Oxalic Acid

Oxalic Acid

SCHEMBL7320960

Clc1ccc(OCCC2CCN(CC=Cc3ccccc3)CC2)cc1Cl.O=C(O)C(=O)O

nearest known ligand 0.53

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 13)

geneUniProtsupporting neighboursconfidence
SLC6A4 known ✓ P31645 1/20 0.49
S1PR1 P21453 1/20 0.51
HRH3 Q9Y5N1 1/20 0.50
KDM4E B2RXH2 4/20 0.49
ALDH1A1 P00352 2/20 0.49
SMN1; SMN2 Q16637 2/20 0.49
SLC6A3 Q01959 1/20 0.49
POLB P06746 1/20 0.49
LMNA P02545 3/20 0.48
MCHR1 Q99705 3/20 0.46
MEN1 O00255 3/20 0.46
KMT2A Q03164 3/20 0.46
HCRTR1 O43613 1/20 0.46

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 SCHEMBL7320957 1.00 S1PR1 (0.51) S1PR1HRH3KDM4EALDH1A1SMN1; SMN2
SCHEMBL7325843 0.95 SLC6A4 (0.53) S1PR1HRH3KDM4ESLC6A4SLC6A3
SCHEMBL7325847 0.95 SLC6A4 (0.53) S1PR1HRH3KDM4ESLC6A4SLC6A3
Oxalic Acid SCHEMBL7327867 0.85 SLC6A4 (0.65) S1PR1HRH3KDM4ESMN1; SMN2SLC6A4
Oxalic Acid SCHEMBL7327873 0.85 SLC6A4 (0.65) S1PR1HRH3KDM4ESMN1; SMN2SLC6A4
Oxalic Acid SCHEMBL7245307 0.82 MCHR1 (0.49) S1PR1HRH3KDM4EALDH1A1SMN1; SMN2
Oxalic Acid SCHEMBL7245310 0.82 MCHR1 (0.49) S1PR1HRH3KDM4EALDH1A1SMN1; SMN2
Oxalic Acid SCHEMBL7243351 0.82 HCRTR1 (0.55) S1PR1HRH3KDM4EALDH1A1SMN1; SMN2
Oxalic Acid SCHEMBL7243355 0.82 HCRTR1 (0.55) S1PR1HRH3KDM4EALDH1A1SMN1; SMN2
Oxalic Acid SCHEMBL9527661 0.82 ALDH1A1 (0.48) HRH3KDM4EALDH1A1SMN1; SMN2POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0542846-A1 N-HYDROCARBYL-4-SUBSTITUTED PIPERIDINES, THEIR PREPARATION AND USE AS CALCIUM BLOCKING AGENTS SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1993-05-26 EP disclosed
WO-1992002502-A1 N-HYDROCARBYL-4-SUBSTITUTED PIPERIDINES, THEIR PREPARATION AND USE AS CALCIUM BLOCKING AGENTS SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1992-02-20 WO disclosed