N-Me-Lys-OH

Name: N-Me-Lys-OH | 7431-89-2
Brand: US-CATO
SKU: S57CPTD787645_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57CPTD787645_10_MG

Vendor: US-CATO

Product Information

Product Name

N-Me-Lys-OH

Brand Name

US-CATO

Product Number

CPTD787645

CAS

7431-89-2

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

7010497

IUPAC Name

(2S)-6-amino-2-(methylamino)hexanoic acid

InChI Key

OLYPWXRMOFUVGH-LURJTMIESA-N

SMILES

CNC@@H(CCCCN)C(=O)O

References Data Source From Pubchem

Addictive drug abuse and depression-a focus on epigenetics

Publication Name: Communications Biology

Publication Date: 2026-02-21

DOI: 10.1038/s42003-026-09705-9

Multi-omics profiling of cachexia-targeted tissues reveals a spatio-temporally coordinated response to cancer

Publication Name: Nature Metabolism

Publication Date: 2026-01-15

DOI: 10.1038/s42255-025-01434-3

Many faces of mammalian NSD methyltransferases

Publication Name: Cellular & Molecular Biology Letters

Publication Date: 2026-01-06

DOI: 10.1186/s11658-025-00848-x

Machine learning-driven prediction of substrates for enzymes introducing or removing protein post-translational modifications

Publication Name: Communications Chemistry

Publication Date: 2025-11-07

DOI: 10.1038/s42004-025-01717-6

Tudor-based proteomic strategy pan-specifically enriches and identifies protein arginine methylation

Publication Name: EMBO Reports

Publication Date: 2025-10-20

DOI: 10.1038/s44319-025-00599-y

N-Me-Lys-OH

Product Information

General Information

References Data Source From Pubchem

Addictive drug abuse and depression-a focus on epigenetics

Multi-omics profiling of cachexia-targeted tissues reveals a spatio-temporally coordinated response to cancer

Many faces of mammalian NSD methyltransferases

Machine learning-driven prediction of substrates for enzymes introducing or removing protein post-translational modifications

Tudor-based proteomic strategy pan-specifically enriches and identifies protein arginine methylation

N-Me-Lys-OH

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Flurbiprofen Impurity 21 (Mixture of Diastereomers)

Docetaxel Impurity 40

H-Met-Glu-OH

Fluticasone Impurity 106

Efavirenz Related Compound C

Cholecalciferol EP Impurity A

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N-Me-Lys-OH

Product Information

General Information

References Data Source From Pubchem

Addictive drug abuse and depression-a focus on epigenetics

Multi-omics profiling of cachexia-targeted tissues reveals a spatio-temporally coordinated response to cancer

Many faces of mammalian NSD methyltransferases

Machine learning-driven prediction of substrates for enzymes introducing or removing protein post-translational modifications

Tudor-based proteomic strategy pan-specifically enriches and identifies protein arginine methylation

N-Me-Lys-OH

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Mycophenolate Mofetil EP Impurity H

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Flurbiprofen Impurity 21 (Mixture of Diastereomers)

Docetaxel Impurity 40

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Fluticasone Impurity 106

Efavirenz Related Compound C

Cholecalciferol EP Impurity A

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