SCHEMBL3979338

SCHEMBL3979338

CC(=O)Nc1ccc(CC(=O)Nc2c(N)[nH]c(=O)n(Cc3ccccc3F)c2=O)cc1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PCK1 P35558 5/20 0.47
KMT2A Q03164 4/20 0.44
MEN1 O00255 3/20 0.44
HTT P42858 1/20 0.44
RORC P51449 2/20 0.43
NLRP3 Q96P20 1/20 0.41
KDM4E B2RXH2 2/20 0.41
USP2 O75604 1/20 0.41
MAPT P10636 1/20 0.41
CASP1 P29466 1/20 0.41
CASP7 P55210 1/20 0.41
PARP1 P09874 1/20 0.39
SIGMAR1 Q99720 1/20 0.38
GAA P10253 1/20 0.38
TDP1 Q9NUW8 2/20 0.38
CTDSP1 Q9GZU7 1/20 0.38
POLB P06746 2/20 0.38
NPSR1 Q6W5P4 1/20 0.38
GNRHR P30968 1/20 0.37
TP53 P04637 1/20 0.37

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
SCHEMBL3983281 0.88 NLRP3 (0.46) KMT2AMEN1HTTNLRP3KDM4E
SCHEMBL4614353 0.88 GLS (0.43) PCK1KMT2AMEN1RORCKDM4E
SCHEMBL4614732 0.81 KDM4E (0.37) PCK1KMT2AMEN1RORCKDM4E
SCHEMBL6386823 0.76 GLS (0.41) PCK1KMT2AMEN1RORCKDM4E
SCHEMBL3980725 0.73 PCK1 (0.41) PCK1KMT2AMEN1HTTRORC
SCHEMBL3980723 0.73 PCK1 (0.42) PCK1KMT2AMEN1HTTRORC
SCHEMBL8392000 0.72 ALDH1A1 (0.45) KMT2AMEN1KDM4EMAPTGAA
SCHEMBL4613128 0.71 PCK1 (0.53) PCK1SIGMAR1TP53
SCHEMBL4614201 0.71 PCK1 (0.48) PCK1KMT2AMEN1KDM4ECTDSP1
SCHEMBL4615986 0.70 L3MBTL1 (0.50) KMT2AMEN1HTTKDM4EUSP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7135475-B2 Antidiabetic agents HOFFMANN-LA ROCHE INC. (US) 2006-11-14 US claimed
US-20040014766-A1 Amide substituted xanthine derivatives HOFFMANN-LA ROCHE INC. 2004-01-22 US claimed
EP-1515972-B1 AMIDE SUBSTITUTED XANTHINE DERIVATIVES WITH GLUCONEOGENESIS MODULATING ACTIVITY HOFFMANN LA ROCHE (CH) 2009-05-13 EP disclosed
US-7135475-B2 Antidiabetic agents HOFFMANN-LA ROCHE INC. (US) 2006-11-14 US disclosed
EP-1515972-A1 AMIDE SUBSTITUTED XANTHINE DERIVATIVES WITH GLUCONEOGENESIS MODULATING ACTIVITY F. HOFFMANN-LA ROCHE AG (CH) 2005-03-23 EP disclosed
US-20040014766-A1 Amide substituted xanthine derivatives HOFFMANN-LA ROCHE INC. 2004-01-22 US disclosed
WO-2003106459-A1 AMIDE SUBSTITUTED XANTHINE DERIVATIVES WITH GLUCONEOGENESIS MODULATING ACTIVITY F. HOFFMANN-LA ROCHE AG (CH) 2003-12-24 WO 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-20040014766-A1 Amide substituted xanthine derivatives GYS2, GLS2, PYGL PCK1 14/4885KMT2A 2893/4885MEN1 2857/4885

“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.