SCHEMBL8991195

SCHEMBL8991195

CCCCC1(C)C(=O)OCCC1(c1ccc(C=NN)cc1)S(=O)(=O)c1ccccc1

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
SCHEMBL8991315 0.73 CRBN (0.32)
SCHEMBL8991475 0.71 CYP19A1 (0.39)
SCHEMBL8991380 0.70 KDM1A (0.35)
SCHEMBL8991007 0.68
SCHEMBL8991191 0.67 KDM1A (0.32)
SCHEMBL8991282 0.67
SCHEMBL8991174 0.65 CYP19A1 (0.30)
SCHEMBL8991217 0.62 POLB (0.32)
SCHEMBL7488740 0.58 OPRM1 (0.40)
SCHEMBL14350785 0.57 MMP2 (0.40)

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-5504106-A Phenyl amidine alkanoic acids and lactones useful as platelet aggregation inhibitors G. D. SEARLE & CO. (US) 1996-04-02 US claimed