SCHEMBL3565164

SCHEMBL3565164

COC(=O)C(C)(C=O)NC(=O)OCc1ccccc1

nearest known ligand 0.60

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.60
KMT2A Q03164 1/20 0.60
SMN1; SMN2 Q16637 2/20 0.47
CA12 O43570 2/20 0.46
CA1 P00915 2/20 0.46
CA2 P00918 2/20 0.46
CA9 Q16790 2/20 0.46
NPC1 O15118 1/20 0.46
RAB9A P51151 1/20 0.46
CTSS P25774 1/20 0.46
PTPN1 P18031 2/20 0.45
ALDH1A1 P00352 1/20 0.45
PTPN2 P17706 1/20 0.45
PTPRB P23467 1/20 0.45
ACP1 P24666 1/20 0.45
LMNA P02545 2/20 0.44
SYK P43405 1/20 0.43
POLB P06746 1/20 0.43
HTT P42858 1/20 0.43

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
SCHEMBL30898810 1.00 MEN1 (0.60) MEN1KMT2ASMN1; SMN2CA12CA1
SCHEMBL6214741 0.89 KMT2A (0.51) MEN1KMT2ASMN1; SMN2CA12CA1
SCHEMBL4707157 0.89 MEN1 (0.52) MEN1KMT2ASMN1; SMN2CA12CA1
SCHEMBL13305932 0.88 MEN1 (0.59) MEN1KMT2ASMN1; SMN2CA12CA1
SCHEMBL13774927 0.88 MEN1 (0.59) MEN1KMT2ASMN1; SMN2CA12CA1
SCHEMBL22468533 0.85 MEN1 (0.66) MEN1KMT2ASMN1; SMN2CA12CA1
SCHEMBL28517383 0.85 HCAR2 (0.47) MEN1KMT2AALDH1A1LMNAHTT
SCHEMBL567435 0.82 MEN1 (0.55) MEN1KMT2ASMN1; SMN2CA12CA1
SCHEMBL10885861 0.81 MEN1 (0.53) MEN1KMT2ASMN1; SMN2CA12CA1
SCHEMBL6538869 0.80 MEN1 (0.63) MEN1KMT2ASMN1; SMN2CA12CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117903004-A Synthesis method of Fmoc-a-methyl-L-glutamic acid (5-tert-butyl ester) 康化(上海)新药研发有限公司 2024-04-19 CN claimed
CN-117903004-A Synthesis method of Fmoc-a-methyl-L-glutamic acid (5-tert-butyl ester) 康化(上海)新药研发有限公司 2024-04-19 CN disclosed
CN-117903004-A Synthesis method of Fmoc-a-methyl-L-glutamic acid (5-tert-butyl ester) 康化(上海)新药研发有限公司 2024-04-19 CN disclosed
US-7652007-B2 Obesity, type II diabetes; such as 6-(4-Chlorobenzyl)-1-(2,4-dichlorobenzenesulfonyl)-8-isopropylhexahydropyrazino[1,2-a]pyrimidine-4,7-dione SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2010-01-26 US disclosed
EP-1597259-B1 NITROGEN-SUBSTITUTED HEXAHYDROPYRAZINO 1,2-A PYRIMIDINE-4,7-DIONE DERIVATIVES, METHOD FOR THE PRODUCTION AND USE THEREOF AS MEDICAMENTS SANOFI AVENTIS DEUTSCHLAND (DE) 2008-04-30 EP disclosed
US-20050085483-A1 Nitrogen-substituted hexahydropyrazino[1,2-a]pyrimidine-4,7-dione derivatives, processes for their preparation and their use as medicaments AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2005-04-21 US 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 (1 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-20050085483-A1 Nitrogen-substituted hexahydropyrazino[1,2-a]pyrimidine-4,7-dione derivatives, processes for their preparation and their use as medicaments DPYD, NUDT1, NT5C2 MEN1 1919/4885KMT2A 4297/4885SMN1; SMN2 1359/4885

“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.