Phenylphosphonic Acid

Phenylphosphonic Acid

SCHEMBL18919337

O=P(O)(O)O.O=P(O)(O)c1ccccc1

nearest known ligand 0.94

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Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Phenylphosphonic 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
▸ CA2 P00918 1/20 0.94
▸ CA4 P22748 1/20 0.94
▸ CA5A P35218 1/20 0.94
▸ CFTR P13569 1/20 0.56
▸ ALOX15 P16050 1/20 0.52
▸ TSHR P16473 1/20 0.52
▸ ALDH1A1 P00352 3/20 0.50
▸ MEN1 O00255 1/20 0.50
▸ KMT2A Q03164 1/20 0.50
▸ PGK1 P00558 1/20 0.47
▸ PGK2 P07205 1/20 0.47
▸ GAA P10253 2/20 0.46
▸ USP2 O75604 1/20 0.46
▸ ESR1 P03372 1/20 0.46
▸ SRC P12931 2/20 0.44
▸ PTPN1 P18031 1/20 0.42
▸ TDP1 Q9NUW8 1/20 0.42
▸ L3MBTL1 Q9Y468 1/20 0.42
▸ MAPT P10636 1/20 0.42
▸ ALPG P10696 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
Phenylphosphonic Acid SCHEMBL269853 0.97 CA2 (1.00) CA2CA4CA5ACFTRALOX15
Phenylphosphonic Acid SCHEMBL28151870 0.97 CA2 (1.00) CA2CA4CA5ACFTRALOX15
Phenylphosphonic Acid SCHEMBL34998 0.97 CA2 (1.00) CA2CA4CA5ACFTRALOX15
Phenylphosphonic Acid SCHEMBL7951127 0.94 CA2 (0.94) CA2CA4CA5ACFTRALOX15
Phenylphosphonic Acid SCHEMBL11422650 0.94 CA2 (0.94) CA2CA4CA5ACFTRALOX15
Phenylphosphonic Acid SCHEMBL16413784 0.94 CA2 (0.94) CA2CA4CA5ACFTRALOX15
Phenylphosphonic Acid SCHEMBL588197 0.94 CA2 (0.94) CA2CA4CA5ACFTRALOX15
Phenylphosphonic Acid SCHEMBL911646 0.94 CA2 (0.94) CA2CA4CA5ACFTRALOX15
Phenylphosphonic Acid SCHEMBL17626563 0.94 CA2 (0.94) CA2CA4CA5ACFTRALOX15
Phenylphosphonic Acid SCHEMBL11847565 0.94 CA2 (0.94) CA2CA4CA5ACFTRALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10428280-B2 Method for manufacturing of multi-level pore zeolite and utilization as catalyst for hydroisomerization of normal paraffins of multi-level pore zeolite prepared thereby S-OIL CORPORATION (KR) 2019-10-01 — — US disclosed
US-20170158970-A1 METHOD FOR MANUFACTURING OF MULTI-LEVEL PORE ZEOLITE AND UTILIZATION AS CATALYST FOR HYDROISOMERIZATION OF NORMAL PARAFFINS OF MULTI-LEVEL PORE ZEOLITE PREPARED THEREBY S-OIL CORPORATION (KR) 2017-06-08 — — US disclosed
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