SCHEMBL6181672

SCHEMBL6181672

O=C(Cc1ccncc1)[N+]1([O-])CCC(=C2c3ccc(Cl)cc3CCc3cccnc32)CC1

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FNTA P49354 10/20 0.69
FNTB P49356 10/20 0.69
HRH1 P35367 6/20 0.62
SLC6A15 Q9H2J7 9/20 0.60
PTAFR P25105 3/20 0.55
MEN1 O00255 2/20 0.54
LMNA P02545 2/20 0.54
CHRM2 P08172 2/20 0.54
ABCB1 P08183 2/20 0.54
CHRM3 P20309 2/20 0.54
TBXA2R P21731 2/20 0.54
HRH2 P25021 2/20 0.54
HTR2A P28223 2/20 0.54
OPRK1 P41145 2/20 0.54
HTR2B P41595 2/20 0.54
SLC6A3 Q01959 2/20 0.54
KMT2A Q03164 2/20 0.54
KCNH2 Q12809 2/20 0.54
ADRB2 P07550 1/20 0.54
CHRM4 P08173 1/20 0.54

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
SCHEMBL6180066 0.91 FNTA (0.70) FNTAFNTBHRH1SLC6A15PTAFR
SCHEMBL7002988 0.88 FNTA (0.60) FNTAFNTBHRH1SLC6A15PTAFR
SCHEMBL6994297 0.87 FNTA (0.71) FNTAFNTBHRH1SLC6A15
SCHEMBL8879934 0.87 FNTA (0.60) FNTAFNTBHRH1SLC6A15PTAFR
SCHEMBL2732013 0.81 FNTA (1.00) FNTAFNTBHRH1SLC6A15PTAFR
SCHEMBL29663139 0.81 FNTA (1.00) FNTAFNTBHRH1SLC6A15PTAFR
SCHEMBL7678148 0.81 SLC6A15 (0.69) FNTAFNTBHRH1SLC6A15PTAFR
SCHEMBL6993110 0.79 FNTA (0.46) FNTAFNTBHRH1SLC6A15PTAFR
SCHEMBL14640320 0.79 FNTA (0.81) FNTAFNTBHRH1SLC6A15PTAFR
SCHEMBL6998864 0.78 FNTA (0.61) FNTAFNTB

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-1123931-B1 Tricylic amide and urea compounds useful for inhibition of G-protein function and for treatment of proliferative diseases SCHERING CORP (US) 2005-06-01 EP disclosed
US-20020068742-A1 Tricyclic amide and urea compounds useful for inhibition of G-protein function and for treatment of proliferative diseases BISHOP W ROBERT (US) 2002-06-06 US disclosed
EP-0723540-B1 TRICYCLIC AMIDE AND UREA COMPOUNDS USEFUL FOR INHIBITION OF G-PROTEIN FUNCTION AND FOR TREATMENT OF PROLIFERATIVE DISEASES SCHERING CORP (US) 2001-12-12 EP disclosed
EP-1123931-A1 Tricylic amide and urea compounds useful for inhibition of G-protein function and for treatment of proliferative diseases SCHERING CORPORATION (US) 2001-08-16 EP disclosed
US-6242458-B1 INHIBITING FARNESYL PROTEIN TRANSFERASE IN A HUMAN SCHERING CORPORATION 2001-06-05 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-20020068742-A1 Tricyclic amide and urea compounds useful for inhibition of G-protein function and for treatment of proliferative diseases RASGRP1, CCNA1, CCNA2 FNTA 516/4885FNTB 1222/4885HRH1 389/4885

“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.