SCHEMBL4945117

SCHEMBL4945117

CCCCC(CC)(CO)COP(O)Cl

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
SCHEMBL6231242 0.86
SCHEMBL4945125 0.81 FDPS (0.33)
SCHEMBL20176145 0.80 SPHK2 (0.37)
SCHEMBL17219655 0.77 TSHR (0.33)
SCHEMBL7099255 0.77 ALDH1A1 (0.33)
SCHEMBL6228437 0.77
SCHEMBL5915888 0.77
SCHEMBL6229516 0.77 FDPS (0.31)
SCHEMBL4841445 0.76
SCHEMBL11276646 0.76 TSHR (0.32)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1583745-A1 1-PROPANOL AND 1-PROPYLAMINE DERIVATIVES AND THEIR USE AS GLUCOCORTICOID LIGANDS BOEHRINGER INGELHEIM PHARMACEUTICALS INC. (US) 2005-10-12 EP claimed
WO-2004063163-A1 1-PROPANOL AND 1-PROPYLAMINE DERIVATIVES AND THEIR USE AS GLUCOCORTICOID LIGANDS BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) 2004-07-29 WO claimed
US-7442732-B2 Hindered amine light stabilizers comprising neoalkanediol phosphites CROMPTON CORPORATION (US) 2008-10-28 US disclosed
US-20060223918-A1 Hindered amine light stabilizers comprising neoalkanediol phosphites ADDIVANT USA, LLC 2006-10-05 US disclosed
WO-2006104867-A1 HINDERED AMINE LIGHT STABILIZERS COMPRISING NEOALKANEDIOL PHOSPHITES CHEMTURA CORPORATION (US) 2006-10-05 WO disclosed
EP-1543015-A1 PROCESS FOR THE PREPARATION OF ACID ESTERS CROMPTON CORPORATION (US) 2005-06-22 EP disclosed
US-20050009967-A1 Phosphite stabilizers and methods to preparation and polymer composition thereof CROMPTON CORPORATION 2005-01-13 US disclosed
WO-2004111158-A1 PHOSPHITE STABILIZERS AND METHODS TO PREPARATION AND POLYMER COMPOSITION THEREOF CHEMTURA CORPORATION (US) 2004-12-23 WO disclosed
EP-1309600-B1 PROCESS FOR THE PREPARATION OF HINDERED PHOSPHITES CROMPTON CORP (US) 2004-08-25 EP disclosed
US-6773624-B2 REACTING GLYCOL SUCH AS PENTAERYTHRITOL WITH PHOSPHORUS TRIHALIDE TO PRODUCE HALO PHOSPHITE ESTER OF GLYCOL, REACTING PRODUCT WITH A PHENOL, REACTING SECOND PRODUCTS COMPRISING ORGANIC PHOSPHITE AND HALO PHOSPHITE WITH METAL PHENOLATE CROMPTON CORPORATION 2004-08-10 US disclosed
US-6747167-B2 REACTING A STERICALLY HINDERED PHENOL AND ACID HALIDE (PCL3) IN THE PRESENCE OF AN AMINE, THEN FURTHER REACTING WITH A CYCLIC ACID ACCEPTOR (DBN, DBU, DMAP OR DABCO) FOR AT LEAST A 98% CONVERSION TO THE PHOSPHITE CROMPTON CORPORATION 2004-06-08 US disclosed
WO-2004026885-A1 PROCESS FOR THE PREPARATION OF ACID ESTERS GENERAL ELECTRIC COMPANY (US) 2004-04-01 WO disclosed
US-20040059151-A1 Process for the preparation of acid esters GENERAL ELECTRIC COMPANY 2004-03-25 US disclosed
EP-0940407-B1 Cyclic bis-phosphites GEN ELECTRIC (US) 2003-12-03 EP disclosed
EP-1309600-A1 PROCESS FOR THE PREPARATION OF HINDERED PHOSPHITES GENERAL ELECTRIC COMPANY (US) 2003-05-14 EP disclosed
US-20020193620-A1 Process for the preparation of hindered phosphites GENERAL ELECTRIC CO. 2002-12-19 US disclosed
US-6444836-B1 PURITY; DESORPTION USING AN INERT GAS; REACTING ALCOHOL WITH PHOSPHOROUS COMPOUND GENERAL ELECTRIC COMPANY 2002-09-03 US disclosed
US-6426429-B1 REACTING A GLYCOL WITH A PHOSPHORUS TRI-HALIDE, REACTING THE HALO PHOSPHITE ESTER PRODUCT WITH A PHENOL, AND FURTHER REACTING ITS PRODUCT WITH A METAL PHENOLATE GENERAL ELECTRIC COMPANY 2002-07-30 US disclosed
WO-2002014335-A1 PROCESS FOR THE PREPARATION OF HINDERED PHOSPHITES GENERAL ELECTRIC COMPANY (US) 2002-02-21 WO disclosed
EP-0940407-A1 Cyclic bis-phosphites GENERAL ELECTRIC COMPANY (US) 1999-09-08 EP disclosed