SCHEMBL9112175

SCHEMBL9112175

CCCCCCCCCCC(CCC)C(C)N

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SPHK1 Q9NYA1 2/20 0.56
OPRM1 P35372 1/20 0.54
TP53 P04637 2/20 0.43
CYP2D6 P10635 2/20 0.42
LMNA P02545 2/20 0.42
LAP3 P28838 2/20 0.42
PLA2G1B P04054 1/20 0.42
PLA2G2A P14555 1/20 0.42
GMNN O75496 1/20 0.42
POLB P06746 1/20 0.42
THPO P40225 1/20 0.42
MTOR P42345 1/20 0.42
BLM P54132 1/20 0.42
KDM4E B2RXH2 1/20 0.42
CYP1A2 P05177 1/20 0.42
CYP3A4 P08684 1/20 0.42
MAPT P10636 1/20 0.42
CETP P11597 1/20 0.42
HTT P42858 1/20 0.42
UBE2N P61088 1/20 0.42

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL30272145 1.00 SPHK1 (0.56) SPHK1OPRM1TP53CYP2D6LMNA
Hydrochloric Acid SCHEMBL30688481 0.98 SPHK1 (0.54) SPHK1OPRM1TP53CYP2D6LMNA
SCHEMBL24107252 0.98 OPRM1 (0.56) SPHK1OPRM1TP53CYP2D6LMNA
SCHEMBL2328466 0.95 SPHK1 (0.60) SPHK1OPRM1TP53CYP2D6LMNA
SCHEMBL21217006 0.95 SPHK1 (0.60) SPHK1OPRM1TP53CYP2D6LMNA
SCHEMBL25831975 0.95 SPHK1 (0.60) SPHK1OPRM1TP53CYP2D6LMNA
SCHEMBL2332779 0.95 SPHK1 (0.60) SPHK1OPRM1TP53CYP2D6LMNA
SCHEMBL2338645 0.95 SPHK1 (0.60) SPHK1OPRM1TP53CYP2D6LMNA
SCHEMBL12728004 0.95 SPHK1 (0.60) SPHK1OPRM1TP53CYP2D6LMNA
SCHEMBL19441327 0.95 SPHK1 (0.60) SPHK1OPRM1TP53CYP2D6LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0647216-A4 INHIBITION OF THE FORMATION OF NITROSAMINES. 1995-05-17 EP disclosed
EP-0647216-A1 INHIBITION OF THE FORMATION OF NITROSAMINES SOLVAY INTEROX (US) 1995-04-12 EP disclosed
US-5324857-A Adding free radical scavenger comprising phenol, aromatic polyol, thiol, or disulfide and chelating agent SOLVAY INTEROX (US) 1994-06-28 US disclosed
WO-1993022273-A1 INHIBITION OF THE FORMATION OF NITROSAMINES SOLVAY INTEROX (US) 1993-11-11 WO disclosed
EP-0409043-B1 REDUCTION OF NITROSAMINE FORMATION SOLVAY INTEROX (US) 1993-01-27 EP disclosed
US-5023376-A Using alkyleneaminopoly(methylene phosphonic acid) compounds INTEROX AMERICA (US) 1991-06-11 US disclosed
EP-0424965-A1 Amine oxide process ETHYL CORPORATION (US) 1991-05-02 EP disclosed
EP-0409043-A1 Reduction of nitrosamine formation SOLVAY INTEROX (US) 1991-01-23 EP disclosed
US-4960934-A Amine oxide process ETHYL CORPORATION (US) 1990-10-02 US disclosed
US-4942260-A REACTION OF A TERT-AMINE WITH HYDROGEN PEROXIDE IN THE PRESENCE OF CATALYTIC CARBON DIOXIDE ETHYL CORPORATION (US) 1990-07-17 US disclosed
EP-0356918-A1 Amine oxide process ETHYL CORPORATION (US) 1990-03-07 EP disclosed
US-4889954-A DIALKYLCARBONATE CATALYST ETHYL CORPORATION (US) 1989-12-26 US disclosed
EP-0307184-A2 Preparation of Amine Oxides ETHYL CORPORATION (US) 1989-03-15 EP disclosed