SCHEMBL3285526

SCHEMBL3285526

Cc1cc(C)c(N2C(=O)c3cccc4c(C#N)ccc(c34)C2=O)c(C)c1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MEN1 O00255 5/20 0.44
▸ KMT2A Q03164 5/20 0.44
▸ USP2 O75604 4/20 0.44
▸ L3MBTL1 Q9Y468 3/20 0.44
▸ KEAP1 Q14145 2/20 0.44
▸ NFE2L2 Q16236 2/20 0.44
▸ LMNA P02545 4/20 0.41
▸ TP53 P04637 2/20 0.41
▸ MAPK1 P28482 2/20 0.41
▸ MAPT P10636 2/20 0.41
▸ HTT P42858 2/20 0.41
▸ THRB P10828 1/20 0.41
▸ TLR9 Q9NR96 1/20 0.41
▸ RGS12 O14924 1/20 0.41
▸ RECQL P46063 1/20 0.41
▸ S1PR2 O95136 1/20 0.41
▸ DPP4 P27487 3/20 0.41
▸ ANPEP P15144 2/20 0.41
▸ ALDH1A1 P00352 3/20 0.41
▸ KDM4E B2RXH2 1/20 0.41

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
SCHEMBL16097347 0.80 L3MBTL1 (0.62) MEN1KMT2AUSP2L3MBTL1KEAP1
SCHEMBL3284832 0.80 ANPEP (0.50) MEN1KMT2AUSP2L3MBTL1KEAP1
SCHEMBL13901466 0.78 KMT2A (0.59) MEN1KMT2AUSP2KEAP1NFE2L2
SCHEMBL3285543 0.77 KMT2A (0.62) MEN1KMT2AUSP2L3MBTL1KEAP1
SCHEMBL14582061 0.77 DPP4 (0.49) MEN1KMT2AUSP2L3MBTL1KEAP1
SCHEMBL23892790 0.76 DPP4 (0.39) MEN1KMT2AUSP2L3MBTL1KEAP1
SCHEMBL19720304 0.75 DPP4 (0.54) MEN1KMT2AUSP2L3MBTL1KEAP1
SCHEMBL19848822 0.75 DPP4 (0.39) MEN1KMT2ALMNAS1PR2DPP4
SCHEMBL6268625 0.74 DPP4 (0.44) MEN1KMT2AUSP2L3MBTL1KEAP1
SCHEMBL29544415 0.74 DPP4 (0.44) MEN1KMT2AUSP2L3MBTL1KEAP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7714044-B2 Use of 4-cyano-naphthalene-1, 8-dicarboximide derivatives and related compounds to protect organic material from the damaging effects of light BASF AKITENGESELLSCHAFT (DE) 2010-05-11 — — US disclosed
EP-1687278-B1 USE OF 4-CYANO-NAPHTHALENE-1, 8-DICARBOXIMIDE DERIVATIVES AND RELATED COMPOUNDS TO PROTECT ORGANIC MATERIAL FROM THE DAMAGING EFFECTS OF LIGHT BASF SE (DE) 2009-03-11 — — EP disclosed
US-20070100033-A1 Use of 4-cyano-naphthalene-1, 8-dicarboximide derivatives and related compounds to protect organic material from the damaging effects of light BAST AKTIENGESELLSCHAFT (DE) 2007-05-03 — — US disclosed
US-20050171252-A1 Use of naphthalin-1,8-dicarboxylic acid monoimides BASF AKTIENGESELLSCHAFT (DE) 2005-08-04 — — 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-20050171252-A1 Use of naphthalin-1,8-dicarboxylic acid monoimides NDC1, NDUFC1, NDUFC2 MEN1 512/4885KMT2A 2786/4885USP2 2968/4885

“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.

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