SCHEMBL993570

SCHEMBL993570

CC(=O)NC(C)C(=O)NCc1ccccc1

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA12 O43570 1/20 0.64
CA1 P00915 1/20 0.64
CA2 P00918 1/20 0.64
CA3 P07451 1/20 0.64
CA4 P22748 1/20 0.64
CA6 P23280 1/20 0.64
CA5A P35218 1/20 0.64
CA7 P43166 1/20 0.64
CACNA1C Q13936 1/20 0.64
SCN9A Q15858 1/20 0.64
CA9 Q16790 1/20 0.64
CA13 Q8N1Q1 1/20 0.64
CA14 Q9ULX7 1/20 0.64
CA5B Q9Y2D0 1/20 0.64
MMP8 P22894 1/20 0.62
ALDH1A1 P00352 4/20 0.58
KMT2A Q03164 2/20 0.58
MME P08473 1/20 0.57
MAPT P10636 2/20 0.55
L3MBTL1 Q9Y468 1/20 0.55

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
SCHEMBL6814514 1.00 CA12 (0.64) CA12CA1CA2CA3CA4
SCHEMBL6813286 1.00 CA12 (0.64) CA12CA1CA2CA3CA4
SCHEMBL24347010 0.97 MMP8 (0.63) CA12CA1CA2CA3CA4
SCHEMBL25214759 0.88 MMP8 (0.63) CA12CA1CA2CA3CA4
SCHEMBL25214750 0.88 MMP8 (0.63) CA12CA1CA2CA3CA4
SCHEMBL25240460 0.88 MMP8 (0.63) CA12CA1CA2CA3CA4
SCHEMBL12436634 0.87 MMP8 (0.59) CA12CA1CA2CA3CA4
SCHEMBL24345983 0.85 MMP8 (0.54) CA12CA1CA2CA3CA4
SCHEMBL8545637 0.85 CA12 (0.66) CA12CA1CA2CA3CA4
SCHEMBL24347008 0.84 MMP8 (0.63) CA12CA1CA2CA3CA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0194464-A1 Amino acid derivatives and use thereof for the preparation of an anticonvulsant Research Corporation Technologies, Inc. (a Delaware corp.) (US) 1986-09-17 EP claimed
EP-2627639-B1 N-OPTIONALLY SUBSTITUTED ARYL-2-OLIGOMER-3-ALKOXYPROPIONAMIDES NEKTAR THERAPEUTICS (US) 2021-12-22 EP disclosed
US-9133101-B2 Processes for the preparation of (R)-2-acetamido-N-benzyl-3-methoxypropionamide and intermediates thereof SIGNA S.A. DE C.V. (MX) 2015-09-15 US disclosed
US-20150025274-A1 PROCESSES FOR THE PREPARATION OF (R)-2-ACETAMIDO-N-BENZYL-3-METHOXYPROPIONAMIDE AND INTERMEDIATES THEREOF SIGNA S.A. DE C.V. (MX) 2015-01-22 US disclosed
US-8933065-B2 N-benzylamide substituted derivatives of 2-(acylamido)acetic acid and 2-(acylamido)propionic acids: potent neurological agents THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2015-01-13 US disclosed
US-8933065-B2 N-benzylamide substituted derivatives of 2-(acylamido)acetic acid and 2-(acylamido)propionic acids: potent neurological agents THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2015-01-13 US disclosed
EP-2262764-B1 NOVEL N-BENZYLAMIDE SUBSTITUTED DERIVATIVES OF 2-(ACYLAMIDO)ACETIC ACID AND 2-(ACYLAMIDO)PROPIONIC ACIDS: POTENT NEUROLOGICAL AGENTS UNIV NORTH CAROLINA (US) 2014-11-12 EP disclosed
EP-2528892-B1 PROCESS FOR THE SYNTHESIS OF LACOSAMIDE EUTICALS SPA (IT) 2014-06-04 EP disclosed
WO-2013030654-A1 PROCESSES FOR THE PREPARATION OF (R)-2-ACETAMIDO-N-BENZYL-3-METHOXYPROPIONAMIDE AND INTERMEDIATES THEREOF SIGNA S.A. DE C.V. (MX) 2013-03-07 WO disclosed
US-20110021482-A1 Novel N-Benzylamide Substituted Derivatives of 2-(Acylamido)acetic Acid and 2-(Acylamido)propionic Acids: Potent Neurological Agents UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL, THE 2011-01-27 US disclosed
EP-0592490-B1 AMINO ACID DERIVATIVE ANTICONVULSANT RES CORP TECHNOLOGIES INC (US) 1998-01-07 EP disclosed
WO-1997033861-A1 ANTICONVULSANT ENANTIOMERIC AMINO ACID DERIVATIVES RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1997-09-18 WO disclosed
US-5654301-A Lacosamide FDA Orange book listed patent RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1997-08-05 US disclosed
US-5378729-A Diamide derivatives RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1995-01-03 US disclosed
EP-0263506-B1 ANTICONVULSANT COMPOSITION CONTAINING AMINO ACID DERIVATIVE AND USE OF SAID AMINO ACID DERIVATIVE RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1993-08-04 EP disclosed
WO-1992021648-A1 AMINO ACID DERIVATIVE ANTICONVULSANT RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1992-12-10 WO disclosed
EP-0194464-B1 AMINO ACID DERIVATIVES AND USE THEREOF FOR THE PREPARATION OF AN ANTICONVULSANT Research Corporation Technologies, Inc. (a Delaware corp.) (US) 1991-04-03 EP disclosed
WO-1990015069-A2 AMINO ACID DERIVATIVE ANTICONVULSANT RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1990-12-13 WO disclosed
EP-0400440-A1 Amino acid derivative anticonvulsant RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1990-12-05 EP disclosed
EP-0194464-A1 Amino acid derivatives and use thereof for the preparation of an anticonvulsant Research Corporation Technologies, Inc. (a Delaware corp.) (US) 1986-09-17 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-20110021482-A1 Novel N-Benzylamide Substituted Derivatives of 2-(Acylamido)acetic Acid and 2-(Acylamido)propionic Acids: Potent Neurological Agents NAAA, AADAC, GBA1 CA12 814/4885CA1 174/4885CA2 296/4885
US-20150025274-A1 PROCESSES FOR THE PREPARATION OF (R)-2-ACETAMIDO-N-BENZYL-3-METHOXYPROPIONAMIDE AND INTERMEDIATES THEREOF NAAA, CYP1A2, REN CA12 2436/4885CA1 1840/4885CA2 1969/4885

“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.