Triphenyl Phosphate

Triphenyl Phosphate

SCHEMBL6852665

O=P(O)(O)O.O=P(Oc1ccccc1)(Oc1ccccc1)Oc1ccccc1.c1ccc(-c2ccccc2)cc1

nearest known ligand 0.61

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

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

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ SRC P12931 1/20 0.61
▸ TDP1 Q9NUW8 1/20 0.48
▸ L3MBTL1 Q9Y468 1/20 0.48
▸ CYP2C9 P11712 1/20 0.45
▸ CYP2C19 P33261 1/20 0.45
▸ CYP3A4 P08684 1/20 0.45
▸ TSHR P16473 1/20 0.45
▸ GPR84 Q9NQS5 1/20 0.44
▸ ACP3 P15309 2/20 0.44
▸ KDM4E B2RXH2 1/20 0.44
▸ ANPEP P15144 2/20 0.43
▸ LAP3 P28838 2/20 0.43
▸ GGPS1 O95749 1/20 0.42
▸ PTPN5 P54829 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
Triphenyl Phosphate SCHEMBL3825293 1.00 SRC (0.61) SRCTDP1L3MBTL1CYP2C9CYP2C19
Triphenyl Phosphate SCHEMBL9622348 0.93 SRC (0.70) SRCTDP1L3MBTL1CYP2C9CYP2C19
Triphenyl Phosphate SCHEMBL7202263 0.93 SRC (0.70) SRCTDP1L3MBTL1CYP2C9CYP2C19
Triphenyl Phosphate SCHEMBL27831754 0.93 SRC (0.56) SRCTDP1L3MBTL1CYP3A4TSHR
Triphenyl Phosphate SCHEMBL4454667 0.92 SRC (0.57) SRCTDP1L3MBTL1CYP2C9CYP2C19
SCHEMBL2137987 0.89 CYP3A4 (0.52) SRCTDP1L3MBTL1CYP2C9CYP2C19
SCHEMBL360818 0.89 CYP3A4 (0.52) SRCTDP1L3MBTL1CYP2C9CYP2C19
Biphenyl SCHEMBL27663828 0.87 SRC (0.61) SRCTDP1L3MBTL1CYP2C9CYP2C19
SCHEMBL473247 0.86 CYP3A4 (0.54) SRCTDP1L3MBTL1CYP2C9CYP2C19
SCHEMBL431694 0.86 CYP3A4 (0.54) SRCTDP1L3MBTL1CYP3A4TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2020213389-A1 THERMOPLASTIC RESIN, MOLDED OBJECT, AND MONOMER FOR THERMOPLASTIC RESIN 三菱瓦斯化学株式会社 2020-10-22 — — WO disclosed
WO-2020189409-A1 POLYESTER CARBONATE RESIN, AND MOLDED BODY WHICH IS OBTAINED BY MOLDING RESIN COMPOSITION CONTAINING SAID RESIN 三菱瓦斯化学株式会社 2020-09-24 — — WO disclosed
WO-2014031530-A1 INHIBITING CORROSION CAUSED BY AQUEOUS ALDEHYDE SOLUTIONS BAKER HUGHES INCORPORATED (US) 2014-02-27 — — WO disclosed
US-20130224092-A1 INHIBITING CORROSION CAUSED BY AQUEOUS ALDEHYDE SOLUTIONS BAKER HUGHES INCORPORATED (US) 2013-08-29 — — US disclosed
US-20130090271-A1 INHIBITING CORROSION CAUSED BY AQUEOUS ALDEHYDE SOLUTIONS BAKER HUGHES INCORPORATED (US) 2013-04-11 — — US disclosed
US-6764540-B2 THE DYE IS DISSOLVED OR DISPERSED IN AN AQUEOUS MEDIUM CONTAINING A COMPOUND CAPABLE OF INCLUDING A DYE, SUCH AS A ROTAXANE MOLECULE OR A MOLECULAR NANOTUBE FUJI PHOTO FILM CO., LTD. (JP) 2004-07-20 — — US disclosed
US-20030061965-A1 Ink compositions and ink jet recording method FUJIFILM CORPORATION (JP) 2003-04-03 — — US disclosed
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