Phosphoric Acid

Phosphoric Acid

SCHEMBL7200448

CC[P+](c1ccccc1C)(c1ccccc1C)c1ccccc1C.CC[P+](c1ccccc1C)(c1ccccc1C)c1ccccc1C.CC[P+](c1ccccc1C)(c1ccccc1C)c1ccccc1C.O=P([O-])([O-])[O-]

nearest known ligand 0.36

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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 13)

geneUniProtsupporting neighboursconfidence
ACP3 P15309 1/20 0.36
HPGD P15428 1/20 0.33
TSHR P16473 1/20 0.33
ACHE P22303 1/20 0.33
ELANE P08246 1/20 0.33
HSD17B10 Q99714 1/20 0.31
NR3C1 P04150 1/20 0.31
PGR P06401 1/20 0.31
NR3C2 P08235 1/20 0.31
TDP1 Q9NUW8 1/20 0.31
FDPS P14324 1/20 0.31
L3MBTL1 Q9Y468 1/20 0.31
GGPS1 O95749 1/20 0.30

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
Bromide SCHEMBL7194996 0.86 TSHR (0.41) TSHRACHENR3C1PGRNR3C2
Hydrochloric Acid SCHEMBL7192621 0.86 TSHR (0.41) TSHRACHENR3C1PGRNR3C2
Iodide SCHEMBL7193553 0.86 TSHR (0.41) TSHRACHENR3C1PGRNR3C2
Phosphoric Acid SCHEMBL9067731 0.85 ACP3 (0.34) ACP3HPGDTDP1
Acetic Acid SCHEMBL8750095 0.83 ALDH1A1 (0.36) HPGDTSHRPGRTDP1
Acetic Acid SCHEMBL2170904 0.83 ALDH1A1 (0.36) HPGDTSHRPGRTDP1
Acetic Acid SCHEMBL7200704 0.80 ERCC5 (0.38) HPGDTSHRTDP1
Phosphoric Acid SCHEMBL7195799 0.80 LAP3 (0.40) ACP3HPGDTSHRL3MBTL1
Succinic Acid SCHEMBL7200700 0.80 HDAC3 (0.40)
Phosphoric Acid SCHEMBL7195775 0.79 ACP3 (0.36) ACP3HPGDTDP1FDPSGGPS1

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 8 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
US-5534565-A DICYANDIAMIDE DERIVATIVES FOR LAMINATES ALLIEDSIGNAL INC. (US) 1996-07-09 US 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