Lysine

Lysine

SCHEMBL614905

NCC(=O)O.NCCCC[C@H](N)C(=O)O.N[C@@H](CC(=O)O)C(=O)O

nearest known ligand 0.74

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PPARDPTGS1PTGS2dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Lysine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GSR P00390 2/20 0.74
ARG2 P78540 4/20 0.47
ARG1 P05089 3/20 0.47
RNPEP Q9H4A4 1/20 0.46
CYP1A2 P05177 3/20 0.45
GRM8 O00222 1/20 0.45
GRM6 O15303 1/20 0.45
GRIN2D O15399 1/20 0.45
GRIN3B O60391 1/20 0.45
GRIK1 P39086 1/20 0.45
GRM5 P41594 1/20 0.45
GRIA1 P42261 1/20 0.45
GRIA2 P42262 1/20 0.45
GRIA3 P42263 1/20 0.45
SLC1A3 P43003 1/20 0.45
SLC1A2 P43004 1/20 0.45
SLC1A1 P43005 1/20 0.45
GRIA4 P48058 1/20 0.45
GRIN1 Q05586 1/20 0.45
GRIN2A Q12879 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
Aspartic Acid SCHEMBL8508699 0.98 GSR (0.71) GSRARG2ARG1RNPEPCYP1A2
Aspartic Acid SCHEMBL8508899 0.98 GSR (0.71) GSRARG2ARG1RNPEPCYP1A2
Aspartic Acid SCHEMBL8508697 0.98 GSR (0.71) GSRARG2ARG1RNPEPCYP1A2
Aspartic Acid SCHEMBL8508901 0.98 GSR (0.71) GSRARG2ARG1RNPEPCYP1A2
Lysine SCHEMBL1425215 0.96 GSR (0.80) GSRARG2ARG1RNPEPCYP1A2
Lysine SCHEMBL20952564 0.96 GSR (0.80) GSRARG2ARG1RNPEPCYP1A2
Lysine SCHEMBL2589784 0.96 GSR (0.80) GSRARG2ARG1RNPEPCYP1A2
Lysine SCHEMBL18528930 0.96 GSR (0.80) GSRARG2ARG1RNPEPCYP1A2
Lysine SCHEMBL1425217 0.96 GSR (0.80) GSRARG2ARG1RNPEPCYP1A2
Lysine SCHEMBL31679370 0.96 GSR (0.80) GSRARG2ARG1RNPEPCYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024140670-A1 CONJUGATE AND USES THEREOF FULL-LIFE TECHNOLOGIES HK LIMITED (CN) 2024-07-04 WO claimed
US-5118669-A Inhibit histamine liberation and antibody production HITACHI CHEMICAL CO., LTD. (JP) 1992-06-02 US claimed
WO-2024140670-A1 CONJUGATE AND USES THEREOF FULL-LIFE TECHNOLOGIES HK LIMITED (CN) 2024-07-04 WO disclosed
US-20220105194-A1 CONJUGATE COMPRISING LIGAND, SPACER, PEPTIDE LINKER, AND BIOMOLECULE ASTELLAS PHARMA INC. (JP) 2022-04-07 US disclosed
EP-3909606-A1 COMPLEX COMPRISING LIGAND AND CEACAM5 ANTIBODY FAB FRAGMENT Astellas Pharma Inc. (JP) 2021-11-17 EP disclosed
EP-3909608-A1 COMPLEX COMPRISING LIGAND, SPACER, PEPTIDE LINKER, AND BIOMOLECULE Astellas Pharma Inc. (JP) 2021-11-17 EP disclosed
CN-113301920-A Complexes comprising ligands, spacers, peptide linkers and biomolecules 安斯泰来制药株式会社 2021-08-24 CN disclosed
CN-113271973-A Complex comprising a ligand and a CEACAM5 antibody Fab fragment 安斯泰来制药株式会社 2021-08-17 CN disclosed
US-20200354403-A1 DUAL MASS SPECTOMETRY-CLEAVABLE CROSSLINKING REAGENTS FOR PROTEIN-PROTEIN INTERACTIONS BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM 2020-11-12 US disclosed
US-10752655-B2 Dual mass spectrometry-cleavable crosslinking reagents for protein-protein interactions BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2020-08-25 US disclosed
WO-2020145227-A1 COMPLEX COMPRISING LIGAND, SPACER, PEPTIDE LINKER, AND BIOMOLECULE アステラス製薬株式会社 2020-07-16 WO disclosed
US-20030186334-A1 KTS-disintegrins TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2003-10-02 US disclosed
EP-1322322-A2 COMPOUNDS AND METHODS FOR INHIBITING ALPHA-1 BETA-1 INTEGRINS Temple University of the Commonwealth System of Higher Education (US) 2003-07-02 EP disclosed
WO-2002022571-A2 COMPOUNDS AND METHODS FOR INHIBITING ALPHA-1 BETA-1 INTEGRINS TEMPLE UNIVERSITY-OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2002-03-21 WO disclosed
US-6022854-A IN SITU TREATMENT OF VASCULAR INJURY, ATHEROSCLEROSIS OR THROMBOSIS BY TARGETED DELIVERY OF A DRUG. E.G. AN ANTICOAGUANT OR ANTITHROMBIN AGENTS, CONJUGATED WITH KISTRIN; WHICH BINDS TO MEGAKARYOCYTES OR PLATELETS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2000-02-08 US disclosed
EP-0421682-B1 Novel peptides, intermediates therefor, process for preparing the same, and antiallergic agents, vasodilators and immunoregulators HITACHI CHEMICAL CO LTD (JP) 1997-03-26 EP disclosed
WO-1994015953-A9 PLATELET-SPECIFIC THERAPEUTIC COMPOUND AND METHOD OF TREATING PLATELET-MOBILIZING DISEASES 1994-09-15 WO disclosed
US-5223487-A Tri-, tetra-, penta- and hexapeptatides of Asp, Gly, Lys, Ser, Ala and salts HITACHI CHEMICAL CO., LTD. (JP) 1993-06-29 US disclosed
US-5118669-A Inhibit histamine liberation and antibody production HITACHI CHEMICAL CO., LTD. (JP) 1992-06-02 US disclosed
EP-0421682-A1 Novel peptides, intermediates therefor, process for preparing the same, and antiallergic agents, vasodilators and immunoregulators HITACHI CHEMICAL CO., LTD. (JP) 1991-04-10 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-20220105194-A1 CONJUGATE COMPRISING LIGAND, SPACER, PEPTIDE LINKER, AND BIOMOLECULE MUC1, CA14, CA13 GSR 4068/4885ARG2 2402/4885ARG1 1809/4885
US-10752655-B2 Dual mass spectrometry-cleavable crosslinking reagents for protein-protein interactions TIMCC, DCLRE1A, MTCL3 GSR 4137/4885ARG2 2959/4885ARG1 3029/4885
US-20200354403-A1 DUAL MASS SPECTOMETRY-CLEAVABLE CROSSLINKING REAGENTS FOR PROTEIN-PROTEIN INTERACTIONS TIMCC, MTCL3, DCLRE1A GSR 4001/4885ARG2 2131/4885ARG1 2279/4885

“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.