SCHEMBL201878

SCHEMBL201878

CCCc1ccc(-c2ccccc2C(=O)N2CC[C@@H](O)[C@H]2C(=O)NO)cc1

nearest known ligand 0.40

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
HCRTR1 O43613 5/20 0.38
HCRTR2 O43614 5/20 0.38
MLNR O43193 3/20 0.37
CYP3A4 P08684 3/20 0.37
MMP13 P45452 3/20 0.37
MMP8 P22894 1/20 0.37
MMP12 P39900 1/20 0.37
LMNA P02545 1/20 0.37
MMP1 P03956 2/20 0.36
MMP9 P14780 1/20 0.36
PPARG P37231 1/20 0.36
MMP2 P08253 1/20 0.36
MMP3 P08254 1/20 0.36
MMP7 P09237 1/20 0.36
KDM2B Q8NHM5 1/20 0.36

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
SCHEMBL201735 0.89 LMNA (0.42) HCRTR1HCRTR2MLNRCYP3A4LMNA
SCHEMBL202856 0.89 HCRTR1 (0.38) HCRTR1HCRTR2MLNRCYP3A4MMP13
SCHEMBL201008 0.89 HCRTR1 (0.38) HCRTR1HCRTR2MLNRCYP3A4MMP13
SCHEMBL202594 0.88 HCRTR1 (0.39) HCRTR1HCRTR2MLNRCYP3A4MMP13
SCHEMBL200867 0.88 HCRTR1 (0.40) HCRTR1HCRTR2MLNRCYP3A4LMNA
SCHEMBL201630 0.87 LMNA (0.38) HCRTR1HCRTR2MLNRCYP3A4MMP13
SCHEMBL203250 0.87 LMNA (0.38) HCRTR1HCRTR2MLNRCYP3A4MMP13
SCHEMBL200909 0.86 CHRNB2 (0.38) HCRTR1HCRTR2MLNRCYP3A4LMNA
SCHEMBL202876 0.86 MMP13 (0.43) MLNRCYP3A4MMP13MMP8MMP1
SCHEMBL200879 0.85 HCRTR1 (0.38) HCRTR1HCRTR2MLNRCYP3A4MMP13

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-8088804-B2 N-hydroxyamide derivatives possessing antibacterial activity PFIZER INC. (US) 2012-01-03 US disclosed
EP-2338878-A2 N-hydroxyamide derivatives possessing antibacterial activity Vicuron Pharmaceuticals, Inc. (US) 2011-06-29 EP disclosed
US-20100022605-A1 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY VICURON PHARMACEUTICALS INC. 2010-01-28 US disclosed
EP-1963262-A2 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY Vicuron Pharmaceuticals, Inc. (US) 2008-09-03 EP disclosed
WO-2007069020-A2 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY VICURON PHARMACEUTICALS INC. (US) 2007-06-21 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 (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-20100022605-A1 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY NAAA, HDHD5, HACL2 HCRTR1 1201/4885HCRTR2 1892/4885MLNR 1501/4885

“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.