SCHEMBL3152227

SCHEMBL3152227

O=C(O)C(COS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)c1ccccc1

nearest known ligand 0.42

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ CA1 P00915 8/20 0.42
▸ CA2 P00918 8/20 0.42
▸ MMP1 P03956 5/20 0.40
▸ MMP2 P08253 5/20 0.40
▸ MMP9 P14780 5/20 0.40
▸ MMP8 P22894 5/20 0.40
▸ MMP13 P45452 5/20 0.40
▸ CYP2C19 P33261 1/20 0.38
▸ SRC P12931 1/20 0.34
▸ POLB P06746 1/20 0.33

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
SCHEMBL1345635 0.86 MAPT (0.40) CA1CA2MMP1MMP2MMP9
SCHEMBL2261974 0.72 CA2 (0.68) CA1CA2MMP1MMP2MMP9
SCHEMBL5916339 0.72 CA1 (0.39) CA1CA2MMP1MMP2MMP9
SCHEMBL28860429 0.70 CA2 (0.44) CA1CA2MMP1MMP2MMP9
SCHEMBL30096771 0.69 CA1 (0.39) CA1CA2MMP1MMP2MMP9
SCHEMBL28498811 0.69 CA1 (0.41) CA1CA2MMP1MMP2MMP9
SCHEMBL25298036 0.69 CA2 (0.44) CA1CA2MMP1MMP2MMP9
SCHEMBL1593152 0.69 CA1 (0.37) CA1CA2MMP1MMP2MMP9
Ammonia Solution, Strong SCHEMBL28221452 0.68 CA2 (0.43) CA1CA2MMP1MMP2MMP9
SCHEMBL6479936 0.68 CA2 (0.45) CA1CA2MMP1MMP2MMP9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7705050-B2 Amides, useful in the inhibition of IL-8-induced chemotaxis of neutrophils DOMPÉ FARMACEUTICI S.P.A. (IT) 2010-04-27 — — US disclosed
EP-1255726-B1 (R)-2-ARYL-PROPIONAMIDES, USEFUL IN THE INHIBITION OF IL-8 INDUCED CHEMIOTAXIS OF NEUTROPHILS DOMPE PHA R MA SPA RES & MFG (IT) 2009-11-11 — — EP disclosed
US-20040181073-A1 Amides, useful in the inhibition of il-8-induced chemotaxis of neutrophils DOMPÉ FARMACEUTICI S.P.A. (IT) 2004-09-16 — — US disclosed
EP-1255726-A2 (R)-2-ARYL-PROPIONAMIDES, USEFUL IN THE INHIBITION OF IL-8 INDUCED CHEMIOTAXIS OF NEUTROPHILS Dompé S.P.A. (IT) 2002-11-13 — — EP disclosed
WO-2001058852-A2 (R)-2-ARYL-PROPIONAMIDES, USEFUL IN THE INHIBITION OF IL-8-INDUCED CHEMIOTAXIS OF NEUTROPHILS Dompé S.p.A. (IT) 2001-08-16 — — 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-20040181073-A1 Amides, useful in the inhibition of il-8-induced chemotaxis of neutrophils CXCL8, MMP8, CCR8 CA1 3350/4885CA2 2998/4885MMP1 77/4885

“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.

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