Oxalic Acid

Oxalic Acid

SCHEMBL1356980

CN(CC(=O)Nc1ccn(-c2ccc(Cl)c(Cl)c2)n1)Cc1ccccc1.O=C(O)C(=O)O

nearest known ligand 0.56

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
ABL1 P00519 1/20 0.56
SIGMAR1 Q99720 3/20 0.53
ELOVL1 Q9BW60 1/20 0.49
RAB9A P51151 1/20 0.48
CACNA1G O43497 1/20 0.48
CACNA1H O95180 1/20 0.48
CACNA1I Q9P0X4 1/20 0.48
ATM Q13315 1/20 0.47
MAPT P10636 2/20 0.47
KDM4E B2RXH2 3/20 0.45
ALDH1A1 P00352 3/20 0.45
MEN1 O00255 2/20 0.45
KMT2A Q03164 2/20 0.45
HTT P42858 2/20 0.42
TSHR P16473 1/20 0.42
HSD17B10 Q99714 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
UBE2M P61081 1/20 0.41
DCUN1D1 Q96GG9 1/20 0.41
LMNA P02545 2/20 0.41

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
SCHEMBL1357515 0.98 ABL1 (0.58) ABL1SIGMAR1ELOVL1RAB9ACACNA1G
Oxalic Acid SCHEMBL1356977 0.80 ABL1 (0.58) ABL1SIGMAR1ELOVL1CACNA1GCACNA1H
SCHEMBL1356743 0.79 ABL1 (0.65) ABL1SIGMAR1ELOVL1CACNA1GCACNA1H
SCHEMBL1356979 0.77 ABL1 (0.48) ABL1SIGMAR1ELOVL1CACNA1GCACNA1H
SCHEMBL1356884 0.76 SIGMAR1 (0.63) ABL1SIGMAR1ATMMAPTKDM4E
SCHEMBL1357656 0.76 ABL1 (0.73) ABL1SIGMAR1ELOVL1MAPTKDM4E
Oxalic Acid SCHEMBL1899223 0.75 SIGMAR1 (0.91) SIGMAR1ATMMAPTKDM4EMEN1
SCHEMBL24685633 0.73 ABL1 (0.66) ABL1SIGMAR1ELOVL1RAB9AMAPT
SCHEMBL20485462 0.73 ELOVL1 (0.73) ABL1SIGMAR1ELOVL1CACNA1GCACNA1H
SCHEMBL20250105 0.73 ELOVL1 (0.68) ABL1SIGMAR1ELOVL1CACNA1GCACNA1H

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1994008-B1 IMIDAZOLE COMPOUNDS HAVING PHARMACEUTICAL ACTIVITY TOWARDS THE SIGMA RECEPTOR ESTEVE LABOR DR (ES) 2016-08-10 EP disclosed
US-8410159-B2 Imidazole compounds having pharmaceutical activity towards the sigma receptor LABORATORIES DEL DR. ESTEVE, S.A. (ES) 2013-04-02 US disclosed
US-20110281848-A1 IMIDAZOLE COMPOUNDS HAVING PHARMACEUTICAL ACTIVITY TOWARDS THE SIGMA RECEPTOR LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2011-11-17 US disclosed
US-7989485-B2 Imidazole compounds having pharmaceutical activity towards the sigma receptor LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2011-08-02 US disclosed
US-20090137560-A1 IMIDAZOLE COMPOUNDS HAVING PHARMACEUTICAL ACTIVITY TOWARDS THE SIGMA RECEPTOR LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2009-05-28 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 (2 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-20090137560-A1 IMIDAZOLE COMPOUNDS HAVING PHARMACEUTICAL ACTIVITY TOWARDS THE SIGMA RECEPTOR SIGMAR1, TMEM97, OPRK1 ABL1 452/4885SIGMAR1 1/4885ELOVL1 3352/4885
US-20110281848-A1 IMIDAZOLE COMPOUNDS HAVING PHARMACEUTICAL ACTIVITY TOWARDS THE SIGMA RECEPTOR SIGMAR1, TMEM97, OPRK1 ABL1 452/4885SIGMAR1 1/4885ELOVL1 3352/4885

“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.