Tetraphenylphosphonium

Tetraphenylphosphonium

SCHEMBL7931797

[Br-].[Cl-].[H+].c1ccc([P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.43

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Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

The experimentally established mechanism targets of Tetraphenylphosphonium. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HIF1A Q16665 1/20 0.43
MAPT P10636 2/20 0.35
HPGD P15428 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
MGLL Q99685 1/20 0.35
HSD17B10 Q99714 1/20 0.35
ALDH1A1 P00352 3/20 0.33
SNCA P37840 1/20 0.32
TSHR P16473 3/20 0.32
CYP1A2 P05177 1/20 0.32
CYP2D6 P10635 1/20 0.32
CYP2C19 P33261 1/20 0.32
MTOR P42345 1/20 0.32
RAB9A P51151 1/20 0.32
GRM7 Q14831 1/20 0.32
SLC6A2 P23975 1/20 0.32
SLC6A4 P31645 1/20 0.32
SLC6A3 Q01959 1/20 0.32
DPP4 P27487 2/20 0.32
F2 P00734 1/20 0.32

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
Tetraphenylphosphonium SCHEMBL7931760 0.97 HIF1A (0.45) HIF1AMAPTHPGDSMN1; SMN2MGLL
Tetraphenylphosphonium SCHEMBL7062601 0.97 HIF1A (0.45) HIF1AMAPTHPGDSMN1; SMN2MGLL
Tetraphenylphosphonium SCHEMBL7934968 0.97 HIF1A (0.45) HIF1AMAPTHPGDSMN1; SMN2MGLL
Tetraphenylphosphonium SCHEMBL126056 0.93 HIF1A (0.47) HIF1AMAPTHPGDSMN1; SMN2MGLL
Tetraphenylphosphonium SCHEMBL17818165 0.93 HIF1A (0.47) HIF1AMAPTHPGDSMN1; SMN2MGLL
Tetraphenylphosphonium SCHEMBL42616 0.93 HIF1A (0.47) HIF1AMAPTHPGDSMN1; SMN2MGLL
Tetraphenylphosphonium SCHEMBL28003445 0.90 HIF1A (0.45) HIF1AMAPTHPGDSMN1; SMN2MGLL
Tetraphenylphosphonium SCHEMBL28003362 0.90 HIF1A (0.45) HIF1AMAPTHPGDSMN1; SMN2MGLL
Tetraphenylphosphonium SCHEMBL28325385 0.90 HIF1A (0.45) HIF1AMAPTHPGDSMN1; SMN2MGLL
Tetraphenylphosphonium SCHEMBL28126789 0.90 HIF1A (0.45) HIF1AMAPTHPGDSMN1; SMN2MGLL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0834496-B1 Preparation of diaryl carbonate UBE INDUSTRIES (JP) 2001-08-16 EP disclosed
EP-0834495-B1 Process for preparing diaryl carbonate UBE INDUSTRIES (JP) 2000-12-27 EP disclosed
US-5892089-A FROM DIARYL OXALATE IN LIQUID PHASE BY DECARBONYLATION USING ORGANIC PHOSHORUS COMPOUND CATALYST UBE INDUSTRIES, LTD. (JP) 1999-04-06 US disclosed
US-5892091-A PHOSPHOROUS CATALYSTS AND HALOGEN ATOMS UBE INDUSTRIES, LTD. (JP) 1999-04-06 US disclosed
EP-0737665-B1 Process for preparation of diaryl carbonate UBE INDUSTRIES (JP) 1998-10-21 EP disclosed
US-5792883-A Preparation of diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1998-08-11 US disclosed
EP-0834496-A1 Preparation of diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1998-04-08 EP disclosed
EP-0834495-A1 Process for preparing diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1998-04-08 EP disclosed
EP-0826658-A1 Catalyst for decarbonylation reaction UBE INDUSTRIES, LTD. (JP) 1998-03-04 EP disclosed
US-5648510-A DECARBONYLATION OF OXALATE UBE INDUSTRIES, LTD. (JP) 1997-07-15 US disclosed
EP-0737665-A1 Process for preparation of diaryl carbonate UBE INDUSTRIES, LTD. (JP) 1996-10-16 EP disclosed