SCHEMBL1926409

SCHEMBL1926409

CN(CC(N)=O)C(=O)OC(C)(C)C

nearest known ligand 0.36

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
HDAC6 Q9UBN7 2/20 0.36
HDAC1 Q13547 1/20 0.36
HDAC2 Q92769 1/20 0.36
MAOA P21397 1/20 0.34
MAOB P27338 1/20 0.34
CTSD P07339 1/20 0.33
CTSL P07711 1/20 0.33
CTSB P07858 1/20 0.33
CTSS P25774 1/20 0.33
CA14 Q9ULX7 1/20 0.33
CACNA1G O43497 1/20 0.32
CACNA1B Q00975 1/20 0.32
CACNA1C Q13936 1/20 0.32
AAK1 Q2M2I8 1/20 0.32
HTR2C P28335 1/20 0.31
SLC6A4 P31645 1/20 0.31
PDK2 Q15119 1/20 0.30
DGAT1 O75907 1/20 0.30
ASGR1 P07306 1/20 0.30

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
SCHEMBL25132906 0.93 HDAC6 (0.36) HDAC6HDAC1HDAC2MAOAMAOB
SCHEMBL256557 0.85 HDAC6 (0.37) HDAC6HDAC1HDAC2CTSDCTSL
SCHEMBL16378479 0.84 HDAC6 (0.34) HDAC6HDAC1HDAC2CTSDCTSL
SCHEMBL1926793 0.84 HDAC6 (0.34) HDAC6HDAC1HDAC2CTSDCTSL
SCHEMBL19544584 0.82 HDAC6 (0.37) HDAC6HDAC1HDAC2CTSDCTSL
SCHEMBL14291315 0.81 HDAC6 (0.33) HDAC6HDAC1HDAC2CTSDCTSL
SCHEMBL6445026 0.81 HDAC6 (0.37) HDAC6HDAC1HDAC2CTSDCTSL
SCHEMBL14224824 0.81 CA14 (0.40) HDAC6HDAC1HDAC2MAOAMAOB
SCHEMBL336495 0.81 HDAC6 (0.37) HDAC6HDAC1HDAC2CTSDCTSL
SCHEMBL1689401 0.81 HDAC6 (0.37) HDAC6HDAC1HDAC2CTSDCTSL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260055121-A1 TYK2 INHIBITORS AND USES THEREOF SUDO BIOSCIENCES LTD (GB) 2026-02-26 US disclosed
US-20250304563-A1 ACTIVATORS OF EFFECTOR T CELLS ORUM THERAPEUTICS, INC. (KR) 2025-10-02 US disclosed
EP-4532485-A1 TYK2 INHIBITORS AND USES THEREOF Sudo Biosciences Limited (GB) 2025-04-09 EP disclosed
EP-4490152-A1 ACTIVATORS OF EFFECTOR T CELLS Orum Therapeutics Inc. (KR) 2025-01-15 EP disclosed
US-20240391934-A1 SUBSTITUTED PYRIDINES AND PYRIDAZINES AS TYK2 INHIBITORS SUDO BIOSCIENCES LTD (GB) 2024-11-28 US disclosed
US-20240383916-A1 SUBSTITUTED PYRIDINES, PYRIDAZINES, AND PYRIMIDINES AS TYK2 INHIBITORS SUDO BIOSCIENCES LTD (GB) 2024-11-21 US disclosed
US-12103937-B2 Substituted pyridines and pyridazines as TYK2 inhibitors SUDO BIOSCIENCES LIMITED (GB) 2024-10-01 US disclosed
US-12084458-B2 Substituted pyridines, pyridazines, and pyrimidines as TYK2 inhibitors SUDO BIOSCIENCES LIMITED (GB) 2024-09-10 US disclosed
EP-4347032-A1 SUBSTITUTED TETRAHYDROFURAN-2-CARBOXAMIDES AS MODULATORS OF SODIUM CHANNELS Vertex Pharmaceuticals Incorporated (US) 2024-04-10 EP disclosed
CN-117813302-A Substituted tetrahydrofuran-2-carboxamides as sodium channel modulators 沃泰克斯药物股份有限公司 2024-04-02 CN disclosed
US-20040014962-A1 1-Methylcarbapenem derivatives SANKYO COMPANY, LIMITED (JP) 2004-01-22 US disclosed
EP-1379514-A2 5-MEMBERED HETEROCYCLES, PREPARATION AND APPLICATION THEREOF AS MEDICAMENTS SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.) (FR) 2004-01-14 EP disclosed
EP-1340757-A1 1-METHYLCARBAPENEM DERIVATIVES Sankyo Company, Limited (JP) 2003-09-03 EP disclosed
WO-2002083656-A2 5-MEMBERED HETEROCYCLES, PREPARATION AND USE THEREOF AS MAO INHIBITORS AND LIPID PEROXIDATION INHIBITORS, PREPARATION THEREOF AND USE THEREOF AS MEDICAMENTS SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.) (FR) 2002-10-24 WO disclosed
EP-1228760-A2 5-membered heterocycle derivatives, production thereof and use thereof as medicaments SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.) (FR) 2002-08-07 EP disclosed
EP-1223933-A2 5-MEMBERED HETEROCYCLE DERIVATIVES, PRODUCTION THEREOF AND USE THEREOF AS MEDICAMENTS SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.) (FR) 2002-07-24 EP disclosed
WO-2001026656-A2 5-MEMBERED HETEROCYCLE DERIVATIVES AND USE THEREOF AS MONOAMINE OXIDASE INHIBITORS SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.) (FR) 2001-04-19 WO disclosed
US-5861429-A MITICIDES AND ANTHELMINTICS SANKYO COMPANY, LIMITED (JP) 1999-01-19 US disclosed
EP-0300189-B1 New amino acid derivatives, processes for the preparation thereof and pharmaceutical composition comprising the same FUJISAWA PHARMACEUTICAL CO (JP) 1994-11-02 EP disclosed
EP-0300189-A2 New amino acid derivatives, processes for the preparation thereof and pharmaceutical composition comprising the same FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1989-01-25 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 (7 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-20040014962-A1 1-Methylcarbapenem derivatives CD14, CPT1A, ACMSD HDAC6 1185/4885HDAC1 370/4885HDAC2 1498/4885
US-12103937-B2 Substituted pyridines and pyridazines as TYK2 inhibitors TYK2, PDXK, TPX2 HDAC6 1240/4885HDAC1 1003/4885HDAC2 360/4885
US-20240383916-A1 SUBSTITUTED PYRIDINES, PYRIDAZINES, AND PYRIMIDINES AS TYK2 INHIBITORS TYK2, PDXK, TPX2 HDAC6 1885/4885HDAC1 1598/4885HDAC2 419/4885
US-20250304563-A1 ACTIVATORS OF EFFECTOR T CELLS CBLB, CBL, CBLC HDAC6 2045/4885HDAC1 4624/4885HDAC2 4678/4885
US-20240391934-A1 SUBSTITUTED PYRIDINES AND PYRIDAZINES AS TYK2 INHIBITORS TYK2, PDXK, TPX2 HDAC6 1240/4885HDAC1 1003/4885HDAC2 360/4885
US-12084458-B2 Substituted pyridines, pyridazines, and pyrimidines as TYK2 inhibitors TYK2, PDXK, TPX2 HDAC6 1885/4885HDAC1 1598/4885HDAC2 419/4885
US-20260055121-A1 TYK2 INHIBITORS AND USES THEREOF TYK2, CSNK2A3, CSNK2B HDAC6 769/4885HDAC1 815/4885HDAC2 362/4885

“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.