SCHEMBL540837

SCHEMBL540837

NC(=O)c1ccc(OBOc2ccc(C(N)=O)cc2)cc1

nearest known ligand 0.64

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PARP10 Q53GL7 18/20 0.64
PARP15 Q460N3 5/20 0.64
PARP4 Q9UKK3 2/20 0.64
PARP14 Q460N5 2/20 0.64
ALDH1A1 P00352 1/20 0.64
KMT2A Q03164 1/20 0.64
PARP16 Q8N5Y8 1/20 0.64
PARP11 Q9NR21 1/20 0.64
PARP2 Q9UGN5 4/20 0.59
CA1 P00915 1/20 0.59
CA2 P00918 1/20 0.59
PARP1 P09874 1/20 0.59
PARP3 Q9Y6F1 1/20 0.50
TNKS O95271 1/20 0.48
TNKS2 Q9H2K2 1/20 0.48
SENP8 Q96LD8 1/20 0.47
SENP6 Q9GZR1 1/20 0.47

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
SCHEMBL3034248 0.88 PARP10 (0.62) PARP10PARP15PARP4PARP14ALDH1A1
SCHEMBL820246 0.84 PARP10 (0.61) PARP10PARP15PARP4PARP14ALDH1A1
SCHEMBL210295 0.79 CA1 (0.58) PARP10PARP15ALDH1A1KMT2ACA1
SCHEMBL3137816 0.78 PARP10 (1.00) PARP10PARP15PARP4PARP14ALDH1A1
SCHEMBL655335 0.77 MAPT (0.64) ALDH1A1KMT2A
Terephthalamide SCHEMBL23774 0.77 PARP1 (0.71) PARP10PARP15PARP4PARP14ALDH1A1
SCHEMBL17226019 0.76 PARP10 (0.70) PARP10PARP15PARP4PARP14ALDH1A1
SCHEMBL191052 0.75 PARP1 (0.65) PARP10PARP15PARP14KMT2APARP2
SCHEMBL17888032 0.74 PARP10 (0.67) PARP10PARP15PARP4PARP14ALDH1A1
SCHEMBL201761 0.74 PARP10 (1.00) PARP10PARP15PARP4PARP14ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250223277-A1 COMPLEMENT FACTOR B INHIBITORS AND USES THEREOF NOVARTIS PHARMA AG (CH) 2025-07-10 US disclosed
CN-115677601-B Compound with anti-tumor activity and application thereof 石药集团中奇制药技术(石家庄)有限公司 2025-06-03 CN disclosed
CN-119790036-A Pyrrolidine-2-carboxamide derivatives as prostaglandin E2 receptor 4 (EP 4) agonists for the treatment of gastrointestinal and pulmonary diseases 奈克斯拉制药英国有限公司 2025-04-08 CN disclosed
CN-119731159-A SARS-CoV2 main proteinase inhibitor 吉利德科学公司 2025-03-28 CN disclosed
CN-119562945-A IKK inhibitors 癌症研究技术有限公司 2025-03-04 CN disclosed
CN-119403554-A Therapeutic or prophylactic agent for amyotrophic lateral sclerosis 东丽株式会社 2025-02-07 CN disclosed
CN-119137099-A Complement factor B inhibitors and uses thereof 诺华股份有限公司 2024-12-13 CN disclosed
CN-112384515-B Imidazopyrimidines and triazolopyrimidines as A2A/A2B inhibitors 因赛特公司 2024-12-10 CN disclosed
US-20240400555-A1 Compounds, Compositions and Methods for Attenuation of Mammalian Translation of C-MYC or N-MYC Proteins of the MYC Proto-Oncogene Family of BHLH Transcription Factors INITIAL THERAPEUTICS, INC. (US) 2024-12-05 US disclosed
EP-4463456-A1 THIAZOLOPYRIDYL AMIDE DERIVATIVES AS DNA POLYMERASE THETA INHIBITORS BeiGene, Ltd. (KY) 2024-11-20 EP disclosed
US-20070281943-A1 Imidazolopyrazine compounds useful for the treatment of degenerative and inflammatory diseases JANSSEN PHARMACEUTICA N.V. (BE) 2007-12-06 US disclosed
WO-2007131991-A1 IMIDAZOLOPYRAZINE COMPOUNDS USEFUL FOR THE TREATMENT OF DEGENERATIVE AND INFLAMMATORY DISEASES GALAPAGOS N.V. (BE) 2007-11-22 WO disclosed
WO-2007130780-A2 BENZIMIDAZOLE MODULATORS OF VR1 JANSSEN PHARMACEUTICA N.V. (BE) 2007-11-15 WO disclosed
WO-2007130468-A2 PYRIDO [2, 3-B] PYRAZINE AND [1, 8] -NAPHTHYRIDINE DERIVATIVES AS ALK AND C-MET INHIBITORS CEPHALON, INC. (US) 2007-11-15 WO disclosed
EP-1831184-A2 PYRAZINES AND PYRIDINES AND DERIVATIVES THEREOF AS THERAPEUTIC COMPOUNDS The Wellcome Trust Limited (GB) 2007-09-12 EP disclosed
WO-2007070816-A2 THIOPHENE DERIVATIVES AS FACTOR XIA INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2007-06-21 WO disclosed
EP-1706395-A1 THIOPHENE AND FURAN COMPOUNDS ELI LILLY AND COMPANY (US) 2006-10-04 EP disclosed
WO-2006067466-A2 PYRAZINES AND PYRIDINES AND DERIVATIVES THEREOF AS THERAPEUTIC COMPOUNDS THE WELLCOME TRUST LIMITED (GB) 2006-06-29 WO disclosed
WO-2006014647-A2 CYCLIC N-HYDROXY IMIDES AS INHIBITORS OF FLAP ENDONUCLEASE AND USES THEREOF ATHERSYS, INC. (US) 2006-02-09 WO disclosed
WO-2005070916-A1 THIOPHENE AND FURAN COMPOUNDS ELI LILLY AND COMPANY (US) 2005-08-04 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 (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-20250223277-A1 COMPLEMENT FACTOR B INHIBITORS AND USES THEREOF CFB, CFH, C1QBP PARP10 1472/4885PARP15 1346/4885PARP4 1064/4885
US-20240400555-A1 Compounds, Compositions and Methods for Attenuation of Mammalian Translation of C-MYC or N-MYC Proteins of the MYC Proto-Oncogene Family of BHLH Transcription Factors MYCBP, MYC, MYCBP2 PARP10 3504/4885PARP15 3181/4885PARP4 3209/4885
US-20070281943-A1 Imidazolopyrazine compounds useful for the treatment of degenerative and inflammatory diseases IKZF3, IRAK2, IRAK1 PARP10 4359/4885PARP15 2427/4885PARP4 4694/4885

“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.