Oxalic Acid

Oxalic Acid

SCHEMBL7632154

O=C(O)C(=O)O.c1ccc([PH](c2ccccc2)(c2ccccc2)C2CCCCCCC2)cc1

nearest known ligand 0.42

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 0.42
KDM4E B2RXH2 6/20 0.41
ALDH1A1 P00352 4/20 0.41
POLB P06746 2/20 0.41
HPGD P15428 1/20 0.41
MEN1 O00255 1/20 0.39
KMT2A Q03164 1/20 0.39
EPHX2 P34913 3/20 0.39
RAB9A P51151 3/20 0.39
SMN1; SMN2 Q16637 2/20 0.39
EPHX1 P07099 1/20 0.39
HDAC4 P56524 1/20 0.37
NPC1 O15118 1/20 0.37
KEAP1 Q14145 1/20 0.37
NFE2L2 Q16236 1/20 0.37
TSHR P16473 1/20 0.36
MCL1 Q07820 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 SCHEMBL7630670 1.00 TAAR1 (0.42) TAAR1KDM4EALDH1A1POLBHPGD
Oxalic Acid SCHEMBL7626635 1.00 TAAR1 (0.42) TAAR1KDM4EALDH1A1POLBHPGD
Oxalic Acid SCHEMBL7635892 0.98 TAAR1 (0.40) TAAR1KDM4EALDH1A1POLBHPGD
Oxalic Acid SCHEMBL7626868 0.94 LMNA (0.37) TAAR1KDM4EALDH1A1POLBHPGD
Oxalic Acid SCHEMBL7627145 0.90 TAAR1 (0.35) TAAR1KDM4EALDH1A1POLBHPGD
SCHEMBL23563764 0.90 IDO1 (0.34) KDM4EALDH1A1HPGDMEN1KMT2A
SCHEMBL3674285 0.90 IDO1 (0.34) KDM4EALDH1A1HPGDMEN1KMT2A
SCHEMBL2445014 0.90 IDO1 (0.34) KDM4EALDH1A1HPGDMEN1KMT2A
Bromide SCHEMBL5723432 0.88 IDO1 (0.33) KDM4EALDH1A1HPGDMEN1KMT2A
Hydrochloric Acid SCHEMBL27574177 0.88 IDO1 (0.36) KDM4EALDH1A1HPGDMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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