Oxalic Acid

Oxalic Acid

SCHEMBL7214633

CC(=O)Nc1ccc2c(c1)C(CCN1CC=C(c3c[nH]c4cc(Cl)ccc34)CC1)CC2.O=C(O)C(=O)O

nearest known ligand 0.55

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
SLC6A4 known ✓ P31645 7/20 0.43
OPRM1 known ✓ P35372 1/20 0.41
HTR1D P28221 3/20 0.52
MTNR1A P48039 1/20 0.44
DRD2 P14416 8/20 0.43
ADRA1D P25100 1/20 0.43
HTR1B P28222 1/20 0.43
ADRA1A P35348 1/20 0.43
ADRA1B P35368 1/20 0.43
HTR1A P08908 6/20 0.42
HTR7 P34969 6/20 0.42
HTR6 P50406 6/20 0.42
OPRK1 P41145 1/20 0.41
LMNA P02545 1/20 0.40
MAPT P10636 1/20 0.40

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
SCHEMBL7219879 0.98 HTR1D (0.54) HTR1DMTNR1ADRD2SLC6A4ADRA1D
Oxalic Acid SCHEMBL7220017 0.96 HTR1D (0.49) HTR1DMTNR1ADRD2SLC6A4HTR1A
Oxalic Acid SCHEMBL7219944 0.95 HTR1D (0.49) HTR1DMTNR1ADRD2SLC6A4HTR1A
SCHEMBL7213738 0.93 HTR1D (0.51) HTR1DMTNR1ADRD2SLC6A4HTR1A
SCHEMBL7216019 0.93 HTR1D (0.51) HTR1DMTNR1ADRD2SLC6A4HTR1A
SCHEMBL6796026 0.90 HTR1D (0.48) HTR1DMTNR1ADRD2SLC6A4HTR1A
SCHEMBL6811593 0.85 HTR1D (0.53) HTR1DDRD2SLC6A4ADRA1DHTR1B
SCHEMBL7219902 0.84 HTR1D (0.52) HTR1DDRD2SLC6A4ADRA1DHTR1B
SCHEMBL6796662 0.84 OPRM1 (0.50) DRD2SLC6A4HTR1AHTR7HTR6
Oxalic Acid SCHEMBL7572885 0.83 HTR1D (0.53) HTR1DDRD2SLC6A4ADRA1DHTR1B

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
US-6552044-B2 Dopamine receptors H. LUNDBECK A/S (DK) 2003-04-22 US disclosed
EP-0946542-B1 INDANE OR DIHYDROINDOLE DERIVATIVES LUNDBECK & CO AS H (DK) 2002-10-09 EP disclosed
US-20010021777-A1 Indane or dihydroindole derivatives H. LUNDBECK A/S (DK) 2001-09-13 US disclosed
US-20010020095-A1 Indane or dihydroindole derivatives H. LUNDBECK A/S (DK) 2001-09-06 US disclosed
US-6262087-B1 HAVE HIGH AFFINITY FOR D4 RECEPTORS; USEFUL IN THE TREATMENT OF CERTAIN PSYCHIATRIC AND NEUROLOGIC DISORDERS, INCLUDING PSYCHOSIS, DEPRESSION AND ANXIETY. H. LUNDBECK A/S (DK) 2001-07-17 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-20010020095-A1 Indane or dihydroindole derivatives HTR4, GPR4, GPR174 SLC6A4 40/4885OPRM1 34/4885HTR1D 4/4885
US-20010021777-A1 Indane or dihydroindole derivatives HTR4, GPR4, GPR174 SLC6A4 40/4885OPRM1 34/4885HTR1D 4/4885

“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.