Phosphoric Acid

Phosphoric Acid

SCHEMBL7197915

Cc1ccc(C[P+](c2ccccc2C)(c2ccccc2C)c2ccccc2C)cc1.Cc1ccc(C[P+](c2ccccc2C)(c2ccccc2C)c2ccccc2C)cc1.Cc1ccc(C[P+](c2ccccc2C)(c2ccccc2C)c2ccccc2C)cc1.O=P([O-])([O-])[O-]

nearest known ligand 0.37

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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 18)

geneUniProtsupporting neighboursconfidence
FDFT1 P37268 4/20 0.37
POLB P06746 1/20 0.34
MEN1 O00255 3/20 0.33
KMT2A Q03164 3/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
LMNA P02545 2/20 0.32
TSHR P16473 1/20 0.32
PLAAT3 P53816 1/20 0.32
PLAAT5 Q96KN8 1/20 0.32
PLAAT2 Q9NWW9 1/20 0.32
PLAAT4 Q9UL19 1/20 0.32
NPC1 O15118 1/20 0.32
RAB9A P51151 1/20 0.32
MAPT P10636 1/20 0.32
ACP3 P15309 1/20 0.32
CA2 P00918 1/20 0.31
CA7 P43166 1/20 0.31
CNR2 P34972 1/20 0.31

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
Phosphoric Acid SCHEMBL7195799 0.90 LAP3 (0.40) POLBSMN1; SMN2LMNATSHRACP3
Iodide SCHEMBL7197262 0.88 IDO1 (0.35) POLBMEN1KMT2ASMN1; SMN2LMNA
Bromide SCHEMBL7197753 0.88 SNCA (0.37) POLBMEN1KMT2ASMN1; SMN2LMNA
Hydrochloric Acid SCHEMBL7200797 0.88 CYP19A1 (0.36) POLBMEN1KMT2ASMN1; SMN2LMNA
Acetic Acid SCHEMBL8750064 0.86 SMN1; SMN2 (0.38) POLBMEN1KMT2ASMN1; SMN2PLAAT3
Phosphoric Acid SCHEMBL7201586 0.85 L3MBTL1 (0.45) MEN1KMT2ATSHRNPC1RAB9A
Succinic Acid SCHEMBL7195814 0.83 HDAC3 (0.38) POLBMEN1KMT2ASMN1; SMN2PLAAT3
Acetic Acid SCHEMBL7195823 0.83 SMN1; SMN2 (0.40) POLBMEN1KMT2ASMN1; SMN2PLAAT3
Phosphoric Acid SCHEMBL7196602 0.78 FDFT1 (0.41) FDFT1MEN1KMT2ALMNATSHR
Phosphoric Acid SCHEMBL7200448 0.78 ACP3 (0.36) TSHRACP3

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