Oxalic Acid

Oxalic Acid

SCHEMBL28535006

CCCCCCCCC(N)(CCCCCCCC)CCCCCCCC.O=C(O)C(=O)O

nearest known ligand 0.50

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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.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GPR84 Q9NQS5 7/20 0.50
PPARG P37231 6/20 0.50
PPARD Q03181 6/20 0.50
PPARA Q07869 6/20 0.50
HDAC11 Q96DB2 5/20 0.50
TSHR P16473 4/20 0.50
ALDH1A1 P00352 2/20 0.50
TLR2 O60603 2/20 0.50
TDP1 Q9NUW8 2/20 0.50
FABP4 P15090 2/20 0.50
PTPN1 P18031 2/20 0.50
SMPD1 P17405 2/20 0.50
SLC22A6 Q4U2R8 1/20 0.50
SLC22A8 Q8TCC7 1/20 0.50
FDPS P14324 1/20 0.50
MEN1 O00255 1/20 0.50
ESR1 P03372 1/20 0.50
ALOX15 P16050 1/20 0.50
PDE4A P27815 1/20 0.50
KMT2A Q03164 1/20 0.50

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
Bicarbonate SCHEMBL829821 0.93 GPR84 (0.52) GPR84PPARGPPARDPPARAHDAC11
Bicarbonate SCHEMBL28711950 0.93 GPR84 (0.52) GPR84PPARGPPARDPPARAHDAC11
Bicarbonate SCHEMBL9751030 0.93 GPR84 (0.52) GPR84PPARGPPARDPPARAHDAC11
Bicarbonate SCHEMBL3271999 0.93 GPR84 (0.52) GPR84PPARGPPARDPPARAHDAC11
Bicarbonate SCHEMBL28426178 0.93 GPR84 (0.52) GPR84PPARGPPARDPPARAHDAC11
Acetic Acid SCHEMBL8065006 0.91 GPR84 (0.50) GPR84PPARGPPARDPPARAHDAC11
Acetic Acid SCHEMBL2204888 0.91 GPR84 (0.50) GPR84PPARGPPARDPPARAHDAC11
Acetic Acid SCHEMBL29060600 0.91 GPR84 (0.50) GPR84PPARGPPARDPPARAHDAC11
Nonanoate SCHEMBL5343938 0.87 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11
Nonadecanoic Acid SCHEMBL7548957 0.87 GPR84 (0.71) GPR84PPARGPPARDPPARAHDAC11

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112662872-B Extraction method of oxalic acid-containing solution 江西理工大学 2022-10-11 CN claimed
CN-115161499-A Method for one-step extraction separation and recovery of rare earth and iron 江西理工大学 2022-10-11 CN claimed
CN-112662872-A Extraction method of oxalic acid-containing solution 江西理工大学 2021-04-16 CN claimed
CN-112608241-A Preparation method of trioctylmethylammonium oxalate 江西理工大学 2021-04-06 CN claimed
CN-112662872-B Extraction method of oxalic acid-containing solution 江西理工大学 2022-10-11 CN disclosed
CN-115161499-A Method for one-step extraction separation and recovery of rare earth and iron 江西理工大学 2022-10-11 CN disclosed
CN-115161499-A Method for one-step extraction separation and recovery of rare earth and iron 江西理工大学 2022-10-11 CN disclosed
CN-112593078-B Synthetic method of organic quaternary ammonium salt 江西理工大学 2022-08-05 CN disclosed
CN-112662872-A Extraction method of oxalic acid-containing solution 江西理工大学 2021-04-16 CN disclosed
CN-112662872-A Extraction method of oxalic acid-containing solution 江西理工大学 2021-04-16 CN disclosed
CN-112608241-A Preparation method of trioctylmethylammonium oxalate 江西理工大学 2021-04-06 CN disclosed
CN-112608241-A Preparation method of trioctylmethylammonium oxalate 江西理工大学 2021-04-06 CN disclosed
CN-112608241-A Preparation method of trioctylmethylammonium oxalate 江西理工大学 2021-04-06 CN disclosed
CN-112593078-A Synthetic method of organic quaternary ammonium salt 江西理工大学 2021-04-02 CN disclosed