Phosphoric Acid

Phosphoric Acid

SCHEMBL7201586

COc1ccc(C[P+](c2ccccc2C)(c2ccccc2C)c2ccccc2C)cc1.COc1ccc(C[P+](c2ccccc2C)(c2ccccc2C)c2ccccc2C)cc1.COc1ccc(C[P+](c2ccccc2C)(c2ccccc2C)c2ccccc2C)cc1.O=P([O-])([O-])[O-]

nearest known ligand 0.45

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Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Phosphoric Acid. 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
SCN8A known ✓ Q9UQD0 1/20 0.37
L3MBTL1 Q9Y468 2/20 0.45
ATM Q13315 1/20 0.45
TDP1 Q9NUW8 1/20 0.45
ACP3 P15309 1/20 0.41
LTA4H P09960 1/20 0.40
LDHA P00338 1/20 0.40
ALDH1A1 P00352 1/20 0.39
TSHR P16473 1/20 0.39
SLC6A4 P31645 1/20 0.38
ANPEP P15144 2/20 0.38
ERAP2 Q6P179 2/20 0.38
HPGD P15428 1/20 0.38
KEAP1 Q14145 1/20 0.38
NPC1 O15118 1/20 0.38
RAB9A P51151 1/20 0.38
PPARG P37231 1/20 0.38
PPARA Q07869 1/20 0.38
SIGMAR1 Q99720 1/20 0.37
MEN1 O00255 1/20 0.37

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
Hydrochloric Acid SCHEMBL7196439 0.90 L3MBTL1 (0.47) L3MBTL1ATMTDP1LTA4HLDHA
Iodide SCHEMBL7200711 0.90 L3MBTL1 (0.47) L3MBTL1ATMTDP1LTA4HLDHA
Bromide SCHEMBL7195760 0.90 L3MBTL1 (0.47) L3MBTL1ATMTDP1LTA4HLDHA
Acetic Acid SCHEMBL8750048 0.87 L3MBTL1 (0.50) L3MBTL1ATMTDP1LTA4HLDHA
Phosphoric Acid SCHEMBL7197915 0.85 FDFT1 (0.37) ACP3TSHRNPC1RAB9AMEN1
Acetic Acid SCHEMBL7198886 0.85 TDP1 (0.48) L3MBTL1ATMTDP1LTA4HLDHA
Phosphoric Acid SCHEMBL7197200 0.85 TAAR1 (0.46) ATMSCN8A
Succinic Acid SCHEMBL7198874 0.85 L3MBTL1 (0.48) L3MBTL1ATMTDP1LDHAALDH1A1
Phosphoric Acid SCHEMBL7195799 0.85 LAP3 (0.40) L3MBTL1ACP3ALDH1A1TSHRANPEP
Phosphoric Acid SCHEMBL9318697 0.77 MAOB (0.39) ATMSCN8AMEN1KMT2AHTT

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
EP-0624173-B2 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 2003-04-09 EP disclosed
EP-0624173-B1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 1997-04-02 EP disclosed
EP-0624173-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS. DOW CHEMICAL CO (US) 1994-11-17 EP disclosed
US-5360886-A Alklyphenylphosphine or phosphonium catalyst THE DOW CHEMICAL COMPANY (US) 1994-11-01 US disclosed
US-5310853-A Epoxy resins THE DOW CHEMICAL COMPANY (US) 1994-05-10 US disclosed
WO-1993015126-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS THE DOW CHEMICAL COMPANY (US) 1993-08-05 WO disclosed
US-5202407-A Phosphonium or phosphine catalyst having at least three alkylphenyl groups attached to phosphorus atom THE DOW CHEMICAL COMPANY (US) 1993-04-13 US disclosed