SCHEMBL6928071

SCHEMBL6928071

N#CCc1cncn1CC1CCN(C(=O)OCc2ccccc2)CC1

nearest known ligand 0.55

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
FNTA P49354 5/20 0.55
FNTB P49356 5/20 0.55
PGGT1B P53609 5/20 0.55
GRIN2B Q13224 9/20 0.51
CYP2D6 P10635 4/20 0.51
CYP2C9 P11712 4/20 0.51
CYP3A4 P08684 3/20 0.51
SMN1; SMN2 Q16637 3/20 0.50
NPC1 O15118 2/20 0.50
RAB9A P51151 2/20 0.50
CYP2C19 P33261 1/20 0.48
GPR119 Q8TDV5 1/20 0.44
FAAH O00519 1/20 0.44
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
NPSR1 Q6W5P4 1/20 0.43

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
SCHEMBL6926261 0.88 GRIN2B (0.54) FNTAFNTBPGGT1BGRIN2BCYP2D6
SCHEMBL6923102 0.87 GRIN2B (0.53) FNTAFNTBPGGT1BGRIN2BCYP2D6
Hydrochloric Acid SCHEMBL6926446 0.86 GRIN2B (0.53) FNTAFNTBPGGT1BGRIN2BCYP2D6
SCHEMBL6929325 0.83 SMN1; SMN2 (0.53) FNTAFNTBPGGT1BGRIN2BCYP2D6
SCHEMBL1290635 0.73 SMN1; SMN2 (0.70) GRIN2BCYP2D6CYP2C9CYP3A4SMN1; SMN2
SCHEMBL5450717 0.73 SMN1; SMN2 (0.59) GRIN2BCYP2D6CYP2C9CYP3A4SMN1; SMN2
SCHEMBL29671511 0.73 SMN1; SMN2 (0.65) GRIN2BCYP2D6CYP2C9CYP3A4SMN1; SMN2
SCHEMBL28690825 0.73 SMN1; SMN2 (0.58) GRIN2BCYP2D6CYP2C9CYP3A4SMN1; SMN2
SCHEMBL15140566 0.72 SMN1; SMN2 (0.72) GRIN2BCYP2D6CYP2C9CYP3A4SMN1; SMN2
SCHEMBL458805 0.72 SMN1; SMN2 (0.72) GRIN2BCYP2D6CYP2C9CYP3A4SMN1; SMN2

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 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.