SCHEMBL6943569

SCHEMBL6943569

COC(=O)[C@H](Cl)CCN

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
SCHEMBL6943574 1.00
Hydrochloric Acid SCHEMBL6950711 0.98 GABRR1 (0.37)
Hydrochloric Acid SCHEMBL6950704 0.98 GABRR1 (0.37)
SCHEMBL2862400 0.85 SMN1; SMN2 (0.42)
SCHEMBL6758586 0.81 CA1 (0.43)
SCHEMBL2862449 0.81 ZDHHC7 (0.45)
SCHEMBL7066443 0.79
SCHEMBL508118 0.79
Hydrochloric Acid SCHEMBL10972875 0.79
SCHEMBL11274815 0.79

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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-20030045730-A1 Process for preparation of optically active n-substituted azetidine-2-carboxylic acids KANEKA CORPORATION (JP) 2003-03-06 US disclosed
EP-1170287-A1 PROCESS FOR PREPARATION OF OPTICALLY ACTIVE N-SUBSTITUTED AZETIDINE-2-CARBOXYLIC ACIDS KANEKA CORPORATION (JP) 2002-01-09 EP disclosed