SCHEMBL4372018

SCHEMBL4372018

O=C(O)c1ccc2[nH]cnc(=O)c2c1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR7 P34969 1/20 0.47
KDM4E B2RXH2 4/20 0.45
ALDH1A1 P00352 3/20 0.45
HPGD P15428 3/20 0.45
THRB P10828 1/20 0.45
PTPN1 P18031 1/20 0.43
CSNK2A1 P68400 2/20 0.43
SLC2A1 P11166 1/20 0.42
HTT P42858 1/20 0.42
RAB9A P51151 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
SIRT2 Q8IXJ6 1/20 0.41
SIRT1 Q96EB6 1/20 0.41
ENPP2 Q13822 1/20 0.41
HSD17B10 Q99714 1/20 0.41
PARP1 P09874 3/20 0.40
HDAC6 Q9UBN7 1/20 0.40
CTNNB1 P35222 1/20 0.39
WNT3A P56704 1/20 0.39
KIF11 P52732 1/20 0.39

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
SCHEMBL8870966 0.87 CSNK2A1 (0.49) KDM4EALDH1A1HPGDTHRBPTPN1
SCHEMBL5947 0.77 KDM4E (0.53) KDM4EALDH1A1HPGDTHRBSLC2A1
SCHEMBL2574527 0.77 LMNA (0.57) HTR7KDM4EALDH1A1HPGDHSD17B10
Hydrochloric Acid SCHEMBL9928726 0.76 KDM4E (0.51) KDM4EALDH1A1HPGDTHRBSLC2A1
SCHEMBL1584889 0.75 PIM1 (0.56) ALDH1A1HPGDCSNK2A1HTTSMN1; SMN2
SCHEMBL8622177 0.75 ACVR1 (0.46) ALDH1A1HPGDHTTRAB9ASMN1; SMN2
SCHEMBL20017862 0.75 IRAK4 (0.36) KDM4EALDH1A1HPGDSLC2A1HTT
SCHEMBL8700858 0.74 PARP1 (0.54) KDM4EALDH1A1HPGDCSNK2A1RAB9A
SCHEMBL2191001 0.74 PARP1 (0.54) ALDH1A1HPGDCSNK2A1PARP1DYRK1A
SCHEMBL2191063 0.74 PARP1 (0.54) KDM4EALDH1A1HTTPARP1

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8367824-B2 Reacting anthranilic acid with formic acid compound in presence of a catalyst and solvent UBE INDUSTRIES LTD. (JP) 2013-02-05 US disclosed
EP-1477481-B1 PROCESS FOR PRODUCING QUINAZOLIN-4-ONE DERIVATIVE UBE INDUSTRIES (JP) 2009-07-22 EP disclosed
US-20050080262-A1 Process for producing quinazolin-4-one derivative UBE INDUSTRIES, LTD. (JP) 2005-04-14 US disclosed
US-6828320-B2 Enzyme inhibitors; anticancer agents SMITHKLINE BEECHAM CORPORATION 2004-12-07 US disclosed
EP-1477481-A1 PROCESS FOR PRODUCING QUINAZOLIN-4-ONE DERIVATIVE Ube Industries, Ltd. (JP) 2004-11-17 EP disclosed
US-20020147214-A1 Heterocyclic compounds NOVARTIS AG (CH) 2002-10-10 US disclosed
US-6391874-B1 ANTICARCINOGENIC AGENTS; SKIN DISORDERS SMITHKLINE BEECHAM CORPORATION 2002-05-21 US disclosed
EP-0912559-A1 FUSED HETEROCYCLIC COMPOUNDS AS PROTEIN TYROSINE KINASE INHIBITORS GLAXO GROUP LIMITED (GB) 1999-05-06 EP disclosed
WO-1998002434-A1 FUSED HETEROCYCLIC COMPOUNDS AS PROTEIN TYROSINE KINASE INHIBITORS GLAXO GROUP LIMITED (GB) 1998-01-22 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 (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-20020147214-A1 Heterocyclic compounds BRAF, ABL1, CSK HTR7 972/4885KDM4E 1461/4885ALDH1A1 4024/4885
US-20050080262-A1 Process for producing quinazolin-4-one derivative NQO2, SDHA, CYP3A4 HTR7 1234/4885KDM4E 879/4885ALDH1A1 477/4885

“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.