Oxalic Acid

Oxalic Acid

SCHEMBL3548154

Clc1ccc(Sc2ccccc2C2CCNCC2)cc1.O=C(O)C(=O)O

nearest known ligand 0.47

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
SLC6A4 known ✓ P31645 2/20 0.39
HTR1A P08908 4/20 0.47
CYP1A2 P05177 2/20 0.47
CYP3A4 P08684 2/20 0.47
CYP2D6 P10635 2/20 0.47
CYP2C9 P11712 2/20 0.47
HTR3A P46098 2/20 0.47
ALDH1A1 P00352 2/20 0.41
KDM4E B2RXH2 2/20 0.41
LMNA P02545 3/20 0.40
BLM P54132 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40
NOD2 Q9HC29 1/20 0.40
HTR2C P28335 3/20 0.40
HTR6 P50406 1/20 0.40
RHEB Q15382 1/20 0.40
SLC6A9 P48067 1/20 0.39
SLC6A2 P23975 2/20 0.39
SLC6A3 Q01959 2/20 0.39
HDAC1 Q13547 1/20 0.39

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
SCHEMBL3541318 0.92 HTR1A (0.54) HTR1ACYP1A2CYP3A4CYP2D6CYP2C9
Oxalic Acid SCHEMBL3539024 0.84 HTR1A (0.49) HTR1AHTR3AKDM4EHTR2CSLC6A9
SCHEMBL3539172 0.83 HTR2C (0.51) HTR1AHTR3AHTR2CSLC6A2SLC6A4
Oxalic Acid SCHEMBL3547180 0.83 SLC6A2 (0.41) HTR1AALDH1A1KDM4ELMNAHTR6
Oxalic Acid SCHEMBL3544184 0.83 MAPK14 (0.41) HTR1AHTR3AALDH1A1KDM4ELMNA
Trifluoroacetic Acid SCHEMBL5742404 0.78 HTR1A (0.48) HTR1AHTR3AALDH1A1KDM4EHTR2C
Tedatioxetine SCHEMBL547653 0.78 HTR2C (0.54) HTR1ACYP1A2CYP3A4CYP2D6CYP2C9
SCHEMBL3542850 0.78 HTR2C (0.45) HTR1AALDH1A1KDM4ELMNANPSR1
SCHEMBL3544136 0.77 HTR2C (0.43) HTR1AHTR2CSLC6A2SLC6A4SLC6A3
Tedatioxetine SCHEMBL3930077 0.77 HTR2C (0.55) HTR1ACYP1A2CYP3A4CYP2D6CYP2C9

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-7732463-B2 4-(2-phenylsulfanyl-phenyl)-piperidine derivatives as serotonin reuptake inhibitors H. LUNDBECK A/S (DK) 2010-06-08 US disclosed
EP-1626720-B1 4-(2-PHENYLSULFANYL-PHENYL)-PIPERIDINE DERIVATIVES AS SEROTONIN REUPTAKE INHIBITORS LUNDBECK & CO AS H (DK) 2008-09-03 EP disclosed
US-20060100242-A1 such as 4-[2-(4-Chloro-phenylsulfanyl)-5-trifluoromethyl-phenyl]-piperidine, used as antidepressants and anxiolytic agents; treatment of panic and obsessive compulsive disorders H.LUNDBECK A/S (DK) 2006-05-11 US disclosed
EP-1626720-A1 4-(2-PHENYLSULFANYL-PHENYL)-PIPERIDINE DERIVATIVES AS SEROTONIN REUPTAKE INHIBITORS H. Lundbeck A/S (DK) 2006-02-22 EP disclosed
WO-2004087156-A1 4-(2-PHENYLSULFANYL-PHENYL)-PIPERIDINE DERIVATIVES AS SEROTONIN REUPTAKE INHIBITORS H. LUNDBECK A/S (DK) 2004-10-14 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-20060100242-A1 such as 4-[2-(4-Chloro-phenylsulfanyl)-5-trifluoromethyl-phenyl]-piperidine, used as antidepressants and anxiolytic agents; treatment of panic and obsessive compulsive disorders HTR4, HTR5A, TPH1 SLC6A4 14/4885HTR1A 11/4885CYP1A2 833/4885

“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.