SCHEMBL6976566

SCHEMBL6976566

COc1ccc(C(=O)c2cn(Cc3c[nH]cn3)cc2-c2cccc3ccccc23)cc1

nearest known ligand 0.57

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
FNTA P49354 13/20 0.57
FNTB P49356 13/20 0.57
GCGR P47871 2/20 0.42
SMN1; SMN2 Q16637 2/20 0.41
ALDH1A1 P00352 2/20 0.41
TP53 P04637 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
CYP1A2 P05177 1/20 0.40
CYP3A4 P08684 1/20 0.40
CYP2D6 P10635 1/20 0.40
CYP2C9 P11712 1/20 0.40
HPGD P15428 1/20 0.40
CYP2C19 P33261 1/20 0.40
HTT P42858 1/20 0.40
CNR2 P34972 1/20 0.40
MEN1 O00255 1/20 0.38
MAPT P10636 1/20 0.38
KMT2A Q03164 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
SCHEMBL6980497 0.91 FNTA (0.52) FNTAFNTBCNR2
SCHEMBL6983449 0.91 FNTA (0.69) FNTAFNTBGCGR
SCHEMBL6982725 0.90 FNTA (0.68) FNTAFNTBSMN1; SMN2ALDH1A1TP53
SCHEMBL6975762 0.90 FNTA (0.66) FNTAFNTBCYP3A4CNR2
SCHEMBL6978634 0.88 FNTA (0.55) FNTAFNTBGCGR
SCHEMBL6972826 0.88 FNTA (0.68) FNTAFNTBCNR2MEN1KMT2A
SCHEMBL6978528 0.88 FNTA (0.56) FNTAFNTBTP53CNR2
SCHEMBL6976425 0.88 FNTA (0.56) FNTAFNTBCNR2
SCHEMBL6978911 0.88 FNTA (0.59) FNTAFNTBNPSR1HTTCNR2
SCHEMBL6972829 0.87 FNTA (0.58) FNTAFNTBCYP3A4CNR2

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 2/4885GCGR 3421/4885

“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.