Oxalic Acid

Oxalic Acid

SCHEMBL7635892

O=C(O)C(=O)O.c1ccc([PH](c2ccccc2)(c2ccccc2)C2CCCC2)cc1

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 17)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 1/20 0.40
KDM4E B2RXH2 5/20 0.38
ALDH1A1 P00352 5/20 0.38
SMN1; SMN2 Q16637 3/20 0.38
RAB9A P51151 3/20 0.38
POLB P06746 2/20 0.38
NPC1 O15118 1/20 0.38
KEAP1 Q14145 1/20 0.38
NFE2L2 Q16236 1/20 0.38
HPGD P15428 1/20 0.38
MEN1 O00255 1/20 0.37
KMT2A Q03164 1/20 0.37
MCL1 Q07820 1/20 0.37
EPHX2 P34913 3/20 0.36
LMNA P02545 1/20 0.36
EPHX1 P07099 1/20 0.36
HDAC4 P56524 1/20 0.36

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 SCHEMBL7632154 0.98 TAAR1 (0.42) TAAR1KDM4EALDH1A1SMN1; SMN2RAB9A
Oxalic Acid SCHEMBL7626635 0.98 TAAR1 (0.42) TAAR1KDM4EALDH1A1SMN1; SMN2RAB9A
Oxalic Acid SCHEMBL7630670 0.98 TAAR1 (0.42) TAAR1KDM4EALDH1A1SMN1; SMN2RAB9A
Oxalic Acid SCHEMBL7626868 0.96 LMNA (0.37) TAAR1KDM4EALDH1A1SMN1; SMN2RAB9A
Oxalic Acid SCHEMBL7627145 0.92 TAAR1 (0.35) TAAR1KDM4EALDH1A1SMN1; SMN2RAB9A
SCHEMBL8299920 0.89 ALDH1A1 (0.34) ALDH1A1POLBKEAP1NFE2L2HPGD
SCHEMBL23563764 0.87 IDO1 (0.34) KDM4EALDH1A1SMN1; SMN2RAB9AHPGD
SCHEMBL2445014 0.87 IDO1 (0.34) KDM4EALDH1A1SMN1; SMN2RAB9AHPGD
Bromide SCHEMBL5723575 0.87 GAA (0.33) ALDH1A1POLBKEAP1NFE2L2HPGD
SCHEMBL3674285 0.87 IDO1 (0.34) KDM4EALDH1A1SMN1; SMN2RAB9AHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0329021-B1 Preparation of advanced epoxy resins and dihydric phenols in the presence of phosphonium compounds DOW CHEMICAL CO (US) 1994-01-26 EP claimed
EP-0329021-A2 Preparation of advanced epoxy resins and dihydric phenols in the presence of phosphonium compounds THE DOW CHEMICAL COMPANY (US) 1989-08-23 EP claimed
US-4808692-A Preparation of advanced epoxy resins from epoxy resins and dihydric phenols in the presence of phosphonium compounds THE DOW CHEMICAL COMPANY (US) 1989-02-28 US claimed
EP-0780452-B1 Aqueous paint TOYO SEIKAN KAISHA LTD (JP) 2002-03-06 EP disclosed
US-5763507-A EPOXY ACRYLATE RESIN TOYO SEIKAN KAISHA, LTD. (JP) 1998-06-09 US disclosed
EP-0780452-A2 Aqueous paint TOYO SEIKAN KAISHA LIMITED (JP) 1997-06-25 EP disclosed
EP-0414160-B1 Process for preparing advanced epoxy resins DOW CHEMICAL CO (US) 1996-09-11 EP disclosed
US-5310854-A Solvent, coatings for beverage cans THE DOW CHEMICAL COMPANY (US) 1994-05-10 US disclosed
EP-0329021-B1 Preparation of advanced epoxy resins and dihydric phenols in the presence of phosphonium compounds DOW CHEMICAL CO (US) 1994-01-26 EP disclosed
EP-0414160-A2 Process for preparing advanced epoxy resins THE DOW CHEMICAL COMPANY (US) 1991-02-27 EP disclosed
EP-0329021-A2 Preparation of advanced epoxy resins and dihydric phenols in the presence of phosphonium compounds THE DOW CHEMICAL COMPANY (US) 1989-08-23 EP disclosed
US-4808692-A Preparation of advanced epoxy resins from epoxy resins and dihydric phenols in the presence of phosphonium compounds THE DOW CHEMICAL COMPANY (US) 1989-02-28 US disclosed