Oxalic Acid

Oxalic Acid

SCHEMBL9336232

C=NO.O=C(O)C(=O)O

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
Bicarbonate SCHEMBL2491825 0.86
Oxalic Acid SCHEMBL615792 0.80
Acetic Acid SCHEMBL29946992 0.78
Oxalic Acid SCHEMBL9227801 0.76
Formaldoxime SCHEMBL11587414 0.75
Oxalic Acid SCHEMBL1029259 0.75 CA1 (0.44)
Oxalic Acid SCHEMBL6968373 0.75
Oxalic Acid SCHEMBL34345 0.75
Oxalic Acid SCHEMBL29462943 0.75 CA1 (0.44)
Oxalic Acid SCHEMBL776 0.74

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0283147-B1 Labile ketone derivatives of 3-substituted-1-alkylamino-2-propanols and their use as beta-adrenergic blockers UNIV FLORIDA (US) 1994-05-11 EP disclosed
US-5017618-A Treatment Of Glaucoma UNIVERSITY OF FLORIDA (US) 1991-05-21 US disclosed
WO-1988007036-A1 LABILE KETONE DERIVATIVES OF 3-SUBSTITUTED-1-ALKYLAMINO-2-PROPANOLS AND THEIR USE AS beta-ADRENERGIC BLOCKERS UNIVERSITY OF FLORIDA (US) 1988-09-22 WO disclosed
EP-0283147-A1 Labile ketone derivatives of 3-substituted-1-alkylamino-2-propanols and their use as beta-adrenergic blockers UNIVERSITY OF FLORIDA (US) 1988-09-21 EP disclosed