Oxalic Acid

Oxalic Acid

SCHEMBL7437494

CC(C)C(=O)Nc1ccc(SCCCN(C)CCc2ccccc2)cc1.O.O=C(O)C(=O)O

nearest known ligand 0.46

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
KMT2A Q03164 5/20 0.44
MEN1 O00255 4/20 0.44
RAB9A P51151 3/20 0.42
NPC1 O15118 2/20 0.42
ALDH1A1 P00352 4/20 0.42
MAPT P10636 1/20 0.42
RXFP1 Q9HBX9 1/20 0.42
ADRB2 P07550 1/20 0.41
LTA4H P09960 1/20 0.41
FDPS P14324 1/20 0.41
HPGD P15428 1/20 0.41
HTT P42858 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
SIGMAR1 Q99720 3/20 0.40
CYP2C9 P11712 2/20 0.40
CYP2C19 P33261 2/20 0.40
CYP2D6 P10635 1/20 0.40
NPY5R Q15761 1/20 0.40
TMEM97 Q5BJF2 1/20 0.40

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
SCHEMBL7441271 0.97 KMT2A (0.47) KMT2AMEN1RAB9ANPC1ALDH1A1
Hydrochloric Acid SCHEMBL7425639 0.85 NPC1 (0.57) KMT2AMEN1RAB9ANPC1ALDH1A1
SCHEMBL7441248 0.85 NPC1 (0.59) KMT2AMEN1RAB9ANPC1ALDH1A1
SCHEMBL7441263 0.83 LTA4H (0.48) KMT2AMEN1RAB9ANPC1ALDH1A1
Oxalic Acid SCHEMBL7431284 0.81 ALDH1A1 (0.49) RAB9ANPC1ALDH1A1MAPTSMN1; SMN2
SCHEMBL7442665 0.78 ALDH1A1 (0.51) RAB9ANPC1ALDH1A1MAPTSMN1; SMN2
SCHEMBL7440692 0.76 SIGMAR1 (0.62) FDPSSIGMAR1CYP2C9CYP2C19CYP2D6
Oxalic Acid SCHEMBL7431270 0.76 SIGMAR1 (0.52) KMT2AMEN1ALDH1A1MAPTFDPS
Oxalic Acid SCHEMBL7445453 0.76 SIGMAR1 (0.52) KMT2AMEN1ALDH1A1MAPTFDPS
Maleic Acid SCHEMBL7430214 0.75 FDPS (0.52) KMT2AMEN1RAB9AALDH1A1FDPS

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0559569-A1 Central nervous system antiischemic agents Bristol-Myers Squibb Company (US) 1993-09-08 EP disclosed