Mibampator

Mibampator

SCHEMBL6660037

CC(C)S(=O)(=O)NC[C@@H](C)c1ccc(-c2ccc(CCNS(C)(=O)=O)cc2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GRIA1GRIA2GRIA3GRIA4

The experimentally established mechanism targets of Mibampator. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
GRIA4 known ✓ P48058 17/20 1.00
GRIA2 known ✓ P42262 3/20 0.59
GRIA1 known ✓ P42261 1/20 0.59
GRIA3 known ✓ P42263 1/20 0.59
POLB P06746 1/20 0.39

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
Mibampator SCHEMBL3045499 1.00 GRIA4 (1.00) GRIA4GRIA2GRIA1GRIA3POLB
Mibampator SCHEMBL3074747 1.00 GRIA4 (1.00) GRIA4GRIA2GRIA1GRIA3POLB
SCHEMBL6563305 0.96 GRIA4 (0.92) GRIA4GRIA2GRIA1GRIA3POLB
SCHEMBL5877913 0.93 GRIA4 (0.87) GRIA4GRIA2GRIA1GRIA3
SCHEMBL6563303 0.89 GRIA4 (0.80) GRIA4GRIA2GRIA1GRIA3
SCHEMBL5878077 0.88 GRIA4 (0.79) GRIA4GRIA2GRIA1GRIA3
SCHEMBL6565213 0.88 GRIA4 (0.79) GRIA4GRIA2GRIA1GRIA3POLB
SCHEMBL719605 0.86 GRIA4 (0.76) GRIA4GRIA2GRIA1GRIA3
SCHEMBL719606 0.86 GRIA4 (0.76) GRIA4GRIA2GRIA1GRIA3
SCHEMBL5878035 0.85 GRIA4 (0.74) GRIA4GRIA2GRIA1GRIA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040235957-A1 Use of sulfonamide derivatives as pharmaceuticals compounds BLEAKMAN DAVID (US) 2004-11-25 US disclosed
EP-1438036-A2 USE OF SULFONAMIDE DERIVATIVES AS PHARMACEUTICALS COMPOUNDS ELI LILLY AND COMPANY (US) 2004-07-21 EP disclosed
WO-2003032974-A2 USE OF SULFONAMIDE DERIVATIVES AS PHARMACEUTICALS COMPOUNDS ELI LILLY AND COMPANY (US) 2003-04-24 WO 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-20040235957-A1 Use of sulfonamide derivatives as pharmaceuticals compounds GABRE, SCN2A, SCN1A GRIA4 212/4885GRIA2 176/4885GRIA1 324/4885

“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.