SCHEMBL29459708

SCHEMBL29459708

Cc1cc(Cn2c(=O)n(Cc3cnc(C)s3)c(=O)c3cc(S(=O)(=O)NC4(C)CC4)ccc32)n(C)n1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
PARG Q86W56 20/20 1.00

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
SCHEMBL17825271 1.00 PARG (1.00) PARG
SCHEMBL17824828 0.91 PARG (1.00) PARG
SCHEMBL17824685 0.87 PARG (1.00) PARG
SCHEMBL17825352 0.86 PARG (1.00) PARG
SCHEMBL19770727 0.86 PARG (1.00) PARG
SCHEMBL17824833 0.86 PARG (1.00) PARG
SCHEMBL24570171 0.85 PARG (0.74) PARG
SCHEMBL31072665 0.85 PARG (1.00) PARG
SCHEMBL19770734 0.85 PARG (1.00) PARG
SCHEMBL17824866 0.84 PARG (1.00) PARG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025233535-A1 METHOD FOR THE DETERMINATION OF CLEAVAGE SITES IN GENOMIC DNA CAUSED BY EXPOSURE TO A SITE DIRECTED NUCLEASE ETH Zürich (CH) 2025-11-13 WO claimed
US-20250255881-A1 Cancer Treatment UNIV OF SOUTH ALABAMA FOUNDATION FOR RESEARCH AND COMMERCIALIZATION (US) 2025-08-14 US claimed
CN-119033940-A Use of PAR hydrolase inhibitors (PDD) for the treatment of peripheral neuropathies associated with DNA damage 中南大学 2024-11-29 CN claimed
WO-2024186926-A1 STRATEGIES TO PREVENT THE EVOLUTION OF LETHAL, MULTI-THERAPY-RESISTANT, WIDELY METASTATIC CUTANEOUS MELANOMA THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2024-09-12 WO claimed
US-20240285647-A1 Cancer Treatment CANAL HOUSE BIOSCIENCES, LLC 2024-08-29 US claimed
EP-4401721-A1 CANCER TREATMENT University of South Alabama Foundation For Research and Commercialization (US) 2024-07-24 EP claimed
WO-2024081789-A2 HISTONE DEMETHYLASE INHIBITORS FOR TREATING CANCERS THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2024-04-18 WO claimed
WO-2023064619-A1 CANCER TREATMENT University of South Alabama Foundation for Research and Commercialization (US) 2023-04-20 WO claimed
CN-122071469-A PARG inhibitor and preparation method and application thereof 烟台新药创制山东省实验室 2026-05-22 CN disclosed
US-20260132140-A1 IMIDAZOLYL-AMINO-PYRAZINE-CARBONITRILS AS CHK-1 INHIBITORS BENEVOLENTAI BIO LTD (GB) 2026-05-14 US disclosed
CN-121971629-A Pharmaceutical composition for combined administration of JNK inhibitor and PARG inhibitor and pharmaceutical application 中国科学院杭州医学研究所 2026-05-05 CN disclosed
US-12601734-B2 Methods and uses of enzymatic labeling of ADP-ribose containing molecules THE JOHNS HOPKINS UNIVERSITY (US) 2026-04-14 US disclosed
EP-3947351-B1 SMALL MOLECULE PARG INHIBITORS AND METHODS OF USE THEREOF UNIV TEXAS (US) 2026-03-11 EP disclosed
US-20260049088-A1 TRICYCLIC HETEROCYCLIC DERIVATIVES, COMPOSITIONS AND USES THEREOF DANATLAS PHARMACEUTICALS CO LTD (CN) 2026-02-19 US disclosed
WO-2022245922-A1 POLY-ADP RIBOSE (PAR) TRACKER OPTIMIZED SPLIT-PROTEIN REASSEMBLY PAR DETECTION REAGENTS THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2022-11-24 WO disclosed
US-20220202821-A1 SMALL MOLECULE PARG INHIBITORS AND METHODS OF USE THEREOF BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2022-06-30 US disclosed
US-20220098196-A1 TRAPPING-FREE PARP INHIBITORS THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2022-03-31 US disclosed
WO-2022060477-A1 METHODS FOR TREATING CANCERS WITH INHIBITORS TARGETING THE ROLE OF GRB2 IN DNA REPAIR BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2022-03-24 WO disclosed
US-20220050112-A1 FLUORESCENT SUBSTRATES FOR POLY(ADP-RIBOSYL) HYDROLASES THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 2022-02-17 US disclosed
EP-3947351-A2 SMALL MOLECULE PARG INHIBITORS AND METHODS OF USE THEREOF Board of Regents, The University of Texas System (US) 2022-02-09 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 (5 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-20260132140-A1 IMIDAZOLYL-AMINO-PYRAZINE-CARBONITRILS AS CHK-1 INHIBITORS CHEK1, CHEK2, BUB1 PARG 4306/4885
US-20220202821-A1 SMALL MOLECULE PARG INHIBITORS AND METHODS OF USE THEREOF PARG, PARP15, PLG PARG 1/4885
US-20220098196-A1 TRAPPING-FREE PARP INHIBITORS PARP1, PARP3, PARP11 PARG 133/4885
US-12601734-B2 Methods and uses of enzymatic labeling of ADP-ribose containing molecules PARP15, PARP12, PARP11 PARG 44/4885
US-20260049088-A1 TRICYCLIC HETEROCYCLIC DERIVATIVES, COMPOSITIONS AND USES THEREOF SRD5A2, CBR1, SRD5A1 PARG 4516/4885

“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.