SCHEMBL11942

SCHEMBL11942

CS(=O)(=O)C(CCc1ccc(OCc2nc(-c3cccnc3)no2)cc1)C(N)=O

nearest known ligand 0.63

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
PSMB5 P28074 2/20 0.55
PSMB8 P28062 1/20 0.55
POLB P06746 1/20 0.53
MAPT P10636 1/20 0.53
FFAR1 O14842 5/20 0.52
KDM4E B2RXH2 1/20 0.48
ADRB2 P07550 2/20 0.47
ADRB1 P08588 2/20 0.47
ADRB3 P13945 2/20 0.47
MAPK1 P28482 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
ALDH1A1 P00352 1/20 0.46
KMT2A Q03164 1/20 0.46

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
SCHEMBL5859 0.90 FFAR1 (0.64) FFAR1MAPK1SMN1; SMN2
SCHEMBL11898792 0.81 ADAMTS4 (0.48) MAPTMAPK1SMN1; SMN2ALDH1A1KMT2A
SCHEMBL11944 0.81 MAPT (0.53) PSMB5PSMB8POLBMAPTFFAR1
SCHEMBL11943 0.79 FFAR1 (0.54) PSMB5PSMB8POLBMAPTFFAR1
SCHEMBL11326 0.77 FFAR1 (0.41) POLBMAPTFFAR1ADRB2
SCHEMBL5950 0.77 FFAR1 (0.43) FFAR1
SCHEMBL11898956 0.75 ADAM17 (0.50) FFAR1SMN1; SMN2KMT2A
SCHEMBL5796 0.75 MAOB (0.46) FFAR1
SCHEMBL4107632 0.73 RAB9A (0.76) POLBMAPTKDM4EMAPK1SMN1; SMN2
SCHEMBL5959943 0.73 RAB9A (0.73) POLBMAPTKDM4EMAPK1SMN1; SMN2

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-20140364398-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents PFIZER INC. (US) 2014-12-11 US disclosed
US-8853258-B2 C-linked hydroxamic acid derivatives useful as antibacterial agents PFIZER INC. (US) 2014-10-07 US disclosed
EP-2488489-A2 C-LINKED HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS Pfizer Inc. (US) 2012-08-22 EP disclosed
US-20120202777-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents BROWN MATTHEW FRANK (US) 2012-08-09 US disclosed
WO-2011045703-A2 C-LINKED HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS PFIZER INC. (US) 2011-04-21 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 (2 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-20120202777-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents HAX1, LPXN, AGXT PSMB5 2563/4885PSMB8 3141/4885POLB 1774/4885
US-20140364398-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents LCT, AGXT, PRXL2A PSMB5 2324/4885PSMB8 3075/4885POLB 2631/4885

“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.