SCHEMBL953455

SCHEMBL953455

COCCC(NC(=O)OC(C)(C)C)C(=O)O

nearest known ligand 0.48

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CTSK P43235 7/20 0.48
CTSS P25774 6/20 0.48
MEN1 O00255 1/20 0.45
GAA P10253 1/20 0.45
KMT2A Q03164 1/20 0.45
PPARA Q07869 7/20 0.45
PPARG P37231 6/20 0.45
CTSL P07711 1/20 0.44
CTSB P07858 1/20 0.44
ITGB3 P05106 1/20 0.44
ITGA2B P08514 1/20 0.44
ACE P12821 1/20 0.44
PPARD Q03181 2/20 0.43
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42
CA7 P43166 1/20 0.42
IDO1 P14902 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
SCHEMBL25262348 1.00 CTSK (0.48) CTSKCTSSMEN1GAAKMT2A
SCHEMBL953453 1.00 CTSK (0.48) CTSKCTSSMEN1GAAKMT2A
SCHEMBL15304806 0.88 PPARA (0.44) CTSKCTSSMEN1GAAKMT2A
SCHEMBL31036464 0.87 CTSK (0.44) CTSKCTSSCTSLCTSBCA1
SCHEMBL21938483 0.87 CTSK (0.44) CTSKCTSSCTSLCTSBCA1
SCHEMBL8270949 0.87 CTSK (0.44) CTSKCTSSCTSLCTSBCA1
SCHEMBL527131 0.86 PPARA (0.53) CTSKCTSSPPARAPPARGCTSL
SCHEMBL580779 0.86 PPARA (0.53) CTSKCTSSPPARAPPARGCTSL
SCHEMBL588912 0.86 PPARA (0.53) CTSKCTSSPPARAPPARGCTSL
SCHEMBL12004419 0.85 HDAC4 (0.50) CTSKCTSSGAAPPARAPPARG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250320234-A1 LONP1 INHIBITOR COMPOUNDS, USES AND METHODS PRETZEL THERAPEUTICS, INC. (US) 2025-10-16 US disclosed
EP-3917527-B1 COMPOUNDS AND USES THEREOF FOGHORN THERAPEUTICS INC (US) 2025-04-23 EP disclosed
US-20250059213-A1 LONP1 INHIBITORS, USES AND METHODS PRETZEL THERAPEUTICS, INC. (US) 2025-02-20 US disclosed
WO-2024163962-A1 3-((1,1-DIOXIDO-2,3,4,5-TETRAHYDROBENZO[F][1,2,5]THIADIAZEPIN-8-YL)OXY)-2-FLUOROACRYLIC ACID DERIVATIVES AS SODIUM TAUROCHOLATE CO-TRANSPORTING POLYPEPTIDE (NTCP) INHIBITORS FOR THE TREATMENT OF CHOLESTASIS Hemoshear Therapeutics, Inc. (US) 2024-08-08 WO disclosed
CN-116813505-A Method for preparing O-methyl-N-carbobenzoxy-L-homoserine 爱斯特(成都)生物制药股份有限公司 2023-09-29 CN disclosed
WO-2023107470-A1 LONP1 INHIBITORS, USES AND METHODS PRETZEL THERAPEUTICS, INC. (US) 2023-06-15 WO disclosed
WO-2023107487-A1 LONP1 INHIBITOR COMPOUNDS, USES AND METHODS PRETZEL THERAPEUTICS, INC. (US) 2023-06-15 WO disclosed
US-20230079819-A1 COMPOUNDS AND USES THEREOF FOGHORN THERAPEUTICS INC. 2023-03-16 US disclosed
EP-3917527-A1 COMPOUNDS AND USES THEREOF Foghorn Therapeutics Inc. (US) 2021-12-08 EP disclosed
CN-113645971-A Compound and use thereof 福宏治疗公司 2021-11-12 CN disclosed
EP-3191112-A2 DIPEPTIDYL KETOAMIDE COMPOUNDS AND THEIR USE FOR THE TREATMENT AND/OR PREVENTION OF FAT ACCUMULATION LANDSTEINER GENMED, S.L. (ES) 2017-07-19 EP disclosed
WO-2016038040-A2 DIPEPTIDYL KETOAMIDE COMPOUNDS AND THEIR USE FOR THE TREATMENT AND/OR PREVENTION OF FAT ACCUMULATION LANDSTEINER GENMED, S.L. (ES) 2016-03-17 WO disclosed
US-8426420-B2 Heterocyclic pyrazole-carboxamidesas P2Y12 antagonists SANOFI (FR) 2013-04-23 US disclosed
EP-2238128-B1 HETEROCYCLIC PYRAZOLE-CARBOXAMIDES AS P2Y12 ANTAGONISTS SANOFI SA (FR) 2012-08-22 EP disclosed
US-20110021537-A1 HETEROCYCLIC PYRAZOLE-CARBOXAMIDESAS P2Y12 ANTAGONISTS SANOFI-AVENTIS (FR) 2011-01-27 US disclosed
EP-2238128-A2 HETEROCYCLIC PYRAZOLE-CARBOXAMIDES AS P2Y12 ANTAGONISTS Sanofi-Aventis (FR) 2010-10-13 EP disclosed
WO-2009080226-A2 HETEROCYCLIC PYRAZOLE-CARBOXAMIDES AS P2Y12 ANTAGONISTS SANOFIS-AVENTIS (FR) 2009-07-02 WO disclosed
EP-1567489-B1 PYRROLIDIN-2-ONE DERIVATIVES AS INHIBITORS OF THROMBIN AND FACTOR XA GLAXO GROUP LTD (GB) 2008-07-23 EP disclosed
US-20060166985-A1 Pyrrolydin-2-one derivatives as inhibitors of thrombin and factor xa GLAXO GROUP LIMITED (GB) 2006-07-27 US disclosed
EP-0402313-A1 Novel endothelin derivative Japat Ltd (CH) 1990-12-12 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 (5 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-20250320234-A1 LONP1 INHIBITOR COMPOUNDS, USES AND METHODS LONP1, NLN, ACAT1 CTSK 1164/4885CTSS 871/4885MEN1 3531/4885
US-20230079819-A1 COMPOUNDS AND USES THEREOF VHL, CLN6, TFEB CTSK 2434/4885CTSS 2010/4885MEN1 1366/4885
US-20250059213-A1 LONP1 INHIBITORS, USES AND METHODS LONP1, ACAT1, ACAA2 CTSK 1102/4885CTSS 736/4885MEN1 3542/4885
US-20110021537-A1 HETEROCYCLIC PYRAZOLE-CARBOXAMIDESAS P2Y12 ANTAGONISTS P2RY1, P2RY12, P2RY11 CTSK 2016/4885CTSS 2459/4885MEN1 2661/4885
US-20060166985-A1 Pyrrolydin-2-one derivatives as inhibitors of thrombin and factor xa TFPI, TFPI2, SERPINC1 CTSK 260/4885CTSS 380/4885MEN1 1732/4885

“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.