SCHEMBL29550002

SCHEMBL29550002

O=C1Cc2ncccc2N1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AHR P35869 1/20 0.48
PDK2 Q15119 1/20 0.48
GSK3B P49841 12/20 0.48
GSK3A P49840 11/20 0.48
CDK5 Q00535 8/20 0.48
CDK5R1 Q15078 8/20 0.48
CCNB2 O95067 2/20 0.47
CDK1 P06493 2/20 0.47
CCNB1 P14635 2/20 0.47
CCNB3 Q8WWL7 2/20 0.47
KDM4E B2RXH2 1/20 0.44
MEN1 O00255 1/20 0.44
LMNA P02545 1/20 0.44
MAPT P10636 1/20 0.44
HTT P42858 1/20 0.44
KMT2A Q03164 1/20 0.44
KDR P35968 2/20 0.43
BRD4 O60885 1/20 0.43
PLCG1 P19174 1/20 0.43
ABL1 P00519 1/20 0.42

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
SCHEMBL659375 1.00 AHR (0.48) AHRPDK2GSK3BGSK3ACDK5
SCHEMBL30493623 0.82 NPC1 (0.50) AHRPDK2GSK3BGSK3ACDK5
SCHEMBL2233893 0.82 NPC1 (0.50) AHRPDK2GSK3BGSK3ACDK5
SCHEMBL3053419 0.79 MAPT (0.53) AHRPDK2GSK3BGSK3ACDK5
SCHEMBL5826323 0.78 GSK3A (0.57) GSK3BGSK3ACDK5CDK5R1CCNB2
SCHEMBL8484211 0.78 CYP1A2 (0.56) GSK3BCDK5CDK5R1CCNB2CDK1
SCHEMBL10558162 0.78 BRD4 (0.40) AHRPDK2GSK3BGSK3ACDK5
SCHEMBL299769 0.77 TDP2 (0.52) GSK3BCDK5CDK5R1CCNB2CDK1
SCHEMBL14852833 0.75 GLO1 (0.43) AHRPDK2GSK3BGSK3ACDK5
SCHEMBL673377 0.74 CYP11B1 (0.42) GSK3BGSK3ACDK5CDK5R1CCNB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250320224-A1 NOVEL PAR-2 INHIBITORS DOMAIN THERAPEUTICS (FR) 2025-10-16 US claimed
EP-4532496-A1 NOVEL PAR-2 INHIBITORS Domain Therapeutics (FR) 2025-04-09 EP claimed
CN-119384420-A Novel PAR-2 inhibitors 多曼治疗学公司 2025-01-28 CN claimed
WO-2023233033-A1 NOVEL PAR-2 INHIBITORS DOMAIN THERAPEUTICS (FR) 2023-12-07 WO claimed
EP-4743078-A2 APOL1 INHIBITORS AND METHODS OF USE Maze Therapeutics, Inc. (US) 2026-05-20 EP disclosed
EP-4735420-A1 ARYL INDOL-3-YL KETONE AND ARYL INDAZOL-3-YL KETONE INHIBITORS OF KIF18A Volastra Therapeutics, Inc. (US) 2026-05-06 EP disclosed
EP-4727548-A1 METHOD OF TREATING CANCER WITH INDOLINE INHIBITORS OF KIF18A Volastra Therapeutics, Inc. (US) 2026-04-22 EP disclosed
EP-4638433-A1 NAMPT MODULATORS Cytokinetics, Inc. (US) 2025-10-29 EP disclosed
US-20250320224-A1 NOVEL PAR-2 INHIBITORS DOMAIN THERAPEUTICS (FR) 2025-10-16 US disclosed
EP-4573080-A1 INDANE AND COUMARAN DERIVATIVES AS FAST SKELETAL MUSCLE MYOSIN INHIBITORS Cytokinetics, Inc. (US) 2025-06-25 EP disclosed
WO-2025090640-A1 SOLID FORMULATIONS AND POLYMORPHIC FORMS OF INDOLINE INHIBITORS OF KIF18A VOLASTRA THERAPEUTICS, INC. (US) 2025-05-01 WO disclosed
CN-115843295-B NAMPT modulators 赛特凯恩蒂克公司 2025-04-15 CN disclosed
EP-4100393-A1 NAMPT MODULATORS Cytokinetics, Inc. (US) 2022-12-14 EP disclosed
CN-111278822-B Crystalline forms 阿雷生物药品公司 2022-10-21 CN disclosed
WO-2022116995-A1 2,3-DIHYDRO-1H-PYRROLO[3,2-B]PYRIDINE DERIVATIVE, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF 上海和誉生物医药科技有限公司 2022-06-09 WO disclosed
WO-2022104348-A1 SMALL MOLECULE INHIBITORS OF NF-KB INDUCING KINASE JANSSEN PHARMACEUTICA NV (BE) 2022-05-19 WO disclosed
CN-110267960-B Substituted pyrazolo [1,5-a ] pyrazine compounds as RET kinase inhibitors 阿雷生物药品公司 2022-04-26 CN disclosed
CN-110357878-B 1, 3-dihydro-2H-pyrrolo [3,2-b ] pyridin-2-one derivatives and medical use thereof 武汉誉祥医药科技有限公司 2022-04-12 CN disclosed
CN-110357878-B 1, 3-dihydro-2H-pyrrolo [3,2-b ] pyridin-2-one derivatives and medical use thereof 武汉誉祥医药科技有限公司 2022-04-12 CN disclosed
US-11299510-B2 Substituted pyridopyrrolopyrimidine ribonucleosides for therapeutic uses USTAV ORGANICKE CHEMIE A BIOCHEMIE AV CR, V.V.I. (CZ) 2022-04-12 US 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-20250320224-A1 NOVEL PAR-2 INHIBITORS F2RL1, F2R, F2RL3 AHR 678/4885PDK2 1096/4885GSK3B 2018/4885
US-11299510-B2 Substituted pyridopyrrolopyrimidine ribonucleosides for therapeutic uses TYMP, DPYD, RRM2 AHR 3225/4885PDK2 445/4885GSK3B 2933/4885

“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.