SCHEMBL8136565

SCHEMBL8136565

OCc1cccc(/C=C/c2ccc3ccc(Cl)cc3n2)c1

nearest known ligand 0.57

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ CYSLTR1 Q9Y271 8/20 0.54
▸ CYSLTR2 Q9NS75 4/20 0.54
▸ ABCC1 P33527 2/20 0.48
▸ MEN1 O00255 1/20 0.48
▸ ABCC3 O15438 1/20 0.48
▸ ABCC4 O15439 1/20 0.48
▸ ABCC5 O15440 1/20 0.48
▸ SLCO2B1 O94956 1/20 0.48
▸ ABCB11 O95342 1/20 0.48
▸ KMT2A Q03164 1/20 0.48
▸ ABCC2 Q92887 1/20 0.48
▸ SLCO1B3 Q9NPD5 1/20 0.48
▸ ABCG2 Q9UNQ0 1/20 0.48
▸ SLCO1B1 Q9Y6L6 1/20 0.48

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
SCHEMBL8136569 1.00 CYSLTR1 (0.54) CYSLTR1CYSLTR2ABCC1MEN1ABCC3
SCHEMBL8138011 0.88 CYSLTR1 (0.53) CYSLTR1CYSLTR2ABCC1MEN1ABCC3
SCHEMBL8138020 0.88 CYSLTR1 (0.53) CYSLTR1CYSLTR2ABCC1MEN1ABCC3
SCHEMBL27352935 0.87 CYSLTR1 (0.54) CYSLTR1CYSLTR2ABCC1MEN1ABCC3
SCHEMBL13513030 0.86 CYSLTR1 (0.59) CYSLTR1CYSLTR2ABCC1MEN1ABCC3
SCHEMBL14843401 0.86 CYSLTR1 (0.53) CYSLTR1CYSLTR2ABCC1MEN1ABCC3
SCHEMBL14843400 0.86 CYSLTR1 (0.53) CYSLTR1CYSLTR2ABCC1MEN1ABCC3
SCHEMBL7496760 0.85 CYSLTR2 (0.68) CYSLTR1CYSLTR2MEN1KMT2A
SCHEMBL7496756 0.85 CYSLTR2 (0.68) CYSLTR1CYSLTR2MEN1KMT2A
SCHEMBL626120 0.84 CYSLTR1 (0.54) CYSLTR1CYSLTR2ABCC1MEN1ABCC3

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 11 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6011033-A ANTILEUKOTRIENIC ACTION AND ANTIHISTAMINIC ACTION KOWA CO., LTD. (JP) 2000-01-04 — — US disclosed
EP-0469833-B1 N-Benzyl-Indoles, processes for their preparation and pharmaceutical compositions containing them LILLY CO ELI (GB) 1999-09-08 — — EP disclosed
CN-1040108-C Pharmaceutical compounds LILLY INDUSTRIES LTD (GB) 1998-10-07 — — CN disclosed
EP-0799826-A1 Heteroaryl substituted phenylene derivatives, their preparation and their use as leukotriene receptor antagonists KOWA CO. LTD. (JP) 1997-10-08 — — EP disclosed
EP-0533695-B1 IMIDAZO (4,5-c) PYRIDINES WITH PAF ANTAGONIST ACTIVITY PFIZER (US) 1994-10-05 — — EP disclosed
US-5322847-A Inhibit platelet activating factor, block leukotriene D4 receptors PFIZER INC. (US) 1994-06-21 — — US disclosed
US-5281593-A Pharmaceuticals LILLY INDUSTRIES LIMITED (GB) 1994-01-25 — — US disclosed
EP-0533695-A1 IMIDAZO (4,5-c) PYRIDINES WITH PAF ANTAGONIST ACTIVITY. PFIZER (US) 1993-03-31 — — EP disclosed
CN-1061413-A Medicinal compound LILLY INDUSTRIES LTD (GB) 1992-05-27 — — CN disclosed
EP-0469833-A1 N-Benzyl-Indoles, processes for their preparation and pharmaceutical compositions containing them LILLY INDUSTRIES LIMITED (GB) 1992-02-05 — — EP disclosed
WO-1991017163-A1 IMIDAZO (4,5-c) PYRIDINES WITH PAF ANTAGONIST ACTIVITY PFIZER INC. (US) 1991-11-14 — — WO disclosed
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