SCHEMBL3087583

SCHEMBL3087583

NC(=O)c1ccc(-c2cccc(F)c2)n2n[c]nc12

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAP4K4 O95819 2/20 0.41
CDC7 O00311 2/20 0.40
HPGDS O60760 1/20 0.40
TLR8 Q9NR97 2/20 0.39
KDM4E B2RXH2 1/20 0.39
FYN P06241 1/20 0.39
EGLN2 Q96KS0 1/20 0.39
PARP1 P09874 1/20 0.37
CHEK2 O96017 2/20 0.36
JAK2 O60674 1/20 0.36
CLK4 Q9HAZ1 2/20 0.36
MAP2K1 Q02750 1/20 0.36
DYRK1B Q9Y463 1/20 0.36
TP53 P04637 1/20 0.36
PIM1 P11309 2/20 0.35
CDK2 P24941 2/20 0.35
GSK3B P49841 2/20 0.35
ROCK2 O75116 1/20 0.35
BACE1 P56817 1/20 0.35
LMNA P02545 1/20 0.35

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
SCHEMBL3104866 0.86 PARP1 (0.42) TLR8KDM4EEGLN2PARP1JAK2
SCHEMBL3082604 0.84 MAP2K1 (0.49) TLR8KDM4EFYNPARP1CLK4
SCHEMBL6876511 0.82 FYN (0.37) MAP4K4CDC7HPGDSTLR8FYN
SCHEMBL3104916 0.82 DYRK1A (0.48) KDM4EFYNPIM1DYRK1AIRAK4
SCHEMBL3099043 0.82 CASP1 (0.48) FYNCSNK1DCHEK1RPS6KB1
SCHEMBL14888540 0.81 FYN (0.46) KDM4EFYNPARP1CHEK2DYRK1B
SCHEMBL3093915 0.79 CHUK (0.47) KDM4EFYNJAK2TP53MAPK1
SCHEMBL3200519 0.78 MAP2K1 (0.36) TLR8KDM4EPARP1CLK4MAP2K1
SCHEMBL3601959 0.78 MAP2K1 (0.36) TLR8KDM4EPARP1CLK4MAP2K1
SCHEMBL3262248 0.78 MAP2K1 (0.34) TLR8FYNPARP1JAK2CLK4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2057158-B1 TRIAZOLE DERIVATIVES AS KINASE INHIBITORS CELLZOME LTD (GB) 2015-08-12 EP claimed
US-9012633-B2 [1,2,4]triazolo[1,5-a]pyridine and [1,2,4]triazolo[1,5-c]pyrimidine compounds and their use CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2015-04-21 US claimed
US-8883820-B2 Triazole derivatives as kinase inhibitors CELLZOME LTD. (GB) 2014-11-11 US claimed
US-20140155594-A1 [1,2,4]Triazolo[1,5-a]Pyridine and [1,2,4]Triazolo[1,5-c]Pyrimidine Compounds and Their Use CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2014-06-05 US claimed
US-8431596-B2 [1,2,4]triazolo[1,5-a]pyridine and [1,2,4]triazolo[1,5-c]pyrimidine compounds and their use CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2013-04-30 US claimed
US-20100298339-A1 [1,2,4]Triazolo[1,5-a]Pyridine and [1,2,4]Triazolo[1,5-c]Pyrimidine Compounds and Their Use CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2010-11-25 US claimed
US-20100227800-A1 TRIAZOLE DERIVATIVES AS KINASE INHIBITORS CELLZOME LIMITED (GB) 2010-09-09 US claimed
EP-2217578-A1 [1,2,4]TRIAZOLO[1,5-A]PYRIDINE AND [1,2,4]TRIAZOLO[1,5-C]PYRIMIDINE COMPOUNDS AND THEIR USE Cancer Research Technology Limited (GB) 2010-08-18 EP claimed
EP-2057158-A1 TRIAZOLE DERIVATIVES AS KINASE INHIBITORS Cellzome Limited (GB) 2009-05-13 EP claimed
WO-2009047514-A1 [1,2,4]TRIAZOLO[1,5-A]PYRIDINE AND [1,2,4]TRIAZOLO[1,5-C]PYRIMIDINE COMPOUNDS AND THEIR USE CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2009-04-16 WO claimed
WO-2008025821-A1 TRIAZOLE DERIVATIVES AS KINASE INHIBITORS CELLZOME LIMITED (GB) 2008-03-06 WO claimed
EP-1894931-A1 Triazole derivatives as kinase inhibitors CELLZOME AG (DE) 2008-03-05 EP claimed
EP-2057158-B1 TRIAZOLE DERIVATIVES AS KINASE INHIBITORS CELLZOME LTD (GB) 2015-08-12 EP disclosed
US-8883820-B2 Triazole derivatives as kinase inhibitors CELLZOME LTD. (GB) 2014-11-11 US disclosed
US-20100227800-A1 TRIAZOLE DERIVATIVES AS KINASE INHIBITORS CELLZOME LIMITED (GB) 2010-09-09 US disclosed
EP-2057158-A1 TRIAZOLE DERIVATIVES AS KINASE INHIBITORS Cellzome Limited (GB) 2009-05-13 EP disclosed
WO-2008025821-A1 TRIAZOLE DERIVATIVES AS KINASE INHIBITORS CELLZOME LIMITED (GB) 2008-03-06 WO disclosed
EP-1894931-A1 Triazole derivatives as kinase inhibitors CELLZOME AG (DE) 2008-03-05 EP 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 (3 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-20100227800-A1 TRIAZOLE DERIVATIVES AS KINASE INHIBITORS ITK, PIK3C3, TXK MAP4K4 249/4885CDC7 641/4885HPGDS 1118/4885
US-20100298339-A1 [1,2,4]Triazolo[1,5-a]Pyridine and [1,2,4]Triazolo[1,5-c]Pyrimidine Compounds and Their Use AXL, TYRO3, FLT3 MAP4K4 147/4885CDC7 1116/4885HPGDS 2164/4885
US-20140155594-A1 [1,2,4]Triazolo[1,5-a]Pyridine and [1,2,4]Triazolo[1,5-c]Pyrimidine Compounds and Their Use AXL, TYRO3, FLT3 MAP4K4 147/4885CDC7 1116/4885HPGDS 2164/4885

“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.