SCHEMBL6685929

SCHEMBL6685929

CC(C)(C)OC(=O)N[C@H](CC(=O)O)CC(=O)OCc1ccccc1

nearest known ligand 0.59

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ SYK P43405 1/20 0.59
▸ KLK5 Q9Y337 3/20 0.53
▸ KLK7 P49862 1/20 0.53
▸ ATM Q13315 1/20 0.53
▸ PPARA Q07869 3/20 0.50
▸ CTSS P25774 3/20 0.47
▸ CTSL P07711 2/20 0.47
▸ MAPT P10636 1/20 0.47
▸ CASP1 P29466 3/20 0.46
▸ CTRB1 P17538 2/20 0.46
▸ PPARG P37231 2/20 0.46
▸ CTSB P07858 1/20 0.46
▸ CTSK P43235 1/20 0.46
▸ APP P05067 1/20 0.44

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
SCHEMBL6685926 1.00 SYK (0.59) SYKKLK5KLK7ATMPPARA
SCHEMBL17207697 0.93 SYK (0.59) SYKKLK5KLK7ATMPPARA
SCHEMBL3108565 0.90 SYK (0.59) SYKKLK5KLK7ATMPPARA
SCHEMBL3276799 0.90 SYK (0.59) SYKKLK5KLK7ATMPPARA
SCHEMBL1262680 0.90 SYK (0.59) SYKKLK5KLK7ATMPPARA
SCHEMBL25301720 0.90 SYK (0.62) SYKATMCTSSCTSLCASP1
SCHEMBL15928906 0.90 ATM (0.62) SYKKLK5KLK7ATMPPARA
SCHEMBL25256638 0.90 SYK (0.62) SYKATMCTSSCTSLCASP1
SCHEMBL14119009 0.90 ATM (0.62) SYKKLK5KLK7ATMPPARA
SCHEMBL25318929 0.89 SYK (0.56) SYKKLK5KLK7ATMPPARA

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 32 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3193904-B1 DIPEPTIDOMIMETICS AS INHIBITORS OF HUMAN IMMUNOPROTEASOMES UNIV CORNELL (US) 2025-10-01 — — EP disclosed
US-20250114428-A1 DIPEPTIDOMIMETICS AS INHIBITORS OF HUMAN IMMUNOPROTEASOMES UNIV CORNELL (US) 2025-04-10 — — US disclosed
US-12016896-B2 Dipeptidomimetics as inhibitors of human immunoproteasomes CORNELL UNIVERSITY (US) 2024-06-25 — — US disclosed
US-20220411385-A1 NOVEL HETEROARYL BUTANOIC ACID DERIVATIVES NOVARTIS AG (CH) 2022-12-29 — — US disclosed
CN-114796207-A Dipeptide mimetics as inhibitors of human immunoproteasome 康奈尔大学 2022-07-29 — — CN disclosed
US-11384051-B2 Ionizable compounds and compositions and uses thereof NITTO DENKO CORPORATION (JP) 2022-07-12 — — US disclosed
US-20220080022-A1 DIPEPTIDOMIMETICS AS INHIBITORS OF HUMAN IMMUNOPROTEASOMES UNIV CORNELL (US) 2022-03-17 — — US disclosed
US-20210340112-A1 NOVEL HETEROARYL BUTANOIC ACID DERIVATIVES NOVARTIS AG (CH) 2021-11-04 — — US disclosed
EP-3313449-B1 IONIZABLE COMPOUNDS AND COMPOSITIONS AND USES THEREOF NITTO DENKO CORP (JP) 2020-09-23 — — EP disclosed
EP-3686184-A2 IONIZABLE COMPOUNDS AND COMPOSITIONS AND USES THEREOF NITTO DENKO CORPORATION (JP) 2020-07-29 — — EP disclosed
US-20170044115-A1 NOVEL DISUBSTITUTED 1, 2, 4-TRIAZINE COMPOUND MITSUBISHI TANABE PHARMA CORPORATION (JP) 2017-02-16 — — US disclosed
US-20170015637-A1 NOVEL HETEROARYL BUTANOIC ACID DERIVATIVES NOVARTIS AG (CH) 2017-01-19 — — US disclosed
US-20170015637-A1 NOVEL HETEROARYL BUTANOIC ACID DERIVATIVES NOVARTIS AG (CH) 2017-01-19 — — US disclosed
US-9290515-B2 Cephem derivative having catechol group SHIONOGI & CO., LTD (JP) 2016-03-22 — — US disclosed
US-9290515-B2 Cephem derivative having catechol group SHIONOGI & CO., LTD (JP) 2016-03-22 — — US disclosed
WO-2015163427-A1 NOVEL DISUBSTITUTED 1, 2, 4-TRIAZINE COMPOUND 田辺三菱製薬株式会社 2015-10-29 — — WO disclosed
WO-2015092740-A1 HETEROARYL BUTANOIC ACID DERIVATIVES AS LTA4H INHIBITORS NOVARTIS AG (CH) 2015-06-25 — — WO disclosed
US-20140256697-A1 CEPHEM DERIVATIVE HAVING CATECHOL GROUP SHIONOGI & CO., LTD. (JP) 2014-09-11 — — US disclosed
US-20140256697-A1 CEPHEM DERIVATIVE HAVING CATECHOL GROUP SHIONOGI & CO., LTD. (JP) 2014-09-11 — — US disclosed
WO-2004089362-A1 2-CYANOPYRROLES AND THEIR ANALOGUES AS DDP-IV INHIBITORS NOVO NORDISK A/S (DK) 2004-10-21 — — 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 (9 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-20220411385-A1 NOVEL HETEROARYL BUTANOIC ACID DERIVATIVES LTA4H, LTC4S, LTB4R SYK 4485/4885KLK5 3017/4885KLK7 4031/4885
US-20170044115-A1 NOVEL DISUBSTITUTED 1, 2, 4-TRIAZINE COMPOUND NR3C2, REN, CYP21A2 SYK 3596/4885KLK5 531/4885KLK7 2445/4885
US-20220080022-A1 DIPEPTIDOMIMETICS AS INHIBITORS OF HUMAN IMMUNOPROTEASOMES PREP, CTSC, DNPEP SYK 3047/4885KLK5 612/4885KLK7 992/4885
US-20250114428-A1 DIPEPTIDOMIMETICS AS INHIBITORS OF HUMAN IMMUNOPROTEASOMES PREP, CTSC, DNPEP SYK 3047/4885KLK5 612/4885KLK7 992/4885
US-20210340112-A1 NOVEL HETEROARYL BUTANOIC ACID DERIVATIVES LTA4H, LTC4S, LTB4R SYK 4485/4885KLK5 3017/4885KLK7 4031/4885
US-20140256697-A1 CEPHEM DERIVATIVE HAVING CATECHOL GROUP COMT, CEP170, SLC6A3 SYK 817/4885KLK5 2516/4885KLK7 3300/4885
US-11384051-B2 Ionizable compounds and compositions and uses thereof NCL, CHMP4B, RNASE1 SYK 3606/4885KLK5 3528/4885KLK7 2341/4885
US-20170015637-A1 NOVEL HETEROARYL BUTANOIC ACID DERIVATIVES LTA4H, LTC4S, LTB4R SYK 4485/4885KLK5 3017/4885KLK7 4031/4885
US-12016896-B2 Dipeptidomimetics as inhibitors of human immunoproteasomes PREP, CTSC, DNPEP SYK 3047/4885KLK5 612/4885KLK7 992/4885

“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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