Oxalic Acid

Oxalic Acid

SCHEMBL10371258

CN1CCC(Oc2c(C#N)ccc3ccccc23)C1.O=C(O)C(=O)O

nearest known ligand 0.44

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
▸ CHRM3 P20309 4/20 0.44
▸ CHRM4 P08173 3/20 0.44
▸ CHRM5 P08912 3/20 0.44
▸ CHRM1 P11229 3/20 0.44
▸ KDM4E B2RXH2 3/20 0.40
▸ NPY1R P25929 1/20 0.40
▸ NPY2R P49146 1/20 0.40
▸ SMN1; SMN2 Q16637 1/20 0.40
▸ CYP2D6 P10635 1/20 0.39
▸ HTT P42858 1/20 0.39
▸ ALDH1A1 P00352 3/20 0.39
▸ CYP1A2 P05177 1/20 0.39
▸ KDM2B Q8NHM5 2/20 0.39
▸ MEN1 O00255 3/20 0.38
▸ KMT2A Q03164 3/20 0.38
▸ PKM P14618 1/20 0.38
▸ NPSR1 Q6W5P4 1/20 0.38
▸ CHRM2 P08172 1/20 0.38
▸ SSTR4 P31391 1/20 0.38
▸ NOS3 P29474 1/20 0.38

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
SCHEMBL10371260 0.93 NOS3 (0.41) CHRM3CHRM4CHRM5CHRM1KDM4E
SCHEMBL10370276 0.77 CHRM4 (0.44) CHRM3CHRM4CHRM5CHRM1ALDH1A1
Oxalic Acid SCHEMBL10672874 0.68 KDM4E (0.50) CHRM3CHRM4CHRM5CHRM1KDM4E
Oxalic Acid SCHEMBL10372028 0.68 KDM4E (0.50) CHRM3CHRM4CHRM5CHRM1KDM4E
SCHEMBL3291578 0.67 PDE10A (0.49) CHRM3CHRM4CHRM5CHRM1CYP2D6
SCHEMBL24476762 0.66 IMPDH2 (0.53) KDM4ESMN1; SMN2CYP2D6ALDH1A1SLC22A12
SCHEMBL31198254 0.66 CHRM3 (0.48) CHRM3CHRM4CHRM5CHRM1CYP2D6
SCHEMBL2422193 0.66 CA1 (0.48) KDM4ECYP2D6ALDH1A1SLC22A12
SCHEMBL10370253 0.65 ALDH1A1 (0.52) CHRM3CHRM4CHRM5CHRM1KDM4E
SCHEMBL18348315 0.65 HTR2C (0.52) —

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-0107930-B1 FUSED AROMATIC OXAZEPINONES AND SULPHUR ANALOGUES THEREOF AND THEIR PREPARATION AND USE IN COUNTERACTING HISTAMINE A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation) (US) 1990-11-28 — — EP disclosed
US-4812565-A ANTIHISTAMINE INTERMEDIATES A. H. ROBINS COMPANY, INCORPORATED (US) 1989-03-14 — — US disclosed
US-4810795-A ANTIHISTAMINES A. H. ROBINS COMPANY, INCORPORATED (US) 1989-03-07 — — US disclosed
US-4727152-A Intermediates useful in the preparation of fused aromatic oxazepinones, thiazepinones, diazepinones and sulfur analogs thereof A. H. ROBINS COMPANY, INC. (US) 1988-02-23 — — US disclosed
US-4705853-A ANTIHISTAMINES A. H. ROBINS COMPANY, INC. (US) 1987-11-10 — — US disclosed
US-4642343-A ANTIHISTAMINES A. H. ROBINS COMPANY, INCORPORATED (US) 1987-02-10 — — US disclosed
US-4604388-A Fused aromatic oxazepinones, thiazepinones, diazepinones and sulfur analogs thereof in a method of counteracting histamine A. H. ROBINS COMPANY, INCORPORATED (US) 1986-08-05 — — US disclosed
US-4592866-A Fused aromatic oxazepinones, thiazepinones, diazepinones and sulfur analogs thereof A. H. ROBINS COMPANY, INC. (US) 1986-06-03 — — US disclosed
EP-0107930-A2 Fused aromatic oxazepinones and sulphur analogues thereof and their preparation and use in counteracting histamine A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation) (US) 1984-05-09 — — EP disclosed
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