SCHEMBL28061322

SCHEMBL28061322

COC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)OC(C)(C)C

nearest known ligand 0.53

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
CTSL P07711 2/20 0.53
CTSB P07858 1/20 0.53
CTSS P25774 1/20 0.53
CTSK P43235 1/20 0.53
CAPN1 P07384 1/20 0.47
BIRC2 Q13490 3/20 0.47
PSEN1 P49768 4/20 0.45
PSEN2 P49810 4/20 0.45
APH1B Q8WW43 4/20 0.45
NCSTN Q92542 4/20 0.45
APH1A Q96BI3 4/20 0.45
PSENEN Q9NZ42 4/20 0.45
CA1 P00915 1/20 0.45
CA2 P00918 1/20 0.45
CA7 P43166 1/20 0.45
REN P00797 2/20 0.44
KMT2A Q03164 1/20 0.43
AAK1 Q2M2I8 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
SCHEMBL12555973 1.00 CTSL (0.53) CTSLCTSBCTSSCTSKCAPN1
SCHEMBL12588811 1.00 CTSL (0.53) CTSLCTSBCTSSCTSKCAPN1
SCHEMBL28061324 1.00 CTSL (0.53) CTSLCTSBCTSSCTSKCAPN1
SCHEMBL30064542 0.93 CTSL (0.55) CTSLCTSBCTSSCTSKCAPN1
SCHEMBL24130734 0.91 CTSL (0.52) CTSLCTSBCTSSCTSKCAPN1
SCHEMBL1176795 0.90 CTSL (0.62) CTSLCTSBCTSSCTSKCAPN1
SCHEMBL1026997 0.90 CTSL (0.62) CTSLCTSBCTSSCTSKCAPN1
SCHEMBL1026994 0.90 CTSL (0.62) CTSLCTSBCTSSCTSKCAPN1
SCHEMBL56907 0.89 CTSL (0.60) CTSLCTSBCTSSCTSKCAPN1
SCHEMBL55832 0.89 CTSL (0.60) CTSLCTSBCTSSCTSKCAPN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240209020-A1 REACTION AGENT FOR AMIDE REACTION AND METHOD FOR PRODUCING AMIDE COMPOUND USING SAME CHUBU UNIVERSITY EDUCATIONAL FOUNDATION (JP) 2024-06-27 US disclosed
EP-3786151-B1 METHOD FOR PRODUCING AMIDE COMPOUND CHUBU UNIV EDUCATIONAL FOUNDATION (JP) 2023-06-07 EP disclosed
CN-112020492-B Method for producing amide compound 学校法人中部大学 2023-05-05 CN disclosed
US-11512108-B2 Method for producing amide compound CHUBU UNIVERSITY EDUCATIONAL FOUNDATION (JP) 2022-11-29 US disclosed
EP-4053101-A1 REACTION AGENT FOR AMIDE REACTION AND METHOD FOR PRODUCING AMIDE COMPOUND USING SAME Chubu University Educational Foundation (JP) 2022-09-07 EP disclosed
CN-105622716-A Cyclic dipeptide used for wound healing GOOD DOCTOR PHARMACEUTICAL GROUP CO LTD 2016-06-01 CN 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-20240209020-A1 REACTION AGENT FOR AMIDE REACTION AND METHOD FOR PRODUCING AMIDE COMPOUND USING SAME NAAA, FAAH, FAAH2 CTSL 1244/4885CTSB 577/4885CTSS 392/4885
US-11512108-B2 Method for producing amide compound BCAT2, ASNS, VIP CTSL 630/4885CTSB 759/4885CTSS 873/4885

“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.