3-Methylpyridine

3-Methylpyridine

SCHEMBL990915

CC.Cc1cccnc1

nearest known ligand 0.00

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⚠ 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.

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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109862873-B Suspension composition 爱客多有限公司 2024-03-08 — — CN disclosed
EP-2272509-A1 New Uses of metabotropic glutamate receptors Novartis AG (CH) 2011-01-12 — — EP disclosed
EP-2069305-A2 NICOTINIC ACID DERIVATIVES AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS Novartis AG (CH) 2009-06-17 — — EP disclosed
EP-1966144-A1 NICOTINIC ACID DERIVATIVES AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS Novartis AG (CH) 2008-09-10 — — EP disclosed
WO-2008031550-A2 NICOTINIC ACID DERIVATIVES AS MODULATORS OF METABOTROPIC GLUTANATE RECEPTORS NOVARTIS AG (CH) 2008-03-20 — — WO disclosed
WO-2007071358-A1 NICOTINIC ACID DERIVATIVES AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS NOVARTIS AG (CH) 2007-06-28 — — WO disclosed
US-6679922-B1 CAPABLE OF DETOXIFYING PESTICIDES; TEXTILES; IMMERSING IN AN AQUEOUS TREATING SOLUTION OF A CATALYST, WETTING AGENT AND A NONAROMATIC HETEROCYCLIC AMINE; TREATING SAID ARTICLE WITH A HALOGENATED AQUEOUS SOLUTION THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2004-01-20 — — US disclosed
WO-2001015778-A1 PESTICIDE PROTECTIVE ARTICLES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2001-03-08 — — WO disclosed
EP-0437290-B1 Process for the preparation of 5-oxohexane nitriles and the compound 2,4-dimethyl-5-oxohexane nitrile DSM NV (NL) 1998-05-06 — — EP disclosed
US-5334721-A Reacting a methyl ketone and an alpha,beta-unsaturated nitrile in the presence of a basic catalyst; preparation of a 2-methyl-3,5-dialkylpyridine; cyclization; dehydrogenation STAMICARBON B.V. (NL) 1994-08-02 — — US disclosed
EP-0437290-A1 Process for the preparation of 5-oxohexane nitriles and the compound 2,4-dimethyl-5-oxohexane nitrile DSM N.V. (NL) 1991-07-17 — — EP disclosed
EP-0025354-B1 METHOD FOR MAKING THIOBISCARBAMATES UNION CARBIDE CORPORATION (US) 1983-09-28 — — EP disclosed
EP-0079991-A1 Method for making thiobiscarbamates UNION CARBIDE CORPORATION (US) 1983-06-01 — — EP disclosed
US-4323516-A BY REACTING A PYRIDINE-SULFUR CHLORIDE ADDUCT WITH A CARBAMATE UNION CARBIDE CORPORATION (US) 1982-04-06 — — US disclosed
WO-1981000713-A1 METHOD FOR MAKING THIOBISCARBAMATES UNION CARBIDE CORP (US) 1981-03-19 — — WO disclosed
EP-0025354-A2 Method for making thiobiscarbamates UNION CARBIDE CORPORATION (US) 1981-03-18 — — EP disclosed
US-4256655-A COMPLEXING AN N-HETEROCYCLIC BASE WITH SULFUR UNION CARBIDE CORPORATION (US) 1981-03-17 — — US disclosed
US-3981879-A Preparation of cyanopyridines MERCK & CO., INC. (US) 1976-09-21 — — US disclosed
US-3970657-A Preparation of cyanopyridines MERCK & CO., INC. (US) 1976-07-20 — — US disclosed
US-3970659-A Preparation of cyanopyridines MERCK & CO., INC. (US) 1976-07-20 — — US disclosed
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