SCHEMBL10164161

SCHEMBL10164161

CC[C@H](NCC=CC(F)(F)F)C(N)=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
SCHEMBL13136715 1.00
SCHEMBL3043575 0.78 TSHR (0.34)
SCHEMBL4970112 0.78 TSHR (0.34)
SCHEMBL28316767 0.74 CTSS (0.41)
SCHEMBL13741705 0.71
SCHEMBL3854088 0.71
SCHEMBL24724789 0.69
Hydrochloric Acid SCHEMBL15413957 0.69 CA1 (0.35)
SCHEMBL21206997 0.67 CA1 (0.39)
SCHEMBL30471284 0.67 EPHX1 (0.36)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120021469-A1 AMIDASES AND METHODS OF THEIR USE CODEXIS, INC. (US) 2012-01-26 US disclosed
US-20120021469-A1 AMIDASES AND METHODS OF THEIR USE CODEXIS, INC. (US) 2012-01-26 US disclosed
US-7612215-B2 Process for preparing 2-oxo-1-pyrrolidine derivatives by intramolecular allylation UCB PHARMA, S.A. (BE) 2009-11-03 US disclosed
US-7612215-B2 Process for preparing 2-oxo-1-pyrrolidine derivatives by intramolecular allylation UCB PHARMA, S.A. (BE) 2009-11-03 US disclosed
US-20080125598-A1 Process for Preparing 2-Oxo-1-Pyrrolidine Derivatives by Intramolecular Allylation UCB, S.A. (BE) 2008-05-29 US disclosed
US-20080125598-A1 Process for Preparing 2-Oxo-1-Pyrrolidine Derivatives by Intramolecular Allylation UCB, S.A. (BE) 2008-05-29 US disclosed