SCHEMBL26010076

SCHEMBL26010076

CCC(C)C(C(=O)O)N(C)C(=O)CN(C)C(=O)[C@@H](NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)NC(=O)OCc1ccccc1)C(C)C

nearest known ligand 0.47

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
CTSK P43235 14/20 0.47
CTSB P07858 9/20 0.47
CTSS P25774 5/20 0.47
CTSL P07711 4/20 0.47
BACE1 P56817 2/20 0.45
CAPN1 P07384 1/20 0.43

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
SCHEMBL29860813 0.93 CTSK (0.44) CTSKCTSBCTSSCTSLBACE1
SCHEMBL30522100 0.89 CTSK (0.54) CTSKCTSBCTSSCTSLBACE1
SCHEMBL23893529 0.87 CTSL (0.54) CTSKCTSBCTSSCTSL
SCHEMBL31388652 0.86 CTSK (0.53) CTSKCTSBCTSSCTSLBACE1
SCHEMBL29860969 0.84 CTSK (0.39) CTSKCTSBCTSSCTSLBACE1
SCHEMBL29861086 0.83 CTSK (0.41) CTSKCTSBCTSSCTSLBACE1
SCHEMBL29860893 0.83 CTSK (0.38) CTSKCTSBCTSSCTSLBACE1
SCHEMBL29973019 0.81 BACE1 (0.38) CTSKCTSBCTSSCTSLBACE1
SCHEMBL29861077 0.81 CTSB (0.48) CTSKCTSBCTSSCTSL
SCHEMBL30763326 0.80 CTSK (0.37) CTSKCTSBCTSSCTSLBACE1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11732002-B2 Deprotection method and resin removal method in solid-phase reaction for peptide compound or amide compound, and method for producing peptide compound CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-08-22 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-11732002-B2 Deprotection method and resin removal method in solid-phase reaction for peptide compound or amide compound, and method for producing peptide compound VIP, PEPD, MLN CTSK 423/4885CTSB 348/4885CTSS 580/4885

“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.