SCHEMBL4017244

SCHEMBL4017244

COC(=O)c1cc(F)cc([N+](=O)[O-])c1Br

nearest known ligand 0.44

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PDGFRB P09619 1/20 0.44
FGFR1 P11362 1/20 0.44
PDGFRA P16234 1/20 0.44
FLT1 P17948 1/20 0.44
FGFR3 P22607 1/20 0.44
KDR P35968 1/20 0.44
SIRT6 Q8N6T7 1/20 0.41
VCAM1 P19320 1/20 0.40
TTR P02766 3/20 0.39
ALDH1A1 P00352 2/20 0.39
TDP1 Q9NUW8 1/20 0.39
MEN1 O00255 2/20 0.38
KMT2A Q03164 2/20 0.38
SOS1 Q07889 1/20 0.37
KDM4E B2RXH2 2/20 0.36
MAPT P10636 1/20 0.36
KCNMA1 Q12791 1/20 0.36

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
SCHEMBL505648 0.85 ALDH1A1 (0.45) PDGFRBFGFR1PDGFRAFLT1FGFR3
SCHEMBL913705 0.84 PDGFRB (0.46) PDGFRBFGFR1PDGFRAFLT1FGFR3
SCHEMBL31159174 0.84 PDGFRB (0.49) PDGFRBFGFR1PDGFRAFLT1FGFR3
SCHEMBL2046728 0.84 PDGFRB (0.49) PDGFRBFGFR1PDGFRAFLT1FGFR3
SCHEMBL4022732 0.84 PDGFRB (0.46) PDGFRBFGFR1PDGFRAFLT1FGFR3
SCHEMBL21357291 0.84 TTR (0.37) VCAM1TTRMAPTKCNMA1
SCHEMBL21357288 0.84 ALDH1A1 (0.50) ALDH1A1KMT2AKDM4EMAPT
SCHEMBL29858635 0.83 TTR (0.50) PDGFRBFGFR1PDGFRAFLT1FGFR3
SCHEMBL205671 0.83 TTR (0.50) PDGFRBFGFR1PDGFRAFLT1FGFR3
SCHEMBL13987139 0.83 ALDH1A1 (0.50) PDGFRBFGFR1PDGFRAFLT1FGFR3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4731631-A1 BENZAMIDAZOLE DIAZAPINONE PARP INHIBITORS AND METHODS OF USE Valo Health, Inc. (US) 2026-04-29 EP disclosed
EP-4731630-A1 HOMOPHTHALAZINONE INDOLE PARP INHIBITORS AND METHODS OF USE Valo Health, Inc. (US) 2026-04-29 EP disclosed
WO-2024261712-A1 BENZAMIDAZOLE DIAZAPINONE PARP INHIBITORS AND METHODS OF USE VALO HEALTH, INC. (US) 2024-12-26 WO disclosed
WO-2024261711-A1 HOMOPHTHALAZINONE INDOLE PARP INHIBITORS AND METHODS OF USE VALO HEALTH, INC. (US) 2024-12-26 WO disclosed
CN-111868060-B Dihydropyridino phthalazinone derivatives, preparation method and application thereof 上海艾力斯医药科技股份有限公司 2023-06-09 CN disclosed
EP-3341375-B1 PROCESS FOR PREPARING PARP INHIBITOR, CRYSTALLINE FORMS, AND USES THEREOF BEIGENE LTD (KY) 2022-04-13 EP disclosed
CN-111868060-A Dihydropyridophthalazinone derivative, preparation method and application thereof 上海艾力斯医药科技股份有限公司 2020-10-30 CN disclosed
US-10457680-B2 Process for preparing a PARP inhibitor, crystalline forms, and uses thereof BEIGENE, LTD. (KY) 2019-10-29 US disclosed
WO-2019174607-A1 DIHYDROPYRIDOPHTHALAZINONE DERIVATIVE, AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF 上海艾力斯医药科技有限公司 2019-09-19 WO disclosed
WO-2019174607-A1 DIHYDROPYRIDOPHTHALAZINONE DERIVATIVE, AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF 上海艾力斯医药科技有限公司 2019-09-19 WO disclosed
CN-101616892-A The tricyclic compound that is used for the treatment of the iron imbalance XENON PHARMACEUTICALS INC 2009-12-30 CN disclosed
EP-2061755-A1 TRICYCLIC COMPOUNDS USEFUL IN TREATING IRON DISORDERS XENON PHARMACEUTICALS INC. (CA) 2009-05-27 EP disclosed
US-20090069408-A1 TRICYCLIC COMPOUNDS USEFUL IN TREATING IRON DISORDERS XENON PHARMACEUTICALS INC. (CA) 2009-03-12 US disclosed
US-20090069408-A1 TRICYCLIC COMPOUNDS USEFUL IN TREATING IRON DISORDERS XENON PHARMACEUTICALS INC. (CA) 2009-03-12 US disclosed
WO-2008109840-A1 TRICYCLIC COMPOUNDS USEFUL IN TREATING IRON DISORDERS XENON PHARMACEUTICALS INC. (CA) 2008-09-12 WO disclosed
WO-2008109840-A1 TRICYCLIC COMPOUNDS USEFUL IN TREATING IRON DISORDERS XENON PHARMACEUTICALS INC. (CA) 2008-09-12 WO disclosed
EP-1208104-B1 TRICYCLIC INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASES AGOURON PHARMA (US) 2005-01-19 EP disclosed
US-6548494-B1 3,4-dihydro-2H-(1,4)diazepino(6,7,1-hi)indol-1-one or 1-thione derivatives where indole C3 could also be N; use treating cancers as well as stroke, head trauma, and neurodegenerative diseases AGOURON PHARMACEUTICALS, INC. 2003-04-15 US disclosed
EP-1208104-A2 TRICYCLIC INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASES AGOURON PHARMACEUTICALS, INC. (US) 2002-05-29 EP disclosed
WO-2001016136-A2 TRICYCLIC INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASES AGOURON PHARMACEUTICALS, INC. (US) 2001-03-08 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-20090069408-A1 TRICYCLIC COMPOUNDS USEFUL IN TREATING IRON DISORDERS TFRC, SLC40A1, FECH PDGFRB 4832/4885FGFR1 1834/4885PDGFRA 4753/4885
US-10457680-B2 Process for preparing a PARP inhibitor, crystalline forms, and uses thereof PARP1, PARP2, PARP11 PDGFRB 490/4885FGFR1 806/4885PDGFRA 272/4885

“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.