SCHEMBL2299151

SCHEMBL2299151

O=C(O)CNS(=O)(=O)c1c(C2(c3ccc(Br)cc3)CCCC2)ccc2ccccc12

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MMP1 P03956 2/20 0.42
MMP2 P08253 1/20 0.42
MMP3 P08254 1/20 0.42
MMP7 P09237 1/20 0.42
MMP9 P14780 1/20 0.42
MMP13 P45452 1/20 0.42
KDM4E B2RXH2 1/20 0.37
TDP1 Q9NUW8 1/20 0.37
AKR1B1 P15121 1/20 0.36
GAA P10253 1/20 0.36
MMP12 P39900 1/20 0.36
POLB P06746 2/20 0.35
MAPK1 P28482 2/20 0.35
ALDH1A1 P00352 1/20 0.35
LMNA P02545 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
CASR P41180 1/20 0.33
KMT2A Q03164 2/20 0.33
ALPL P05186 1/20 0.33

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
SCHEMBL2296460 0.83 MMP1 (0.42) MMP1MMP2MMP3MMP7MMP9
SCHEMBL8973405 0.68 MMP1 (0.47) MMP1MMP2MMP3MMP7MMP9
SCHEMBL6077738 0.65 CASP1 (0.56) MMP1KDM4EGAAMMP12POLB
SCHEMBL8972679 0.63 TPSAB1 (0.50) MMP1GAAMMP12POLBLMNA
SCHEMBL2299153 0.63 KEAP1 (0.49) MMP1MMP2MMP9MMP13ITGB1
SCHEMBL20535409 0.61 CA12 (0.46) LMNASMN1; SMN2L3MBTL1KMT2AMEN1
SCHEMBL7870635 0.61 MMP1 (1.00) MMP1MMP2MMP3MMP7MMP9
SCHEMBL28108213 0.60 SLC6A3 (0.54) ALOX5AP
SCHEMBL6438335 0.60 ALDH1A1 (0.69) MMP1KDM4ETDP1GAAMMP12
SCHEMBL14804300 0.60 ESR1 (0.58) POLBMAPK1ALDH1A1LMNASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2536694-B1 Glycine sulfonamides for use as inhibitors of diacylglycerol lipase BRISTOL MYERS SQUIBB CO (US) 2014-01-22 EP claimed
US-8404741-B2 Glycine chroman-6-sulfonamides for use as inhibitors of diacylglycerol lipase BRISTOL-MYERS SQUIBB COMPANY (US) 2013-03-26 US claimed
EP-2536694-A1 GLYCINE SULFONAMIDES FOR USE AS INHIBITORS OF DIACYLGLYCEROL LIPASE Bristol-Myers Squibb Company (US) 2012-12-26 EP claimed
US-20110207749-A1 Glycine Chroman-6-Sulfonamides for Use as Inhibitors of Diacylglycerol Lipase BRISTOL-MYERS SQUIBB COMPANY 2011-08-25 US claimed
WO-2011103055-A1 GLYCINE SULFONAMIDES FOR USE AS INHIBITORS OF DIACYLGLYCEROL LIPASE BRISTOL-MYERS SQUIBB COMPANY (US) 2011-08-25 WO claimed
EP-2536694-B1 Glycine sulfonamides for use as inhibitors of diacylglycerol lipase BRISTOL MYERS SQUIBB CO (US) 2014-01-22 EP disclosed
US-8404741-B2 Glycine chroman-6-sulfonamides for use as inhibitors of diacylglycerol lipase BRISTOL-MYERS SQUIBB COMPANY (US) 2013-03-26 US disclosed
US-20110207749-A1 Glycine Chroman-6-Sulfonamides for Use as Inhibitors of Diacylglycerol Lipase BRISTOL-MYERS SQUIBB COMPANY 2011-08-25 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 (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-20110207749-A1 Glycine Chroman-6-Sulfonamides for Use as Inhibitors of Diacylglycerol Lipase DAGLB, DAGLA, MGLL MMP1 2630/4885MMP2 1091/4885MMP3 1674/4885

“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.