SCHEMBL5099688

SCHEMBL5099688

CCCN1CCC[C@H](NC(=O)[CH]CC(C)C(N)=O)C(=O)C1

nearest known ligand 0.35

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ACHE P22303 1/20 0.34
DRD3 P35462 3/20 0.32
PARP1 P09874 1/20 0.32
KDM2B Q8NHM5 4/20 0.31
BCHE P06276 1/20 0.31
CTSK P43235 1/20 0.31
BIRC2 Q13490 1/20 0.31
CHRNB4 P30926 1/20 0.31
CHRNA3 P32297 1/20 0.31
DRD2 P14416 2/20 0.30
DRD1 P21728 2/20 0.30
DRD4 P21917 2/20 0.30
DRD5 P21918 2/20 0.30
MEN1 O00255 1/20 0.30
KMT2A Q03164 1/20 0.30

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
SCHEMBL5098964 0.94 BIRC2 (0.37) BCHECTSKBIRC2
SCHEMBL5098998 0.93 BCHE (0.41) BCHECTSKBIRC2
SCHEMBL5092868 0.83 CTSK (0.35) CTSKCHRNB4CHRNA3KMT2A
SCHEMBL4687324 0.83 ALDH1A1 (0.41) ACHEBCHECTSKBIRC2
SCHEMBL5099657 0.82 LMNA (0.39) KMT2A
SCHEMBL5099273 0.82 CTSK (0.40) CTSK
SCHEMBL5098864 0.82 KMT2A (0.39) CTSKMEN1KMT2A
SCHEMBL4310035 0.81
SCHEMBL5096703 0.80 ALDH1A1 (0.41) PARP1
SCHEMBL5096735 0.80 KMT2A (0.43) MEN1KMT2A

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 ACHE 618/4885DRD3 3743/4885PARP1 352/4885
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 ACHE 1144/4885DRD3 4447/4885PARP1 487/4885
US-20020147188-A1 Protease inhibitors CTSK, MMP13, CTSZ ACHE 618/4885DRD3 3743/4885PARP1 352/4885
US-20040002487-A1 Protease inhibitors CTSK, MMP13, CTSZ ACHE 618/4885DRD3 3743/4885PARP1 352/4885
US-20030144175-A1 Protease inhibitors CTSK, MMP13, CTSZ ACHE 618/4885DRD3 3743/4885PARP1 352/4885

“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.