SCHEMBL31023

SCHEMBL31023

Oc1cc(O)n2nccc2n1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE10A Q9Y233 1/20 0.46
PIM1 P11309 2/20 0.38
PIM3 Q86V86 1/20 0.38
PLK3 Q9H4B4 1/20 0.38
PIM2 Q9P1W9 1/20 0.38
KCNN3 Q9UGI6 8/20 0.37
KCNN1 Q92952 2/20 0.37
KCNN2 Q9H2S1 2/20 0.37
PRKAA1 Q13131 2/20 0.37
AURKA O14965 1/20 0.37
JAK2 O60674 1/20 0.37
NTRK1 P04629 1/20 0.37
RET P07949 1/20 0.37
FGFR1 P11362 1/20 0.37
PRKACA P17612 1/20 0.37
LTK P29376 1/20 0.37
KDR P35968 1/20 0.37
MAP2K2 P36507 1/20 0.37
FLT3 P36888 1/20 0.37
MAPK8 P45983 1/20 0.37

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
SCHEMBL20664459 0.80 PDE10A (0.43) PDE10APIM1PIM3PLK3PIM2
SCHEMBL16828091 0.80 PDE10A (0.43) PDE10APIM1PIM3PLK3PIM2
SCHEMBL4102510 0.80 PDE10A (0.43) PDE10AKCNN3PRKAA1KDRPRKAB2
SCHEMBL12364000 0.80 PDE10A (0.43) PDE10APIM1PIM3PLK3PIM2
SCHEMBL1934445 0.76 PDE10A (0.40) PDE10APIM1PIM3PLK3PIM2
SCHEMBL7431490 0.76 PRKAB2 (0.54) PDE10AKCNN3KCNN1KCNN2PRKAA1
SCHEMBL19953388 0.76 LOXL2 (0.46) PDE10APIM1PIM3PLK3PIM2
SCHEMBL4253867 0.76 PIM1 (0.56) PDE10APIM1PIM3PLK3PIM2
SCHEMBL30443263 0.73 CCR1 (0.47) PDE10AKCNN3KDRMAPK14CDK2
SCHEMBL12953626 0.73 PIM1 (0.53) PIM1PIM3PLK3PIM2KCNN3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110016036-B Pyrazolo [1,5-a ] pyrimidine compound and preparation method and application thereof 辽宁大学 2022-06-03 CN claimed
EP-3778604-B1 LRRK2 INHIBITORS AND METHODS OF MAKING AND USING THE SAME DANA FARBER CANCER INST INC (US) 2026-01-07 EP disclosed
CN-117486885-A Use of pyrazolopyrimidines 中国科学院上海药物研究所 2024-02-02 CN disclosed
US-20230348478-A1 TYK2 PSEUDOKINASE LIGANDS VENTYX BIOSCIENCES, INC. 2023-11-02 US disclosed
US-20230348478-A1 TYK2 PSEUDOKINASE LIGANDS VENTYX BIOSCIENCES, INC. 2023-11-02 US disclosed
US-11753411-B2 Substituted pyrazolo[1,5-a]pyrimidines as TYK2 pseudokinase ligands VENTYX BIOSCIENCES, INC. (US) 2023-09-12 US disclosed
US-11753411-B2 Substituted pyrazolo[1,5-a]pyrimidines as TYK2 pseudokinase ligands VENTYX BIOSCIENCES, INC. (US) 2023-09-12 US disclosed
US-20230056447-A1 TYK2 INHIBITORS AND USES THEREOF TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2023-02-23 US disclosed
CN-110016036-B Pyrazolo [1,5-a ] pyrimidine compound and preparation method and application thereof 辽宁大学 2022-06-03 CN disclosed
CN-110016036-B Pyrazolo [1,5-a ] pyrimidine compound and preparation method and application thereof 辽宁大学 2022-06-03 CN disclosed
US-20070037824-A1 Enzyme inhibitors from pyrazolo[1,5a]pyrimidine as enzyme inhibitors SCHERING CORPORATION 2007-02-15 US disclosed
US-20070037824-A1 Enzyme inhibitors from pyrazolo[1,5a]pyrimidine as enzyme inhibitors SCHERING CORPORATION 2007-02-15 US disclosed
US-7161003-B1 Pyrazolopyrimidines as cyclin dependent kinase inhibitors SCHERING CORPORATION (US) 2007-01-09 US disclosed
US-7161003-B1 Pyrazolopyrimidines as cyclin dependent kinase inhibitors SCHERING CORPORATION (US) 2007-01-09 US disclosed
US-20060135514-A1 Pyrazolo[1,5-a]pyrimidine derivatives TEIJIN PHARMA LIMITED 2006-06-22 US disclosed
US-20050080260-A1 Preparation of prodrugs for selective drug delivery LUMINIDE 2005-04-14 US disclosed
US-6555663-B1 Pharmaceuticals which are activated intracellularly by reaction with cellular electron carriers or free radicals to cause release of a free and active drug molecule MILLS RANDELL LEE (US) 2003-04-29 US disclosed
EP-0414730-B1 Chemical Compounds and pharmaceutical compositions capable of releasing a drug MILLS RANDELL L (US) 1999-12-15 EP disclosed
US-5773592-A COMPRISES A CHEMILUMINESCENT MOIETY, A PHOTOCHROMIC MOIETY AND A BIOLOGICALLY ACTIVE AGENT CAPABLE OF BEING RELEASED MILLS RANDELL LEE (US) 1998-06-30 US disclosed
US-5428163-A Luminides; chemiluminescence; redox system, releasing free drug MILLS RANDELL L (US) 1995-06-27 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 (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-20050080260-A1 Preparation of prodrugs for selective drug delivery APEH, PAH, ALAD PDE10A 3189/4885PIM1 2880/4885PIM3 3769/4885
US-11753411-B2 Substituted pyrazolo[1,5-a]pyrimidines as TYK2 pseudokinase ligands TYK2, JAK1, JAK2 PDE10A 2917/4885PIM1 450/4885PIM3 610/4885
US-20230348478-A1 TYK2 PSEUDOKINASE LIGANDS TYK2, JAK2, PTK2B PDE10A 4296/4885PIM1 460/4885PIM3 521/4885
US-20230056447-A1 TYK2 INHIBITORS AND USES THEREOF TYK2, JAK2, JAK1 PDE10A 4705/4885PIM1 244/4885PIM3 273/4885
US-20070037824-A1 Enzyme inhibitors from pyrazolo[1,5a]pyrimidine as enzyme inhibitors CDK2, CDK5, CDKN1A PDE10A 1177/4885PIM1 453/4885PIM3 856/4885
US-20060135514-A1 Pyrazolo[1,5-a]pyrimidine derivatives MAPKAPK2, MAPKAPK5, MAP4K2 PDE10A 1284/4885PIM1 1208/4885PIM3 2061/4885

“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.