SCHEMBL1025474

SCHEMBL1025474

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

nearest known ligand 0.37

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 3/20 0.35
KDM4E B2RXH2 1/20 0.35
GRM4 Q14833 1/20 0.35
TLR2 O60603 1/20 0.34
TLR1 Q15399 1/20 0.34
CYP2C9 P11712 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
F2 P00734 1/20 0.34
CTSK P43235 2/20 0.33
CTSB P07858 1/20 0.33
CTSS P25774 1/20 0.33
HSD17B10 Q99714 1/20 0.33
BCHE P06276 1/20 0.33

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
SCHEMBL1029070 0.88 GRM4 (0.47) TAAR1KDM4EGRM4TLR2TLR1
SCHEMBL1028998 0.86 POLB (0.45) KDM4EGRM4CYP2C9
SCHEMBL1074002 0.84 TAAR1 (0.44) TAAR1KDM4ESMN1; SMN2HSD17B10
SCHEMBL1028652 0.83 GRM4 (0.41) KDM4EGRM4CYP2C9SMN1; SMN2HSD17B10
SCHEMBL1027699 0.80 ALDH1A1 (0.58) TAAR1CYP2C9SMN1; SMN2F2HSD17B10
SCHEMBL1029850 0.80 KCNQ3 (0.39) KDM4ESMN1; SMN2HSD17B10
SCHEMBL1027865 0.80 ALDH1A1 (0.35)
SCHEMBL1028011 0.79 LMNA (0.36) KDM4EHSD17B10
SCHEMBL1025056 0.78 TAAR1 (0.64) TAAR1HSD17B10
SCHEMBL1026383 0.77 SLC6A1 (0.31)

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 TAAR1 4781/4885KDM4E 2233/4885GRM4 1689/4885
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 TAAR1 4769/4885KDM4E 1805/4885GRM4 1600/4885
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 TAAR1 4799/4885KDM4E 1750/4885GRM4 1649/4885

“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.