SCHEMBL4894778

SCHEMBL4894778

BN(C)C.[NaH]

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
SCHEMBL34801 0.93
SCHEMBL6754664 0.86
Water SCHEMBL28143155 0.86
SCHEMBL8610296 0.86
Hydrochloric Acid SCHEMBL27868053 0.86
SCHEMBL990627 0.86
SCHEMBL10172352 0.77
Benzene SCHEMBL27719523 0.76 TSHR (0.33)
Trimethylammonium SCHEMBL11615551 0.68
SCHEMBL21609889 0.67

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5912352-A CATALYTIC REDUCTION OF HYDRAZIDE TO HYDRAZINE DERIVATIVE IN PRESENCE OF COMPLEX HYDRIDE; ACYL MIGRATION; HYDROGENATION; CATALYST SELECTIVITY NOVARTIS FINANCE CORPORATION (US) 1999-06-15 US claimed
WO-1997046514-A1 PROCESS FOR THE PREPARATION OF HYDRAZINE DERIVATIVES USEFUL AS INTERMEDIATES FOR THE PREPARATION OF PEPTIDE ANALOGUES NOVARTIS AG (CH) 1997-12-11 WO claimed
CN-112895361-A Oxyhydrogen atomizer casing injection mold 上海利劲塑胶模具有限公司 2021-06-04 CN disclosed
EP-3065743-B1 PRODUCTION OF 6-HYDROXY MORPHINANS WITHOUT THE ISOLATION OF INTERMEDIATES SpecGx LLC (US) 2019-05-29 EP disclosed
EP-3065743-A1 PRODUCTION OF 6-HYDROXY MORPHINANS WITHOUT THE ISOLATION OF INTERMEDIATES Mallinckrodt LLC (US) 2016-09-14 EP disclosed
US-9193737-B2 Production of 6-hydroxy morphinans without the isolation of intermediates MALLINCKRODT LLC (US) 2015-11-24 US disclosed
WO-2015069717-A1 PRODUCTION OF 6-HYDROXY MORPHINANS WITHOUT THE ISOLATION OF INTERMEDIATES MALLINCKRODT LLC (US) 2015-05-14 WO disclosed
US-20150126742-A1 PRODUCTION OF 6-HYDROXY MORPHINANS WITHOUT THE ISOLATION OF INTERMEDIATES OCERA THERAPEUTICS LLC 2015-05-07 US disclosed
US-20080052904-A1 Method Of Manufacturing An Electronic Circuit Assembly ATOTECH DEUTSCHLAND GMBH (DE) 2008-03-06 US disclosed
WO-2006010639-A2 METHOD OF MANUFACTURING AN ELECTRONIC CIRCUIT DEVICE THROUGH A DIRECT WRITE TECHNIQUE ATOTECH DEUTSCHLAND GMBH (DE) 2006-02-02 WO disclosed
EP-1622435-A1 Method of manufacturing an electronic circuit assembly using direct write techniques ATOTECH Deutschland GmbH (DE) 2006-02-01 EP disclosed
EP-0876336-B1 AZAHEXANE DERIVATIVES AS SUBSTRATE ISOSTERS OF RETROVIRAL ASPARATE PROTEASES NOVARTIS AG (CH) 2002-06-05 EP disclosed
US-6225345-B1 FOR THERAPY OF ACQUIRED IMMUNODEFICIENCY SYNDROME NOVARTIS AG (CH) 2001-05-01 US disclosed
US-5912352-A CATALYTIC REDUCTION OF HYDRAZIDE TO HYDRAZINE DERIVATIVE IN PRESENCE OF COMPLEX HYDRIDE; ACYL MIGRATION; HYDROGENATION; CATALYST SELECTIVITY NOVARTIS FINANCE CORPORATION (US) 1999-06-15 US disclosed
EP-0876336-A1 AZAHEXANE DERIVATIVES AS SUBSTRATE ISOSTERS OF RETROVIRAL ASPARATE PROTEASES Novartis AG (CH) 1998-11-11 EP disclosed
US-5808070-A Process for preparing alkaline aminoborohydrides and alkaline aminoborohydride complexes METALLGESELLSCHAFT AKTIENGESELLSCHAFT (DE) 1998-09-15 US disclosed
WO-1997046514-A1 PROCESS FOR THE PREPARATION OF HYDRAZINE DERIVATIVES USEFUL AS INTERMEDIATES FOR THE PREPARATION OF PEPTIDE ANALOGUES NOVARTIS AG (CH) 1997-12-11 WO disclosed
WO-1997019055-A1 AZAHEXANE DERIVATIVES AS SUBSTRATE ISOSTERS OF RETROVIRAL ASPARATE PROTEASES NOVARTIS AG (CH) 1997-05-29 WO disclosed
US-5466798-A Reducing agents THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1995-11-14 US disclosed