SCHEMBL2177052

SCHEMBL2177052

C[C@]1(C(=O)N2CCN(c3ccccc3)CC2)N(C(=O)O)C[C@H](OS(C)(=O)=O)C[C@]1(C)C(=O)O

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 5/20 0.43
ALDH1A1 P00352 3/20 0.43
KMT2A Q03164 5/20 0.38
HSD11B1 P28845 1/20 0.37
HTT P42858 3/20 0.37
MAPT P10636 3/20 0.37
TSHR P16473 2/20 0.37
POLB P06746 1/20 0.37
RAB9A P51151 1/20 0.37
ADAM10 O14672 1/20 0.36
MMP2 P08253 1/20 0.36
MMP9 P14780 1/20 0.36
MEN1 O00255 4/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
NPSR1 Q6W5P4 1/20 0.36
USP2 O75604 1/20 0.36
GAA P10253 1/20 0.35
CYP1A2 P05177 1/20 0.35
CYP3A4 P08684 1/20 0.35
CYP2C9 P11712 1/20 0.35

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
SCHEMBL2173082 0.88 ALDH1A1 (0.46) LMNAALDH1A1KMT2AHSD11B1HTT
SCHEMBL2173080 0.85 ALDH1A1 (0.44) LMNAALDH1A1KMT2AHSD11B1HTT
SCHEMBL2173178 0.84 LMNA (0.49) LMNAALDH1A1KMT2AHSD11B1HTT
SCHEMBL2173564 0.84 LMNA (0.49) LMNAALDH1A1KMT2AHSD11B1HTT
SCHEMBL2177320 0.82 LMNA (0.41) LMNAALDH1A1KMT2AHSD11B1HTT
SCHEMBL2176908 0.81 ALDH1A1 (0.43) LMNAALDH1A1KMT2AHTTMAPT
SCHEMBL2174272 0.79 ALOX15 (0.41) LMNAALDH1A1KMT2AHTTMAPT
SCHEMBL4476420 0.79 GPR119 (0.39) LMNAALDH1A1KMT2AHSD11B1HTT
SCHEMBL2172907 0.78 LMNA (0.45) LMNAALDH1A1KMT2AHSD11B1HTT
SCHEMBL2174752 0.77 ADAM10 (0.37) LMNAALDH1A1KMT2AHTTMAPT

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-9440958-B2 Substituted cyclic hydroxamates as inhibitors of matrix metalloproteinases INCYTE CORPORATION (US) 2016-09-13 US disclosed
US-20110224189-A1 SUBSTITUTED CYCLIC HYDROXAMATES AS INHIBITORS OF MATRIX METALLOPROTEINASES INCYTE CORPORATION 2011-09-15 US disclosed
US-7973041-B2 Antiarthritic agents; psoriasis; anticancer agents;antiallergens; metalloprotease inhibitors. INCYTE CORPORATION (US) 2011-07-05 US disclosed
US-7491724-B2 Substituted cyclic hydroxamates as inhibitors of matrix metalloproteinases INCYTE CORPORATION (US) 2009-02-17 US disclosed
US-20050113344-A1 Substituted cyclic hydroxamates as inhibitors of matrix metalloproteinases INCYTE CORPORATION 2005-05-26 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 (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-20110224189-A1 SUBSTITUTED CYCLIC HYDROXAMATES AS INHIBITORS OF MATRIX METALLOPROTEINASES MMP25, MMP14, MMP9 LMNA 2321/4885ALDH1A1 673/4885KMT2A 1912/4885
US-20050113344-A1 Substituted cyclic hydroxamates as inhibitors of matrix metalloproteinases MMP25, MMP2, MMP14 LMNA 2198/4885ALDH1A1 497/4885KMT2A 1880/4885

“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.