Oxalic Acid

Oxalic Acid

SCHEMBL1968009

C=CCN[C@@H]1CCc2ccccc21.O=C(O)C(=O)O

nearest known ligand 0.54

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 20)

geneUniProtsupporting neighboursconfidence
HTR1A P08908 1/20 0.54
MAOA P21397 3/20 0.50
MAOB P27338 3/20 0.50
BCHE P06276 1/20 0.50
ADRA2B P18089 1/20 0.50
ADRA2C P18825 1/20 0.50
ACHE P22303 1/20 0.50
ADRA1A P35348 1/20 0.50
HTR6 P50406 1/20 0.50
KDM4E B2RXH2 5/20 0.47
ALDH1A1 P00352 3/20 0.47
PDPK1 O15530 1/20 0.46
EPHX2 P34913 2/20 0.46
TAS1R3 Q7RTX0 2/20 0.46
TAS1R1 Q7RTX1 2/20 0.46
KMT2A Q03164 2/20 0.45
MEN1 O00255 1/20 0.45
CA1 P00915 1/20 0.44
CA2 P00918 1/20 0.44
TAS1R2 Q8TE23 1/20 0.44

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
Oxalic Acid SCHEMBL1974437 1.00 HTR1A (0.54) HTR1AMAOAMAOBBCHEADRA2B
SCHEMBL31046300 0.91 HTR1A (0.62) HTR1AMAOAMAOBBCHEADRA2B
SCHEMBL1971780 0.91 HTR1A (0.62) HTR1AMAOAMAOBBCHEADRA2B
SCHEMBL1969755 0.91 HTR1A (0.62) HTR1AMAOAMAOBBCHEADRA2B
Cadaverine Tartrate SCHEMBL6521196 0.90 HTR1A (0.50) HTR1AMAOAMAOBBCHEADRA2B
Cadaverine Tartrate SCHEMBL1971585 0.90 HTR1A (0.50) HTR1AMAOAMAOBBCHEADRA2B
SCHEMBL361398 0.82 HTR1A (0.56) HTR1AMAOAMAOBBCHEADRA2B
Oxalic Acid SCHEMBL3421257 0.80 MAOA (0.49) MAOAMAOBBCHEADRA2BADRA2C
SCHEMBL92713 0.78 MAOA (0.56) MAOAMAOBBCHEADRA2BADRA2C
SCHEMBL2467861 0.78 MAOA (0.56) MAOAMAOBBCHEADRA2BADRA2C

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-8461388-B2 Process for the synthesis of propargylated aminoindan derivatives CIPLA LIMITED (IN) 2013-06-11 US disclosed
EP-2231582-B1 PROCESS FOR THE SYNTHESIS OF PROPARGYLATED AMINOINDAN DERIVATIVES CIPLA LTD (IN) 2011-06-22 EP disclosed
US-20110054218-A1 Process for the Synthesis of Propargylated Aminoindan Derivatives CIPLA LIMITED (IN) 2011-03-03 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20110054218-A1 Process for the Synthesis of Propargylated Aminoindan Derivatives DAO, DDC, HRH2 HTR1A 402/4885MAOA 811/4885MAOB 549/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.