SCHEMBL7861818

SCHEMBL7861818

O=P([O-])(OCc1ccccc1)OCc1ccccc1.[Cs+]

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.61
FUCA1 P04066 1/20 0.49
CETP P11597 3/20 0.46
IDO1 P14902 1/20 0.43
SRC P12931 1/20 0.42
PDPK1 O15530 1/20 0.42
MTOR P42345 1/20 0.42
ALPG P10696 1/20 0.42
PTK2B Q14289 1/20 0.42
AGXT P21549 1/20 0.41
ALDH1A1 P00352 2/20 0.41
CA1 P00915 1/20 0.41
CA2 P00918 1/20 0.41
CA9 Q16790 1/20 0.41
FOLH1 Q04609 1/20 0.41
NPC1 O15118 1/20 0.40
RAB9A P51151 1/20 0.40
NR4A1 P22736 1/20 0.40
NR4A2 P43354 1/20 0.40
NR4A3 Q92570 1/20 0.40

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
SCHEMBL5437520 0.96 TSHR (0.61) TSHRFUCA1CETPIDO1SRC
Silver SCHEMBL216224 0.96 TSHR (0.61) TSHRFUCA1CETPIDO1SRC
Lithium Ion SCHEMBL9446519 0.96 TSHR (0.61) TSHRFUCA1CETPIDO1SRC
Potassium Ion SCHEMBL4956047 0.96 TSHR (0.61) TSHRFUCA1CETPIDO1SRC
SCHEMBL11756561 0.96 TSHR (0.61) TSHRFUCA1CETPIDO1SRC
SCHEMBL10689581 0.96 TSHR (0.61) TSHRFUCA1CETPIDO1SRC
SCHEMBL28669438 0.96 TSHR (0.61) TSHRFUCA1CETPIDO1SRC
Tetramethylammonium Ion SCHEMBL9937868 0.90 TSHR (0.55) TSHRFUCA1CETPIDO1SRC
SCHEMBL11741735 0.84 TSHR (0.63) TSHRFUCA1CETPIDO1SRC
SCHEMBL28648736 0.83 TSHR (0.61) TSHRFUCA1CETPIDO1SRC

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0900227-B1 IMPROVED PROCESS FOR THE SYNTHESIS OF DIESTERS OF PHOSPHORIC ACID 2,5-DIOXO-4,4-DIPHENYL-IMIDAZOLIDIN-1-YLMETHYL ESTER WARNER LAMBERT CO (US) 2001-12-12 EP claimed
US-6022975-A Process for the synthesis of diesters of phosphoric acid 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl ester WARNER-LAMBERT COMPANY (US) 2000-02-08 US claimed
EP-0900227-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF DIESTERS OF PHOSPHORIC ACID 2,5-DIOXO-4,4-DIPHENYL-IMIDAZOLIDIN-1-YLMETHYL ESTER WARNER-LAMBERT COMPANY (US) 1999-03-10 EP claimed
WO-1997041132-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF DIESTERS OF PHOSPHORIC ACID 2,5-DIOXO-4,4-DIPHENYL-IMIDAZOLIDIN-1-YLMETHYL ESTER WARNER-LAMBERT COMPANY (US) 1997-11-06 WO claimed
CN-117699747-A Difluorosulfonyl imide alkali metal salt and preparation method and application thereof 龙子湖新能源实验室 2024-03-15 CN disclosed
EP-0900227-B1 IMPROVED PROCESS FOR THE SYNTHESIS OF DIESTERS OF PHOSPHORIC ACID 2,5-DIOXO-4,4-DIPHENYL-IMIDAZOLIDIN-1-YLMETHYL ESTER WARNER LAMBERT CO (US) 2001-12-12 EP disclosed
US-6255492-B1 CHEMICAL INTERMEDIATES IN PRODUCTION OF 5,5-DIPHENYL-((3-PHOSPHONOOXY)METHYL)-2,4-IMIDAZOLIDINEDIONE DISODIUM SALT; USEFUL AS ANTICONVULSANT, ANTIEPILEPTIC, AND ANTIARRHYTHMIC AGENTS WARNER-LAMBERT COMPANY 2001-07-03 US disclosed
US-6022975-A Process for the synthesis of diesters of phosphoric acid 2,5-dioxo-4,4-diphenyl-imidazolidin-1-ylmethyl ester WARNER-LAMBERT COMPANY (US) 2000-02-08 US disclosed
EP-0900227-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF DIESTERS OF PHOSPHORIC ACID 2,5-DIOXO-4,4-DIPHENYL-IMIDAZOLIDIN-1-YLMETHYL ESTER WARNER-LAMBERT COMPANY (US) 1999-03-10 EP disclosed
WO-1997041132-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF DIESTERS OF PHOSPHORIC ACID 2,5-DIOXO-4,4-DIPHENYL-IMIDAZOLIDIN-1-YLMETHYL ESTER WARNER-LAMBERT COMPANY (US) 1997-11-06 WO disclosed