Oxalic Acid

Oxalic Acid

SCHEMBL7201736

O.O.O.O=C(O)C(=O)O.[Cr].[KH]

nearest known ligand 0.40

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 14)

geneUniProtsupporting neighboursconfidence
CA1 P00915 1/20 0.40
CA2 P00918 1/20 0.40
CA9 Q16790 1/20 0.40
LDHA P00338 1/20 0.39
LDHB P07195 1/20 0.39
ALDH1A1 P00352 1/20 0.36
TP53 P04637 1/20 0.36
TSHR P16473 1/20 0.36
KDM5B Q9UGL1 1/20 0.33
ACHE P22303 1/20 0.33
FFAR3 O14843 1/20 0.33
LCK P06239 1/20 0.33
FYN P06241 1/20 0.33
OR51E2 Q9H255 1/20 0.31

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 SCHEMBL786271 0.94
Oxalic Acid SCHEMBL785518 0.94 CA1 (0.44) CA1CA2CA9LDHALDHB
Oxalic Acid SCHEMBL7064622 0.94 CA1 (0.44) CA1CA2CA9LDHALDHB
Oxalic Acid SCHEMBL3416798 0.94
Oxalic Acid SCHEMBL28387559 0.94 CA1 (0.44) CA1CA2CA9LDHALDHB
Oxalic Acid SCHEMBL28604188 0.94
Oxalic Acid SCHEMBL2722477 0.94
Oxalic Acid SCHEMBL236657 0.94
Oxalic Acid SCHEMBL14694752 0.89 CA1 (0.40) CA1CA2CA9LDHALDHB
Oxalic Acid SCHEMBL3837051 0.89

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113603488-A Production method of novel environment-friendly anode carbon block 河南中孚铝业有限公司 2021-11-05 CN disclosed
CN-109400163-B Carbon anode and preparation method and application thereof 山东圣泉新材料股份有限公司 2020-02-04 CN disclosed
US-6589751-B2 Antibody specific for homocystamide adducts, such as those formed by dehydrating homocysteine to homocysteine thiolactone and reaction this with a carrier such as low density lipoprotein (LDL) to form homocystamide-LDL adduct MCW RESEARCH FOUNDATION 2003-07-08 US disclosed
US-20020015968-A1 IMMUNOLOGICAL DETECTION OF THE HOMOCYSTAMIDE ADDUCT AND A THIOLACTONE IMMUNOASSAY FOR ENDOGENEOUS HOMOCYSTEINE NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2002-02-07 US disclosed