SCHEMBL7918141

SCHEMBL7918141

NC1(O)C=CC([N+](=O)[O-])=CC1

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
SCHEMBL9711596 0.78
SCHEMBL9763476 0.78 CYP19A1 (0.30)
SCHEMBL15399539 0.78
SCHEMBL4754696 0.78
SCHEMBL4953742 0.78
SCHEMBL6689289 0.78
SCHEMBL27472037 0.78
SCHEMBL10659257 0.74 HTT (0.30)
SCHEMBL27545401 0.73 CYP3A4 (0.38)
SCHEMBL28363279 0.71

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6222044-B1 REACTING AN AROMATIC ALDEHYDE WITH HYDROXYLAMINE TO FORM AN AROMATIC ALDEHYDE OXIME, HALOGENATING OXIME TO FORM AROMATIC HYDROXAMOYL HALIDE, AND REACTING WITH AROMATIC AMINE COMPOUNDS TO FORM BENZOXAZOLE, BENZOTHIAXOLE, BENZIMIDAZOLES THE DOW CHEMICAL COMPANY 2001-04-24 US disclosed
EP-0820447-B1 PROCESS FOR MAKING 2-ARYL BENZ(OX, THI, IMID)AZOLES AND 2-AMINOARYL AMINOBENZ(OX, THI, IMID)AZOLES DOW CHEMICAL CO (US) 2000-08-23 EP disclosed
EP-0820447-A1 PROCESS FOR MAKING 2-ARYL BENZ(OX, THI, IMID)AZOLES AND 2-AMINOARYL AMINOBENZ(OX, THI, IMID)AZOLES THE DOW CHEMICAL COMPANY (US) 1998-01-28 EP disclosed
US-5567843-A Process for making 2-aryl benz (ox, thi, imid)azoles and 2-aminoaryl aminobenz(ox, thi, imid)azoles THE DOW CHEMICAL COMPANY (US) 1996-10-22 US disclosed
WO-1996029319-A1 PROCESS FOR MAKING 2-ARYL BENZ(OX, THI, IMID)AZOLES AND 2-AMINOARYL AMINOBENZ(OX, THI, IMID)AZOLES THE DOW CHEMICAL COMPANY (US) 1996-09-26 WO disclosed