Lysine

Lysine

SCHEMBL8562830

NCCCCC(N)C(=O)O.O=CO

nearest known ligand 0.83

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 0.83
ARG2 P78540 4/20 0.52
ARG1 P05089 3/20 0.52
RNPEP Q9H4A4 1/20 0.50
NOS2 P35228 5/20 0.46
CYP1A2 P05177 3/20 0.46
NOS1 P29475 3/20 0.46
NOS3 P29474 2/20 0.46
TSHR P16473 2/20 0.46
CYP3A4 P08684 1/20 0.46
CPB2 Q96IY4 2/20 0.46
GLA P06280 1/20 0.46
NFKB1 P19838 1/20 0.46
APEX1 P27695 1/20 0.46
CYP2C19 P33261 1/20 0.46
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

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
Lysine SCHEMBL2324976 1.00 GSR (0.83) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL28331087 0.96 GSR (0.77) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL445453 0.92 GSR (0.83) GSRARG2ARG1RNPEPNOS2
Ornithine Aketoglutarate SCHEMBL27686822 0.92 GSR (0.69) GSRARG2ARG1NOS2CYP1A2
Lysine SCHEMBL17102268 0.92 GSR (0.83) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL22534312 0.92 GSR (0.83) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL7343 0.91 GSR (1.00) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL1645 0.91 GSR (1.00) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL456381 0.91 GSR (1.00) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL20362357 0.91 GSR (1.00) GSRARG2ARG1RNPEPNOS2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118616094-A Artificial enzyme with laccase-like catalytic activity, and preparation method and application thereof 天津大学 2024-09-10 CN disclosed
US-8791129-B2 Phenylquinazoline derivatives MERCK PATENT GMBH (DE) 2014-07-29 US disclosed
US-20130178443-A1 PHENYLQUINAZOLINE DERIVATIVES MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 2013-07-11 US disclosed
EP-0844890-A1 THE USE OF BILE ACID DERIVATIVES THE UNIVERSITY OF BIRMINGHAM (GB) 1998-06-03 EP disclosed
WO-1997006829-A1 THE USE OF BILE ACID DERIVATIVES THE UNIVERSITY OF BIRMINGHAM (GB) 1997-02-27 WO 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 (1 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-20130178443-A1 PHENYLQUINAZOLINE DERIVATIVES HSP90B1, HSP90AB1, HSP90AA1 GSR 704/4885ARG2 176/4885ARG1 848/4885

“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.