Sugi Predict

Sugi Predict / Compounds / SCHEMBL6347385

SCHEMBL6347385

SCHEMBL6347385

O=C1C(=O)c2cc(Br)cnc2-c2ncc(Br)cc21

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ S100A4 P26447 1/20 0.44
▸ DYRK1A Q13627 3/20 0.39
▸ ABL1 P00519 2/20 0.39
▸ AURKA O14965 1/20 0.39
▸ DAPK3 O43293 1/20 0.39
▸ JAK2 O60674 1/20 0.39
▸ PRKD3 O94806 1/20 0.39
▸ MAP4K4 O95819 1/20 0.39
▸ PAK4 O96013 1/20 0.39
▸ NTRK1 P04629 1/20 0.39
▸ FYN P06241 1/20 0.39
▸ RET P07949 1/20 0.39
▸ MET P08581 1/20 0.39
▸ PDGFRB P09619 1/20 0.39
▸ PIM1 P11309 1/20 0.39
▸ FGFR1 P11362 1/20 0.39
▸ PDGFRA P16234 1/20 0.39
▸ FLT1 P17948 1/20 0.39
▸ LTK P29376 1/20 0.39
▸ GRK5 P34947 1/20 0.39

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
SCHEMBL29407380 1.00 S100A4 (0.44) S100A4DYRK1AABL1AURKADAPK3
SCHEMBL22066823 0.95 KMT2A (0.41) S100A4DYRK1AABL1AURKADAPK3
SCHEMBL28112787 0.86 DYRK1A (0.39) S100A4DYRK1AABL1AURKADAPK3
SCHEMBL13292088 0.85 TDP2 (0.66) S100A4ABL1PTPRCKMT2ACES1
SCHEMBL22065879 0.81 GAA (0.66) S100A4ABL1PTPRCKMT2ACES1
SCHEMBL29291252 0.78 S100A4 (0.40) S100A4DYRK1AABL1AURKADAPK3
SCHEMBL31346196 0.77 NSD2 (0.40) S100A4ABL1PTPRCKMT2ACES1
SCHEMBL30029120 0.76 NPSR1 (0.41) DYRK1AABL1AURKADAPK3JAK2
SCHEMBL20672203 0.76 NPSR1 (0.41) DYRK1AABL1AURKADAPK3JAK2
SCHEMBL29291251 0.74 S100A4 (0.40) S100A4DYRK1AABL1AURKADAPK3

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 23 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114106353-B Four polymerization complexes using phenanthroline imidazole derivative as ligand, preparation method and application thereof 湘潭大学 2023-03-21 — — CN claimed
CN-114196035-B Four polymerization complexes using phenanthroline derivative as ligand, preparation method and application thereof 湘潭大学 2022-12-09 — — CN claimed
CN-114196035-A Four polymerization complexes using phenanthroline derivative as ligand, preparation method and application thereof 湘潭大学 2022-03-18 — — CN claimed
CN-114106353-A Four polymerization complexes using phenanthroline imidazole derivative as ligand, preparation method and application thereof 湘潭大学 2022-03-01 — — CN claimed
CN-110283209-B Phosphino-oxygen group modified bipyridyl-phenazinyl red/near-infrared thermal excitation delayed fluorescence material, and synthesis method and application thereof 黑龙江大学 2021-11-26 — — CN claimed
CN-114106353-B Four polymerization complexes using phenanthroline imidazole derivative as ligand, preparation method and application thereof 湘潭大学 2023-03-21 — — CN disclosed
CN-114196035-B Four polymerization complexes using phenanthroline derivative as ligand, preparation method and application thereof 湘潭大学 2022-12-09 — — CN disclosed
US-11283026-B2 Compound having tetraazatriphenylene ring structure, light-emitting material, and organic electroluminescent device HODOGAYA CHEMICAL CO., LTD. (JP) 2022-03-22 — — US disclosed
CN-114196035-A Four polymerization complexes using phenanthroline derivative as ligand, preparation method and application thereof 湘潭大学 2022-03-18 — — CN disclosed
CN-114106353-A Four polymerization complexes using phenanthroline imidazole derivative as ligand, preparation method and application thereof 湘潭大学 2022-03-01 — — CN disclosed
CN-110283209-B Phosphino-oxygen group modified bipyridyl-phenazinyl red/near-infrared thermal excitation delayed fluorescence material, and synthesis method and application thereof 黑龙江大学 2021-11-26 — — CN disclosed
CN-111825672-A Partial triazine phenanthroline derivative, electronic device and application 苏州久显新材料有限公司 2020-10-27 — — CN disclosed
US-8632931-B2 Electrophotographic photosensitive member, process cartridge, and electrophotographic apparatus CANON KABUSHIKI KAISHA (JP) 2014-01-21 — — US disclosed
US-8524429-B2 — — 2013-09-03 — — US disclosed
US-8524429-B2 — — 2013-09-03 — — US disclosed
US-20110143273-A1 ELECTROPHOTOGRAPHIC PHOTOSENSITIVE MEMBER, PROCESS CARTRIDGE, AND ELECTROPHOTOGRAPHIC APPARATUS CANON KABUSHIKI KAISHA (JP) 2011-06-16 — — US disclosed
US-20110143273-A1 ELECTROPHOTOGRAPHIC PHOTOSENSITIVE MEMBER, PROCESS CARTRIDGE, AND ELECTROPHOTOGRAPHIC APPARATUS CANON KABUSHIKI KAISHA (JP) 2011-06-16 — — US disclosed
EP-2317391-A1 Electrophotographic photosensitive member, process cartridge, and electrophotographic apparatus Canon Kabushiki Kaisha (JP) 2011-05-04 — — EP disclosed
US-6929873-B2 Electroluminescent device using metal coordination compound CANON KABUSHIKI KAISHA (JP) 2005-08-16 — — US disclosed
US-20040013905-A1 Electroluminescent device using metal coordination compound CANON KABUSHIKI KAISHA (JP) 2004-01-22 — — 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-11283026-B2 Compound having tetraazatriphenylene ring structure, light-emitting material, and organic electroluminescent device LEF1, TEAD1, LAGE3 S100A4 2698/4885DYRK1A 3056/4885ABL1 2322/4885

“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.