SCHEMBL5261067

SCHEMBL5261067

NCCCC[C@H](NC(=O)Oc1ccccc1)C(=O)O

nearest known ligand 0.51

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SLC1A3 P43003 1/20 0.51
SIRT1 Q96EB6 3/20 0.50
MMP2 P08253 1/20 0.50
MMP9 P14780 1/20 0.50
FOLH1 Q04609 1/20 0.49
ITGB3 P05106 6/20 0.47
ITGA2B P08514 6/20 0.47
SIRT2 Q8IXJ6 3/20 0.47
CPB2 Q96IY4 2/20 0.46
ECE1 P42892 1/20 0.46
CPB1 P15086 1/20 0.46
CA1 P00915 1/20 0.45
CA2 P00918 1/20 0.45

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
SCHEMBL5261062 1.00 SLC1A3 (0.51) SLC1A3SIRT1MMP2MMP9FOLH1
SCHEMBL5854507 0.96 SLC1A3 (0.52) SLC1A3SIRT1MMP2MMP9FOLH1
SCHEMBL5854503 0.96 SLC1A3 (0.52) SLC1A3SIRT1MMP2MMP9FOLH1
SCHEMBL5855554 0.96 SLC1A3 (0.52) SLC1A3SIRT1MMP2MMP9FOLH1
SCHEMBL29233071 0.90 SIRT1 (0.49) SLC1A3SIRT1MMP2MMP9ITGB3
SCHEMBL29233069 0.90 SIRT1 (0.49) SLC1A3SIRT1MMP2MMP9ITGB3
SCHEMBL25409269 0.88 TGM2 (0.47) MMP2MMP9FOLH1ITGB3ITGA2B
SCHEMBL21891962 0.84 SIRT1 (0.61) SIRT1FOLH1SIRT2
SCHEMBL11436844 0.84 FAAH (0.55) SLC1A3SIRT1SIRT2
SCHEMBL30544863 0.83 TGM2 (0.50) MMP2MMP9FOLH1ITGB3ITGA2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119060325-B Polylysine rich in 1, 3-dicarbonyl side chains and preparation method and application thereof 浙江农林大学 2025-03-11 CN disclosed
CN-119060325-A Polylysine rich in 1, 3-dicarbonyl side chains and preparation method and application thereof 浙江农林大学 2024-12-03 CN disclosed
CN-118215651-A Method for producing isocyanate compound, method for producing urethane compound, method for recovering amine compound, and isocyanate composition 旭化成株式会社 2024-06-18 CN disclosed
CN-112438905-B Moisturizing and skin-brightening composition and application thereof 澳思美日用化工(广州)有限公司 2021-09-07 CN disclosed
CN-112438905-A Moisturizing and skin-brightening composition and application thereof 澳思美日用化工(广州)有限公司 2021-03-05 CN disclosed
CN-110546135-A Method for producing isocyanate ASAHI CHEMICAL IND 2019-12-06 CN disclosed
EP-1338588-B1 METHOD OF RESOLVING OPTICAL ISOMERS OF AMINO ACID DERIVATIVE TOKUYAMA CORP (JP) 2007-09-26 EP disclosed
US-7199264-B2 Method of resolving optical isomers of amino acid derivative TOKUYAMA CORPORATION (JP) 2007-04-03 US disclosed
US-7030214-B2 Ureins derived from α, ω, diamino acids and process for their preparation SOLVAY (SOCIETE ANONYME) (BE) 2006-04-18 US disclosed
EP-0922696-B1 Urea derivatives of alpha, omega-diaminoacids and peptides SOLVAY (BE) 2005-04-20 EP disclosed
US-20040102646-A1 Method of resolving optical isomers of amino acid derivative TOKUYAMA CORPORATION (JP) 2004-05-27 US disclosed
EP-1338588-A1 METHOD OF RESOLVING OPTICAL ISOMERS OF AMINO ACID DERIVATIVE TOKUYAMA CORPORATION (JP) 2003-08-27 EP disclosed
US-20020058784-A1 Ureins derived from alpha, omega, -diamond acids and process for their preparation CALLENS ROLAND (BE) 2002-05-16 US disclosed
US-6310178-B1 AS THE N-TERMINAL RESIDUE OF BIOLOGICALLY ACTIVE PEPTIDES, E.G, THYROTROPIN RELEASING HORMONE (BY REPLACING THE N-TERMINAL PYROGLUTAMYL GROUP); IMPARTING INCREASED RESISTANCE TO PROTEOLYTIC DIGESTION SOLVAY, S.A. (BE) 2001-10-30 US disclosed
EP-0633267-B1 Process for the preparation of alpha-amino acid amide for use in peptide synthesis SOLVAY (BE) 2001-09-26 EP disclosed
EP-0629612-B1 Process for the preparation of ureas derived from alpha, omega-diaminoacids SOLVAY (BE) 1999-12-01 EP disclosed
EP-0922696-A2 Urea derivatives of alpha, omega-diaminoacids and peptides SOLVAY (Société Anonyme) (BE) 1999-06-16 EP disclosed
EP-0633267-A1 Process for the preparation of an alpha-amino acid amide for use in peptide synthesis SOLVAY (Société Anonyme) (BE) 1995-01-11 EP disclosed
EP-0629612-A1 Ureas derived from alpha, omega-diaminoacids and process for their preparation SOLVAY (Société Anonyme) (BE) 1994-12-21 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-20040102646-A1 Method of resolving optical isomers of amino acid derivative ALAD, AAAS, BCAT1 SLC1A3 105/4885SIRT1 4595/4885MMP2 2787/4885
US-20020058784-A1 Ureins derived from alpha, omega, -diamond acids and process for their preparation UPP1, URB2, UFM1 SLC1A3 3925/4885SIRT1 4310/4885MMP2 3854/4885

“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.