Phosphoric Acid

Phosphoric Acid

SCHEMBL474409

CC(=O)[C@@]1(n2cnc3c(N)ncnc32)O[C@H](CO)[C@@H](O)[C@H]1O.O=P(O)(O)O

nearest known ligand 0.48

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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
DPP4 known ✓ P27487 1/20 0.46
ADRB2 known ✓ P07550 1/20 0.43
KCNH2 known ✓ Q12809 1/20 0.43
ADORA1 P30542 3/20 0.48
PI4KA P42356 2/20 0.46
PI4K2B Q8TCG2 2/20 0.46
PI4K2A Q9BTU6 2/20 0.46
PI4KB Q9UBF8 2/20 0.46
ADORA3 P0DMS8 4/20 0.46
ADORA2A P29274 3/20 0.46
SLC28A1 O00337 2/20 0.46
SMN1; SMN2 Q16637 2/20 0.46
MEN1 O00255 1/20 0.46
MAP3K7 O43318 1/20 0.46
SLC28A2 O43868 1/20 0.46
GAPDH P04406 1/20 0.46
MAPK1 P28482 1/20 0.46
ADORA2B P29275 1/20 0.46
STAT6 P42226 1/20 0.46
KMT2A Q03164 1/20 0.46

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
SCHEMBL219553 0.96 ADORA3 (0.49) ADORA1PI4KAPI4K2BPI4K2API4KB
Acetaldehyde SCHEMBL27678170 0.92 ADORA3 (0.48) ADORA1PI4KAPI4K2BPI4K2API4KB
Phosphoric Acid SCHEMBL18486577 0.89 ADORA1 (0.45) ADORA1PI4KAPI4K2BPI4K2API4KB
SCHEMBL474415 0.87 P2RY1 (0.56) ADORA1SMN1; SMN2DNPH1PRKAB2TRPM2
Phosphoric Acid SCHEMBL9394402 0.87 ADORA1 (0.44) ADORA1PI4KAPI4K2BPI4K2API4KB
Phosphoric Acid SCHEMBL20505441 0.87 ADORA1 (0.44) ADORA1PI4KAPI4K2BPI4K2API4KB
SCHEMBL5742074 0.87 EGFR (0.49) ADORA1PI4KAPI4K2BPI4K2API4KB
SCHEMBL29655156 0.86 ADORA3 (0.50) ADORA1PI4KAPI4K2BPI4K2API4KB
SCHEMBL2463541 0.86 ADORA3 (0.50) ADORA1PI4KAPI4K2BPI4K2API4KB
SCHEMBL28215296 0.85 ADORA3 (0.49) ADORA1PI4KAPI4K2BPI4K2API4KB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250243168-A1 ACETYL-COA SYNTHETASE 2 (ACSS2) INHIBITORS AND METHODS USING SAME THE WISTAR INST (US) 2025-07-31 US disclosed
US-12281084-B2 Acetyl-CoA synthetase 2 (ACSS2) inhibitors and methods using same THE WISTAR INSTITUTE (US) 2025-04-22 US disclosed
US-20220281826-A1 ACETYL-COA SYNTHETASE 2 (ACSS2) INHIBITORS AND METHODS USING SAME THE WISTAR INSTITUTE 2022-09-08 US disclosed
EP-3983391-A1 ACETYL-COA SYNTHETASE 2 (ACSS2) INHIBITORS AND METHODS USING SAME The Wistar Institute (US) 2022-04-20 EP disclosed
WO-2020252407-A1 ACETYL-COA SYNTHETASE 2 (ACSS2) INHIBITORS AND METHODS USING SAME THE WISTAR INSTITUTE (US) 2020-12-17 WO disclosed
US-8518635-B2 Regulation of protein activity by reversible acetylation THE J. DAVID GLADSTONE INSTITUTES (US) 2013-08-27 US disclosed
EP-2029731-B1 REGULATION OF PROTEIN ACTIVITY BY REVERSIBLE ACETYLATION DAVID GLADSTONE INST (US) 2012-02-01 EP disclosed
US-20090061015-A1 Regulation of Protein Activity By Reversible Acetylation THE J. DAVID GLADSTONE INSTITUTES (US) 2009-03-05 US disclosed
EP-2029731-A2 REGULATION OF PROTEIN ACTIVITY BY REVERSIBLE ACETYLATION The J. David Gladstone Institutes (US) 2009-03-04 EP disclosed
WO-2007149270-A9 REGULATION OF PROTEIN ACTIVITY BY REVERSIBLE ACETYLATION DAVID GLADSTONE INST (US) 2008-03-06 WO disclosed
WO-2007149270-A2 REGULATION OF PROTEIN ACTIVITY BY REVERSIBLE ACETYLATION THE J. DAVID GLADSTONE INSTITUTES (US) 2007-12-27 WO 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 (3 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-12281084-B2 Acetyl-CoA synthetase 2 (ACSS2) inhibitors and methods using same ACSS2, ACACB, ACACA DPP4 1824/4885ADRB2 4010/4885KCNH2 4706/4885
US-20220281826-A1 ACETYL-COA SYNTHETASE 2 (ACSS2) INHIBITORS AND METHODS USING SAME ACSS2, ACACB, ACACA DPP4 1824/4885ADRB2 4010/4885KCNH2 4706/4885
US-20250243168-A1 ACETYL-COA SYNTHETASE 2 (ACSS2) INHIBITORS AND METHODS USING SAME ACSS2, ACACB, ACACA DPP4 1824/4885ADRB2 4010/4885KCNH2 4706/4885

“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.