SCHEMBL29918073

SCHEMBL29918073

CSCC[C@H](NC(=O)[C@H](C)NC(=O)OC(C)(C)C)C(=O)N[C@@H](C)C(=O)OC(C)(C)C

nearest known ligand 0.56

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ CTSS P25774 1/20 0.56
▸ CTSK P43235 1/20 0.56
▸ REN P00797 1/20 0.47
▸ CA2 P00918 1/20 0.47
▸ BACE1 P56817 11/20 0.46
▸ TSHR P16473 1/20 0.41
▸ BACE2 Q9Y5Z0 1/20 0.41
▸ METAP2 P50579 1/20 0.41
▸ METAP1 P53582 1/20 0.41
▸ KDM4E B2RXH2 2/20 0.41
▸ ALDH1A1 P00352 1/20 0.41
▸ MAPT P10636 1/20 0.41

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
SCHEMBL30064531 0.94 CTSS (0.63) CTSSCTSKRENCA2BACE1
SCHEMBL29918303 0.92 CTSS (0.55) CTSSCTSKRENCA2BACE1
SCHEMBL30064525 0.91 CTSS (0.56) CTSSCTSKRENCA2BACE1
SCHEMBL10144023 0.85 CTSS (0.59) CTSSCTSKRENCA2BACE1
SCHEMBL29918031 0.82 KMT2A (0.47) CTSSCTSKCA2KDM4EMAPT
SCHEMBL29918107 0.82 KMT2A (0.47) CTSSCTSKCA2KDM4EMAPT
SCHEMBL27704332 0.80 CTSK (0.64) CTSSCTSKCA2TSHRKDM4E
SCHEMBL27688713 0.80 CTSK (0.64) CTSSCTSKCA2TSHRKDM4E
SCHEMBL27483577 0.80 CTSK (0.64) CTSSCTSKCA2TSHRKDM4E
SCHEMBL29865883 0.79 CTSS (0.58) CTSSCTSKRENCA2BACE1

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
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

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 CTSS 392/4885CTSK 593/4885REN 1111/4885
US-11512108-B2 Method for producing amide compound BCAT2, ASNS, VIP CTSS 873/4885CTSK 812/4885REN 172/4885

“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.

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