Phosphoric Acid

Phosphoric Acid

SCHEMBL6794536

O=P(O)(O)O.O=P(O)(O)O.O=P(O)(O)O.O=c1c2ccoc2ccn1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

nearest known ligand 0.67

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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 17)

geneUniProtsupporting neighboursconfidence
P2RY2 P41231 10/20 0.67
SLC28A1 O00337 1/20 0.50
SLC28A2 O43868 1/20 0.50
SLC29A1 Q99808 1/20 0.50
SLC28A3 Q9HAS3 1/20 0.50
LMNA P02545 1/20 0.48
THRB P10828 1/20 0.48
MTOR P42345 1/20 0.48
MDM2 Q00987 1/20 0.48
NCOA1 Q15788 1/20 0.48
NCOA3 Q9Y6Q9 1/20 0.48
SLC5A2 P31639 2/20 0.47
SLC5A1 P13866 1/20 0.47
MAPT P10636 1/20 0.45
CDA P32320 1/20 0.45
P2RY4 P51582 2/20 0.45
ADK P55263 1/20 0.43

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
SCHEMBL6797497 0.95 P2RY2 (0.62) P2RY2SLC28A1SLC28A2SLC29A1SLC28A3
SCHEMBL6797491 0.95 P2RY2 (0.62) P2RY2SLC28A1SLC28A2SLC29A1SLC28A3
Triphosphate SCHEMBL6794540 0.92 P2RY2 (0.80) P2RY2P2RY4
Benzoic Acid SCHEMBL6795922 0.86 P2RY2 (0.54) P2RY2SLC28A1SLC28A2SLC29A1SLC28A3
SCHEMBL6794538 0.80 P2RY2 (1.00) P2RY2P2RY4
Phosphoric Acid SCHEMBL6803088 0.77 P2RY2 (0.68) P2RY2SLC28A1SLC28A2SLC29A1SLC28A3
SCHEMBL6800943 0.76 P2RY2 (0.62) P2RY2SLC28A1SLC28A2SLC29A1SLC28A3
SCHEMBL6800949 0.76 P2RY2 (0.62) P2RY2SLC28A1SLC28A2SLC29A1SLC28A3
SCHEMBL6795846 0.74 P2RY2 (0.62) P2RY2SLC28A1SLC28A2SLC29A1SLC28A3
SCHEMBL6795708 0.74 P2RY2 (0.62) P2RY2SLC28A1SLC28A2SLC29A1SLC28A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040122223-A1 Non-natural nucleotides and dinucleotides CELLTECH R & D LIMITED (GB) 2004-06-24 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20040122223-A1 Non-natural nucleotides and dinucleotides P2RY1, P2RY11, P2RY13 P2RY2 8/4885SLC28A1 7/4885SLC28A2 10/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.