SCHEMBL5096437

SCHEMBL5096437

CC(C[CH]C(=O)N[C@H]1CCCN(S(=O)(=O)c2cccc(F)c2)CC1=O)C(N)=O

nearest known ligand 0.45

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
POLB P06746 1/20 0.45
PKM P14618 1/20 0.42
TSHR P16473 1/20 0.42
KMT2A Q03164 4/20 0.41
ALDH1A1 P00352 2/20 0.39
MAPT P10636 1/20 0.39
MAPK1 P28482 1/20 0.39
MEN1 O00255 2/20 0.38
CTSK P43235 5/20 0.38
CTSL P07711 3/20 0.38
CTSS P25774 3/20 0.38
CTSV O60911 1/20 0.38
CTSB P07858 1/20 0.38
NPSR1 Q6W5P4 1/20 0.37
CACNA1B Q00975 1/20 0.36
F10 P00742 1/20 0.36
HTR2A P28223 1/20 0.36
HTR2C P28335 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
SCHEMBL5096578 0.91 POLB (0.48) POLBPKMTSHRKMT2AALDH1A1
SCHEMBL5099202 0.90 KMT2A (0.43) POLBPKMKMT2AALDH1A1MAPT
SCHEMBL4767047 0.90 CTSK (0.42) CTSKCTSLCTSSCTSVCTSB
SCHEMBL5105882 0.86 CTSK (0.41) CTSKCTSLCTSSCTSVCTSB
SCHEMBL5098737 0.85 ALDH1A1 (0.41) TSHRKMT2AALDH1A1MAPK1MEN1
SCHEMBL6404947 0.85 CTSK (0.44) CTSKCTSLCTSSCTSVCTSB
SCHEMBL5096603 0.85 HSD17B10 (0.45) TSHRALDH1A1MAPK1CTSKCTSL
SCHEMBL4767024 0.84 MEN1 (0.40) POLBKMT2AMEN1CTSKNPSR1
SCHEMBL5092882 0.83 POLB (0.49) POLBPKMTSHRKMT2AALDH1A1
SCHEMBL6631525 0.83 TSHR (0.45) POLBPKMTSHRALDH1A1CTSK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050256104-A1 substituted 1,1,4-1l6-trioxo[1,2]thiazepan-4-ylamide-derived protease inhibitors which inhibit the likes of cathepsin K; treating osteoporosis, osteo- and rheumatoid arthritis and periodontal disease; inhibiting excessive cartilage or matrix degradation SMITHKLINE BEECHAM CORPORATION 2005-11-17 US claimed
US-20040002487-A1 Protease inhibitors MARQUIS ROBERT WELLS (US) 2004-01-01 US claimed
US-20030225061-A1 Protease inhibitors MARQUIS ROBERT WELLS (US) 2003-12-04 US claimed
US-20030144175-A1 Protease inhibitors SMITHKLINE BEECHAM CORPORATION 2003-07-31 US claimed
US-20020147188-A1 Protease inhibitors SMITHKLINE BEECHAM CORPORATION 2002-10-10 US claimed
US-7405209-B2 e.g. 2-Benzyloxycarbonylamino-4-methyl-pentanoyl)-3-oxo-azepan-4-ylcarbamoyl}carbamic acid benzyl ester; protease inhibitors like cathepsin K; osteoporosis, osteo- and rheumatoid arthritis and periodontal disease; inhibiting excessive cartilage or matrix degradation SMITHKLINE BEECHAM CORPORATION (US) 2008-07-29 US disclosed
US-20050256104-A1 substituted 1,1,4-1l6-trioxo[1,2]thiazepan-4-ylamide-derived protease inhibitors which inhibit the likes of cathepsin K; treating osteoporosis, osteo- and rheumatoid arthritis and periodontal disease; inhibiting excessive cartilage or matrix degradation SMITHKLINE BEECHAM CORPORATION 2005-11-17 US disclosed
US-20040002487-A1 Protease inhibitors MARQUIS ROBERT WELLS (US) 2004-01-01 US disclosed
US-20030225061-A1 Protease inhibitors MARQUIS ROBERT WELLS (US) 2003-12-04 US disclosed
US-20030144175-A1 Protease inhibitors SMITHKLINE BEECHAM CORPORATION 2003-07-31 US disclosed
US-20020147188-A1 Protease inhibitors SMITHKLINE BEECHAM CORPORATION 2002-10-10 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 (5 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-20030225061-A1 Protease inhibitors CTSK, MMP13, CTSZ POLB 3510/4885PKM 1809/4885TSHR 4016/4885
US-20050256104-A1 substituted 1,1,4-1l6-trioxo[1,2]thiazepan-4-ylamide-derived protease inhibitors which inhibit the likes of cathepsin K; treating osteoporosis, osteo- and rheumatoid arthritis and periodontal disease; inhibiting excessive cartilage or matrix degradation CTSK, CTSZ, CTSE POLB 3793/4885PKM 1315/4885TSHR 2596/4885
US-20020147188-A1 Protease inhibitors CTSK, MMP13, CTSZ POLB 3510/4885PKM 1809/4885TSHR 4016/4885
US-20040002487-A1 Protease inhibitors CTSK, MMP13, CTSZ POLB 3510/4885PKM 1809/4885TSHR 4016/4885
US-20030144175-A1 Protease inhibitors CTSK, MMP13, CTSZ POLB 3510/4885PKM 1809/4885TSHR 4016/4885

“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.