SCHEMBL524782

SCHEMBL524782

O=C(c1cc(Cc2n[nH]c(=O)c3ccccc23)ccc1F)N1CCNCC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
PARP1 P09874 20/20 1.00
PARP3 Q9Y6F1 2/20 0.93
TNKS O95271 1/20 0.76
ADORA1 P30542 1/20 0.76
CDK6 Q00534 1/20 0.76
PDE3A Q14432 1/20 0.76
PARP6 Q2NL67 1/20 0.76
PARP15 Q460N3 1/20 0.76
PARP14 Q460N5 1/20 0.76
PARP10 Q53GL7 1/20 0.76
TIPARP Q7Z3E1 1/20 0.76
PARP8 Q8N3A8 1/20 0.76
PARP16 Q8N5Y8 1/20 0.76
PARP12 Q9H0J9 1/20 0.76
TNKS2 Q9H2K2 1/20 0.76
PARP11 Q9NR21 1/20 0.76
PARP2 Q9UGN5 1/20 0.76
PARP4 Q9UKK3 1/20 0.76

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
SCHEMBL30205023 1.00 PARP1 (1.00) PARP1PARP3TNKSADORA1CDK6
SCHEMBL29463415 1.00 PARP1 (1.00) PARP1PARP3TNKSADORA1CDK6
Hydrochloric Acid SCHEMBL29536089 0.99 PARP1 (0.98) PARP1PARP3TNKSADORA1CDK6
Hydrochloric Acid SCHEMBL23113141 0.99 PARP1 (0.98) PARP1PARP3TNKSADORA1CDK6
Hydrochloric Acid SCHEMBL22656793 0.99 PARP1 (0.98) PARP1PARP3TNKSADORA1CDK6
SCHEMBL864319 0.96 PARP1 (1.00) PARP1PARP3
SCHEMBL29434944 0.96 PARP1 (1.00) PARP1PARP3
SCHEMBL19569971 0.94 PARP1 (0.90) PARP1PARP3TNKSADORA1CDK6
SCHEMBL17781907 0.93 PARP1 (0.86) PARP1PARP3TNKSADORA1CDK6
SCHEMBL30293115 0.92 PARP1 (0.89) PARP1PARP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116803990-A Preparation method of Olaparib 天津法莫西医药科技有限公司 2023-09-26 CN claimed
CN-113603647-B PARP inhibitor-alkylation bifunctional molecule and preparation method and application thereof 潍坊医学院 2023-01-31 CN claimed
CN-106554316-B A method of preparing 1- [5- [(3,4- dihydro -4- oxo -1- phthalazinyl) methyl] -2- fluoro benzoyl] piperazine 上海医药集团股份有限公司 2019-03-08 CN claimed
CN-106554316-A The method that one kind prepares 1- [5- [(3,4- dihydro -4- oxo -1- phthalazinyls) methyl] -2- fluoro benzoyls] piperazine 上海医药集团股份有限公司 2017-04-05 CN claimed
EP-2374800-A2 Methods for the preparation of 4-[3-(4-cyclopropanecarbonyl- piperazine-1-carbonyl)-4-fluoro-benzyl]-2H-phthalazin-1-one Kudos Pharmaceuticals Limited (GB) 2011-10-12 EP claimed
US-7692006-B2 Phthalazinone derivatives KUDOS PHARMACEUTICALS LIMITED (GB) 2010-04-06 US claimed
EP-2064189-A2 POLYMORPHIC FORM OF 4-[3-(4-CYCLOPROPANECARBONYL-PIPERAZINE-1-CARBONYL)-4-FLUORO-BENZYL]-2H-PHTHALAZIN-1-ONE Kudos Pharmaceuticals Limited (GB) 2009-06-03 EP claimed
US-20080146575-A1 4-[3-(4-cyclopropanecarbonyl-piperazine-1-carbonyl)-4-fluoro-benzyl]-2H-phthalazin-1-one as crystalline; enzyme poly(ADP-ribose)polymerase (synthase)-1 or poly ADP-ribosyltransferase (PARP-1) inhibitor; anticarcinogenic with BRCA2 deficient phenotype; septic shock, ischemic injury, multiple sclerosis KUDOS PHARMACEUTICALS LIMITED (GB) 2008-06-19 US claimed
