SCHEMBL867264

SCHEMBL867264

Nc1cccc2c1CNC2=O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP1 P09874 5/20 0.68
CDK5 Q00535 2/20 0.61
DYRK1A Q13627 2/20 0.61
CLK4 Q9HAZ1 2/20 0.61
PIM1 P11309 1/20 0.61
CSNK1A1 P48729 1/20 0.61
ROCK1 Q13464 1/20 0.61
LRRK2 Q5S007 1/20 0.61
DYRK1B Q9Y463 1/20 0.61
LTK P29376 1/20 0.53
MST1R Q04912 1/20 0.53
CA12 O43570 1/20 0.48
CA9 Q16790 1/20 0.48
PIK3CD O00329 1/20 0.46
PIK3CA P42336 1/20 0.46
PIK3CB P42338 1/20 0.46
PARP10 Q53GL7 3/20 0.44
PARP11 Q9NR21 3/20 0.44
KDR P35968 3/20 0.44
MAP3K9 P80192 1/20 0.41

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
SCHEMBL30914266 1.00 PARP1 (0.68) PARP1CDK5DYRK1ACLK4PIM1
SCHEMBL7581623 0.81 PARP1 (1.00) PARP1CDK5DYRK1ACLK4PIM1
SCHEMBL1333209 0.78 KDR (0.57) PARP1CDK5DYRK1ACLK4PIM1
SCHEMBL6297545 0.78 PARP1 (0.70) PARP1CDK5DYRK1ACLK4PIM1
SCHEMBL29532218 0.78 PARP1 (0.70) PARP1CDK5DYRK1ACLK4PIM1
SCHEMBL13964372 0.77 PARP1 (0.50) PARP1CDK5DYRK1ACLK4PIM1
SCHEMBL24148319 0.76 CDK5 (0.61) PARP1CDK5DYRK1ACLK4PIM1
SCHEMBL2379452 0.76 CDK5 (0.61) PARP1CDK5DYRK1ACLK4PIM1
SCHEMBL1078443 0.76 CDK5 (0.61) PARP1CDK5DYRK1ACLK4PIM1
SCHEMBL9475196 0.76 PARP1 (0.68) PARP1CDK5DYRK1ACLK4PIM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230364243-A1 CANCER-SELECTIVE TARGET DEGRADATION BY TARGETING GROUP CAGED PROTACS BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2023-11-16 US claimed
WO-2022165185-A9 CANCER-SELECTIVE TARGET DEGRADATION BY TARGETING GROUP CAGED PROTACS BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2022-12-01 WO claimed
WO-2022165185-A1 CANCER-SELECTIVE TARGET DEGRADATION BY TARGETING GROUP CAGED PROTACS BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2022-08-04 WO claimed
EP-4027995-B1 HPK1 ANTAGONISTS AND USES THEREOF NIMBUS SATURN INC (US) 2026-05-27 EP disclosed
CN-119874700-A HPK1 antagonists and uses thereof 林伯士萨顿公司 2025-04-25 CN disclosed
US-12215105-B2 HPK1 antagonists and uses thereof Nimbus Saturn, Inc. (US) 2025-02-04 US disclosed
CN-114945366-B HPK1 antagonists and uses thereof 林伯士萨顿公司 2025-01-07 CN disclosed
EP-4393547-A2 METHODS FOR DOSING AND TREATMENT OF B CELL MALIGNANCIES IN ADOPTIVE CELL THERAPY Juno Therapeutics, Inc. (US) 2024-07-03 EP disclosed
US-12018021-B2 Thiophene derivatives for the treatment of disorders caused by IgE UCB Biopharma SRL (BE) 2024-06-25 US disclosed
US-20240131173-A1 PROTACS WITH TRANSCRIPTION FACTOR TARGETING MOIETIES BETH ISRAEL DEACONESS MEDICAL CENTER, INC. (US) 2024-04-25 US disclosed
EP-4327878-A2 COMBINATION OF A CELL THERAPY AND AN IMMUNOMODULATORY COMPOUND Juno Therapeutics, Inc. (US) 2024-02-28 EP disclosed
WO-2004007458-A1 SUBSTITUTED 2-ALKYLAMINE NICOTINIC AMIDE DERIVATIVES AND USE THERE OF AMGEN INC. (US) 2004-01-22 WO disclosed
WO-2003093249-A1 THIAZOLIDINONES AND THE USE THEREOF AS POLO-LIKE KINASE INHIBITORS SCHERING AKTIENGESELLSCHAFT (DE) 2003-11-13 WO disclosed
US-20030203922-A1 Substituted amine derivatives and methods of use AMGEN INC. 2003-10-30 US disclosed
US-20030149050-A1 Inhibitors of inflammation and reperfusion injury and methods of use thereof INOTEK CORP. 2003-08-07 US disclosed
US-6534651-B2 Substituted isoindolinone derivatives INOTEK PHARMACEUTICALS CORP. 2003-03-18 US disclosed
US-6534651-B2 Substituted isoindolinone derivatives INOTEK PHARMACEUTICALS CORP. 2003-03-18 US disclosed
US-6534651-B2 Substituted isoindolinone derivatives INOTEK PHARMACEUTICALS CORP. 2003-03-18 US disclosed
US-20020095044-A1 Inhibitors of inflammation and reperfusion injury and methods of use thereof INOTEK PHARMACEUTICALS CORPORATION 2002-07-18 US disclosed
WO-2001077075-A2 INHIBITORS OF INFLAMMATION AND REPERFUSION INJURY INOTEK CORPORATION (US) 2001-10-18 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 (7 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-20020095044-A1 Inhibitors of inflammation and reperfusion injury and methods of use thereof IL1B, PTGS1, MMP8 PARP1 505/4885CDK5 411/4885DYRK1A 3592/4885
US-20230364243-A1 CANCER-SELECTIVE TARGET DEGRADATION BY TARGETING GROUP CAGED PROTACS ADRM1, MYC, SKP2 PARP1 1231/4885CDK5 101/4885DYRK1A 3095/4885
US-20030203922-A1 Substituted amine derivatives and methods of use MAOB, HNMT, FLT4 PARP1 758/4885CDK5 504/4885DYRK1A 2254/4885
US-12018021-B2 Thiophene derivatives for the treatment of disorders caused by IgE TSLP, CYSLTR1, CYSLTR2 PARP1 3854/4885CDK5 4141/4885DYRK1A 4096/4885
US-20030149050-A1 Inhibitors of inflammation and reperfusion injury and methods of use thereof IL1B, PTGS1, MMP8 PARP1 505/4885CDK5 411/4885DYRK1A 3592/4885
US-20240131173-A1 PROTACS WITH TRANSCRIPTION FACTOR TARGETING MOIETIES VHL, UBTF, RELA PARP1 1503/4885CDK5 514/4885DYRK1A 1307/4885
US-12215105-B2 HPK1 antagonists and uses thereof PDXK, HIPK1, PCK1 PARP1 2477/4885CDK5 934/4885DYRK1A 860/4885

“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.