Orthocresol

Orthocresol

SCHEMBL2951271

Cc1ccccc1O.[K]

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.

Compoundsimilaritytop predictedshared targets
Orthocresol SCHEMBL16002 0.97 — —
Orthocresol SCHEMBL10419161 0.97 TRPA1 (0.60) —
Orthocresol SCHEMBL8710164 0.97 TRPA1 (0.60) —
Orthocresol SCHEMBL170162 0.97 TRPA1 (0.60) —
Orthocresol SCHEMBL29395276 0.97 — —
Orthocresol SCHEMBL8995948 0.94 — —
Orthocresol SCHEMBL3890279 0.94 TRPA1 (0.57) —
Orthocresol SCHEMBL18173954 0.94 — —
Orthocresol SCHEMBL5481807 0.94 — —
Orthocresol SCHEMBL11055588 0.94 TRPA1 (0.57) —

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
CN-113308267-B Oxidation process 摩瑞奇曼公司 2022-09-06 — — CN disclosed
CN-113308267-A Oxidation process 摩瑞奇曼公司 2021-08-27 — — CN disclosed
CN-109415636-B Oxidation process 摩瑞奇曼公司 2021-06-08 — — CN disclosed
US-7767825-B2 2,2′,6,6′-tetraoxazolinyl biphenyl ligand and method for preparing the same SHANGHAI JIAOTONG UNIVERSITY (CN) 2010-08-03 — — US disclosed
US-7754891-B2 chiral ligand may coordinate with metal ions, such as copper, palladium and the like, to catalyze such reactions as asymmetric cyclopropylation reaction, intramolecular Wacker-Type cyclization reaction, asymmetric oxidation reaction of olefin, and intramolecular [2+1] ring addition reaction SHANGHAI JIAOTONG UNIVERSITY (CN) 2010-07-13 — — US disclosed
US-20090156829-A1 5,5'- POSITION LINKED 1,1'- BIPHENYL AXIAL CHIRAL LIGAND AND METHOD FOR PREPARING THE SAME SHANGHAI JIAOTONG UNIVERSITY (CN) 2009-06-18 — — US disclosed
US-20090043104-A1 2,2',6,6' - TETRAOXAZOLINYL BIPHENYL LIGAND AND METHOD FOR PREPARING THE SAME SHANGHAI JIAOTONG UNIVERSITY (CN) 2009-02-12 — — US disclosed
US-7309452-B2 Phenolate-containing formulation with low freezing point OMYA DEVELOPMENT AG (CH) 2007-12-18 — — US disclosed
US-20070191494-A1 PHENOLATE-CONTAINING FORMULATION WITH LOW FREEZING POINT OMYA AG (CH) 2007-08-16 — — US disclosed
US-20060065875-A1 Phenolate-containing formulation with low freezing point OMYA AG (CH) 2006-03-30 — — US disclosed
US-6994798-B2 Phenolate-containing formulation with low freezing point OMYA AG (CH) 2006-02-07 — — US disclosed
US-20040259955-A1 New pharmaceutical compositions containing ambroxol and isopropamide iodide BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2004-12-23 — — US disclosed
WO-2004041263-A1 NEW PHARMACEUTICAL COMPOSITIONS CONTAINING AMBROXOL AND ISOPROPAMIDE IODIDE BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2004-05-21 — — WO disclosed
EP-1417961-A1 New pharmaceutical compositions containing a combination of ambroxol or bromhexine and isopropamide iodide Boehringer Ingelheim International GmbH (DE) 2004-05-12 — — EP disclosed
US-20040023939-A1 Phenolates-containing formulation with low freezing point OMYA DEVELOPMENT AG (CH) 2004-02-05 — — US disclosed
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