SCHEMBL7188927

SCHEMBL7188927

CCOC(C)Oc1cc(OC(C)OCC)c(PC(=O)c2c(C)cc(C(C)(C)C)cc2C)c(OC(C)OCC)c1.[LiH]

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
SCHEMBL7175013 0.90
SCHEMBL7183112 0.87 NR1H4 (0.31)
SCHEMBL7178289 0.86 NLRP3 (0.31)
SCHEMBL7183619 0.85
SCHEMBL7175539 0.84 HDAC1 (0.31)
SCHEMBL7174641 0.83 NR1H4 (0.36)
SCHEMBL7180393 0.83 NR1H4 (0.35)
SCHEMBL7177739 0.81 CYP3A4 (0.39)
Lithium SCHEMBL7175779 0.80 NR1H4 (0.32)
SCHEMBL7180504 0.80 TRPM4 (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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6579663-B2 Chemical intermediates such as lithium 2,6-dimethylbenzoyl phenylphosphine for preparation of acylphosphines, acylphosphine oxides or acylphosphine sulfides CIBA SPECIALTY CHEMICALS CORPORATION 2003-06-17 US disclosed
US-20020107413-A1 Organometallic monoacylarylphosphines WOLF JEAN-PIERRE (CH) 2002-08-08 US disclosed
US-6399805-B2 SUCH AS LITHIUM 2,6-DIMETHYLBENZOYLPHENYLPHOSPHINE, USE AS PHOTOINITIATORS IN PHOTOCURABLE COMPOSITIONS SUCH AS FOR PHOTOGRAPHIC PRODUCTION OF RELIEF IMAGES CIBA SPECIALTY CHEMICALS CORPORATION 2002-06-04 US disclosed
US-20010031898-A1 Organometallic monoacylarylphosphines CIBA SPECIALTY CHEMICALS CORP. 2001-10-18 US disclosed