Phosphoric Acid

Phosphoric Acid

SCHEMBL851329

Cc1ncc(CO)c(N)n1.O=P(O)(O)O.O=P(O)(O)O

nearest known ligand 0.54

Full drug profile on Sugi Atlas →

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 4)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.53
TKT P29401 6/20 0.46
TDP1 Q9NUW8 1/20 0.45
HSP90AA1 P07900 1/20 0.44

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 SCHEMBL1533803 1.00 LMNA (0.53) LMNATKTTDP1HSP90AA1
SCHEMBL479344 0.91 LMNA (0.61) LMNATKTHSP90AA1
Pyrophosphoric Acid SCHEMBL851327 0.91 LMNA (0.51) LMNATKTTDP1
SCHEMBL8445448 0.89 LMNA (0.59) LMNATKTHSP90AA1
Hydrochloric Acid SCHEMBL6520994 0.89 LMNA (0.59) LMNATKTHSP90AA1
SCHEMBL849877 0.83 LMNA (0.53) LMNATKTTDP1
SCHEMBL3371360 0.79 LMNA (0.61) LMNATKTTDP1
SCHEMBL12346332 0.77 LMNA (0.63) LMNATKT
SCHEMBL5916304 0.76 LMNA (0.50) LMNATKTTDP1
SCHEMBL851328 0.74 LMNA (0.57) LMNATKTTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040006040-A1 Method for the identification and treatment of pathogenic microorganism infections by inhibiting one or more enzymes in an essential metabolic pathway and compounds and pharmaceutical compositions useful therefor PYRO PHARMACEUTICALS, INC. 2004-01-08 US claimed
EP-2463654-B1 Compositions and methods for modeling saccharomyces cerevisiae metabolism UNIV CALIFORNIA (US) 2020-06-03 EP disclosed
US-8311790-B2 Reverse engineering genome-scale metabolic network reconstructions for organisms with incomplete genome annotation and developing constraints using proton flux states and numerically-determined sub-systems UNIVERSITY OF DELAWARE (US) 2012-11-13 US disclosed
EP-2463654-A1 Compositions and methods for modeling saccharomyces cerevisiae metabolism The Regents of The University of California (US) 2012-06-13 EP disclosed
EP-2434421-A2 Compositions and methods for modeling saccharomyces cerevisiae metabolism The Regents of The University of California (US) 2012-03-28 EP disclosed
US-20100280803-A1 Compositions and Methods for Modeling Saccharomyces cerevisiae Metabolism THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2010-11-04 US disclosed
EP-2230312-A1 Probe compound for detecting and isolating enzymes and means and methods using the same Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2010-09-22 EP disclosed
US-20090259451-A1 REVERSE ENGINEERING GENOME-SCALE METABOLIC NETWORK RECONSTRUCTIONS FOR ORGANISMS WITH INCOMPLETE GENOME ANNOTATION AND DEVELOPING CONSTRAINTS USING PROTON FLUX STATES AND NUMERICALLY-DETERMINED SUB-SYSTEMS UNIVERSITY OF DELAWARE (US) 2009-10-15 US disclosed
US-20060252113-A1 Methods for identifying compounds that modulate an enzyme in the glucose metabolic pathway of a pathogenic microorganism SCHECHTER ALAN M 2006-11-09 US disclosed
US-20060252112-A1 Methods for indentifying compounds that modulate an enzyme involved in biotin metabolism in a pathogenic microorganism SCHECHTER ALAN M 2006-11-09 US disclosed
US-20060178322-A1 Methods for indentifying compounds that modulate an enzyme involved in riboflavin metabolism in a pathogenic microorganism SCHECHTER ALAN M 2006-08-10 US disclosed
US-20060178320-A1 Methods for indentifying compounds that modulate an enzyme involved in thiamine metabolism in a pathogenic microorganism SCHECHTER ALAN M 2006-08-10 US disclosed
US-20060178321-A1 Methods for indentifying compounds that modulate an enzyme involved in reductive carboxylation in a pathogenic microorganism SCHECHTER ALAN M 2006-08-10 US disclosed
US-20060094075-A1 Methods for indentifying compounds that modulate an enzyme in the coenzyme a biosynthetic pathway in a pathogenic microoganism SCHECHTER ALAN M 2006-05-04 US disclosed
US-20060063224-A1 Method for the identification and treatment of pathogenic microorganism infections by inhibiting one or more enzymes in an essential metabolic pathway SCHECHTER ALAN M 2006-03-23 US disclosed
US-6955890-B2 Method for the identification and treatment of pathogenic microorganisms infections by inhibiting one or more enzymes in an essential metabolic pathway PYRO PHARMACEUTICALS, INC. (US) 2005-10-18 US disclosed
US-20040006040-A1 Method for the identification and treatment of pathogenic microorganism infections by inhibiting one or more enzymes in an essential metabolic pathway and compounds and pharmaceutical compositions useful therefor PYRO PHARMACEUTICALS, INC. 2004-01-08 US disclosed
US-20030180830-A1 Method for the identification and treatment of pathogenic microorganism infections by inhibiting one or more enzymes in an essential metabolic pathway PYRO PHARMACEUTICALS, INC. 2003-09-25 US disclosed
CN-1317051-A HMP-P rinase and TMP-PPase from arabidopsis thaliana and their use in herbicide screening SINGENPE AG (CH) 2001-10-10 CN 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 (7 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-20060252113-A1 Methods for identifying compounds that modulate an enzyme in the glucose metabolic pathway of a pathogenic microorganism MGAM, G6PD, UGDH LMNA 3781/4885TKT 33/4885TDP1 3499/4885
US-20060094075-A1 Methods for indentifying compounds that modulate an enzyme in the coenzyme a biosynthetic pathway in a pathogenic microoganism COASY, BPGM, ME1 LMNA 3658/4885TKT 233/4885TDP1 3203/4885
US-20060178320-A1 Methods for indentifying compounds that modulate an enzyme involved in thiamine metabolism in a pathogenic microorganism IMPDH1, SLC19A2, IMPDH2 LMNA 2045/4885TKT 11/4885TDP1 2410/4885
US-20060178322-A1 Methods for indentifying compounds that modulate an enzyme involved in riboflavin metabolism in a pathogenic microorganism BLVRB, IMPDH1, IMPDH2 LMNA 2663/4885TKT 162/4885TDP1 3097/4885
US-20040006040-A1 Method for the identification and treatment of pathogenic microorganism infections by inhibiting one or more enzymes in an essential metabolic pathway and compounds and pharmaceutical compositions useful therefor CYP51A1, ME1, BPGM LMNA 3872/4885TKT 24/4885TDP1 3936/4885
US-20060252112-A1 Methods for indentifying compounds that modulate an enzyme involved in biotin metabolism in a pathogenic microorganism BTD, BLVRB, BPGM LMNA 1995/4885TKT 133/4885TDP1 4162/4885
US-20060178321-A1 Methods for indentifying compounds that modulate an enzyme involved in reductive carboxylation in a pathogenic microorganism CYP2E1, POR, BLVRB LMNA 4306/4885TKT 344/4885TDP1 4211/4885

“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.