SCHEMBL6923020

SCHEMBL6923020

O=C(c1cccs1)c1c[nH]cc1-c1cccc2ccccc12

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 7/20 0.50
MEN1 O00255 4/20 0.50
KMT2A Q03164 4/20 0.50
NPSR1 Q6W5P4 3/20 0.50
HTT P42858 2/20 0.50
L3MBTL1 Q9Y468 2/20 0.50
TDP1 Q9NUW8 1/20 0.50
ALOX15 P16050 4/20 0.47
LMNA P02545 1/20 0.47
RORC P51449 1/20 0.45
RORB Q92753 1/20 0.45
NPC1 O15118 4/20 0.44
RAB9A P51151 3/20 0.44
HPGDS O60760 1/20 0.43
TSHR P16473 1/20 0.41
RXFP1 Q9HBX9 1/20 0.41
SMN1; SMN2 Q16637 2/20 0.41
MAPK1 P28482 1/20 0.41
CTNNB1 P35222 1/20 0.40
WNT3A P56704 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
SCHEMBL11195206 0.79 ALOX15 (0.62) MAPTMEN1KMT2ANPSR1L3MBTL1
SCHEMBL14627581 0.79 ALDH1A1 (0.61) MAPTMEN1KMT2ANPSR1HTT
SCHEMBL6599085 0.76 MEN1 (0.56) MAPTMEN1KMT2ANPSR1HTT
SCHEMBL6924882 0.74 FNTA (0.48) MAPTNPSR1TSHRRXFP1SMN1; SMN2
SCHEMBL6928721 0.74 MEN1 (0.51) MAPTMEN1KMT2ANPSR1HTT
SCHEMBL976142 0.73 HDAC8 (0.60) MAPTMEN1KMT2ANPSR1HTT
SCHEMBL6930105 0.71 BCL2 (0.59) MAPTMEN1KMT2ANPSR1HTT
SCHEMBL27610085 0.70 ALOX15 (0.62) MAPTMEN1KMT2ANPSR1ALOX15
SCHEMBL9148337 0.70 LMNA (0.85) MAPTMEN1KMT2ANPSR1HTT
SCHEMBL30897296 0.70 CTNNB1 (0.70) MAPTMEN1KMT2ANPSR1ALOX15

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 MAPT 2463/4885MEN1 523/4885KMT2A 3370/4885

“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.