Odanacatib

Odanacatib

SCHEMBL3479347

CC(C)(F)C[C@H](NC(c1ccc(-c2ccc(S(C)(=O)=O)cc2)cc1)C(F)(F)F)C(=O)NC1(C#N)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CTSK

The experimentally established mechanism targets of Odanacatib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
CTSK known ✓ P43235 16/20 1.00
CTSL P07711 8/20 1.00
CTSB P07858 7/20 1.00
CTSS P25774 5/20 1.00
CTSF Q9UBX1 3/20 1.00
CTSV O60911 1/20 1.00

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
Odanacatib SCHEMBL1496266 1.00 CTSK (1.00) CTSKCTSLCTSBCTSSCTSF
Odanacatib SCHEMBL18540595 1.00 CTSK (1.00) CTSKCTSLCTSBCTSSCTSF
Odanacatib SCHEMBL15827397 1.00 CTSK (1.00) CTSKCTSLCTSBCTSSCTSF
SCHEMBL2155573 0.94 CTSK (0.90) CTSKCTSLCTSBCTSSCTSF
Odanacatib SCHEMBL21828714 0.94 CTSK (0.88) CTSKCTSLCTSBCTSSCTSF
Odanacatib SCHEMBL21828716 0.94 CTSK (0.88) CTSKCTSLCTSBCTSSCTSF
SCHEMBL2155279 0.94 CTSK (0.88) CTSKCTSLCTSBCTSSCTSF
SCHEMBL2156790 0.92 CTSK (0.85) CTSKCTSLCTSBCTSSCTSF
SCHEMBL22733918 0.91 CTSK (0.83) CTSKCTSLCTSBCTSSCTSF
SCHEMBL22733917 0.91 CTSK (0.83) CTSKCTSLCTSBCTSSCTSF

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230148179-A1 SMALL MOLECULE INHIBITORS OF SARS-CoV-2 VIRAL REPLICATION AND USES THEREOF NATIONAL INSTITUTES OF HEALTH 2023-05-11 US disclosed
US-20210300863-A1 PROCESS TO MAKE A SELECTIVE CATHEPSIN CYSTEINE PROTEASE INHIBITOR INTERVET INC. (US) 2021-09-30 US disclosed
EP-2144871-A1 AMIDATION PROCESS FOR THE PREPARATION OF CATHEPSIN K INHIBITORS Merck Frosst Canada Ltd. (CA) 2010-01-20 EP disclosed
WO-2008119176-A1 AMIDATION PROCESS FOR THE PREPARATION OF CATHEPSIN K INHIBITORS MERCK FROSST CANADA LTD. (CA) 2008-10-09 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 (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-20230148179-A1 SMALL MOLECULE INHIBITORS OF SARS-CoV-2 VIRAL REPLICATION AND USES THEREOF ACE2, ACE, SARS1 CTSK 86/4885CTSL 6/4885CTSB 31/4885
US-20210300863-A1 PROCESS TO MAKE A SELECTIVE CATHEPSIN CYSTEINE PROTEASE INHIBITOR CTSB, CTSF, CTSZ CTSK 8/4885CTSL 11/4885CTSB 1/4885

“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.