SCHEMBL2143334

SCHEMBL2143334

CC(=O)C1CCCC(=O)N1

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC3 O15379 9/20 0.36
HDAC11 Q96DB2 9/20 0.36
HDAC6 Q9UBN7 9/20 0.36
HDAC1 Q13547 8/20 0.36
HDAC2 Q92769 8/20 0.36
HDAC10 Q969S8 8/20 0.36
HDAC8 Q9BY41 8/20 0.36
HDAC4 P56524 1/20 0.36
HDAC7 Q8WUI4 1/20 0.36
HDAC9 Q9UKV0 1/20 0.36
HDAC5 Q9UQL6 1/20 0.36
ABL1 P00519 1/20 0.35
NCOR2 Q9Y618 2/20 0.34
LMNA P02545 1/20 0.33
MEN1 O00255 1/20 0.33
KMT2A Q03164 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
CRBN Q96SW2 1/20 0.32
TRHR P34981 1/20 0.32
POLB P06746 1/20 0.31

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
SCHEMBL8426408 1.00 HDAC3 (0.36) HDAC3HDAC11HDAC6HDAC1HDAC2
SCHEMBL17995 0.94 HDAC3 (0.36) HDAC3HDAC11HDAC6HDAC1HDAC2
SCHEMBL2132866 0.87
SCHEMBL3134625 0.87
SCHEMBL8920712 0.87
SCHEMBL15347243 0.83 HDAC3 (0.38) HDAC3HDAC11HDAC6HDAC1HDAC2
SCHEMBL630497 0.81 CAD (0.43) HDAC3HDAC11HDAC6HDAC1HDAC2
SCHEMBL3625069 0.81 CAD (0.43) HDAC3HDAC11HDAC6HDAC1HDAC2
SCHEMBL2344195 0.81 CAD (0.43) HDAC3HDAC11HDAC6HDAC1HDAC2
SCHEMBL14374129 0.79 GLI1 (0.44) HDAC3HDAC11HDAC6HDAC1HDAC2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2445874-B1 PROCESS OF PREPARATION OF 2-ACETYL-1-PYRROLINE AND A STABLE PRECURSOR THEREOF, ISOTOPICALLY LABELLED OR NOT CENTRE NAT DE LA RECH SCIENT (C N R S ) (FR) 2017-11-29 EP disclosed
EP-2445874-B1 PROCESS OF PREPARATION OF 2-ACETYL-1-PYRROLINE AND A STABLE PRECURSOR THEREOF, ISOTOPICALLY LABELLED OR NOT CENTRE NAT DE LA RECH SCIENT (C N R S ) (FR) 2017-11-29 EP disclosed
US-8597706-B2 Method for synthesizing 2-acetyl-1-pyrroline, stable ketal precursors thereof, and isotopically marked analogs CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2013-12-03 US disclosed
EP-2445874-A1 METHOD FOR SYNTHESISING 2-ACETYL-1-PYRROLINE AND THE STABLE PRECURSOR THEREOF, OPTIONALLY ISOTOPICALLY MARKED Centre National De La Recherche Scientifique CNRS (FR) 2012-05-02 EP disclosed
US-20120100274-A1 METHOD FOR SYNTHESISING 2-ACETYL-1-PYRROLINE AND THE STABLE PRECURSOR THEREOF, OPTIONALLY ISOTOPICALLY MARKED UNIVERSITE DE MONTPELLIER (FR) 2012-04-26 US disclosed
US-20120100274-A1 METHOD FOR SYNTHESISING 2-ACETYL-1-PYRROLINE AND THE STABLE PRECURSOR THEREOF, OPTIONALLY ISOTOPICALLY MARKED UNIVERSITE DE MONTPELLIER (FR) 2012-04-26 US disclosed
US-20120100274-A1 METHOD FOR SYNTHESISING 2-ACETYL-1-PYRROLINE AND THE STABLE PRECURSOR THEREOF, OPTIONALLY ISOTOPICALLY MARKED UNIVERSITE DE MONTPELLIER (FR) 2012-04-26 US disclosed
WO-2010149744-A1 METHOD FOR SYNTHESISING 2-ACETYL-1-PYRROLINE AND THE STABLE PRECURSOR THEREOF, OPTIONALLY ISOTOPICALLY MARKED CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2010-12-29 WO disclosed
WO-2010149744-A1 METHOD FOR SYNTHESISING 2-ACETYL-1-PYRROLINE AND THE STABLE PRECURSOR THEREOF, OPTIONALLY ISOTOPICALLY MARKED CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2010-12-29 WO disclosed
US-7829561-B2 Caspase inhibitors and uses thereof VERTEX PHARMACEUTICALS INCORPORATED (US) 2010-11-09 US disclosed
US-20090156572-A1 Nitrogen-containing heterocyclic compound and use thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED 2009-06-18 US disclosed
US-20090156572-A1 Nitrogen-containing heterocyclic compound and use thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED 2009-06-18 US disclosed
WO-2009072643-A1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUND AND USE THEREOF TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2009-06-11 WO disclosed
US-20090023739-A1 interleukin-1B converting enzyme inhibitors such as 3-(6,11-Dioxo-1,2,3,4-tetrahydro-pyridazino[1,2-b]phthalazin-1-carboxamido)-5-fluoro-4-oxo-pentanoic acid, that mediate cell apoptosis and inflammation, used for cell or organ preservation and the treatment of osteoarthritis and rheumatoid arthritis VERTEX PHARMACEUTICALS, INCORPORATED (US) 2009-01-22 US disclosed
US-7407964-B2 Caspase inhibitors and uses thereof VERTEX PHARMACEUTICALS INCORPORATED (US) 2008-08-05 US disclosed
EP-0522533-A1 Process for polymerizing epsilon-caprolactam UNITIKA LTD. (JP) 1993-01-13 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 (3 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-20090023739-A1 interleukin-1B converting enzyme inhibitors such as 3-(6,11-Dioxo-1,2,3,4-tetrahydro-pyridazino[1,2-b]phthalazin-1-carboxamido)-5-fluoro-4-oxo-pentanoic acid, that mediate cell apoptosis and inflammation, used for cell or organ preservation and the treatment of osteoarthritis and rheumatoid arthritis IL1B, IL1RN, CASP1 HDAC3 595/4885HDAC11 1050/4885HDAC6 1636/4885
US-20120100274-A1 METHOD FOR SYNTHESISING 2-ACETYL-1-PYRROLINE AND THE STABLE PRECURSOR THEREOF, OPTIONALLY ISOTOPICALLY MARKED SAT1, PDHA1, PTMS HDAC3 464/4885HDAC11 285/4885HDAC6 721/4885
US-20090156572-A1 Nitrogen-containing heterocyclic compound and use thereof NTSR2, NTSR1, HNMT HDAC3 452/4885HDAC11 365/4885HDAC6 780/4885

“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.