SCHEMBL26312607

SCHEMBL26312607

CC[C@@H](CC(C)C)C(=O)N1C[C@]2(C[C@H]1C(N)=O)C(=O)Nc1ccccc12

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
SCHEMBL25656362 0.88 BACE1 (0.41) —
SCHEMBL25656364 0.88 BACE1 (0.41) —
SCHEMBL24403330 0.86 BACE1 (0.41) —
SCHEMBL24403208 0.86 BACE1 (0.41) —
Hydrochloric Acid SCHEMBL30631305 0.85 BACE1 (0.41) —
Hydrochloric Acid SCHEMBL30631308 0.85 BACE1 (0.41) —
SCHEMBL26312560 0.85 — —
SCHEMBL24447558 0.84 BACE1 (0.39) —
SCHEMBL24447982 0.84 BACE1 (0.39) —
SCHEMBL27034725 0.83 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230295175-A1 PROCESSES FOR THE PREPARATION OF SUBSTITUTED SPIROOXINDOLE DERIVATIVES ENANTA PHARMACEUTICALS, INC. 2023-09-21 — — US disclosed
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