Oxalic Acid

Oxalic Acid

SCHEMBL28604188

O.O=C(O)C(=O)O.[KH].[KH]

nearest known ligand 0.00

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Known targets — ChEMBL curated mechanism

OPRM1SLC6A4

The experimentally established mechanism targets of Oxalic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
Oxalic Acid SCHEMBL2722477 1.00
Oxalic Acid SCHEMBL28387559 1.00 CA1 (0.44)
Oxalic Acid SCHEMBL236657 1.00
Oxalic Acid SCHEMBL29237689 0.94
Oxalic Acid SCHEMBL29253639 0.94 CA1 (0.40)
Oxalic Acid SCHEMBL28708653 0.94 CA1 (0.40)
Oxalic Acid SCHEMBL7201736 0.94 CA1 (0.40)
Oxalic Acid SCHEMBL3837051 0.94
Oxalic Acid SCHEMBL14694752 0.94 CA1 (0.40)
Oxalic Acid SCHEMBL1054534 0.94 CA1 (0.40)

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 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113198418-B Method for preparing efficient phosphorus removal activated carbon by using edible fungus residues 贵州民族大学 2022-08-05 CN disclosed
CN-113198418-A Method for preparing efficient phosphorus removal activated carbon by using edible fungus residues 贵州民族大学 2021-08-03 CN disclosed