SCHEMBL4827171

SCHEMBL4827171

Cc1cccc(C)c1OP(=O)(Oc1c(C)cccc1C)N1CCN(P(=O)(Oc2c(C)cccc2C)Oc2c(C)cccc2C)CC1

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 3/20 0.40
▸ NPSR1 Q6W5P4 1/20 0.40
▸ ALDH1A1 P00352 2/20 0.38
▸ LMNA P02545 3/20 0.36
▸ GAA P10253 1/20 0.36
▸ SMN1; SMN2 Q16637 1/20 0.36
▸ SCN4A P35499 6/20 0.35
▸ SCN1A P35498 2/20 0.35
▸ SCN5A Q14524 2/20 0.35
▸ SCN9A Q15858 2/20 0.35
▸ CYP1A2 P05177 1/20 0.35
▸ CYP3A4 P08684 1/20 0.35
▸ CYP2D6 P10635 1/20 0.35
▸ CYP2C9 P11712 1/20 0.35
▸ TSHR P16473 1/20 0.35
▸ NFKB1 P19838 1/20 0.35
▸ KCNK3 O14649 1/20 0.35
▸ CACNA1F O60840 1/20 0.35
▸ KCNK2 O95069 1/20 0.35
▸ GBA1 P04062 1/20 0.35

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
SCHEMBL132931 0.80 MAPT (0.59) MAPTNPSR1ALDH1A1LMNAGAA
SCHEMBL130226 0.79 MAPT (0.45) MAPTNPSR1ALDH1A1LMNAGAA
SCHEMBL940949 0.74 MAPT (0.45) MAPTALDH1A1LMNAGAASMN1; SMN2
SCHEMBL14204629 0.73 LMNA (0.44) MAPTALDH1A1LMNAGAASMN1; SMN2
SCHEMBL19084451 0.72 SCN4A (0.41) MAPTALDH1A1LMNAGAASMN1; SMN2
SCHEMBL3757859 0.71 MAPT (0.42) MAPTALDH1A1LMNAGAASMN1; SMN2
SCHEMBL1486673 0.71 MAPT (0.42) MAPTALDH1A1LMNAGAASMN1; SMN2
SCHEMBL28397604 0.71 MAPT (0.42) MAPTALDH1A1LMNAGAASMN1; SMN2
SCHEMBL272850 0.71 INPPL1 (0.43) MAPTALDH1A1LMNAGAASMN1; SMN2
SCHEMBL2220467 0.71 INPPL1 (0.59) MAPTALDH1A1LMNAGAASMN1; SMN2

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 37 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1259519-B1 METHOD FOR PREPARING STERICALLY HINDERED PHOSPHORAMIDATES GEN ELECTRIC (US) 2003-12-17 — — EP claimed
JP-2003524014-A — — 2003-08-12 — — JP claimed
JP-2003508404-A — — 2003-03-04 — — JP claimed
EP-1259519-A1 METHOD FOR PREPARING STERICALLY HINDERED PHOSPHORAMIDATES GENERAL ELECTRIC COMPANY (US) 2002-11-27 — — EP claimed
WO-2001062766-A1 METHOD FOR PREPARING STERICALLY HINDERED PHOSPHORAMIDATES GENERAL ELECTRIC COMPANY (US) 2001-08-30 — — WO claimed
US-6277988-B1 REACTING STERICALLY HINDERED DIARYL CHLOROPHOSPHATE WITH A BASIC NITROGEN COMPOUND CONTAINING TWO SECONDARY AMINE GROUPS IN LIQUID SOLVENT-FREE REACTION MIXTURE TO FORM PHOSPHORAMIDATE AND HYDROGEN CHLORIDE BY-PRODUCT GENERAL ELECTRIC COMPANY 2001-08-21 — — US claimed
WO-2001016143-A1 SOLVENT-FREE METHOD FOR PREPARING STERICALLY HINDERED PHOSPHORAMIDATES GENERAL ELECTRIC COMPANY (US) 2001-03-08 — — WO claimed
US-9884961-B2 Phosphazene flame retardant polycarbonate compounds POLYONE CORPORATION (US) 2018-02-06 — — US disclosed
US-9884961-B2 Phosphazene flame retardant polycarbonate compounds POLYONE CORPORATION (US) 2018-02-06 — — US disclosed
US-20160272812-A1 PHOSPHAZENE FLAME RETARDANT POLYCARBONATE COMPOUNDS POLYONE CORPORATION (US) 2016-09-22 — — US disclosed
US-20160272812-A1 PHOSPHAZENE FLAME RETARDANT POLYCARBONATE COMPOUNDS POLYONE CORPORATION (US) 2016-09-22 — — US disclosed
US-20160122534-A1 COMPLETELY NON-HALOGENATED FLAME RETARDANT POLYCARBONATE COMPOUNDS POLYONE CORPORATION (US) 2016-05-05 — — US disclosed
US-20160122534-A1 COMPLETELY NON-HALOGENATED FLAME RETARDANT POLYCARBONATE COMPOUNDS POLYONE CORPORATION (US) 2016-05-05 — — US disclosed
WO-2001016143-A1 SOLVENT-FREE METHOD FOR PREPARING STERICALLY HINDERED PHOSPHORAMIDATES GENERAL ELECTRIC COMPANY (US) 2001-03-08 — — WO disclosed
US-6191276-B1 SUCH AS N,N'-BIS(DI-(2,6-XYLYL)PHOSPHORYL)PIPERAZINE, BY CONTACTING DI-(2,6-XYLYL) CHLOROPHOSPHATE WITH PIPERAZINE IN THE PRESENCE OF CALCIUM OXIDE AS ACID ACCEPTOR IN A DIPOLAR APORTIC SOLVENT; HIGH YIELD; USE AS FLAME RETARDANTS GENERAL ELECTRIC COMPANY 2001-02-20 — — US disclosed
US-6191276-B1 SUCH AS N,N'-BIS(DI-(2,6-XYLYL)PHOSPHORYL)PIPERAZINE, BY CONTACTING DI-(2,6-XYLYL) CHLOROPHOSPHATE WITH PIPERAZINE IN THE PRESENCE OF CALCIUM OXIDE AS ACID ACCEPTOR IN A DIPOLAR APORTIC SOLVENT; HIGH YIELD; USE AS FLAME RETARDANTS GENERAL ELECTRIC COMPANY 2001-02-20 — — US disclosed
US-6166115-A Flame resistant polyphenylene ether-polyamide resin blends GENERAL ELECTRIC COMPANY (US) 2000-12-26 — — US disclosed
WO-2000012610-A1 FLAME RESISTANT POLYPHENYLENE ETHER-POLYAMIDE RESIN BLENDS GENERAL ELECTRIC COMPANY (US) 2000-03-09 — — WO disclosed
US-5973041-A THEMROPLASTIC RESIN BLENDED WITH AN AROMATIC BISPHOSPHORAMIDATE OF GIVNE FORMULA HAVING ACCEPTABLE FIRE RETARDING PROPERTIES AND A HIGHER HEAT DEFLECTION TEMPERTURE GENERAL ELECTRIC COMPANY (US) 1999-10-26 — — US disclosed
US-5973041-A THEMROPLASTIC RESIN BLENDED WITH AN AROMATIC BISPHOSPHORAMIDATE OF GIVNE FORMULA HAVING ACCEPTABLE FIRE RETARDING PROPERTIES AND A HIGHER HEAT DEFLECTION TEMPERTURE GENERAL ELECTRIC COMPANY (US) 1999-10-26 — — US disclosed
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