SCHEMBL1243720

SCHEMBL1243720

COc1cccc(OC)c1C(=O)NCCc1csc(-c2ccccc2)n1

nearest known ligand 0.82

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.71
SMN1; SMN2 Q16637 3/20 0.71
MAPT P10636 9/20 0.66
TP53 P04637 3/20 0.64
TAAR1 Q96RJ0 1/20 0.62
HSD17B10 Q99714 2/20 0.62
ATM Q13315 1/20 0.61
RXFP1 Q9HBX9 1/20 0.61
HPGD P15428 2/20 0.59
ALDH1A1 P00352 1/20 0.59
TSHR P16473 1/20 0.59
L3MBTL1 Q9Y468 1/20 0.59
POLB P06746 1/20 0.58

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
SCHEMBL17261472 0.89 MAPT (0.80) LMNASMN1; SMN2MAPTTP53HSD17B10
SCHEMBL1243672 0.83 LMNA (1.00) LMNASMN1; SMN2MAPTTP53HSD17B10
SCHEMBL17274015 0.82 MAPT (0.80) LMNASMN1; SMN2MAPTTP53HSD17B10
SCHEMBL17273863 0.80 HSD17B10 (0.67) LMNASMN1; SMN2MAPTTP53HSD17B10
SCHEMBL17261500 0.79 HSD17B10 (0.70) LMNASMN1; SMN2MAPTTP53HSD17B10
SCHEMBL1243060 0.78 SMN1; SMN2 (1.00) LMNASMN1; SMN2MAPTTP53HSD17B10
SCHEMBL17261498 0.78 MAPT (0.74) LMNASMN1; SMN2MAPTTP53HSD17B10
SCHEMBL17273820 0.77 LMNA (0.68) LMNASMN1; SMN2MAPTTP53HSD17B10
SCHEMBL17273757 0.77 HSD17B10 (0.67) LMNASMN1; SMN2MAPTTP53HSD17B10
SCHEMBL17273821 0.76 HSD17B10 (0.63) LMNASMN1; SMN2MAPTTP53HSD17B10

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7888289-B2 2,6-Difluoro-N-[2-(2-methyl-4-thiazolyl)ethyl]benzamide; applying an effective and nonphytotoxic amount of the fungicide composition to the plant seeds,leaves and/or fruits of the plants or to the soil; crops; Alternaria BAYER CROPSCIENCE AG (DE) 2011-02-15 US claimed
US-20090156651-A1 Heterocyclylethylbenzamide Derivatives BAYER INTELLECTUAL PROPERTY GMBH (DE) 2009-06-18 US claimed
EP-1871744-B1 NEW HETEROCYCLYLETHYLBENZAMIDE DERIVATIVES BAYER CROPSCIENCE SA (FR) 2009-01-07 EP claimed
EP-1871744-A1 NEW HETEROCYCLYLETHYLBENZAMIDE DERIVATIVES BAYER CROPSCIENCE SA (FR) 2008-01-02 EP claimed
WO-2006108792-A1 NEW HETEROCYCLYLETHYLBENZAMIDE DERIVATIVES BAYER CROPSCIENCE SA (FR) 2006-10-19 WO claimed
US-7888289-B2 2,6-Difluoro-N-[2-(2-methyl-4-thiazolyl)ethyl]benzamide; applying an effective and nonphytotoxic amount of the fungicide composition to the plant seeds,leaves and/or fruits of the plants or to the soil; crops; Alternaria BAYER CROPSCIENCE AG (DE) 2011-02-15 US disclosed
US-20090156651-A1 Heterocyclylethylbenzamide Derivatives BAYER INTELLECTUAL PROPERTY GMBH (DE) 2009-06-18 US disclosed
EP-1871744-B1 NEW HETEROCYCLYLETHYLBENZAMIDE DERIVATIVES BAYER CROPSCIENCE SA (FR) 2009-01-07 EP disclosed
EP-1871744-A1 NEW HETEROCYCLYLETHYLBENZAMIDE DERIVATIVES BAYER CROPSCIENCE SA (FR) 2008-01-02 EP disclosed
WO-2006108792-A1 NEW HETEROCYCLYLETHYLBENZAMIDE DERIVATIVES BAYER CROPSCIENCE SA (FR) 2006-10-19 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-20090156651-A1 Heterocyclylethylbenzamide Derivatives CYP1A2, CYP51A1, CYP1B1 LMNA 2574/4885SMN1; SMN2 3511/4885MAPT 2385/4885

“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.