SCHEMBL4970677

SCHEMBL4970677

O=C(O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ncncc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CSNK2A2 P19784 20/20 1.00
CSNK2A1 P68400 20/20 1.00
CSNK2B P67870 15/20 1.00
CSNK2A3 Q8NEV1 3/20 0.74
CHEK1 O14757 1/20 0.71
GAK O14976 1/20 0.71
DAPK3 O43293 1/20 0.71
DYRK3 O43781 1/20 0.71
ULK1 O75385 1/20 0.71
STK10 O94804 1/20 0.71
CCNB2 O95067 1/20 0.71
CDK1 P06493 1/20 0.71
PIM1 P11309 1/20 0.71
CCNB1 P14635 1/20 0.71
PHKG2 P15735 1/20 0.71
CCNE1 P24864 1/20 0.71
CDK2 P24941 1/20 0.71
TYK2 P29597 1/20 0.71
FLT3 P36888 1/20 0.71
CSNK1A1 P48729 1/20 0.71

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
SCHEMBL16838022 0.91 CSNK2A1 (0.83) CSNK2A2CSNK2A1CSNK2BCSNK2A3CHEK1
SCHEMBL11932184 0.88 CSNK2A1 (0.80) CSNK2A2CSNK2A1CSNK2BCSNK2A3
SCHEMBL4972019 0.88 CSNK2A1 (1.00) CSNK2A2CSNK2A1CSNK2BCSNK2A3
SCHEMBL4972016 0.86 CSNK2A1 (1.00) CSNK2A2CSNK2A1CSNK2BCSNK2A3
SCHEMBL4970117 0.86 CSNK2A1 (0.80) CSNK2A2CSNK2A1CSNK2BCSNK2A3CHEK1
SCHEMBL16838028 0.85 CSNK2A1 (0.86) CSNK2A2CSNK2A1CSNK2BCSNK2A3
SCHEMBL10134688 0.85 CSNK2A1 (0.80) CSNK2A2CSNK2A1CSNK2BCSNK2A3CHEK1
SCHEMBL12268708 0.85 CSNK2A1 (0.82) CSNK2A2CSNK2A1CSNK2BCSNK2A3
SCHEMBL1928082 0.85 CSNK2A1 (1.00) CSNK2A2CSNK2A1CSNK2BCSNK2A3
SCHEMBL4974001 0.85 CSNK2A1 (1.00) CSNK2A2CSNK2A1CSNK2BCSNK2A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3458047-B1 METHODS AND PHARMACEUTICAL COMPOSITIONS FOR TREATING MICROBIOME DYSREGULATIONS ASSOCIATED WITH CIRCADIAN CLOCK DISRUPTION INST NAT SANTE RECH MED (FR) 2022-08-03 EP disclosed
US-11364219-B2 Methods and pharmaceutical compositions for treating microbiome dysregulations associated with circadian clock disruption INSERM (INSTITUT NATION DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (FR) 2022-06-21 US disclosed
US-20200390740-A1 METHODS AND PHARMACEUTICAL COMPOSITIONS FOR TREATING MICROBIOME DYSREGULATIONS ASSOCIATED WITH CIRCADIAN CLOCK DISRUPTION INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE) (FR) 2020-12-17 US disclosed
US-20190002569-A1 Methods and Pharmaceutical Compositions for the Treatment of Diseases Mediated by the NRP-1/OBR Complex Signaling Pathway UNIVERSITÉ PARIS CITÉ (FR) 2019-01-03 US disclosed
US-20170051062-A1 Methods and Pharmaceutical Compositions for the Treatment of Diseases Mediated by the NRP-1/OBR Complex Signaling Pathway CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2017-02-23 US disclosed
US-20170051062-A1 Methods and Pharmaceutical Compositions for the Treatment of Diseases Mediated by the NRP-1/OBR Complex Signaling Pathway CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2017-02-23 US disclosed
US-9062043-B2 Fused tricyclic compounds as serine-threonine protein kinase and PARP modulators SENHWA BIOSCIENCES, INC. (TW) 2015-06-23 US disclosed
US-9062043-B2 Fused tricyclic compounds as serine-threonine protein kinase and PARP modulators SENHWA BIOSCIENCES, INC. (TW) 2015-06-23 US disclosed
