Lysine

Lysine

SCHEMBL5060018

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

nearest known ligand 0.91

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 1/20 0.91
ARG2 P78540 4/20 0.55
ARG1 P05089 3/20 0.55
RNPEP Q9H4A4 1/20 0.54
NOS2 P35228 6/20 0.53
CYP1A2 P05177 2/20 0.53
TSHR P16473 2/20 0.53
CYP2C19 P33261 2/20 0.53
GLA P06280 1/20 0.53
NFKB1 P19838 1/20 0.53
APEX1 P27695 1/20 0.53
NOS1 P29475 4/20 0.53
NOS3 P29474 3/20 0.53
CYP3A4 P08684 1/20 0.53
BLM P54132 2/20 0.52
KMT2A Q03164 2/20 0.52
ALOX15 P16050 1/20 0.52
PMP22 Q01453 1/20 0.52
MEN1 O00255 1/20 0.50
DDAH1 O94760 1/20 0.50

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 SCHEMBL4641859 1.00 GSR (0.91) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL31644218 1.00 GSR (0.91) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL31039861 1.00 GSR (0.91) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL8937983 0.98 GSR (0.87) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL15286920 0.95 GSR (0.91) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL1042282 0.95 GSR (0.91) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL9439278 0.95 GSR (1.00) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL12867528 0.95 GSR (1.00) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL7343 0.95 GSR (1.00) GSRARG2ARG1RNPEPNOS2
Lysine SCHEMBL8613373 0.95 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 40 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117479946-A Dry powder compositions containing treprostinil and its prodrug and further comprising (E) -3,6-bis [4- (N-carbonyl-2-propenyl) amide butyl ] -2,5-diketopiperazine (FDKP) 联合治疗公司 2024-01-30 CN claimed
EP-3727600-B1 AMINO ACID CARBAMATE COMPLEXES COLGATE PALMOLIVE CO (US) 2023-09-20 EP claimed
US-10857083-B2 Amino acid carbamate complexes COLGATE-PALMOLIVE COMPANY (US) 2020-12-08 US claimed
EP-3727600-A1 AMINO ACID CARBAMATE COMPLEXES Colgate-Palmolive Company (US) 2020-10-28 EP claimed
CN-111479614-A Amino acid carbamate complexes 高露洁-棕榄公司 2020-07-31 CN claimed
US-20190183765-A1 Amino Acid Carbamate Complexes COLGATE-PALMOLIVE COMPANY (US) 2019-06-20 US claimed
CN-1213058-C FAP-activated anti-tumor compounds BOEHRINGER INGELHEIM PHARMA (DE) 2005-08-03 CN claimed
EP-1439820-A2 METHODS AND DOSAGE FORMS FOR IMPROVING THE BIOAVAILABILITY OF THERAPEUTIC AGENTS LABOPHARM INC. (CA) 2004-07-28 EP claimed
US-20030138486-A1 Methods and dosage forms for improving the bioavailability of therapeutic agents KING PHARMACEUTICALS RESEARCH 2003-07-24 US claimed
WO-2003037301-A2 ORAL DOSAGE FORMS FOR IMPROVING THE BIOAVAILABILITY OF THERAPEUTIC AGENTS KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC (US) 2003-05-08 WO claimed
WO-2003037296-A2 METHODS AND DOSAGE FORMS FOR IMPROVING THE BIOAVAILABILITY OF THERAPEUTIC AGENTS LABOPHARM INC. (CA) 2003-05-08 WO claimed
EP-0162043-B1 METHOD AND APPARATUS FOR PRODUCING EFFERVESCENT TABLETS AND GRANULATED PRODUCTS BRU, Jean (FR) 1989-12-13 EP claimed
US-4614648-A Process for manufacturing effervescent granules and tablets BRU JEAN (FR) 1986-09-30 US claimed
CN-117479946-A Dry powder compositions containing treprostinil and its prodrug and further comprising (E) -3,6-bis [4- (N-carbonyl-2-propenyl) amide butyl ] -2,5-diketopiperazine (FDKP) 联合治疗公司 2024-01-30 CN disclosed
EP-3727600-B1 AMINO ACID CARBAMATE COMPLEXES COLGATE PALMOLIVE CO (US) 2023-09-20 EP disclosed
US-11739055-B2 Process for preparing diisocyanates based on lysine EVONIK OPERATIONS GMBH (DE) 2023-08-29 US disclosed
WO-2003037301-A2 ORAL DOSAGE FORMS FOR IMPROVING THE BIOAVAILABILITY OF THERAPEUTIC AGENTS KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, INC (US) 2003-05-08 WO disclosed
WO-2003037296-A2 METHODS AND DOSAGE FORMS FOR IMPROVING THE BIOAVAILABILITY OF THERAPEUTIC AGENTS LABOPHARM INC. (CA) 2003-05-08 WO disclosed
US-RE33086-E HIGH PURITY; FOR PHARMACEUTICALS RECHERCHE ET PROPRIETE INDUSTRIELLE (FR) 1989-10-10 US disclosed
US-4614648-A Process for manufacturing effervescent granules and tablets BRU JEAN (FR) 1986-09-30 US 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-11739055-B2 Process for preparing diisocyanates based on lysine KDM7A, KDM8, JMJD6 GSR 2994/4885ARG2 328/4885ARG1 50/4885
US-10857083-B2 Amino acid carbamate complexes CPS1, GLUL, PROC GSR 1816/4885ARG2 57/4885ARG1 27/4885
US-20190183765-A1 Amino Acid Carbamate Complexes CPS1, GLUL, PROC GSR 1816/4885ARG2 57/4885ARG1 27/4885

“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.