SCHEMBL3547387

SCHEMBL3547387

C=CCOc1c(CC=C)cc(C(=O)O)cc1OC

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 6/20 0.57
ALDH1A1 P00352 5/20 0.57
SMN1; SMN2 Q16637 4/20 0.57
HPGD P15428 3/20 0.57
NPC1 O15118 3/20 0.57
RAB9A P51151 3/20 0.57
HSP90AA1 P07900 1/20 0.57
HTT P42858 1/20 0.57
TPMT P51580 2/20 0.48
MAPT P10636 3/20 0.47
POLB P06746 3/20 0.47
L3MBTL1 Q9Y468 2/20 0.47
MEN1 O00255 1/20 0.47
GAA P10253 1/20 0.47
CASP6 P55212 1/20 0.47
KMT2A Q03164 1/20 0.47
MCL1 Q07820 1/20 0.47
GPR55 Q9Y2T6 1/20 0.47
HSD17B10 Q99714 2/20 0.45
TDP1 Q9NUW8 1/20 0.45

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
SCHEMBL3549570 0.88 TPMT (0.57) KDM4EALDH1A1SMN1; SMN2HPGDNPC1
SCHEMBL3543262 0.88 KDM4E (0.50) KDM4EALDH1A1SMN1; SMN2HPGDNPC1
SCHEMBL8542113 0.87 KDM4E (0.55) KDM4EALDH1A1SMN1; SMN2HPGDNPC1
SCHEMBL27317680 0.84 TPMT (0.55) KDM4EALDH1A1SMN1; SMN2HPGDNPC1
SCHEMBL3548321 0.82 KDM4E (0.49) KDM4EALDH1A1SMN1; SMN2HPGDNPC1
SCHEMBL3547337 0.81 CA12 (0.62) KDM4EALDH1A1HPGDHTTTPMT
SCHEMBL16077697 0.79 CA12 (0.46) KDM4EALDH1A1HTTTPMTMAPT
SCHEMBL5572235 0.79 GAA (0.50) KDM4EALDH1A1SMN1; SMN2HPGDNPC1
SCHEMBL31737057 0.78 KDM4E (0.74) KDM4EALDH1A1SMN1; SMN2HPGDNPC1
SCHEMBL14907128 0.78 KDM4E (0.74) KDM4EALDH1A1SMN1; SMN2HPGDNPC1

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-7691843-B2 N-hydroxyamide derivatives possessing antibacterial activity PFIZER INC. (US) 2010-04-06 US disclosed
US-20080058304-A1 N-hydroxyamide derivatives possessing antibacterial activity VICURON HOLDINGS LLC 2008-03-06 US disclosed
EP-1539744-A4 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY VICURON PHARM INC (US) 2007-06-06 EP disclosed
EP-1539744-A2 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY Vicuron Pharmaceuticals, Inc. (US) 2005-06-15 EP disclosed
WO-2004007444-A2 N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY VICURON PHARMACEUTICALS, INC. (US) 2004-01-22 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-20080058304-A1 N-hydroxyamide derivatives possessing antibacterial activity AMDHD2, OGA, ENGASE KDM4E 2323/4885ALDH1A1 2309/4885SMN1; SMN2 3846/4885

“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.