SCHEMBL6971909

SCHEMBL6971909

O=C(c1ccccc1Cl)c1cn(Cc2c[nH]cn2)cc1-c1cccc2ccccc12

nearest known ligand 0.52

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
FNTA P49354 15/20 0.52
FNTB P49356 15/20 0.52
RORC P51449 1/20 0.47
RORB Q92753 1/20 0.47
CNR2 P34972 2/20 0.37
CNR1 P21554 1/20 0.37
MEN1 O00255 1/20 0.36
MAPT P10636 1/20 0.36
HTT P42858 1/20 0.36
KMT2A Q03164 1/20 0.36
NPSR1 Q6W5P4 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
L3MBTL1 Q9Y468 1/20 0.36
CYP3A4 P08684 1/20 0.35
PGGT1B P53609 1/20 0.35

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
SCHEMBL6984623 0.92 FNTA (0.56) FNTAFNTBCNR2CNR1MEN1
SCHEMBL6979860 0.91 FNTA (0.47) FNTAFNTBRORCRORBCNR2
SCHEMBL6979313 0.88 FNTA (0.52) FNTAFNTBCNR2MEN1MAPT
SCHEMBL6982646 0.88 FNTA (0.67) FNTAFNTBCNR2CNR1MEN1
SCHEMBL6976425 0.87 FNTA (0.56) FNTAFNTBCNR2
SCHEMBL6975762 0.87 FNTA (0.66) FNTAFNTBCNR2CYP3A4PGGT1B
SCHEMBL6925142 0.86 FNTA (0.53) FNTAFNTBMEN1KMT2A
SCHEMBL6978528 0.83 FNTA (0.56) FNTAFNTBCNR2
SCHEMBL6978911 0.83 FNTA (0.59) FNTAFNTBCNR2CNR1MEN1
SCHEMBL6972826 0.83 FNTA (0.68) FNTAFNTBCNR2MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1045846-B1 IMIDAZOLE DERIVATIVES HAVING AN INHIBITORY ACTIVITY FOR FARNESYL TRANSFERASE AND PROCESS FOR PREPARATION THEREOF LG CHEMICAL LTD (KR) 2003-05-02 EP claimed
US-20020137769-A1 Imidazole derivatives having an inhibitory activity for farnesyl transferase and process for preparation thereof LG CHEMICAL LTD. 2002-09-26 US claimed
US-6268363-B1 ANTITUMOR LG CHEMICAL LTD. (KR) 2001-07-31 US claimed

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-20020137769-A1 Imidazole derivatives having an inhibitory activity for farnesyl transferase and process for preparation thereof FNTA, FNTB, FDPS FNTA 1/4885FNTB 2/4885RORC 1627/4885

“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.