SCHEMBL2520169

SCHEMBL2520169

CC(C)(C)N(CCC[C@H](N)CNS(C)(=O)=O)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
SCHEMBL149146 0.77 POLB (0.38)
SCHEMBL6245968 0.77 NOS3 (0.33)
SCHEMBL1852682 0.77 NOS3 (0.33)
SCHEMBL6665323 0.77 ALDH1A1 (0.35)
SCHEMBL5618639 0.76 POLB (0.37)
SCHEMBL1853569 0.76 ALDH1A1 (0.34)
Methane SCHEMBL30958396 0.76 ALDH1A1 (0.40)
SCHEMBL6670962 0.74 GABRP (0.41)
SCHEMBL930036 0.74 KDM4D (0.34)
SCHEMBL2514613 0.72 CYP2D6 (0.33)

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-8034938-B2 Imidazo[4,5-c]quinolines, 6,7,8,9-tetrahydroimidazo[4,5-c]quinolines, imidazo[4,5-c]naphthyridines, and 6,7,8,9-tetrahydroimidazo[4,5-c]naphthyridines) with a CH( R1) group in the fused ring at 1-position of imidazo ring; modulate immune response, by induction of cytokine biosynthesis or other mechanism 3M INNOVATIVE PROPERTIES COMPANY (US) 2011-10-11 US disclosed