Oxalic Acid

Oxalic Acid

SCHEMBL5863295

CN(C)CCNC(=O)c1cccc(-c2ccc(CSCCOc3ccccc3)cc2)c1.O=C(O)C(=O)O

nearest known ligand 0.47

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
FYN P06241 2/20 0.47
PRKD3 O94806 1/20 0.46
PRKD1 Q15139 1/20 0.46
PRKD2 Q9BZL6 1/20 0.46
LMNA P02545 2/20 0.45
CAMK2D Q13557 1/20 0.45
KIFC1 Q9BW19 1/20 0.44
KDR P35968 1/20 0.44
SMN1; SMN2 Q16637 3/20 0.44
ALOX5 P09917 1/20 0.44
MAP4K4 O95819 1/20 0.44
RAD52 P43351 2/20 0.44
MAPT P10636 1/20 0.43
NPC1 O15118 1/20 0.43
HPGD P15428 1/20 0.43
RAB9A P51151 1/20 0.43
ROCK2 O75116 2/20 0.42
ROCK1 Q13464 2/20 0.42
ABL1 P00519 1/20 0.42
CYP3A4 P08684 1/20 0.42

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
SCHEMBL5863110 0.98 FYN (0.48) FYNPRKD3PRKD1PRKD2LMNA
Oxalic Acid SCHEMBL5863207 0.95 FYN (0.49) FYNLMNAKDRSMN1; SMN2MAPT
Oxalic Acid SCHEMBL5863223 0.94 KDR (0.47) FYNLMNAKDRSMN1; SMN2MAPT
SCHEMBL5863289 0.93 FYN (0.50) FYNLMNAKDRSMN1; SMN2MAPT
Oxalic Acid SCHEMBL5863159 0.92 ALDH1A1 (0.51) FYNLMNASMN1; SMN2ALOX5RAD52
SCHEMBL5863380 0.89 ROCK2 (0.50) FYNLMNASMN1; SMN2ALOX5RAD52
Oxalic Acid SCHEMBL5863234 0.88 SIGMAR1 (0.49) FYNLMNAKDRSMN1; SMN2MAPT
Oxalic Acid SCHEMBL5863143 0.86 FYN (0.46) FYNPRKD3PRKD1PRKD2CAMK2D
Oxalic Acid SCHEMBL5863123 0.86 CYP3A4 (0.51) FYNSMN1; SMN2NPC1RAB9AROCK2
Oxalic Acid SCHEMBL5863058 0.85 ROCK2 (0.48) FYNLMNASMN1; SMN2NPC1HPGD

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 FYN 3249/4885PRKD3 1637/4885PRKD1 2795/4885

“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.