SCHEMBL6977393

SCHEMBL6977393

CN1CCN(C(=O)c2cn(Cc3c[nH]cn3)cc2-c2cccc3ccccc23)CC1

nearest known ligand 0.57

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
FNTA P49354 15/20 0.57
FNTB P49356 15/20 0.57
PGGT1B P53609 2/20 0.53
CYP3A4 P08684 1/20 0.53
KDM4E B2RXH2 2/20 0.46
HTR2C P28335 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.41
ALDH1A1 P00352 1/20 0.40
GLA P06280 1/20 0.40
GAA P10253 1/20 0.40
CASP1 P29466 1/20 0.40
CASP7 P55210 1/20 0.40
HSD17B10 Q99714 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
SCHEMBL6982870 0.91 FNTA (0.68) FNTAFNTBPGGT1BCYP3A4KDM4E
SCHEMBL6984228 0.91 FNTA (0.55) FNTAFNTBPGGT1BCYP3A4KDM4E
SCHEMBL6979480 0.91 FNTA (0.57) FNTAFNTBPGGT1BCYP3A4HTR2C
SCHEMBL6975190 0.90 FNTA (0.69) FNTAFNTBPGGT1BCYP3A4HTR2C
SCHEMBL6975380 0.90 FNTA (0.56) FNTAFNTBPGGT1BCYP3A4KDM4E
SCHEMBL6982219 0.89 FNTA (0.57) FNTAFNTBPGGT1BCYP3A4HTR2C
SCHEMBL6980781 0.86 FNTA (0.52) FNTAFNTBPGGT1BCYP3A4HTR2C
SCHEMBL6925142 0.84 FNTA (0.53) FNTAFNTBKDM4EALDH1A1
SCHEMBL6984623 0.82 FNTA (0.56) FNTAFNTBL3MBTL1
SCHEMBL6975762 0.81 FNTA (0.66) FNTAFNTBPGGT1BCYP3A4

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 5 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
EP-1045846-A1 IMIDAZOLE DERIVATIVES HAVING AN INHIBITORY ACTIVITY FOR FARNESYL TRANSFERASE AND PROCESS FOR PREPARATION THEREOF LG CHEMICAL LIMITED (KR) 2000-10-25 EP claimed
WO-1999028315-A1 IMIDAZOLE DERIVATIVES HAVING AN INHIBITORY ACTIVITY FOR FARNESYL TRANSFERASE AND PROCESS FOR PREPARATION THEREOF LG CHEMICAL LTD. (KR) 1999-06-10 WO 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 2/4885PGGT1B 32/4885

“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.