Phosphoric Acid

Phosphoric Acid

SCHEMBL2777264

O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].[Ta+5].[Ta+5].[Ta+5]

nearest known ligand 0.46

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Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRB1ADRB2ADRB3CYP11B1DPP4FGFR1FGFR2FGFR3FGFR4HRH1JAK1JAK2JAK3KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITNAOPRD1OPRK1OPRM1PPDGFRBPIK3CDSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASMOTYK2polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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 SCHEMBL29272737 0.94 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL31206823 0.94
Phosphoric Acid SCHEMBL31207180 0.94
Phosphoric Acid SCHEMBL14939300 0.94 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL20599796 0.94 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL29049270 0.94 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL28628618 0.88 SLC34A1 (0.39) SLC34A1LMNA
Phosphoric Acid SCHEMBL31206872 0.88
Phosphoric Acid SCHEMBL25395731 0.86
Phosphoric Acid SCHEMBL21951285 0.86 SLC34A1 (0.46) SLC34A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260142188-A1 ANODE MATERIAL AND BATTERY BTR NEW MATERIAL GROUP CO., LTD. (CN) 2026-05-21 US claimed
EP-4648131-A2 MATRIX, ANODE MATERIAL, AND SECONDARY BATTERY BTR New Material Group Co., Ltd. (CN) 2025-11-12 EP claimed
US-20250333310-A1 MATRIX, ANODE MATERIAL, AND SECONDARY BATTERY BTR NEW MATERIAL GROUP CO., LTD. (CN) 2025-10-30 US claimed
EP-4589680-A2 ANODE MATERIAL, ANODE SHEET, AND SECONDARY BATTERY BTR New Material Group Co., Ltd. (CN) 2025-07-23 EP claimed
CN-119843365-A Tantalum phosphate nonlinear optical crystal, preparation method and application thereof 中国科学院理化技术研究所 2025-04-18 CN claimed
US-20250046797-A1 Coated Single Crystalline Metal Oxide Materials and Method for Producing The Same Action Battery Technologies, Inc. 2025-02-06 US claimed
CN-119108525-A Negative electrode material, negative electrode sheet, and secondary battery 贝特瑞新材料集团股份有限公司 2024-12-10 CN claimed
CN-119092692-A Negative electrode material, negative electrode sheet, and secondary battery 贝特瑞新材料集团股份有限公司 2024-12-06 CN claimed
CN-119092693-A Matrix, negative electrode material, and secondary battery 贝特瑞新材料集团股份有限公司 2024-12-06 CN claimed
CN-119050328-A Negative electrode material, negative electrode plate and battery 贝特瑞新材料集团股份有限公司 2024-11-29 CN claimed
US-6897027-B2 Method for desalting nucleic acids DECODE GENETICS EHF. (IS) 2005-05-24 US claimed
EP-0384766-B1 Process of preparing linearly-extended polyalkylenepolyamines DOW CHEMICAL CO (US) 1994-07-06 EP claimed
EP-0375355-B1 Process for the catalytic reforming of alkylene amines to linearly-extended polyalkylene polyamines DOW CHEMICAL CO (US) 1994-02-02 EP claimed
US-5011999-A Amination of difunctional aliphatic alcohols with amines; catalyst of niobium or tantalum phosphates, group 5 oxides; efficiency THE DOW CHEMICAL COMPANY (US) 1991-04-30 US claimed
EP-0384766-A2 Process of preparing linearly-extended polyalkylenepolyamines THE DOW CHEMICAL COMPANY (US) 1990-08-29 EP claimed
EP-0375355-A2 Process for the catalytic reforming of alkylene amines to linearly-extended polyalkylene polyamines THE DOW CHEMICAL COMPANY (US) 1990-06-27 EP claimed
EP-0170383-B1 IMPROVED AROMATIC CARBOXYLIC ANHYDRIDE CATALYSTS EXXON RESEARCH AND ENGINEERING COMPANY (US) 1989-07-19 EP claimed
US-4791092-A SEQUENTIAL DEPOSITION AND CALCINING OF A TANTALUM COMPOUND AND A VANADIUM COMPOUND ON TITANIUM DIOXIDE EXXON RESEARCH & ENGINEERING CO. (US) 1988-12-13 US claimed
US-4582911-A VANADIUM AND TANTALUM OXIDES ON TITANIUM DIOXIDE SUPPORT EXXON RESEARCH & ENGINEERING CO. (US) 1986-04-15 US claimed
EP-0170383-A1 Improved aromatic carboxylic anhydride catalysts EXXON RESEARCH AND ENGINEERING COMPANY (US) 1986-02-05 EP claimed

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-20260142188-A1 ANODE MATERIAL AND BATTERY CACNA2D4, CACNA2D1, CACNA2D2 SLC34A1 898/4885LMNA 913/4885

“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.