SCHEMBL4668252

SCHEMBL4668252

NCC[C@@H](Cl)C(=O)O

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
SCHEMBL4671396 1.00
SCHEMBL3381251 1.00
Hydrochloric Acid SCHEMBL4669861 0.97
Hydrochloric Acid SCHEMBL4669857 0.97
SCHEMBL29054582 0.84
SCHEMBL29054583 0.84
SCHEMBL2193910 0.82 LMNA (0.50)
SCHEMBL28070224 0.78
SCHEMBL10943349 0.77
SCHEMBL628995 0.77 LMNA (0.44)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1193253-B1 PROCESS FOR PRODUCING OPTICALLY ACTIVE AZETIDINE-2-CARBOXYLIC ACIDS KANEKA CORP (JP) 2008-06-25 EP disclosed
EP-1927588-A2 Process for producing optically active azetidine-2-carboxylic acids KANEKA CORPORATION (JP) 2008-06-04 EP disclosed
US-7262308-B2 Process for producing optically active azetidine-2-carboxylic acids KANEKA CORPORATION (JP) 2007-08-28 US disclosed
US-20050043547-A1 Process for producing optically active azetidine-2-carboxylic acids HONDA TATSUYA (JP) 2005-02-24 US disclosed
EP-1253140-B1 PROCESS FOR CYCLIZING OPTICALLY ACTIVE 4-AMINO-2-HALOGENOBUTYRIC ACIDS KANEKA CORP (JP) 2005-01-12 EP disclosed
US-6838567-B1 Process for producing optically active azetidine-2-carboxylic acids KANEKA CORPORATION (JP) 2005-01-04 US disclosed
US-20040171849-A1 Process for producing optically active azetidine-2-carboxylic acid KANEKA CORPORATION (JP) 2004-09-02 US disclosed
US-6747161-B2 AZETIDINE-2-CARBOXYLIC ACID; ALKALINE EARTH METAL OXIDE OR HYDROXIDE, OR AMINE; HIGH OPTICAL YIELD KANEKA CORPORATION (JP) 2004-06-08 US disclosed
EP-1415985-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE AZETIDINE-2-CARBOXYLIC ACID KANEKA CORPORATION (JP) 2004-05-06 EP disclosed
EP-1170287-B1 PROCESS FOR PREPARATION OF OPTICALLY ACTIVE N-SUBSTITUTED AZETIDINE-2-CARBOXYLIC ACIDS KANEKA CORP (JP) 2003-12-03 EP disclosed
US-6617461-B2 Cyclizing an optically active 4-substituted amino-2-halobutyric acid containing substituted oxycarbonyl or sulfonyl type protective group in presence of a base KANEKA CORPORATION (JP) 2003-09-09 US disclosed
US-20030109719-A1 Process for cyclizing optically active 4-amino-2-halogenobutyric acids SAKA YASUHIRO (JP) 2003-06-12 US disclosed
US-20030045730-A1 Process for preparation of optically active n-substituted azetidine-2-carboxylic acids KANEKA CORPORATION (JP) 2003-03-06 US disclosed
EP-1253140-A1 PROCESS FOR CYCLIZING OPTICALLY ACTIVE 4-AMINO-2-HALOGENOBUTYRIC ACIDS KANEKA CORPORATION (JP) 2002-10-30 EP disclosed
EP-1193253-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE AZETIDINE-2-CARBOXYLIC ACIDS KANEKA CORPORATION (JP) 2002-04-03 EP disclosed
EP-1170287-A1 PROCESS FOR PREPARATION OF OPTICALLY ACTIVE N-SUBSTITUTED AZETIDINE-2-CARBOXYLIC ACIDS KANEKA CORPORATION (JP) 2002-01-09 EP disclosed