Oxalic Acid

Oxalic Acid

SCHEMBL5863102

CN(C)CCCCNC(=O)c1cccc(-c2ccccc2CSCCOc2ccccc2)c1.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
KDR P35968 1/20 0.44
FYN P06241 3/20 0.43
KDM4E B2RXH2 4/20 0.42
ALDH1A1 P00352 4/20 0.42
SMN1; SMN2 Q16637 3/20 0.42
KMT2A Q03164 3/20 0.42
MAPT P10636 1/20 0.42
SIGMAR1 Q99720 1/20 0.41
CD274 Q9NZQ7 1/20 0.41
MEN1 O00255 1/20 0.41
POLB P06746 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
HDAC3 O15379 1/20 0.41
HDAC4 P56524 1/20 0.41
HDAC1 Q13547 1/20 0.41
HDAC7 Q8WUI4 1/20 0.41
HDAC2 Q92769 1/20 0.41
HDAC10 Q969S8 1/20 0.41
HDAC11 Q96DB2 1/20 0.41
HDAC8 Q9BY41 1/20 0.41

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 SCHEMBL5863262 0.97 FYN (0.46) KDRFYNKDM4EALDH1A1SMN1; SMN2
Oxalic Acid SCHEMBL5863143 0.94 FYN (0.46) KDRFYNKDM4EALDH1A1SMN1; SMN2
SCHEMBL6252851 0.89 KDM4E (0.43) KDRKDM4EALDH1A1SMN1; SMN2KMT2A
SCHEMBL5863072 0.89 NPC1 (0.45) FYNKDM4EALDH1A1SMN1; SMN2KMT2A
Oxalic Acid SCHEMBL5863223 0.87 KDR (0.47) KDRFYNKDM4EALDH1A1SMN1; SMN2
SCHEMBL5863100 0.86 FYN (0.46) FYNKDM4EALDH1A1SMN1; SMN2KMT2A
Oxalic Acid SCHEMBL5863234 0.85 SIGMAR1 (0.49) KDRFYNKDM4EALDH1A1SMN1; SMN2
Oxalic Acid SCHEMBL5863178 0.85 KDM4E (0.43) KDM4EALDH1A1SMN1; SMN2KMT2AMAPT
Oxalic Acid SCHEMBL5863207 0.84 FYN (0.49) KDRFYNKDM4EALDH1A1SMN1; SMN2
SCHEMBL5863289 0.82 FYN (0.50) KDRFYNSMN1; SMN2KMT2AMAPT

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
US-7132456-B2 MCH receptor antagonists ELI LILLY AND COMPANY (US) 2006-11-07 US disclosed
US-20060052449-A1 Novel mch receptor antagonists ELI LILLY AND COMPANY 2006-03-09 US 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 (1 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-20060052449-A1 Novel mch receptor antagonists MCHR1, MCHR2, MC1R KDR 2060/4885FYN 3249/4885KDM4E 2532/4885

“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.