SCHEMBL48519

SCHEMBL48519

CCOC(=O)CCNC(=O)Nc1nc(C)c(-c2ccc(S(C)(=O)=O)cc2)s1

nearest known ligand 0.61

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
PIK3CD O00329 15/20 0.61
PIK3CA P42336 14/20 0.61
PIK3CG P48736 14/20 0.61
PIK3CB P42338 13/20 0.61
PI4KB Q9UBF8 4/20 0.53
CLK2 P49760 2/20 0.47
CLK1 P49759 1/20 0.47
DYRK3 O43781 1/20 0.45
MAP4K4 O95819 1/20 0.45
DYRK1A Q13627 1/20 0.45
MINK1 Q8N4C8 1/20 0.45
CLK4 Q9HAZ1 1/20 0.45
PTGS2 P35354 1/20 0.44
ALDH1A1 P00352 2/20 0.41
GAA P10253 1/20 0.41
LMNA P02545 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
SCHEMBL48491 0.90 PIK3CD (0.64) PIK3CDPIK3CAPIK3CGPIK3CBPI4KB
SCHEMBL48676 0.89 PIK3CD (0.53) PIK3CDPIK3CAPIK3CGPIK3CBPI4KB
SCHEMBL48707 0.89 PIK3CD (0.59) PIK3CDPIK3CAPIK3CGPIK3CBPI4KB
SCHEMBL1786151 0.88 PIK3CD (0.76) PIK3CDPIK3CAPIK3CGPIK3CBPI4KB
SCHEMBL49803 0.88 PIK3CD (0.66) PIK3CDPIK3CAPIK3CGPIK3CBPI4KB
SCHEMBL1883394 0.85 PIK3CG (0.54) PIK3CDPIK3CAPIK3CGPIK3CBPI4KB
SCHEMBL1784577 0.85 PIK3CD (0.69) PIK3CDPIK3CAPIK3CGPIK3CBPI4KB
SCHEMBL48623 0.85 PIK3CD (0.72) PIK3CDPIK3CAPIK3CGPIK3CBPI4KB
SCHEMBL48948 0.85 PIK3CD (0.64) PIK3CDPIK3CAPIK3CGPIK3CBPI4KB
SCHEMBL2339914 0.85 PIK3CD (0.82) PIK3CDPIK3CAPIK3CGPIK3CBPI4KB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2311818-B1 Combination of a 5-phenylthiazole compound as PI3 kinase inhibitor with an antiinflammatory, bronchodilatory or antihistamine drug NOVARTIS AG (CH) 2013-01-16 EP disclosed
US-8129541-B2 5-phenylthiazole derivatives and use as PI3 kinase inhibitors NOVARTIS AG (CH) 2012-03-06 US disclosed
EP-1480962-B1 5-PHENYLTHIAZOLE DERIVATIVES AND USE AS PI3 KINASE INHIBITORS NOVARTIS AG (CH) 2011-08-24 EP disclosed
EP-2311818-A1 Combination of a 5-phenylthiazole compound as PI3 kinase inhibitor with an antiinflammatory, bronchodilatory or antihistamine drug Novartis AG (CH) 2011-04-20 EP disclosed
US-20100093690-A1 5-PHENYLTHIAZOLE DERIVATIVES AND USE AS PI3 KINASE INHIBITORS BRUCE IAN 2010-04-15 US disclosed
US-7687637-B2 5-phenylthiazole derivatives and use as Pi3 kinase inhibitors NOVARTIS AG (CH) 2010-03-30 US disclosed
US-20050119320-A1 5-phenylthiazole derivatives and use as pi3 kinase inhibitors NOVARTIS AG (CH) 2005-06-02 US disclosed
EP-1480962-A1 5-PHENYLTHIAZOLE DERIVATIVES AND USE AS PI3 KINASE INHIBITORS Novartis AG (CH) 2004-12-01 EP disclosed
WO-2003072557-A1 5-PHENYLTHIAZOLE DERIVATIVES AND USE AS PI3 KINASE INHIBITORS NOVARTIS AG (CH) 2003-09-04 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 (2 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-20100093690-A1 5-PHENYLTHIAZOLE DERIVATIVES AND USE AS PI3 KINASE INHIBITORS PIK3CA, PIK3R5, PIP5K1B PIK3CD 4/4885PIK3CA 1/4885PIK3CG 8/4885
US-20050119320-A1 5-phenylthiazole derivatives and use as pi3 kinase inhibitors PIK3CA, PIK3R5, PIP5K1B PIK3CD 4/4885PIK3CA 1/4885PIK3CG 8/4885

“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.