SCHEMBL6983262

SCHEMBL6983262

COCCN(C)C(=O)c1cn(C(C)c2cnc[nH]2)nc1-c1cccc2ccccc12

nearest known ligand 0.45

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
HTR2C P28335 1/20 0.45
FNTA P49354 12/20 0.45
FNTB P49356 12/20 0.45
PGGT1B P53609 1/20 0.45
ADRA2A P08913 5/20 0.38
ADRA2B P18089 5/20 0.38
ADRA2C P18825 5/20 0.38
ADRA1A P35348 3/20 0.37
ADRA1D P25100 2/20 0.37
ADRA1B P35368 2/20 0.37

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
SCHEMBL6980621 0.85 FNTA (0.42) HTR2CFNTAFNTBPGGT1BADRA2A
SCHEMBL6973808 0.85 FNTA (0.42) HTR2CFNTAFNTBPGGT1BADRA2A
SCHEMBL7087759 0.84 FNTA (0.40) HTR2CFNTAFNTBPGGT1BADRA2A
SCHEMBL6983089 0.84 FNTA (0.41) HTR2CFNTAFNTBPGGT1B
SCHEMBL6927139 0.82 FNTA (0.39) HTR2CFNTAFNTBPGGT1B
SCHEMBL6978464 0.79 FNTA (0.38) HTR2CFNTAFNTBPGGT1B
SCHEMBL7084119 0.79 FNTA (0.44) HTR2CFNTAFNTBPGGT1BADRA2A
SCHEMBL7084240 0.79 FNTA (0.44) HTR2CFNTAFNTBPGGT1BADRA2A
SCHEMBL6927124 0.76 FNTA (0.47) HTR2CFNTAFNTBPGGT1BADRA2A
SCHEMBL7512901 0.76 FNTA (0.45) HTR2CFNTAFNTBPGGT1BADRA2A

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 7 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
US-6472526-B1 SHOWS AN INHIBITORY ACTIVITY AGAINST FARNESYL TRANSFERASE OR PHARMACEUTICALLY ACCEPTABLE SALTS OR ISOMERS THEREOF, IN PHARMACEUTICAL COMPOSITION AND INTERMEDIATES LG CHEMICAL LTD. (KR) 2002-10-29 US disclosed
US-6268363-B1 ANTITUMOR LG CHEMICAL LTD. (KR) 2001-07-31 US disclosed
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 disclosed
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 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-20020137769-A1 Imidazole derivatives having an inhibitory activity for farnesyl transferase and process for preparation thereof FNTA, FNTB, FDPS HTR2C 4873/4885FNTA 1/4885FNTB 2/4885

“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.