EP-2061765-B1 Serine-threonine protein kinase and PARP modulators SENHWA BIOSCIENCES INC (TW) 2014-10-22 EP disclosed
US-20120208792-A1 PROTEIN KINASE MODULATORS CYLENE PHARMACEUTICALS, INC. (US) 2012-08-16 US disclosed
US-7956064-B2 Fused tricyclic compounds as serine-threonine protein kinase and PARP modulators CYLENE PHARMACEUTICALS, INC. (US) 2011-06-07 US disclosed
WO-2011041785-A1 BIOMARKERS FOR PREDICTING THE SENSITIVITY AND RESPONSE OF PROTEIN KINASE CK2-MEDIATED DISEASES TO CK2 INHIBITORS CYLENE PHARMACEUTICALS, INC. (US) 2011-04-07 WO disclosed
US-20090264423-A2 SERINE-THREONINE PROTEIN KINASE AND PARP MODULATORS CYLENE PHARMACEUTICALS, INC. (US) 2009-10-22 US disclosed
US-20090264423-A2 SERINE-THREONINE PROTEIN KINASE AND PARP MODULATORS CYLENE PHARMACEUTICALS, INC. (US) 2009-10-22 US disclosed
US-20090239859-A1 PROTEIN KINASE MODULATORS SENHWA BIOSCIENCES, INC. (TW) 2009-09-24 US disclosed
US-20090239859-A1 PROTEIN KINASE MODULATORS SENHWA BIOSCIENCES, INC. (TW) 2009-09-24 US disclosed
WO-2009108912-A1 PROTEIN KINASE MODULATORS CYLENE PHARMACEUTICALS, INC. (US) 2009-09-03 WO disclosed
US-20090105233-A1 SERINE-THREONINE PROTEIN KINASE AND PARP MODULATORS SENHWA BIOSCIENCES, INC. (TW) 2009-04-23 US disclosed
US-20090105233-A1 SERINE-THREONINE PROTEIN KINASE AND PARP MODULATORS SENHWA BIOSCIENCES, INC. (TW) 2009-04-23 US disclosed
WO-2008028168-A2 SERINE-THREONINE PROTEIN KINASE AND PARP MODULATORS CYLENE PHARMACEUTICALS, INC. (US) 2008-03-06 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 (8 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-20170051062-A1 Methods and Pharmaceutical Compositions for the Treatment of Diseases Mediated by the NRP-1/OBR Complex Signaling Pathway NR0B1, NRP1, NR0B2 CSNK2A2 1183/4885CSNK2A1 1045/4885CSNK2B 897/4885
US-11364219-B2 Methods and pharmaceutical compositions for treating microbiome dysregulations associated with circadian clock disruption PER2, CRY1, CRY2 CSNK2A2 4/4885CSNK2A1 5/4885CSNK2B 7/4885
US-20190002569-A1 Methods and Pharmaceutical Compositions for the Treatment of Diseases Mediated by the NRP-1/OBR Complex Signaling Pathway NR0B1, NRP1, NR0B2 CSNK2A2 1183/4885CSNK2A1 1045/4885CSNK2B 897/4885
US-20090264423-A2 SERINE-THREONINE PROTEIN KINASE AND PARP MODULATORS PACSIN2, TNKS, PARP1 CSNK2A2 37/4885CSNK2A1 24/4885CSNK2B 39/4885
US-20120208792-A1 PROTEIN KINASE MODULATORS PIM1, PIM2, PIM3 CSNK2A2 810/4885CSNK2A1 680/4885CSNK2B 772/4885
US-20090105233-A1 SERINE-THREONINE PROTEIN KINASE AND PARP MODULATORS PACSIN2, TNKS, PARP1 CSNK2A2 37/4885CSNK2A1 24/4885CSNK2B 39/4885
US-20090239859-A1 PROTEIN KINASE MODULATORS PIM1, PIM2, PIM3 CSNK2A2 810/4885CSNK2A1 680/4885CSNK2B 772/4885
US-20200390740-A1 METHODS AND PHARMACEUTICAL COMPOSITIONS FOR TREATING MICROBIOME DYSREGULATIONS ASSOCIATED WITH CIRCADIAN CLOCK DISRUPTION PER2, CRY1, CRY2 CSNK2A2 4/4885CSNK2A1 5/4885CSNK2B 7/4885

“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.