Phosphoric Acid

Phosphoric Acid

SCHEMBL647323

CCCCN(CCCC)CCCC.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 20)

geneUniProtsupporting neighboursconfidence
OPRM1 known ✓ P35372 1/20 0.39
MMP1 P03956 1/20 0.54
MMP2 P08253 1/20 0.54
MMP3 P08254 1/20 0.54
MMP8 P22894 1/20 0.54
CA12 O43570 2/20 0.46
CA1 P00915 2/20 0.46
CA9 Q16790 2/20 0.46
LPAR3 Q9UBY5 4/20 0.44
LPAR2 Q9HBW0 1/20 0.44
MEN1 O00255 1/20 0.44
KMT2A Q03164 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
S1PR2 O95136 1/20 0.43
S1PR1 P21453 1/20 0.43
S1PR3 Q99500 1/20 0.43
S1PR5 Q9H228 1/20 0.43
KDM5A P29375 3/20 0.42
FDPS P14324 5/20 0.42
GGPS1 O95749 4/20 0.41

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 SCHEMBL5052603 1.00 MMP1 (0.54) MMP1MMP2MMP3MMP8CA12
Phosphoric Acid SCHEMBL310173 1.00 MMP1 (0.54) MMP1MMP2MMP3MMP8CA12
Phosphoric Acid SCHEMBL6233901 1.00 MMP1 (0.54) MMP1MMP2MMP3MMP8CA12
Phosphoric Acid SCHEMBL4363976 1.00 MMP1 (0.54) MMP1MMP2MMP3MMP8CA12
Phosphoric Acid SCHEMBL5052596 1.00 MMP1 (0.54) MMP1MMP2MMP3MMP8CA12
Phosphoric Acid SCHEMBL1334842 1.00 MMP1 (0.54) MMP1MMP2MMP3MMP8CA12
Phosphoric Acid SCHEMBL4713937 1.00 MMP1 (0.54) MMP1MMP2MMP3MMP8CA12
Phosphoric Acid SCHEMBL31442966 0.97 MMP1 (0.52) MMP1MMP2MMP3MMP8CA12
Phosphoric Acid SCHEMBL28193980 0.97 MMP1 (0.52) MMP1MMP2MMP3MMP8CA12
Phosphoric Acid SCHEMBL17726983 0.93 S1PR2 (0.53) MMP1MMP2MMP3MMP8LPAR3

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 327 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025111479-A1 FLUOROGENIC SUBSTRATES AND METHODS OF USE ABBOTT LABORATORIES (US) 2025-05-30 WO claimed
CN-119331478-A Water-based heat-resistant paint, preparation method and application 金隅微观(沧州)化工有限公司 2025-01-21 CN claimed
CN-107710462-B Electrochemical hydrogen storage electrode and battery 巴斯夫公司 2022-08-02 CN claimed
CN-107615556-B Electrolyte and metal hydride battery 巴斯夫公司 2021-11-02 CN claimed
US-20200283833-A1 POLYMER TAGGED NUCLEOTIDES FOR SINGLE MOLECULE ELECTRONIC SNP ASSAY THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2020-09-10 US claimed
US-20180112257-A1 POLYMER TAGGED NUCLEOTIDES FOR SINGLE MOLECULE ELECTRONIC SNP ASSAY THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2018-04-26 US claimed
CN-107922968-A Nucleotide for the polymeric marker of unimolecule electronics SNP measure 哥伦比亚大学董事会 2018-04-17 CN claimed
EP-3274471-A1 POLYMER TAGGED NUCLEOTIDES FOR SINGLE MOLECULE ELECTRONIC SNP ASSAY The Trustees of Columbia University in the City of New York (US) 2018-01-31 EP claimed
WO-2016154215-A1 POLYMER TAGGED NUCLEOTIDES FOR SINGLE MOLECULE ELECTRONIC SNP ASSAY THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2016-09-29 WO claimed
US-8614312-B2 Method for preparing nucleotides and related analogues by synthesis on soluble substrate, and biological tools thus prepared CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2013-12-24 US claimed
US-20110118454-A1 METHOD FOR PREPARING NUCLEOTIDES AND RELATED ANALOGUES BY SYNTHESIS ON SOLUBLE SUBSTRATE, AND BIOLOGICAL TOOLS THUS PREPARED CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2011-05-19 US claimed
US-5990303-A REACTING 7-DEAZA-2-DEOXY GUANOSINE WITH A PHOSPHORYLATING AGENT TO FORM NUCLEOTIDE; USED AS GUANOSINE NUCLEOTIDE ANALOGUES FOR SEQUENCE DETERMINATION; COMPOUNDS ARE STABLE AND NONAGGREGATING ROCHE DIAGNOSTICS GMBH (DE) 1999-11-23 US claimed
US-4565868-A PHOSPHORYLATION, ESTERIFICATION TO PRODUCE PHOSPHATE ESTERS SYNTEX (U.S.A.) INC. (US) 1986-01-21 US claimed
CN-122080984-A Borate extreme pressure agent with core-shell structure, wide-temperature-range industrial lubricating grease and application thereof 2026-05-26 CN disclosed
EP-4094767-B1 NUCLEOTIDE AND NUCLEOSIDE THERAPEUTIC COMPOSITIONS AND USES RELATED THERETO UNIV EMORY (US) 2026-05-20 EP disclosed
EP-4717779-A2 COMPOSITIONS AND METHODS FOR SYNTHESIZING 5'-CAPPED RNAS TriLink BioTechnologies, LLC (US) 2026-04-01 EP disclosed
EP-0235301-A1 PYRIDOPYRIMIDINE NUCLEOTIDE DERIVATIVES TEIJIN LIMITED (JP) 1987-09-09 EP disclosed
US-4565868-A PHOSPHORYLATION, ESTERIFICATION TO PRODUCE PHOSPHATE ESTERS SYNTEX (U.S.A.) INC. (US) 1986-01-21 US disclosed
EP-0105486-A2 1-Monophosphate esters, 1,3-bisphosphate esters and cyclic phosphate esters of 9-(1,3-dihydroxy-2-propoxymethyl)-guanine as antiviral agents SYNTEX (U.S.A.) INC. (US) 1984-04-18 EP disclosed
US-4247328-A TRISODIUM CITRATE, AMINE PHOSPHATES VICKERS LIMITED (GB) 1981-01-27 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-20110118454-A1 METHOD FOR PREPARING NUCLEOTIDES AND RELATED ANALOGUES BY SYNTHESIS ON SOLUBLE SUBSTRATE, AND BIOLOGICAL TOOLS THUS PREPARED PNP, NUDT1, DUT OPRM1 3126/4885MMP1 3916/4885MMP2 3557/4885

“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.