SCHEMBL6930105

SCHEMBL6930105

O=C(c1ccc(Oc2ccccc2)cc1)c1c[nH]cc1-c1cccc2ccccc12

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BCL2 P10415 3/20 0.59
MCL1 Q07820 3/20 0.59
BAD Q92934 1/20 0.59
FNTA P49354 2/20 0.54
FNTB P49356 2/20 0.54
SMN1; SMN2 Q16637 2/20 0.52
ALDH1A1 P00352 2/20 0.52
MEN1 O00255 2/20 0.51
MAPT P10636 2/20 0.51
KMT2A Q03164 2/20 0.51
HTT P42858 1/20 0.51
NPSR1 Q6W5P4 1/20 0.51
TDP1 Q9NUW8 1/20 0.51
L3MBTL1 Q9Y468 1/20 0.51
MAPK1 P28482 1/20 0.50
SRD5A2 P31213 2/20 0.47
ENPP2 Q13822 1/20 0.44
GCGR P47871 2/20 0.42
PARP10 Q53GL7 1/20 0.41
POLB P06746 1/20 0.41

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
SCHEMBL6928721 0.83 MEN1 (0.51) BCL2MCL1BADFNTAFNTB
SCHEMBL15313717 0.81 MCL1 (0.76) BCL2MCL1BADFNTAFNTB
SCHEMBL6599085 0.77 MEN1 (0.56) MCL1SMN1; SMN2ALDH1A1MEN1MAPT
SCHEMBL15313720 0.74 BCL2 (1.00) BCL2MCL1BADFNTAFNTB
SCHEMBL8398501 0.73 NR4A1 (0.53) BCL2MCL1BADFNTAFNTB
SCHEMBL10537061 0.72 SRD5A2 (0.71) BCL2MCL1BADSRD5A2PARP10
SCHEMBL6923020 0.71 MAPT (0.50) SMN1; SMN2ALDH1A1MEN1MAPTKMT2A
SCHEMBL976142 0.71 HDAC8 (0.60) MCL1SMN1; SMN2MEN1MAPTKMT2A
SCHEMBL31254507 0.70 SRD5A2 (0.59) BCL2MCL1BADSMN1; SMN2ALDH1A1
SCHEMBL27527408 0.70 FNTA (0.52) BCL2MCL1BADFNTAFNTB

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 disclosed
US-6518429-B2 Anticancer agents, treating restenosis, atherosclerosis and hepatitis virus LG CHEMICAL, LTD. (KR) 2003-02-11 US disclosed
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-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 BCL2 4618/4885MCL1 1991/4885BAD 3823/4885

“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.