SCHEMBL1723503

SCHEMBL1723503

C1CNC2CNC[C@@H]2C1

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
SCHEMBL1724943 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 23 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112010851-A Preparation method of moxifloxacin hydrochloride 浙江美诺华药物化学有限公司 2020-12-01 CN claimed
EP-2403831-B1 SYNTHESIS OF (4aS,7aS)-OCTAHYDRO-1H-PYRROLOÝ3,4-b¨PYRIDINE ITALIANA SINT SPA (IT) 2015-05-20 EP claimed
US-20110137036-A1 SYNTHESIS OF (4aS,7aS)-OCTAHYDRO-1H-PYRROLO[3,4-b]PYRIDINE F.I.S. FABBRICA ITALIANA SINTETICI S.P.A (IT) 2011-06-09 US claimed
CN-118147101-A Method for preparing moxifloxacin intermediate by enzyme catalysis 湖州颐盛生物科技有限公司 2024-06-07 CN disclosed
CN-111024831-B Method for separating moxifloxacin hydrochloride and impurities thereof by high performance liquid chromatography 江苏正大丰海制药有限公司 2023-05-02 CN disclosed
CN-110746334-B Method for preparing 3- (3-chloropropyl) -4-oxopyrrolidine-1-carboxylic ester 上海朴颐化学科技有限公司 2023-03-14 CN disclosed
CN-112010851-A Preparation method of moxifloxacin hydrochloride 浙江美诺华药物化学有限公司 2020-12-01 CN disclosed
CN-112010851-A Preparation method of moxifloxacin hydrochloride 浙江美诺华药物化学有限公司 2020-12-01 CN disclosed
CN-111024831-A Method for separating moxifloxacin hydrochloride and impurities thereof by high performance liquid chromatography 江苏正大丰海制药有限公司 2020-04-17 CN disclosed
EP-2403831-B1 SYNTHESIS OF (4aS,7aS)-OCTAHYDRO-1H-PYRROLOÝ3,4-b¨PYRIDINE ITALIANA SINT SPA (IT) 2015-05-20 EP disclosed
CN-102964346-B Preparation method of (S, S)-octahydro-6H-pyrrolo[3, 4-b]pyridine SINOCHEM CORP 2015-04-22 CN disclosed
US-8680276-B2 Synthesis of (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine F.I.S. FABBRICA ITALIANA SINTETICI S.P.A (IT) 2014-03-25 US disclosed
EP-2599386-A1 2-aminopyrimidine modulators of the histamine h4 receptor Janssen Pharmaceutica N.V. (BE) 2013-06-05 EP disclosed
CN-102964346-A Preparation method of (S, S)-octahydro-6H-pyrrolo[3, 4-b]pyridine SINOCHEM CORP 2013-03-13 CN disclosed
CN-102964346-A Preparation method of (S, S)-octahydro-6H-pyrrolo[3, 4-b]pyridine SINOCHEM CORP 2013-03-13 CN disclosed
EP-2403831-A1 SYNTHESIS OF (4aS,7aS)-OCTAHYDRO-1H-PYRROLOÝ3,4-b¨PYRIDINE F.I.S. Fabbrica Italiana Sintetici S.p.A. (IT) 2012-01-11 EP disclosed
US-20110137036-A1 SYNTHESIS OF (4aS,7aS)-OCTAHYDRO-1H-PYRROLO[3,4-b]PYRIDINE F.I.S. FABBRICA ITALIANA SINTETICI S.P.A (IT) 2011-06-09 US disclosed
US-20110137036-A1 SYNTHESIS OF (4aS,7aS)-OCTAHYDRO-1H-PYRROLO[3,4-b]PYRIDINE F.I.S. FABBRICA ITALIANA SINTETICI S.P.A (IT) 2011-06-09 US disclosed
WO-2010100215-A1 SYNTHESIS OF (4aS,7aS)-OCTAHYDRO-1H-PYRROLO[3,4-b]PYRIDINE F.I.S. FABBRICA ITALIANA SINTETICI S.P.A. (IT) 2010-09-10 WO disclosed
US-20080306105-A1 DEUTERIUM-ENRICHED MOXIFLOXACIN PROTIA, LLC (US) 2008-12-11 US disclosed