SCHEMBL5126325

SCHEMBL5126325

O=C1c2c(O)c3n(c2CCN1Cc1ccc(F)cc1)CCN(Cc1ccc(F)cc1)C3=O

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNH2 Q12809 2/20 0.47
GRM2 Q14416 1/20 0.47
AKR1B1 P15121 1/20 0.44
RAB9A P51151 1/20 0.42
ALDH1A1 P00352 2/20 0.42
POLB P06746 1/20 0.42
LMNA P02545 4/20 0.41
SMN1; SMN2 Q16637 3/20 0.41
L3MBTL1 Q9Y468 3/20 0.41
HTT P42858 2/20 0.41
CLPP Q16740 1/20 0.41
TP53 P04637 2/20 0.39
NCOA3 Q9Y6Q9 1/20 0.39
MEN1 O00255 2/20 0.39
KMT2A Q03164 2/20 0.39
NPC1 O15118 1/20 0.39
HDAC3 O15379 1/20 0.38
HDAC4 P56524 1/20 0.38
HDAC1 Q13547 1/20 0.38
HDAC7 Q8WUI4 1/20 0.38

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
SCHEMBL4750297 0.94 KCNH2 (0.43) KCNH2GRM2AKR1B1RAB9AALDH1A1
SCHEMBL4746127 0.93 KCNH2 (0.44) KCNH2GRM2AKR1B1RAB9AALDH1A1
SCHEMBL4743883 0.92 KCNH2 (0.43) KCNH2GRM2AKR1B1ALDH1A1LMNA
SCHEMBL4745898 0.91 KCNH2 (0.43) KCNH2GRM2AKR1B1RAB9AALDH1A1
SCHEMBL4744312 0.91 KCNH2 (0.41) KCNH2GRM2AKR1B1RAB9AALDH1A1
SCHEMBL4746444 0.89 CLPP (0.44) KCNH2GRM2AKR1B1ALDH1A1LMNA
SCHEMBL4746501 0.89 KCNH2 (0.43) KCNH2GRM2AKR1B1ALDH1A1POLB
SCHEMBL4748853 0.89 CLPP (0.44) KCNH2GRM2AKR1B1ALDH1A1LMNA
SCHEMBL4746845 0.88 ALDH1A1 (0.49) KCNH2GRM2AKR1B1ALDH1A1POLB
SCHEMBL4743154 0.87 RAB9A (0.44) KCNH2GRM2AKR1B1RAB9AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7435735-B2 Hydroxy pyridopyrrolopyrazine dione compounds useful as HIV integrase inhibitors MERCK & CO., INC. (US) 2008-10-14 US claimed
US-20070093496-A1 Hydroxy pyridopyrrolopyrazine dione compounds useful as hiv integrase inhibitors MERCK SHARP & DOHME CORP. 2007-04-26 US claimed
US-7435735-B2 Hydroxy pyridopyrrolopyrazine dione compounds useful as HIV integrase inhibitors MERCK & CO., INC. (US) 2008-10-14 US disclosed
US-7435735-B2 Hydroxy pyridopyrrolopyrazine dione compounds useful as HIV integrase inhibitors MERCK & CO., INC. (US) 2008-10-14 US disclosed
US-7435735-B2 Hydroxy pyridopyrrolopyrazine dione compounds useful as HIV integrase inhibitors MERCK & CO., INC. (US) 2008-10-14 US disclosed
US-20070093496-A1 Hydroxy pyridopyrrolopyrazine dione compounds useful as hiv integrase inhibitors MERCK SHARP & DOHME CORP. 2007-04-26 US disclosed
US-20070093496-A1 Hydroxy pyridopyrrolopyrazine dione compounds useful as hiv integrase inhibitors MERCK SHARP & DOHME CORP. 2007-04-26 US disclosed
US-20070093496-A1 Hydroxy pyridopyrrolopyrazine dione compounds useful as hiv integrase inhibitors MERCK SHARP & DOHME CORP. 2007-04-26 US 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-20070093496-A1 Hydroxy pyridopyrrolopyrazine dione compounds useful as hiv integrase inhibitors DHPS, DPYD, TYMP KCNH2 1318/4885GRM2 4487/4885AKR1B1 318/4885

“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.