SCHEMBL5787744

SCHEMBL5787744

Cc1cccc(-c2c(-c3ccncc3)nc(Cl)n(C)c2=O)c1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CSNK1D P48730 3/20 0.55
MAPK9 P45984 3/20 0.55
MAP4K4 O95819 2/20 0.55
CDC42BPA Q5VT25 2/20 0.55
MINK1 Q8N4C8 2/20 0.55
FRK P42685 1/20 0.55
CSNK1A1 P48729 1/20 0.55
MAP4K5 Q9Y4K4 1/20 0.55
TDP2 O95551 1/20 0.42
NPC1 O15118 1/20 0.41
RAB9A P51151 1/20 0.41
MAPK14 Q16539 7/20 0.40
TGFBR1 P36897 1/20 0.40
CSNK1E P49674 1/20 0.40
KDM1A O60341 2/20 0.40
MAPK13 O15264 2/20 0.40
EGFR P00533 1/20 0.40
ERBB2 P04626 1/20 0.40
LYN P07948 1/20 0.40
PRKACA P17612 1/20 0.40

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
SCHEMBL5847664 0.87 MAPK14 (0.49) CSNK1DMAPK9MAP4K4CDC42BPAMINK1
SCHEMBL5847952 0.86 MAPK9 (0.43) CSNK1DMAPK9MAP4K4CDC42BPAMINK1
SCHEMBL5788934 0.83 GRIN1 (0.45) CSNK1DMAPK9MAP4K4CDC42BPAMINK1
SCHEMBL27507564 0.83 MAPK9 (0.49) CSNK1DMAPK9MAP4K4CDC42BPAMINK1
SCHEMBL6932152 0.83 CSNK1D (0.53) CSNK1DMAPK9MAP4K4CDC42BPAMINK1
SCHEMBL4826188 0.82 MAPK9 (0.56) CSNK1DMAPK9MAP4K4CDC42BPAMINK1
Hydrochloric Acid SCHEMBL6935269 0.82 GRIN1 (0.45) CSNK1DMAPK9MAP4K4CDC42BPAMINK1
SCHEMBL5849136 0.80 ADORA1 (0.45) MAPK9TDP2NPC1RAB9AMAPK14
SCHEMBL5786878 0.78 MAPK14 (0.50) CSNK1DMAPK9MAP4K4CDC42BPAMINK1
SCHEMBL5789108 0.78 MAPK14 (0.57) CSNK1DMAPK14CSNK1EMAPK13EGFR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1448564-B1 SUBSTITUTED INDOLIZINE-LIKE COMPOUNDS AND METHODS OF USE AMGEN INC (US) 2006-04-19 EP disclosed
US-7026326-B2 Substituted heterocyclic compounds and methods of use AMGEN INC. (US) 2006-04-11 US disclosed
US-6921762-B2 Substituted indolizine-like compounds and methods of use AMGEN INC. (US) 2005-07-26 US disclosed
US-20050038010-A1 Substituted heterocyclic compounds and methods of use AMGEN, INC. 2005-02-17 US disclosed
EP-1506186-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AND METHODS OF USE Amgen Inc. (US) 2005-02-16 EP disclosed
EP-1448564-A2 SUBSTITUTED INDOLIZINE-LIKE COMPOUNDS AND METHODS OF USE Amgen Inc. (US) 2004-08-25 EP disclosed
WO-2003099808-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS AND METHODS OF USE AMGEN INC. (US) 2003-12-04 WO disclosed
US-6649604-B2 Analgesics; antidiabetic agents; antiinflamamtory agents AMGEN INC. 2003-11-18 US disclosed
US-20030195221-A1 Substituted indolizine-like compounds and methods of use AMGEN INC. 2003-10-16 US disclosed
WO-2003044021-A2 SUBSTITUTED INDOLIZINE-LIKE COMPOUNDS AND METHODS OF USE AMGEN INC. (US) 2003-05-30 WO disclosed
US-20030073704-A1 Substituted pyridone compounds and methods of use AMGEN INC. 2003-04-17 US disclosed
US-6420385-B1 INFLAMMATORY, PAIN AND DIABETES DISEASES, AMGEN INC. 2002-07-16 US disclosed
US-6096753-A Substituted pyrimidinone and pyridone compounds and methods of use AMGEN INC. (US) 2000-08-01 US disclosed
EP-0948496-A2 SUBSTITUTED PYRIMIDINONE AND PYRIDONE COMPOUNDS AND METHODS OF USE Amgen inc. (US) 1999-10-13 EP disclosed
WO-1998024780-A2 SUBSTITUTED PYRIMIDINONE AND PYRIDINONE COMPOUNDS AND THEIR USE AMGEN INC. (US) 1998-06-11 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 (3 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-20050038010-A1 Substituted heterocyclic compounds and methods of use MYLK2, MYLK, MCL1 CSNK1D 1643/4885MAPK9 1787/4885MAP4K4 1286/4885
US-20030195221-A1 Substituted indolizine-like compounds and methods of use IL1A, IL1B, IL6 CSNK1D 558/4885MAPK9 1455/4885MAP4K4 368/4885
US-20030073704-A1 Substituted pyridone compounds and methods of use IL6, IL1B, IL1A CSNK1D 1761/4885MAPK9 1247/4885MAP4K4 761/4885

“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.