SCHEMBL12049

SCHEMBL12049

CS(=O)(=O)NC(=O)CCCc1ccc(OCCc2ccncc2)cc1

nearest known ligand 0.55

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 2/20 0.50
CYP4F2 P78329 1/20 0.48
CYP4A11 Q02928 1/20 0.48
ACACB O00763 1/20 0.47
HDAC1 Q13547 1/20 0.46
ATM Q13315 1/20 0.45
EPHX2 P34913 1/20 0.45
LMNA P02545 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
TSHR P16473 1/20 0.43
MAPK1 P28482 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
FFAR1 O14842 2/20 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
SCHEMBL5797 0.91 EPHX2 (0.53) LTA4HCYP4F2CYP4A11EPHX2FFAR1
SCHEMBL6073 0.85 L3MBTL1 (0.56) LTA4HCYP4F2CYP4A11ACACBATM
SCHEMBL11899994 0.84 LTA4H (0.61) LTA4HHDAC1LMNAFFAR1
SCHEMBL11898793 0.80 CYP4F2 (0.51) LTA4HCYP4F2CYP4A11ACACBLMNA
SCHEMBL12984882 0.78 LTA4H (0.40) LTA4HCYP4F2CYP4A11HDAC1
SCHEMBL6158 0.77 LTA4H (0.46) LTA4HCYP4F2CYP4A11SMN1; SMN2FFAR1
SCHEMBL6212 0.77 MAOB (0.54) FFAR1
SCHEMBL11593 0.76 LTA4H (0.45) LTA4HCYP4F2CYP4A11ACACBL3MBTL1
SCHEMBL5811 0.74 MMP2 (0.54) LTA4HCYP4F2CYP4A11SMN1; SMN2FFAR1
SCHEMBL452538 0.74 S1PR1 (0.70) LTA4HFFAR1

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 LTA4H 115/4885CYP4F2 3646/4885CYP4A11 4699/4885
US-20140364398-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents LCT, AGXT, PRXL2A LTA4H 352/4885CYP4F2 3971/4885CYP4A11 4790/4885

“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.