SCHEMBL6182064

SCHEMBL6182064

CC(C)CC(NC(=O)c1ccc(NC(=O)OCCN2CCOCC2)cc1)C(=O)N(C)C#N

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CTSB P07858 4/20 0.45
HRH3 Q9Y5N1 1/20 0.44
CD274 Q9NZQ7 1/20 0.43
KDM4E B2RXH2 1/20 0.42
ALDH1A1 P00352 1/20 0.42
HPGD P15428 1/20 0.42
SMN1; SMN2 Q16637 3/20 0.42
MAPT P10636 2/20 0.42
RAB9A P51151 2/20 0.42
MAPK1 P28482 2/20 0.42
LMNA P02545 1/20 0.42
TSHR P16473 1/20 0.42
STAT3 P40763 1/20 0.42
CTSL P07711 2/20 0.41
CTSS P25774 2/20 0.41
CTSK P43235 2/20 0.41
NPC1 O15118 1/20 0.41
POLB P06746 1/20 0.40
EPHX2 P34913 3/20 0.39
ATM Q13315 1/20 0.39

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
SCHEMBL6185393 0.92 CTSB (0.47) CTSBHRH3HPGDSMN1; SMN2MAPT
SCHEMBL6182071 0.85 CTSL (0.55) CTSBHRH3CD274CTSLCTSS
SCHEMBL6181621 0.85 SMN1; SMN2 (0.55) CTSBALDH1A1SMN1; SMN2MAPTLMNA
SCHEMBL7488759 0.84 CTSK (0.49) CTSBHRH3CD274ALDH1A1LMNA
SCHEMBL6182460 0.83 CHRM3 (0.46) CTSB
SCHEMBL6182883 0.82 CTSB (0.55) CTSBCTSLCTSSCTSK
SCHEMBL6182200 0.81 CHRM3 (0.45) CTSB
SCHEMBL6183226 0.81 CTSB (0.43) CTSBCTSLCTSSCTSK
SCHEMBL6184173 0.80 BCHE (0.46) CTSBCTSLCTSSCTSK
SCHEMBL6182114 0.79 CTSB (0.58) CTSBCTSLCTSSCTSK

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
EP-1161415-B1 N-CYANOMETHYLAMIDES AS PROTEASE INHIBITORS AXYS PHARM INC (US) 2005-07-13 EP disclosed
US-6593327-B2 N-cyanomethyl amides which are cysteine protease inhibitors; treating osteoporosis; mixtures with bisphosphonates AXYS PHARMACEUTICALS, INC. 2003-07-15 US disclosed
US-20030119788-A1 Novel compounds and compositions as protease inhibitors AXYS PHARMACEUTICALS, INC. (US) 2003-06-26 US disclosed
US-6476026-B1 Compounds and compositions as protease inhibitors AXYS PHARMACEUTICALS, INC. 2002-11-05 US disclosed
US-20020086996-A1 Novel compounds and compositions as protease inhibitors AXYS PHARMACEUTICALS, INC. (US) 2002-07-04 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 (2 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-20020086996-A1 Novel compounds and compositions as protease inhibitors CTRL, SERPINB1, CPN1 CTSB 11/4885HRH3 2461/4885CD274 4830/4885
US-20030119788-A1 Novel compounds and compositions as protease inhibitors CTRL, SERPINB1, CPN1 CTSB 11/4885HRH3 2461/4885CD274 4830/4885

“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.