Phosphoric Acid

Phosphoric Acid

SCHEMBL9099370

O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].[H+].[H+].[H+].[H+].[H+].[H+].[H+].[H+].[H+]

nearest known ligand 0.46

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 2)

geneUniProtsupporting neighboursconfidence
SLC34A1 Q06495 1/20 0.46
LMNA P02545 2/20 0.39

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 SCHEMBL436 1.00
Phosphoric Acid SCHEMBL7743392 1.00 SLC34A1 (0.46) SLC34A1LMNA
Phosphoric Acid SCHEMBL2989706 0.94
Phosphoric Acid SCHEMBL1979287 0.94 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL6540946 0.94
Phosphoric Acid SCHEMBL2181871 0.94
Phosphoric Acid SCHEMBL1291546 0.94
Phosphoric Acid SCHEMBL1835681 0.94
Phosphoric Acid SCHEMBL7525209 0.94 LMNA (0.43) SLC34A1LMNA
Phosphoric Acid SCHEMBL15066667 0.94

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-11576413-B2 Compositions comprising ionized cannabidiol Natural Extraction Systems, LLC (US) 2023-02-14 US claimed
EP-4066302-A1 STABLE AQUEOUS COMPOSITIONS COMPRISING QUINONES, AND USE THEREOF IN REDOX FLOW BATTERIES Technische Universität Graz (AT) 2022-10-05 EP claimed
US-20200315229-A1 COMPOSITIONS COMPRISING IONIZED CANNABIDIOL Natural Extraction Systems, LLC 2020-10-08 US claimed
CN-116539892-B Renal clear cell carcinoma protein marker and auxiliary diagnosis model construction method 上海交通大学医学院附属新华医院 2024-03-26 CN disclosed
CN-116539892-A Renal clear cell carcinoma protein marker and auxiliary diagnosis model construction method 上海交通大学医学院附属新华医院 2023-08-04 CN disclosed
WO-2023131254-A1 PSEUDOURIDINE MODIFIED AT N1 POSITION AND USE THEREOF IN MRNA SYNTHESIS 上海吉量医药工程有限公司 2023-07-13 WO disclosed
US-11576413-B2 Compositions comprising ionized cannabidiol Natural Extraction Systems, LLC (US) 2023-02-14 US disclosed
EP-4066302-A1 STABLE AQUEOUS COMPOSITIONS COMPRISING QUINONES, AND USE THEREOF IN REDOX FLOW BATTERIES Technische Universität Graz (AT) 2022-10-05 EP disclosed
US-20220023773-A1 COMPOSITIONS COMPRISING 2-[(1R,6R)-6-ISOPROPENYL-3-METHYLCYCLOHEX-2-EN-1-YL]-3-HYDROXY-5-PENTYLPHENOLATE WAGNER ROBERT C (US) 2022-01-27 US disclosed
US-20200315229-A1 COMPOSITIONS COMPRISING IONIZED CANNABIDIOL Natural Extraction Systems, LLC 2020-10-08 US disclosed
US-5489420-A SELECTIVE NONCATALYTIC REDUCTION IN GAS PHASE AT HIGH TEMPERATURES BY USING AN NH-CONTAINING REDUCING AGENT SUCH AS UREA NALCO FUEL TECH (US) 1996-02-06 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 (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-20200315229-A1 COMPOSITIONS COMPRISING IONIZED CANNABIDIOL CNR1, CNR2, PLCB3 SLC34A1 4262/4885LMNA 2464/4885
US-20220023773-A1 COMPOSITIONS COMPRISING 2-[(1R,6R)-6-ISOPROPENYL-3-METHYLCYCLOHEX-2-EN-1-YL]-3-HYDROXY-5-PENTYLPHENOLATE HTR6, UGT1A6, MPHOSPH6 SLC34A1 4109/4885LMNA 2479/4885
US-11576413-B2 Compositions comprising ionized cannabidiol CNR1, CNR2, PLCB3 SLC34A1 4262/4885LMNA 2464/4885

“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.