Oxalic Acid

Oxalic Acid

SCHEMBL4769280

CCN1CCN(c2nc(Sc3ccccn3)cc3ccccc23)CC1.O=C(O)C(=O)O

nearest known ligand 0.50

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
SMN1; SMN2 Q16637 5/20 0.50
KMT2A Q03164 4/20 0.50
CYP1A2 P05177 2/20 0.50
CYP2C19 P33261 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.50
LMNA P02545 1/20 0.46
MAPT P10636 1/20 0.46
RAD52 P43351 1/20 0.44
TSHR P16473 1/20 0.41
ALDH1A1 P00352 3/20 0.40
CYP2D6 P10635 2/20 0.40
MEN1 O00255 2/20 0.40
KDM4E B2RXH2 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40
GBA1 P04062 1/20 0.40
POLB P06746 1/20 0.40
HPGD P15428 1/20 0.40
HTT P42858 1/20 0.40
PAX8 Q06710 1/20 0.40
HIF1A Q16665 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
SCHEMBL4770851 0.94 SMN1; SMN2 (0.53) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
Oxalic Acid SCHEMBL4767453 0.87 SMN1; SMN2 (0.47) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
SCHEMBL4771301 0.81 SMN1; SMN2 (0.51) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
Oxalic Acid SCHEMBL4764739 0.80 SMN1; SMN2 (0.50) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
SCHEMBL4763604 0.74 SMN1; SMN2 (0.65) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
Oxalic Acid SCHEMBL4763598 0.74 HRH4 (0.42) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
Hydrochloric Acid SCHEMBL4763437 0.74 SMN1; SMN2 (0.64) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
SCHEMBL4769898 0.74 KMT2A (0.55) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
SCHEMBL4770409 0.73 SMN1; SMN2 (0.54) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
SCHEMBL4770401 0.73 SMN1; SMN2 (0.54) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1020445-B1 FUSED PYRIDINE DERIVATIVES EISAI R&D MAN CO LTD (JP) 2008-08-13 EP disclosed
US-6875761-B2 Certain 1,3-disubstituted isoquinoline derivatives EISAI CO., LTD. (JP) 2005-04-05 US disclosed
US-20040204421-A1 Certain 1,3-disubstituted isoquinoline derivatives EISAI CO., LTD. 2004-10-14 US disclosed
US-6790844-B2 MUSCLE RELAXANTS; ANTISEROTONINE AGENT EISAI CO., LTD (JP) 2004-09-14 US disclosed
US-20020013460-A1 Condensed pyridine compound EISAI CO., LTD 2002-01-31 US disclosed
US-6340759-B1 ANTISPASMODIC AGENTS EISAI CO., LTD. (JP) 2002-01-22 US disclosed
EP-1020445-A1 FUSED PYRIDINE DERIVATIVES Eisai Co., Ltd. (JP) 2000-07-19 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20020013460-A1 Condensed pyridine compound MUSK, HTR1A, PAX3 SMN1; SMN2 27/4885KMT2A 1240/4885CYP1A2 2126/4885
US-20040204421-A1 Certain 1,3-disubstituted isoquinoline derivatives MUSK, HTR1A, RYR1 SMN1; SMN2 37/4885KMT2A 1300/4885CYP1A2 1489/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.