SCHEMBL6983372

SCHEMBL6983372

COC(=O)c1sc(Cc2cncn2Cc2ccc(Cl)cc2)nc1-c1cccc2ccccc12

nearest known ligand 0.48

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
FNTA P49354 9/20 0.48
FNTB P49356 9/20 0.48
CYP11B1 P15538 3/20 0.46
CYP11B2 P19099 3/20 0.46
PGGT1B P53609 4/20 0.41
KDM4E B2RXH2 1/20 0.39
GAA P10253 1/20 0.39
KMT2A Q03164 1/20 0.39
NPSR1 Q6W5P4 1/20 0.39

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
SCHEMBL7071192 0.86 CYP11B1 (0.46) FNTAFNTBCYP11B1CYP11B2PGGT1B
SCHEMBL6981190 0.83 FNTA (0.56) FNTAFNTBPGGT1B
SCHEMBL6982813 0.77 GRIN2B (0.40) FNTAFNTBPGGT1B
SCHEMBL6923539 0.76 FNTA (0.51) FNTAFNTBCYP11B1CYP11B2PGGT1B
SCHEMBL7672122 0.76 CYP11B1 (0.46) FNTAFNTBCYP11B1CYP11B2KDM4E
SCHEMBL6980878 0.73 FNTA (0.58) FNTAFNTBPGGT1B
SCHEMBL6983374 0.70 KDM4E (0.38) FNTAFNTBPGGT1BKDM4EGAA
SCHEMBL7086800 0.69 FNTA (0.59) FNTAFNTBCYP11B1CYP11B2PGGT1B
SCHEMBL7050806 0.66 FNTA (0.61) FNTAFNTBCYP11B1CYP11B2PGGT1B
SCHEMBL6610051 0.66 FNTA (0.54) FNTAFNTBCYP11B1CYP11B2PGGT1B

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
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 disclosed
US-6518429-B2 Anticancer agents, treating restenosis, atherosclerosis and hepatitis virus LG CHEMICAL, LTD. (KR) 2003-02-11 US disclosed
US-20020137769-A1 Imidazole derivatives having an inhibitory activity for farnesyl transferase and process for preparation thereof LG CHEMICAL LTD. 2002-09-26 US disclosed
US-6268363-B1 ANTITUMOR LG CHEMICAL LTD. (KR) 2001-07-31 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-20020137769-A1 Imidazole derivatives having an inhibitory activity for farnesyl transferase and process for preparation thereof FNTA, FNTB, FDPS FNTA 1/4885FNTB 2/4885CYP11B1 74/4885

“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.