Oxalic Acid

Oxalic Acid

SCHEMBL4776290

CNN.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
Carbamic Acid SCHEMBL28270441 0.83
Acetic Acid SCHEMBL17582502 0.83
Oxalic Acid SCHEMBL5874592 0.82 FFAR3 (0.42)
Oxalic Acid SCHEMBL1401724 0.82
Methylhydrazine SCHEMBL29108676 0.82
Acetic Acid SCHEMBL9331464 0.80
Acetone SCHEMBL2194029 0.78
Oxalic Acid SCHEMBL8859767 0.78
Oxalic Acid SCHEMBL9685885 0.77 LDHA (0.44)
Oxalic Acid SCHEMBL9685888 0.77 LDHA (0.44)

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
WO-2022259210-A1 NOVEL PROCESS FOR PREPARATION OF 1-METHYL-3-(TRIFLUOROMETHYL)-1H-PYRAZOL-5-OL INCOR RENOVIS PHARMA PRIVATE LIMITED (IN) 2022-12-15 WO claimed
WO-2022259210-A1 NOVEL PROCESS FOR PREPARATION OF 1-METHYL-3-(TRIFLUOROMETHYL)-1H-PYRAZOL-5-OL INCOR RENOVIS PHARMA PRIVATE LIMITED (IN) 2022-12-15 WO disclosed
EP-1907372-A1 SUBSTITUTED CYCLOHEXYL DERIVATIVES AS NK-3 RECEPTOR ANTAGONISTS MERCK SHARP &amp; DOHME LTD. (GB) 2008-04-09 EP disclosed
WO-2007003965-A1 SUBSTITUTED CYCLOHEXYL DERIVATIVES AS NK-3 RECEPTOR ANTAGONISTS MERCK SHARP & DOHME LIMITED (GB) 2007-01-11 WO disclosed