SCHEMBL3980844

SCHEMBL3980844

CC(=O)Nc1ccc(C(Cc2ccccc2F)c2nc3c([nH]2)c(=O)[nH]c(=O)n3CC=C(C)C)cc1

nearest known ligand 0.41

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
PCK1 P35558 4/20 0.41
PARP1 P09874 2/20 0.36
KMT2A Q03164 4/20 0.35
MEN1 O00255 3/20 0.35
HTT P42858 1/20 0.35
GAA P10253 1/20 0.34
HPGD P15428 1/20 0.34
USP1 O94782 1/20 0.34
ADORA2B P29275 2/20 0.33
TPH1 P17752 1/20 0.33
TPH2 Q8IWU9 1/20 0.33
ADORA2A P29274 1/20 0.33
PARP2 Q9UGN5 1/20 0.33
CTDSP1 Q9GZU7 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
ALDH1A1 P00352 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
SCHEMBL3985140 0.89 PCK1 (0.47) PCK1ADORA2BADORA2A
SCHEMBL3978792 0.89 PCK1 (0.42) PCK1PARP1KMT2AMEN1HTT
SCHEMBL3976949 0.87 PCK1 (0.53) PCK1PARP1KMT2AMEN1HTT
SCHEMBL3985334 0.87 PCK1 (0.42) PCK1PARP1KMT2AMEN1HTT
SCHEMBL3978661 0.87 PCK1 (0.53) PCK1PARP1KMT2AMEN1HTT
SCHEMBL4285441 0.87 PCK1 (0.42) PCK1PARP1KMT2AMEN1HTT
SCHEMBL3987439 0.87 PCK1 (0.45) PCK1PARP1KMT2AMEN1HTT
SCHEMBL3978051 0.86 PCK1 (0.50) PCK1PARP1KMT2AMEN1HTT
SCHEMBL3986615 0.85 PARP1 (0.43) PCK1PARP1KMT2AMEN1HTT
SCHEMBL3987357 0.85 PCK1 (0.41) PCK1PARP1KMT2AMEN1HTT

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 14/4885PARP1 3467/4885KMT2A 2893/4885

“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.