SCHEMBL14969022

SCHEMBL14969022

CCn1cc(C(=O)O)c(=O)n(-c2ccccc2)c1=O

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PGR P06401 2/20 0.46
LMNA P02545 2/20 0.44
KMT2A Q03164 2/20 0.44
MEN1 O00255 1/20 0.44
ABCC4 O15439 1/20 0.44
PKM P14618 1/20 0.44
PTGS1 P23219 1/20 0.44
BRD4 O60885 1/20 0.43
NOTUM Q6P988 2/20 0.43
ALDH1A1 P00352 2/20 0.43
MET P08581 1/20 0.42
MAPK8 P45983 1/20 0.42
GSK3B P49841 4/20 0.42
GSK3A P49840 3/20 0.42
KDM4E B2RXH2 2/20 0.42
TSHR P16473 3/20 0.41
HIF1A Q16665 1/20 0.41
HPGD P15428 1/20 0.39
RAB9A P51151 1/20 0.39
HSD17B10 Q99714 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
SCHEMBL31091429 0.88 NOTUM (0.47) LMNAKMT2AMEN1ABCC4PKM
SCHEMBL14968894 0.87 NOTUM (0.47) LMNANOTUMMETKDM4E
SCHEMBL31091421 0.85 KDM4E (0.52) LMNAALDH1A1METKDM4ETSHR
SCHEMBL31091480 0.83 NOTUM (0.49) LMNAKMT2AMEN1ABCC4PKM
SCHEMBL19377741 0.83 MERTK (0.40) PGRKMT2ANOTUMALDH1A1GSK3B
SCHEMBL21785474 0.81 HTT (0.45) LMNAKMT2AMEN1ABCC4PKM
SCHEMBL16401887 0.80 GSK3A (0.47) PGRKMT2AMEN1BRD4NOTUM
SCHEMBL29288016 0.77 PGR (0.46) PGRLMNAPKMBRD4ALDH1A1
SCHEMBL14967274 0.76 MET (0.46) LMNANOTUMMETGSK3BGSK3A
SCHEMBL14969331 0.76 KMT2A (0.44) PGRKMT2ANOTUMALDH1A1MET

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2780338-B1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS IGNYTA INC (US) 2016-11-09 EP claimed
US-20140275077-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2014-09-18 US claimed
US-10017496-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2018-07-10 US disclosed
US-20180148447-A1 PYRAZOLO[1,5-A]PYRIDINE DERIVATIVES AND METHODS OF THEIR USE IGNYTA, INC. (US) 2018-05-31 US disclosed
EP-3309160-A1 PYRAZOLO[1,5-A]PYRIDINE DERIVATIVES AND METHODS OF THEIR USE Ignyta, Inc. (US) 2018-04-18 EP disclosed
US-9914731-B2 Pyrazolo[1,5-a]pyridine derivatives and methods of their use IGNYTA, INC. (US) 2018-03-13 US disclosed
US-20170320853-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS IGNYTA, INC. (US) 2017-11-09 US disclosed
EP-3087070-B1 PYRAZOLO[1,5-A]PYRIDINE DERIVATIVES AND METHODS OF THEIR USE IGNYTA INC (US) 2017-11-08 EP disclosed
US-9745283-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2017-08-29 US disclosed
US-20170050949-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. 2017-02-23 US disclosed
US-9522902-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2016-12-20 US disclosed
EP-3045453-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2016-07-20 EP disclosed
US-9120778-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2015-09-01 US disclosed
US-20150210670-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. 2015-07-30 US disclosed
US-20150209358-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. 2015-07-30 US disclosed
WO-2015100117-A1 PYRAZOLO[1,5-A]PYRIDINE DERIVATIVES AND METHODS OF THEIR USE CEPHALON, INC. (US) 2015-07-02 WO disclosed
US-9029538-B2 Uracil derivatives as AXL and c-MET kinase inhibitors IGNYTA, INC. (US) 2015-05-12 US disclosed
EP-2780338-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS Cephalon, Inc. (US) 2014-09-24 EP disclosed
US-20140275077-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2014-09-18 US disclosed
WO-2013074633-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS CEPHALON, INC. (US) 2013-05-23 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-20180148447-A1 PYRAZOLO[1,5-A]PYRIDINE DERIVATIVES AND METHODS OF THEIR USE AXL, FLT3, ERBB2 PGR 936/4885LMNA 4583/4885KMT2A 2091/4885
US-20150210670-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF PGR 2909/4885LMNA 3405/4885KMT2A 822/4885
US-20170050949-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF PGR 2909/4885LMNA 3405/4885KMT2A 822/4885
US-20170320853-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, FLT3 PGR 3158/4885LMNA 3883/4885KMT2A 792/4885
US-20140275077-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF PGR 2909/4885LMNA 3405/4885KMT2A 822/4885
US-10017496-B2 Uracil derivatives as AXL and c-MET kinase inhibitors AXL, RET, FLT3 PGR 3158/4885LMNA 3883/4885KMT2A 792/4885
US-20150209358-A1 URACIL DERIVATIVES AS AXL AND C-MET KINASE INHIBITORS AXL, RET, BRAF PGR 2909/4885LMNA 3405/4885KMT2A 822/4885

“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.