WO-2008047082-A2 POLYMORPHIC FORM OF 4-[3-(4-CYCLOPROPANECARBONYL-PIPERAZINE-1-CARBONYL)-4-FLUORO-BENZYL]-2H-PHTHALAZIN-1-ONE KUDOS PHARMACEUTICALS LIMITED (GB) 2008-04-24 WO claimed
EP-3504196-B1 PROCESSES FOR PREPARING OLAPARIB SCINOPHARM TAIWAN LTD (TW) 2026-04-08 EP disclosed
US-12441757-B2 Platform for screening NAD+ binding proteins in a cellular context OREGON HEALTH & SCIENCE UNIVERSITY (US) 2025-10-14 US disclosed
US-12398121-B2 Anti-cancer nuclear hormone receptor-targeting compounds NUVATION BIO INC. (US) 2025-08-26 US disclosed
US-20250127907-A1 PARP INHIBITORS Stablix, Inc. 2025-04-24 US disclosed
EP-4446324-A1 LIGAND COMPOUNDS FOR E3 UBIQUITIN LIGASE, PROTEIN DEGRADERS DEVELOPED ON BASIS OF LIGAND COMPOUNDS, AND USES THEREOF Gluetacs Therapeutics (Shanghai) Co., Ltd. (CN) 2024-10-16 EP disclosed
WO-2008047082-A2 POLYMORPHIC FORM OF 4-[3-(4-CYCLOPROPANECARBONYL-PIPERAZINE-1-CARBONYL)-4-FLUORO-BENZYL]-2H-PHTHALAZIN-1-ONE KUDOS PHARMACEUTICALS LIMITED (GB) 2008-04-24 WO disclosed
WO-2008047082-A2 POLYMORPHIC FORM OF 4-[3-(4-CYCLOPROPANECARBONYL-PIPERAZINE-1-CARBONYL)-4-FLUORO-BENZYL]-2H-PHTHALAZIN-1-ONE KUDOS PHARMACEUTICALS LIMITED (GB) 2008-04-24 WO disclosed
US-20060149059-A1 Phthalazinone derivatives KUDOS PHARMACEUTICALS LIMITED (GB) 2006-07-06 US disclosed
EP-1633724-A1 PHTHALAZINONE DERIVATIVES Kudos Pharmaceuticals Limited (GB) 2006-03-15 EP disclosed
US-20050059663-A1 Phthalazinone derivatives KUDOS PHARMACEUTICALS LIMITED (GB) 2005-03-17 US disclosed
WO-2004080976-A1 PHTHALAZINONE DERIVATIVES KUDOS PHARMACEUTICALS LIMITED (GB) 2004-09-23 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 (6 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-12398121-B2 Anti-cancer nuclear hormone receptor-targeting compounds NCOA1, NCOR1, NCOA3 PARP1 1873/4885PARP3 1005/4885TNKS 2187/4885
US-20050059663-A1 Phthalazinone derivatives NR0B1, NR0B2, NR2E1 PARP1 3029/4885PARP3 3491/4885TNKS 4048/4885
US-20060149059-A1 Phthalazinone derivatives NR0B1, NR0B2, NR2E1 PARP1 3176/4885PARP3 3644/4885TNKS 4111/4885
US-20080146575-A1 4-[3-(4-cyclopropanecarbonyl-piperazine-1-carbonyl)-4-fluoro-benzyl]-2H-phthalazin-1-one as crystalline; enzyme poly(ADP-ribose)polymerase (synthase)-1 or poly ADP-ribosyltransferase (PARP-1) inhibitor; anticarcinogenic with BRCA2 deficient phenotype; septic shock, ischemic injury, multiple sclerosis PARP1, PARP11, PARP2 PARP1 1/4885PARP3 4/4885TNKS 129/4885
US-12441757-B2 Platform for screening NAD+ binding proteins in a cellular context SARM1, PARP16, PARP15 PARP1 24/4885PARP3 28/4885TNKS 189/4885
US-20250127907-A1 PARP INHIBITORS PARP1, PARP2, PARP3 PARP1 1/4885PARP3 3/4885TNKS 14/4885

“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.