SCHEMBL642477

SCHEMBL642477

C[C@@H]1C(=O)OC(=O)N1C

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
SCHEMBL640792 1.00
SCHEMBL640791 1.00
SCHEMBL18074135 0.75
SCHEMBL18074131 0.75
SCHEMBL13762165 0.72
SCHEMBL13762169 0.72
SCHEMBL5028673 0.72
SCHEMBL12660411 0.69 KDM4E (0.31)
SCHEMBL31293584 0.69
SCHEMBL18911283 0.69

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250382307-A1 IMPROVED METHODS FOR PREPARING N-METHYL ALANINE ESTERS OF MAYTANSINOL IMMUNOGEN, INC. 2025-12-18 US disclosed
EP-4587445-A1 IMPROVED METHODS FOR PREPARING N-METHYL ALANINE ESTERS OF MAYTANSINOL ImmunoGen, Inc. (US) 2025-07-23 EP disclosed
WO-2024059267-A1 IMPROVED METHODS FOR PREPARING N-METHYL ALANINE ESTERS OF MAYTANSINOL IMMUNOGEN, INC. (US) 2024-03-21 WO disclosed
EP-2152680-B1 METHOD FOR PREPARING ENANTIOMERICALLY ENRICHED N-CARBOXYANHYDRIDE SANOFI SA (FR) 2015-06-24 EP disclosed
EP-2152680-B1 METHOD FOR PREPARING ENANTIOMERICALLY ENRICHED N-CARBOXYANHYDRIDE SANOFI SA (FR) 2015-06-24 EP disclosed
US-20120215007-A1 METHOD FOR PREPARING ENANTIOMERICALLY ENRICHED N-CARBOXYANHYDRIDE SANOFI (FR) 2012-08-23 US disclosed
US-20120215007-A1 METHOD FOR PREPARING ENANTIOMERICALLY ENRICHED N-CARBOXYANHYDRIDE SANOFI (FR) 2012-08-23 US disclosed
US-20120215007-A1 METHOD FOR PREPARING ENANTIOMERICALLY ENRICHED N-CARBOXYANHYDRIDE SANOFI (FR) 2012-08-23 US disclosed
US-8119813-B2 Method for preparing enantiomerically enriched N-carboxyanhydride SANOFI-AVENTIS (FR) 2012-02-21 US disclosed
US-8119813-B2 Method for preparing enantiomerically enriched N-carboxyanhydride SANOFI-AVENTIS (FR) 2012-02-21 US disclosed
US-8119813-B2 Method for preparing enantiomerically enriched N-carboxyanhydride SANOFI-AVENTIS (FR) 2012-02-21 US disclosed
EP-1838715-B1 METHOD FOR THE PREPARATION OF MAYTANSINOID ESTERS IMMUNOGEN INC (US) 2010-10-27 EP disclosed
US-20100113797-A1 METHOD FOR PREPARING ENANTIOMERICALLY ENRICHED N-CARBOXYANHYDRIDE SANOFI-AVENTIS (FR) 2010-05-06 US disclosed
US-20100113797-A1 METHOD FOR PREPARING ENANTIOMERICALLY ENRICHED N-CARBOXYANHYDRIDE SANOFI-AVENTIS (FR) 2010-05-06 US disclosed
US-20100113797-A1 METHOD FOR PREPARING ENANTIOMERICALLY ENRICHED N-CARBOXYANHYDRIDE SANOFI-AVENTIS (FR) 2010-05-06 US disclosed
EP-2152680-A2 METHOD FOR PREPARING ENANTIOMERICALLY ENRICHED&lt;I&gt;N&lt;/I&gt;-CARBOXYANHYDRIDE Sanofi-Aventis (FR) 2010-02-17 EP disclosed
WO-2009004141-A2 METHOD FOR PREPARING ENANTIOMERICALLY ENRICHED N-CARBOXYANHYDRIDE SANOFI-AVENTIS (FR) 2009-01-08 WO disclosed
WO-2009004141-A2 METHOD FOR PREPARING ENANTIOMERICALLY ENRICHED N-CARBOXYANHYDRIDE SANOFI-AVENTIS (FR) 2009-01-08 WO disclosed
US-7301019-B2 Method for the preparation of maytansinoid esters IMMUNOGEN, INC. (US) 2007-11-27 US disclosed
US-7301019-B2 Method for the preparation of maytansinoid esters IMMUNOGEN, INC. (US) 2007-11-27 US disclosed