SCHEMBL6177448

SCHEMBL6177448

CCOC(=O)N1CCC(=C2c3ccc(Cl)cc3CCc3c2ncc(Br)c3Cl)CC1

nearest known ligand 0.74

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC6A15 Q9H2J7 9/20 0.74
HRH1 P35367 7/20 0.71
MEN1 O00255 1/20 0.68
NPC1 O15118 1/20 0.68
CACNA1F O60840 1/20 0.68
NR1I2 O75469 1/20 0.68
GMNN O75496 1/20 0.68
USP2 O75604 1/20 0.68
ABCB11 O95342 1/20 0.68
LMNA P02545 1/20 0.68
TP53 P04637 1/20 0.68
CHRM2 P08172 1/20 0.68
ABCB1 P08183 1/20 0.68
CYP3A4 P08684 1/20 0.68
ADORA3 P0DMS8 1/20 0.68
CYP2C8 P10632 1/20 0.68
CYP2D6 P10635 1/20 0.68
MAPT P10636 1/20 0.68
CYP2C9 P11712 1/20 0.68
ADRB3 P13945 1/20 0.68

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
SCHEMBL6178414 0.92 SLC6A15 (0.75) SLC6A15HRH1MEN1NPC1CACNA1F
SCHEMBL12550607 0.87 SLC6A15 (0.82) SLC6A15HRH1MEN1NPC1CACNA1F
SCHEMBL5473193 0.85 SLC6A15 (0.82) SLC6A15HRH1MEN1NPC1CACNA1F
SCHEMBL6178317 0.84 SLC6A15 (0.80) SLC6A15HRH1MEN1NPC1CACNA1F
SCHEMBL31294067 0.83 SLC6A15 (1.00) SLC6A15HRH1MEN1NPC1CACNA1F
SCHEMBL7675089 0.83 SLC6A15 (1.00) SLC6A15HRH1MEN1NPC1CACNA1F
SCHEMBL14370721 0.82 SLC6A15 (0.60) SLC6A15HRH1FNTAFNTB
SCHEMBL24363099 0.81 HRH1 (0.76) SLC6A15HRH1MEN1NPC1CACNA1F
SCHEMBL29687620 0.81 HRH1 (0.76) SLC6A15HRH1MEN1NPC1CACNA1F
SCHEMBL29687346 0.81 HRH1 (1.00) SLC6A15HRH1MEN1NPC1CACNA1F

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-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
US-6365588-B1 AS ANTINEOPLASTIC AGENT AND A POTENTIATING SCHERING CORPORATION 2002-04-02 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
WO-1995010516-A1 TRICYCLIC AMIDE AND UREA COMPOUNDS USEFUL FOR INHIBITION OF G-PROTEIN FUNCTION AND FOR TREATMENT OF PROLIFERATIVE DISEASES SCHERING CORPORATION (US) 1995-04-20 WO 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 SLC6A15 1804/4885HRH1 389/4885MEN1 485/4885

“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.