Phosphoric Acid

Phosphoric Acid

SCHEMBL6889996

O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].[Al+3].[Co+2].[Co+2].[Co+2]

nearest known ligand 0.42

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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 2)

geneUniProtsupporting neighboursconfidence
SLC34A1 Q06495 1/20 0.42
LMNA P02545 2/20 0.36

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 SCHEMBL6856496 0.94 SLC34A1 (0.39) SLC34A1LMNA
Phosphoric Acid SCHEMBL9600604 0.94 SLC34A1 (0.39) SLC34A1LMNA
Phosphoric Acid SCHEMBL31147691 0.94 SLC34A1 (0.39) SLC34A1LMNA
Phosphoric Acid SCHEMBL10750036 0.94 SLC34A1 (0.46) SLC34A1LMNA
Phosphoric Acid SCHEMBL22451 0.94
Phosphoric Acid SCHEMBL37194 0.94 SLC34A1 (0.46) SLC34A1LMNA
Phosphoric Acid SCHEMBL8720297 0.94 SLC34A1 (0.46) SLC34A1LMNA
Phosphoric Acid SCHEMBL10746522 0.94 SLC34A1 (0.46) SLC34A1LMNA
Phosphoric Acid SCHEMBL217686 0.94 SLC34A1 (0.46) SLC34A1LMNA
Phosphoric Acid SCHEMBL14353952 0.88

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0325141-B1 Process for the preparation of phenyl ethanols BASF AG (DE) 1993-11-10 EP claimed
US-5130435-A Elimination of alcohol from an acetal or ketal in the presence of phosphates BASF AKTIENGESELLSCHAFT (DE) 1992-07-14 US claimed
US-4943667-A DECYCLIZATION OF STYRENE OXIDE, HYDROGENATION CATALYST BASF AKTIENGESELLSCHAFT (DE) 1990-07-24 US claimed
EP-0325141-A2 Process for the preparation of phenyl ethanols BASF Aktiengesellschaft (DE) 1989-07-26 EP claimed
US-3932421-A FROM ACETALDEHYDE AND AMMONIA, METAL PHOSPHATE AS CATALYST KOEI CHEMICAL COMPANY, LTD. (JA) 1976-01-13 US claimed
CN-119798144-A Preparation method of 2-methylpyridine derivative 湖南大学 2025-04-11 CN disclosed
CN-118877908-B Aluminum phosphate LTA molecular sieve and preparation method and application thereof 聊城大学 2025-02-25 CN disclosed
CN-119080022-A Lamellar AEL molecular sieve and preparation method and application thereof 聊城大学 2024-12-06 CN disclosed
CN-119080023-A AEL structure hollow molecular sieve and preparation method and application thereof 聊城大学 2024-12-06 CN disclosed
CN-118877908-A Aluminum phosphate LTA molecular sieve and preparation method and application thereof 聊城大学 2024-11-01 CN disclosed
CN-117342572-B Preparation method and application of magnetic cobalt phosphate molecular sieve 内蒙古工业大学 2024-02-13 CN disclosed
CN-117342572-A Preparation method and application of magnetic cobalt phosphate molecular sieve 内蒙古工业大学 2024-01-05 CN disclosed
US-5130435-A Elimination of alcohol from an acetal or ketal in the presence of phosphates BASF AKTIENGESELLSCHAFT (DE) 1992-07-14 US disclosed
US-4943667-A DECYCLIZATION OF STYRENE OXIDE, HYDROGENATION CATALYST BASF AKTIENGESELLSCHAFT (DE) 1990-07-24 US disclosed
EP-0349859-A2 Process for the preparation of 1,4-diazabicyclo [2,2,2]octanes BASF Aktiengesellschaft (DE) 1990-01-10 EP disclosed
EP-0327985-A1 Process for the preparation of vinyl ethers BASF Aktiengesellschaft (DE) 1989-08-16 EP disclosed
EP-0325141-A2 Process for the preparation of phenyl ethanols BASF Aktiengesellschaft (DE) 1989-07-26 EP disclosed
US-4158741-A CATALYSTIC DECYCLIZATION AND ISOMERIZATION OF GAMMA-VINYL-GAMMA-BUTYROLACTONE NIPPON GOHSEI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1979-06-19 US disclosed
US-3932421-A FROM ACETALDEHYDE AND AMMONIA, METAL PHOSPHATE AS CATALYST KOEI CHEMICAL COMPANY, LTD. (JA) 1976-01-13 US disclosed
US-3932421-A FROM ACETALDEHYDE AND AMMONIA, METAL PHOSPHATE AS CATALYST KOEI CHEMICAL COMPANY, LTD. (JA) 1976-01-13 US disclosed