SCHEMBL16185207

SCHEMBL16185207

CC(C)c1c(CN)n2c(c(O)c1=O)C(=O)N(Cc1ccc(F)c(Cl)c1)CC2

nearest known ligand 0.43

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
ERCC1 P07992 1/20 0.34
ERCC4 Q92889 1/20 0.34
GRM2 Q14416 2/20 0.34
HTR2A P28223 1/20 0.34
TNIK Q9UKE5 1/20 0.33
HRH3 Q9Y5N1 2/20 0.33
CLPP Q16740 2/20 0.33
CYP2D6 P10635 1/20 0.33
TP53 P04637 1/20 0.33
KCNH2 Q12809 2/20 0.32
MAOB P27338 1/20 0.32
SOS1 Q07889 1/20 0.32
PIK3CA P42336 1/20 0.31
P2RX7 Q99572 1/20 0.31
AKR1B1 P15121 1/20 0.31
TRAP1 Q12931 1/20 0.31

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
Trifluoroacetic Acid SCHEMBL17537045 0.94 DPP4 (0.35) ERCC1ERCC4GRM2HTR2ACLPP
SCHEMBL17537046 0.86 GRM2 (0.31) GRM2HTR2ATP53KCNH2P2RX7
SCHEMBL17537011 0.84 UBE2M (0.32) ERCC1ERCC4GRM2HTR2ACLPP
SCHEMBL16185232 0.83 P2RX7 (0.35) TP53P2RX7
SCHEMBL16180376 0.83 PIK3CB (0.34) ERCC1ERCC4GRM2HTR2ATNIK
SCHEMBL16185201 0.81 NAMPT (0.37) TNIK
SCHEMBL2895650 0.79 MAOB (0.38) ERCC1ERCC4GRM2HTR2ATNIK
SCHEMBL3907766 0.77 ERCC1 (0.44) ERCC1ERCC4GRM2HTR2ATNIK
SCHEMBL5522450 0.73 ERCC1 (0.39) ERCC1ERCC4CLPPKCNH2PIK3CA
SCHEMBL16185299 0.73 ERCC1 (0.36) ERCC1ERCC4GRM2HTR2ATNIK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2986291-B1 4-PYRIDONE DERIVATIVE COMPOUNDS AND USES THEREOF AS HIV INTEGRASE INHIBITORS MERCK SHARP & DOHME (US) 2020-05-27 EP disclosed
US-9493479-B2 Substituted pyrido[1,2-a]pyrazines as HIV integrase inhibitors MERCK SHARP & DOHME CORP. (US) 2016-11-15 US disclosed
US-9493479-B2 Substituted pyrido[1,2-a]pyrazines as HIV integrase inhibitors MERCK SHARP & DOHME CORP. (US) 2016-11-15 US disclosed
US-20160060272-A1 4-PYRIDONE DERIVATIVE COMPOUNDS AND USES THEREOF AS HIV INTEGRASE INHIBITORS MERCK SHARP & DOHME CORP. (US) 2016-03-03 US disclosed
US-20160060272-A1 4-PYRIDONE DERIVATIVE COMPOUNDS AND USES THEREOF AS HIV INTEGRASE INHIBITORS MERCK SHARP & DOHME CORP. (US) 2016-03-03 US disclosed
WO-2014172188-A2 4-PYRIDONE DERIVATIVE COMPOUNDS AND USES THEREOF AS HIV INTEGRASE INHIBITORS MERCK SHARP & DOHME CORP. (US) 2014-10-23 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 (1 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-20160060272-A1 4-PYRIDONE DERIVATIVE COMPOUNDS AND USES THEREOF AS HIV INTEGRASE INHIBITORS PNPO, TYMP, PDXK ERCC1 1908/4885ERCC4 809/4885GRM2 4171/4885

“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.