Oxalic Acid

Oxalic Acid

SCHEMBL3202744

O=C([O-])C(=O)[O-].[F-].[K+].[K+].[Na+]

nearest known ligand 0.89

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
CA4 P22748 5/20 0.89
FAHD1 Q6P587 1/20 0.89
MEN1 O00255 1/20 0.54
LDHA P00338 1/20 0.54
BLM P54132 1/20 0.54
KMT2A Q03164 1/20 0.54
CA1 P00915 2/20 0.50
LMNA P02545 2/20 0.40
CASP1 P29466 1/20 0.40
FFAR3 O14843 1/20 0.33
HDAC3 O15379 1/20 0.33
HDAC1 Q13547 1/20 0.33
HDAC2 Q92769 1/20 0.33
HDAC8 Q9BY41 1/20 0.33
CA2 P00918 1/20 0.32

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 SCHEMBL11574957 1.00 CA4 (0.89) CA4FAHD1MEN1LDHABLM
Oxalic Acid SCHEMBL1330792 0.94
Oxalic Acid SCHEMBL28222674 0.94 CA4 (1.00) CA4FAHD1MEN1LDHABLM
Oxalic Acid SCHEMBL7776891 0.94
Oxalic Acid SCHEMBL40019 0.94
Oxalic Acid SCHEMBL16029775 0.89
Oxalic Acid SCHEMBL17511334 0.89 CA4 (0.70) CA4FAHD1MEN1LDHABLM
Oxalic Acid SCHEMBL7530049 0.89 CA4 (0.89) CA4FAHD1MEN1LDHABLM
Oxalic Acid SCHEMBL5909741 0.89 CA4 (0.89) CA4FAHD1MEN1LDHABLM
Oxalic Acid SCHEMBL694299 0.89 CA4 (0.89) CA4FAHD1MEN1LDHABLM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100029710-A1 COMPOUNDS HAVING BOTH ANGIOTENSIN II RECEPTOR ANTAGONISM AND PPARy ACTIVATING ACTIVITIES PFIZER PRODUCTS INC. (US) 2010-02-04 US disclosed
US-20080090829-A1 SUBSTITUTED HETEROARYL- AND PHENYLSULFAMOYL COMPOUNDS PFIZER INC. 2008-04-17 US disclosed
US-20070191429-A1 PPAR ACTIVATORS PFIZER INC. (US) 2007-08-16 US disclosed
EP-1633709-A1 ANTI-DIABETIC AGENTS Pfizer Products Inc. (US) 2006-03-15 EP disclosed
EP-1620427-A1 CARBOXAMIDE DERIVATIVES AS ANTI-DIABETIC AGENTS Pfizer Products Inc. (US) 2006-02-01 EP disclosed
US-6992092-B2 substituted N-(indole-2-carbonyl)amides; antiischemic, anticholesterol, hypoglycemic, hypotensive agents; 5-chloro-1H-indole-2-carboxylic acid-[5-(1,2-dihydroxy-1-methyl-ethyl)-3-ethoxy-pyridin-2-yl]-amide PFIZER INC. (US) 2006-01-31 US disclosed
US-6992101-B2 N-(indole-2-carbonyl) and H-thieno[2,3-b]pyrrole-5-carboxamide anti-diabetic agents PFIZER, INC. (US) 2006-01-31 US disclosed
EP-1562899-A2 N-(INDOLE-2-CARBONYL)AMIDES AS ANTI-DIABETIC AGENTS Pfizer Products Inc. (US) 2005-08-17 EP disclosed
US-20040229916-A1 Anti-diabetic agents PFIZER INC 2004-11-18 US disclosed
WO-2004096768-A1 ANTI-DIABETIC AGENTS PFIZER PRODUCTS INC. (US) 2004-11-11 WO disclosed
US-20040220229-A1 insulin resistance; central nervous system disorders; vision defects; anticholesterol agents;antilipemic agents; antiischemic agents PFIZER INC 2004-11-04 US disclosed
WO-2004092158-A1 CARBOXAMIDE DERIVATIVES AS ANTI-DIABETIC AGENTS PFIZER PRODUCTS INC. (US) 2004-10-28 WO disclosed
US-20040157907-A1 Anti-diabetic agents PFIZER INC 2004-08-12 US disclosed
WO-2004041780-A2 N-(INDOLE-2-CARBONYL) AMIDES AS ANTI-DIABETIC AGENTS PFIZER PRODUCTS INC. (US) 2004-05-21 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 (6 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-20070191429-A1 PPAR ACTIVATORS PPARA, PPARG, PPARD CA4 4857/4885FAHD1 1745/4885MEN1 4872/4885
US-20040157907-A1 Anti-diabetic agents GPR119, INSR, IRS1 CA4 2580/4885FAHD1 2194/4885MEN1 2918/4885
US-20040229916-A1 Anti-diabetic agents GPR119, SLC5A1, GLP1R CA4 1382/4885FAHD1 3430/4885MEN1 3379/4885
US-20040220229-A1 insulin resistance; central nervous system disorders; vision defects; anticholesterol agents;antilipemic agents; antiischemic agents IRS1, INSR, GPR119 CA4 3412/4885FAHD1 926/4885MEN1 1810/4885
US-20100029710-A1 COMPOUNDS HAVING BOTH ANGIOTENSIN II RECEPTOR ANTAGONISM AND PPARy ACTIVATING ACTIVITIES AGTR2, AGTR1, AGT CA4 4142/4885FAHD1 3145/4885MEN1 4523/4885
US-20080090829-A1 SUBSTITUTED HETEROARYL- AND PHENYLSULFAMOYL COMPOUNDS PPARA, PPARG, PPARD CA4 4869/4885FAHD1 1548/4885MEN1 4855/4885

“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.