSOH CORPORATION (JP) 2010-01-12 US disclosed
US-20080230482-A1 Optically active polymaleimide derivatives and process for their production TOSOH CORPORATION (JP) 2008-09-25 US disclosed
US-7381742-B2 Optically active polymaleimide derivatives and process for their production TOSOH CORPORATION (JP) 2008-06-03 US disclosed
US-20070131616-A1 Optically active maleimide derivatives, optically active polymaleimide derivatives, process for their production, separating media comprising the optically active polymaleimide derivatives and method of separating optically active compounds using them TOSOH CORPORATION (JP) 2007-06-14 US disclosed
US-7186750-B2 Optically active maleimide derivatives, optically active polymaleimide derivatives, process for their production, separating media comprising the optically active polymaleimide derivatives and method of separating optically active compounds using them TOSOH CORPORATION (JP) 2007-03-06 US disclosed
US-20040235937-A1 Optically active maleimide derivatives, optically active polymaleimide derivatives, process for their production, separating media comprising the optically active polymaleimide derivatives and method of separating optically active compounds using them TOSOH CORPORATION (JP) 2004-11-25 US disclosed
EP-1479669-A1 Optically active maleimide derivatives and polymaleimides for use as chiral adsorbent in chromatography Tosoh Corporation (JP) 2004-11-24 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 (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-20080230482-A1 Optically active polymaleimide derivatives and process for their production CYBA, COASY, MEP1B PTGS1 1062/4885PTGS2 998/4885MGLL 2036/4885
US-20040235937-A1 Optically active maleimide derivatives, optically active polymaleimide derivatives, process for their production, separating media comprising the optically active polymaleimide derivatives and method of separating optically active compounds using them MACF1, MEP1B, CYBA PTGS1 860/4885PTGS2 852/4885MGLL 2056/4885
US-20070131616-A1 Optically active maleimide derivatives, optically active polymaleimide derivatives, process for their production, separating media comprising the optically active polymaleimide derivatives and method of separating optically active compounds using them MACF1, MEP1B, ACMSD PTGS1 1162/4885PTGS2 861/4885MGLL 1868/4885

“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.