Phosphoric Acid

Phosphoric Acid

SCHEMBL9600604

O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].[Al+3].[Co+2].[Co+2].[Co+2].[SiH4]

nearest known ligand 0.39

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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 0.39
LMNA P02545 2/20 0.33

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 SCHEMBL6889996 0.94 SLC34A1 (0.42) SLC34A1LMNA
Phosphoric Acid SCHEMBL1790065 0.94
Phosphoric Acid SCHEMBL10385414 0.94
Phosphoric Acid SCHEMBL31147691 0.89 SLC34A1 (0.39) SLC34A1LMNA
Phosphoric Acid SCHEMBL6856496 0.89 SLC34A1 (0.39) SLC34A1LMNA
Phosphoric Acid SCHEMBL8371246 0.89 SLC34A1 (0.39) SLC34A1LMNA
Phosphoric Acid SCHEMBL9159256 0.89
Phosphoric Acid SCHEMBL5948560 0.89
Phosphoric Acid SCHEMBL15778794 0.89 SLC34A1 (0.39) SLC34A1LMNA
Phosphoric Acid SCHEMBL22451 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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116987528-A Method for preparing naphtha by catalytic cracking of heavy fuel oil 浙江美福石油化工有限责任公司 2023-11-03 CN claimed
EP-0325141-B1 Process for the preparation of phenyl ethanols BASF AG (DE) 1993-11-10 EP claimed
US-4943667-A DECYCLIZATION OF STYRENE OXIDE, HYDROGENATION CATALYST BASF AKTIENGESELLSCHAFT (DE) 1990-07-24 US claimed
CN-116987528-B Method for preparing naphtha by catalytic cracking of heavy fuel oil 浙江美福石油化工有限责任公司 2025-10-21 CN disclosed
CN-116987528-A Method for preparing naphtha by catalytic cracking of heavy fuel oil 浙江美福石油化工有限责任公司 2023-11-03 CN disclosed
CN-116987528-A Method for preparing naphtha by catalytic cracking of heavy fuel oil 浙江美福石油化工有限责任公司 2023-11-03 CN disclosed
US-4943667-A DECYCLIZATION OF STYRENE OXIDE, HYDROGENATION CATALYST BASF AKTIENGESELLSCHAFT (DE) 1990-07-24 US disclosed