Oxalic Acid

Oxalic Acid

SCHEMBL5157364

Cc1[nH]cnc1CCO.O=C(O)C(=O)O

nearest known ligand 0.61

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 15)

geneUniProtsupporting neighboursconfidence
GABRR1 P24046 1/20 0.61
HRH4 Q9H3N8 2/20 0.55
HRH3 Q9Y5N1 2/20 0.55
HRH2 P25021 1/20 0.55
HRH1 P35367 1/20 0.55
TDP1 Q9NUW8 1/20 0.53
FDPS P14324 1/20 0.45
HTR3A P46098 3/20 0.42
HTR3E A5X5Y0 2/20 0.42
HTR3B O95264 2/20 0.42
HTR3D Q70Z44 2/20 0.42
HTR3C Q8WXA8 2/20 0.42
F2 P00734 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.36

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
SCHEMBL6569238 0.91
SCHEMBL6678869 0.79 HRH4 (0.60) GABRR1HRH4HRH3HRH2HRH1
Hydrochloric Acid SCHEMBL1310204 0.79 GABRR1 (0.66) GABRR1HRH4HRH3HRH2HRH1
Hydrochloric Acid SCHEMBL6741572 0.78 TDP1 (0.61) GABRR1HRH4HRH3HRH2HRH1
SCHEMBL9237536 0.76 GABRR1 (1.00) GABRR1HRH4HRH3HRH2HRH1
SCHEMBL5157359 0.75 GABRR1 (0.56) GABRR1HRH4HRH3HRH2HRH1
SCHEMBL711376 0.74
SCHEMBL31421461 0.74 GABRR1 (0.54) GABRR1HRH4HRH3HRH2HRH1
Hydrochloric Acid SCHEMBL917 0.72
SCHEMBL14131260 0.72

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1472232-B1 PROCESSES FOR PREPARING IMIDAZOLE DERIVATIVES AND SALTS THEREOF YUHAN CORP (KR) 2007-01-24 EP disclosed
EP-1472232-A4 PROCESSES FOR PREPARING IMIDAZOLE DERIVATIVES AND SALTS THEREOF YUHAN CORP (KR) 2006-02-01 EP disclosed
EP-1472232-A1 PROCESSES FOR PREPARING IMIDAZOLE DERIVATIVES AND SALTS THEREOF Yuhan Corporation (KR) 2004-11-03 EP disclosed
US-6706888-B2 REACTING A 3-HALOTETRAHYDROFURAN OR TETRAHYDROPYRAN COMPOUND WITH FORMAMIDINE OR ITS SALT IN THE PRESENCE OF A BASE TO PRODUCE A 3-(1H-IMIDAZOL-4-YL)PROPANOL DERIVATIVE; EFFICIENCY; INTERMEDIATES; ANTICARCINOGENIC AGENTS; VIRICIDES; YUHAN CORPORATION (KR) 2004-03-16 US disclosed
US-20030153769-A1 Processes for preparing imidazole derivatives and salts thereof YUHAN CORPORATION 2003-08-14 US disclosed
WO-2003066600-A1 PROCESSES FOR PREPARING IMIDAZOLE DERIVATIVES AND SALTS THEREOF YUHAN CORPORATION (KR) 2003-08-14 WO 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-20030153769-A1 Processes for preparing imidazole derivatives and salts thereof NISCH, INF2, SRI GABRR1 4012/4885HRH4 193/4885HRH3 730/4885

“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.