SCHEMBL7127030

SCHEMBL7127030

CC(C)(C)NC(=O)C(CCc1ccccc1)NS(=O)(=O)c1ccc(C(=O)NCCOCc2ccccc2)cc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PSMB8 P28062 8/20 0.51
PSMB5 P28074 7/20 0.51
PLAU P00749 1/20 0.47
HPN P05981 1/20 0.47
CA2 P00918 2/20 0.45
MMP2 P08253 2/20 0.44
MMP9 P14780 2/20 0.44
MMP1 P03956 1/20 0.44
MMP14 P50281 1/20 0.44
F2 P00734 2/20 0.44
TMPRSS6 Q8IU80 2/20 0.44
ITGB3 P05106 2/20 0.43
ITGA2B P08514 2/20 0.43
MEN1 O00255 1/20 0.43
CYP3A4 P08684 1/20 0.43
CYP2D6 P10635 1/20 0.43
KMT2A Q03164 1/20 0.43
ALDH1A1 P00352 1/20 0.42
MAPT P10636 1/20 0.42
MMP3 P08254 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
SCHEMBL7117861 0.86 PSMB8 (0.54) PSMB8PSMB5PLAUHPNMMP2
SCHEMBL7124501 0.84 PLAU (0.54) PSMB8PSMB5PLAUHPNMMP2
SCHEMBL7127817 0.81 MMP2 (0.53) PSMB8PSMB5PLAUHPNMMP2
SCHEMBL7124459 0.81 ALDH1A1 (0.57) PSMB8PSMB5PLAUHPNMMP2
SCHEMBL7127019 0.81 PLAU (0.60) PSMB8PSMB5PLAUHPNMMP2
SCHEMBL7118677 0.79 MMP2 (0.49) PSMB8PSMB5PLAUHPNMMP2
SCHEMBL7121669 0.79 ALDH1A1 (0.63) PLAUHPNMMP2MMP9MMP1
SCHEMBL7118405 0.76 MMP2 (0.50) PSMB8PSMB5PLAUHPNMMP2
SCHEMBL7125293 0.76 PLAU (0.59) PSMB8PLAUHPNMMP2MMP9
SCHEMBL7126168 0.71 MMP2 (0.49) PLAUHPNCA2MMP2MMP9

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-6583318-B2 Carrying out a four component condensation reaction between components consisting of a sulfonamide, an aldehyde or ketone, an isocyanide and a carboxylic acid, and one of such components being attached to a solid support ADVANCED SYNTECH, LLC 2003-06-24 US disclosed
US-20030013910-A1 Method for synthesis of alpha-sulfonamido amide, carboxylic acid and hydroxamic acid derivatives ADVANCED SYNTECH LLC 2003-01-16 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-20030013910-A1 Method for synthesis of alpha-sulfonamido amide, carboxylic acid and hydroxamic acid derivatives ASPH, COASY, HAAO PSMB8 2820/4885PSMB5 3386/4885PLAU 1115/4885

“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.