SCHEMBL1724943

SCHEMBL1724943

C1CN[C@@H]2CNCC2C1

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
SCHEMBL606391 1.00
SCHEMBL7496575 1.00
SCHEMBL1726593 1.00
SCHEMBL7496569 1.00
SCHEMBL64396 1.00
SCHEMBL1723503 1.00
SCHEMBL606385 1.00
SCHEMBL29208889 1.00
Hydrochloric Acid SCHEMBL3332500 0.98 CCR5 (0.36)
SCHEMBL8704625 0.93 EPAS1 (0.37)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115536658-B Preparation method of moxifloxacin hydrochloride monohydrate 天方药业有限公司 2024-06-28 CN claimed
CN-117230091-B Imine reductase IR11 or mutant and application thereof 四川大学华西第二医院 2024-01-19 CN claimed
CN-115322191-B Synthetic method of moxifloxacin hydrochloride 苏州汉德创宏生化科技有限公司 2023-12-26 CN claimed
CN-117230091-A Imine reductase IR11 or mutant and application thereof 四川大学华西第二医院 2023-12-15 CN claimed
WO-2022166436-A1 METHOD FOR PREPARING MOXIFLOXACIN INTERMEDIATE (S, S)-2, 8-DIAZABICYCLO [4, 3, 0] NONANE 台州市生物医化产业研究院有限公司 2022-08-11 WO claimed
WO-2022166440-A1 METHOD FOR PREPARING MOXIFLOXACIN INTERMEDIATE, (S,S)-2,8-DIAZABICYCLO[4,3,0]NONANE 台州市生物医化产业研究院有限公司 2022-08-11 WO claimed
EP-2089388-B1 PROCESS FOR THE SYNTHESIS OF MOXIFLOXACIN HYDROCHLORIDE CIPLA LTD (IN) 2014-01-29 EP claimed
US-8198451-B2 Process for the synthesis of moxifloxacin hydrochloride CIPLA LIMITED (IN) 2012-06-12 US claimed
US-20100152229-A1 Process for the Synthesis of Moxifloxacin Hydrochloride CIPLA LIMITED (IN) 2010-06-17 US claimed
US-7692015-B2 Economical process for preparing (S, S)-2, 8-diazabicyclo[4.3.0]nonane and its enantiomer LIANYUNGANG JINKANG PHARMACEUTICAL TECHNOLOGY CO. LTD. (CN) 2010-04-06 US claimed
EP-2121680-A1 A NOVEL AND ECONOMICAL PROCESS FOR PREPARING (S,S)-2, 8-DIAZABICYCLOÝ4.3.0¨NONANE AND ITS ENANTIOMER Wang, Zheqing (US) 2009-11-25 EP claimed
US-20090259041-A1 QUINOLINE CARBOXYLIC ACID-O,O BIS-ACYLOXY BORATE AND PROCESS OF MAKING SATYANARAYANA CHAVA 2009-10-15 US claimed
WO-2009125425-A2 IMPROVED PROCESS FOR THE PREPARATION OF (S.S)-2.8-DIAZABICYCLO[4.3.0]NONANE NEULAND LABORATORIES LTD (IN) 2009-10-15 WO claimed
US-20080221329-A1 Novel and economical process for preparing (S, S)-2, 8-diazabicyclo[4.3.0]nonane and its enantiomer LIANYUNGANG JINKANG PHARMACEUTICAL TECHNOLOGY CO. LTD. (CN) 2008-09-11 US claimed
WO-2008085480-A1 A NOVEL AND ECONOMICAL PROCESS FOR PREPARING (S,S)-2, 8-DIAZABICYCLO[4.3.0]NONANE AND ITS ENANTIOMER WANG ZHEQING (US) 2008-07-17 WO claimed
EP-1832587-A1 Method for preparing moxifloxacin and moxifloxacin hydrochloride Quimica Sintetica, S.A. (ES) 2007-09-12 EP claimed
US-20060264635-A1 Process for the preparation of moxifloxacin hydrochloride MATRIX LABORATORIES LTD. (IN) 2006-11-23 US claimed
EP-1077979-B1 METHOD FOR PRODUCING (S,S)-BENZYL-2,8-DIAZABICYCLO 4.3.0]NONANE BAYER HEALTHCARE AG (DE) 2005-07-06 EP claimed
US-20040044205-A1 Process for the enantiomeric enrichment of cis-8-benzyl-7,9-dioxo-2,8-diazabicyclo[4.3.0]nonane LANXESS DEUTSCHLAND GMBH (DE) 2004-03-04 US claimed
US-6235908-B1 PREPARATION OF TARTRATE BAYER AKTIENGESELLSCHAFT (DE) 2001-05-22 US claimed