SCHEMBL2998543

SCHEMBL2998543

[Li]c1cccn1C

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL197196 0.69 PCSK9 (0.60) —
SCHEMBL143814 0.67 — —
SCHEMBL196709 0.65 — —
SCHEMBL3766047 0.65 — —
SCHEMBL12074519 0.65 — —
SCHEMBL4282205 0.65 — —
SCHEMBL15272985 0.65 — —
SCHEMBL3092636 0.65 — —
SCHEMBL2971700 0.65 — —
SCHEMBL12754884 0.65 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100184977-A1 Nickel or Iron Catalysed Carbon-Carbon Coupling Reaction of Arylenes, Alkenes and Alkines SALTIGO GMBH (DE) 2010-07-22 — — US disclosed
CN-101300209-A Nickel-or iron-catalyzed carbon-carbon coupling of arylenes, alkenes and alkynes SALTIGO GMBH (DE) 2008-11-05 — — CN disclosed
EP-1924539-A1 NICKEL OR IRON CATALYSED CARBON-CARBON COUPLING REACTION OF ARYLENES, ALKENES AND ALKINES Saltigo GmbH (DE) 2008-05-28 — — EP disclosed
WO-2007031511-A1 NICKEL OR IRON CATALYSED CARBON-CARBON COUPLING REACTION OF ARYLENES, ALKENES AND ALKINES SALTIGO GMBH (DE) 2007-03-22 — — WO disclosed
US-6884801-B1 Imidazoline derivatives as alpha-1A adrenoceptor ligands SMITHKLINE BEECHAM CORPORATION (US) 2005-04-26 — — US disclosed
WO-2000061134-A9 ANTIMICROBIAL AGENTS BRITISH BIOTECH PHARM (GB) 2004-04-22 — — WO disclosed
US-6716878-B1 BACTERICIDE, ANTIPROTOZOAL; VANCOMYCIN RESISTANT ENTEROCOCCI AND BETA-LACTAM ANTIBIOTIC-RESISTANT BACTERIA, METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS; HYDROXAMIC ACID AND N-FORMYL SUBTITUTED ALKYLAMIDES VERNALIS (OXFORD) LIMITED (GB) 2004-04-06 — — US disclosed
US-6509474-B1 Metallization with lithium in ether solvent in presence of conjugated diene hydrogen acceptor CHEMETALL GMBH (DE) 2003-01-21 — — US disclosed
EP-1124819-B1 METHOD OF LITHIATING FIVE-MEMBERED HETEROCYCLES CHEMETALL GMBH (DE) 2003-01-08 — — EP disclosed
EP-1169031-A1 ANTIMICROBIAL AGENTS BRITISH BIOTECH PHARMACEUTICALS LIMITED (GB) 2002-01-09 — — EP disclosed
WO-2000061134-A1 ANTIMICROBIAL AGENTS BRITISH BIOTECH PHARMACEUTICALS LIMITED (GB) 2000-10-19 — — WO disclosed
EP-0146348-B1 SUBSTITUTED NAPHTHALENES, INDOLES, BENZOFURANS AND BENZOTHIOPHENES AS LIPOXYGENASE INHIBITORS THE UPJOHN COMPANY (US) 1991-07-31 — — EP disclosed
US-4737519-A Substituted naphthalenes, indoles, benzofurans, and benzothiophenes as lipoxygenase inhibitors THE UPJOHN COMPANY (US) 1988-04-12 — — US disclosed
EP-0146348-A2 Substituted naphthalenes, indoles, benzofurans and benzothiophenes as lipoxygenase inhibitors THE UPJOHN COMPANY (US) 1985-06-26 — — EP disclosed
US-4173640-A Hypotensive perhydro naphthalene pentol derivatives E. R. SQUIBB & SONS, INC. (US) 1979-11-06 — — US disclosed
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