SCHEMBL30201670

SCHEMBL30201670

NC(=O)NN=Cc1ccc(O)cc1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GFER P55789 2/20 0.68
MIF P14174 4/20 0.64
KMT2A Q03164 3/20 0.61
GAA P10253 2/20 0.61
MEN1 O00255 2/20 0.61
SMN1; SMN2 Q16637 2/20 0.61
USP2 O75604 1/20 0.61
L3MBTL1 Q9Y468 1/20 0.61
KDM4E B2RXH2 3/20 0.59
ALDH1A1 P00352 2/20 0.59
HPGD P15428 2/20 0.59
GLA P06280 1/20 0.59
MAPT P10636 1/20 0.59
SCN4A P35499 1/20 0.59
SCN9A Q15858 1/20 0.59
CA12 O43570 1/20 0.55
CA1 P00915 1/20 0.55
CA2 P00918 1/20 0.55
CA9 Q16790 1/20 0.55
ESRRG P62508 3/20 0.54

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
SCHEMBL12641934 0.84 GFER (0.72) GFERMIFKMT2AGAAMEN1
SCHEMBL15718835 0.83 KMT2A (0.63) GFERKMT2AGAAMEN1SMN1; SMN2
SCHEMBL17560984 0.83 SCN4A (0.82) GFERKMT2AGAAMEN1SMN1; SMN2
SCHEMBL17560986 0.83 SCN4A (0.82) GFERKMT2AGAAMEN1SMN1; SMN2
SCHEMBL15718834 0.83 KMT2A (0.63) GFERKMT2AGAAMEN1SMN1; SMN2
SCHEMBL24000970 0.83 KMT2A (0.71) GFERKMT2AGAAMEN1SMN1; SMN2
SCHEMBL17560884 0.83 PRMT5 (0.61) GFERKMT2AGAAMEN1SMN1; SMN2
SCHEMBL17560882 0.83 PRMT5 (0.61) GFERKMT2AGAAMEN1SMN1; SMN2
Phenylsemicarbazone SCHEMBL11882629 0.82 MEN1 (0.71) GFERKMT2AGAAMEN1SMN1; SMN2
Phenylsemicarbazone SCHEMBL9018897 0.82 MEN1 (0.71) GFERKMT2AGAAMEN1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11565995-B2 Methods of forming imines, imine-related and imine-derived compounds using green solvents THE RESEARCH FOUNDATION FOR THE STATE UNIVERSITY OF NEW YORK (US) 2023-01-31 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-11565995-B2 Methods of forming imines, imine-related and imine-derived compounds using green solvents IK, LDHB, IDH3B GFER 2269/4885MIF 83/4885KMT2A 2431/4885

“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.