Oxalic Acid

Oxalic Acid

SCHEMBL9307684

CCCCCN[C@@H](CO)C(N)=O.O=C(O)C(=O)O

nearest known ligand 0.44

Full drug profile on Sugi Atlas →

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 14)

geneUniProtsupporting neighboursconfidence
ALOX15 P16050 1/20 0.44
NOD1 Q9Y239 1/20 0.41
DPP7 Q9UHL4 2/20 0.38
EPHX1 P07099 7/20 0.37
TLR2 O60603 1/20 0.37
NAAA Q02083 1/20 0.36
KDM4E B2RXH2 2/20 0.36
ALDH1A1 P00352 1/20 0.36
CA1 P00915 1/20 0.35
CA2 P00918 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
RRM1 P23921 1/20 0.35
CASP2 P42575 1/20 0.34
TGFBR1 P36897 1/20 0.34

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
SCHEMBL9802585 0.95 EPHX1 (0.41) NOD1DPP7EPHX1TLR2NAAA
SCHEMBL8055730 0.95 EPHX1 (0.41) NOD1DPP7EPHX1TLR2NAAA
SCHEMBL248427 0.93 EPHX1 (0.44) NOD1DPP7EPHX1TLR2NAAA
SCHEMBL248429 0.93 EPHX1 (0.44) NOD1DPP7EPHX1TLR2NAAA
Phosphoric Acid SCHEMBL8213494 0.87 ANPEP (0.44) NOD1EPHX1TLR2NAAAKDM4E
SCHEMBL2282993 0.82 NOD1 (0.48) NOD1EPHX1NAAAKDM4EALDH1A1
SCHEMBL7342396 0.82 CA1 (0.44) ALOX15NOD1DPP7EPHX1CA1
SCHEMBL2282988 0.82 NOD1 (0.48) NOD1EPHX1NAAAKDM4EALDH1A1
SCHEMBL14367745 0.82 CA1 (0.44) ALOX15NOD1DPP7EPHX1CA1
SCHEMBL21206958 0.81 TGFBR1 (0.36) TLR2KDM4ECA1CA2SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5347007-A Mesylated hydroxymethyl compound treated with alkali metal chloride or quaternary ammonium chloride to form chloromethylamide compound E. R. SQUIBB & SONS, INC. (US) 1994-09-13 US disclosed
US-5260448-A Treating a vinyl bromide containing compound with a metal carbonate cyclizing agent E. R. SQUIBB & SONS, INC. (US) 1993-11-09 US disclosed
US-5260449-A Method for preparing 7-oxabicycloheptyl substituted bromooxazole amide prostaglandin analog intermediates useful in the preparation of anti-thrombotic and anti-vasospastic compounds E. R. SQUIBB & SONS, INC. (US) 1993-11-09 US disclosed