Iodoacetamide - Moligand™, ≥98% , Activator of TRPA1, CAS No.144-48-9, Activator of TRPA1

Name: Iodoacetamide - Moligand™, ≥98% , Activator of TRPA1, CAS No.144-48-9, Activator of TRPA1
Brand: Aladdin Scientific
SKU: I105563
Availability: InStock

CAS: 144-48-9 Cat. No.: I105563 Formula: C₂H₄INO Peso molecolare: 184.96 Beilstein Registry Number: 1739080 Numero EC: 205-630-1

112 Citations COA

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QUALITÀ & PUREZZA Moligand™ ? ≥98%

Synonyms

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Scheda delle specifiche

Panoramica Specifiche Nomi e identificatori Documentazione Dati avanzati Taxonomic Classification Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Domande frequenti e articoli Citations of This Product Calcolatori di soluzioni Recensioni

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Perché questa qualità

Moligand™, ≥98% Moligand™ per flussi di lavoro cromatografici e analitici sensibili che richiedono un'interferenza minima della linea di base.

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Stoccaggio e spedizione

Store at 2-8°C,Protected from light Spedizione Wet ice. Consultare il COA specifico del lotto per le specifiche esatte.

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Documenti di qualità

SDS, COA, scheda tecnica e scheda delle specifiche disponibili per il download. COA specifico del lotto accessibile tramite ricerca per numero di lotto.

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Prova documentale

Citato in 112 pubblicazioni peer-reviewed su cromatografia, sintesi organica e reazioni di accoppiamento incrociato.

Panoramica

Alkylating reagent for cysteine residues in peptide sequencing.

Specifiche

Sinonimi

Specifiche e purezza

Moligand™, ≥98%

Meccanismi biochimici e fisiologici

Iodoacetamide acts as an alkylating reagent for cysteine residues in peptide sequencing. It is an irreversible inhibitor of enzymes with cysteine at the active site. It reacts much more slowly with histidine residues, but that activity is responsible for

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Protected from light

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Moligand™

Tipo di azione

ACTIVATOR

Meccanismo d'azione

Activator of TRPA1

Purezza

≥98%

Nomi e identificatori

Pubchem Sid

508815490

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508815490

Sorrisi canonici

C(C(=O)N)I

IUPAC Name

2-iodoacetamide

InChIKey

PGLTVOMIXTUURA-UHFFFAOYSA-N

INCHI

1S/C2H4INO/c3-1-2(4)5/h1H2,(H2,4,5)

Isomeri SMILES

C(C(=O)N)I

WGK Germania

RTECS

AC4200000

Numero UN

2811

Gruppo di imballaggio

III

Peso molecolare

184.96

Beilstein

1739080

Reaxy-Rn

1739080

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1739080&ln=

Documentazione

📋 Scheda di dati di sicurezza (SDS)

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Riepilogo di riferimento rapido delle specifiche e applicazioni del prodotto.

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Dati avanzati

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Classe Carboxylic acids and derivatives
    - Subclass Carboxylic acid derivatives
      - Level5 Carboxylic acid amides
        Level6 Primary carboxylic acid amides

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Classe	Carboxylic acids and derivatives
Subclass	Carboxylic acid derivatives
Intermediate Tree Nodes	Carboxylic acid amides
Direct Parent	Primary carboxylic acid amides
Alternative Parents	Organopnictogen compounds Organonitrogen compounds Organoiodides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl iodides
Molecular Framework	Aliphatic acyclic compounds
Substituents	Primary carboxylic acid amide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organoiodide - Organohalogen compound - Carbonyl group - Alkyl iodide - Alkyl halide - Aliphatic acyclic compound
Descrizione	This compound belongs to the class of organic compounds known as primary carboxylic acid amides. These are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2.
External Descriptors	an iodide
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Struttura 3D

Obiettivi associati (umani)

CYP3A4 Tclin Cytochrome P450 3A4 (1 Activities)

Discover Target: CYP3A4

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TRPA1 Tclin Transient receptor potential cation channel subfamily A member 1 (1 Activities)

Discover Target: TRPA1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TYMS Tclin Thymidylate synthase (1651 Activities)

Discover Target: TYMS

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

Discover Target: CHRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AK2 Tbio Adenylate kinase 2 (264 Activities)

Discover Target: AK2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

POLB Tchem DNA polymerase beta (23632 Activities)

Discover Target: POLB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GLA Tclin Alpha-galactosidase A (5444 Activities)

Discover Target: GLA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ARSA Tbio Cerebroside-sulfatase (655 Activities)

Discover Target: ARSA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALOX15B Tchem Arachidonate 15-lipoxygenase, type II (7244 Activities)

Discover Target: ALOX15B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)

Discover Target: CYP2D6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)

Discover Target: ALOX15

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

Discover Target: CYP1A2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)

Discover Target: CYP2C9

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)

Discover Target: CYP2C19

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TP53 Tchem Cellular tumor antigen p53 (48468 Activities)

Discover Target: TP53

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

F13A1 Tchem Coagulation factor XIII (223 Activities)

Discover Target: F13A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)

Discover Target: HSD17B10

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)

Discover Target: KDM4E

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

USP2 Tbio Ubiquitin carboxyl-terminal hydrolase 2 (8818 Activities)

Discover Target: USP2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

LMNA Tbio Prelamin-A/C (36751 Activities)

Discover Target: LMNA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RECQL Tbio ATP-dependent DNA helicase Q1 (5575 Activities)

Discover Target: RECQL

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

BLM Tchem Bloom syndrome protein (4248 Activities)

Discover Target: BLM

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)

Discover Target: HPGD

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

THPO Tbio Thrombopoietin (834 Activities)

Discover Target: THPO

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PMP22 Tbio Peripheral myelin protein 22 (699 Activities)

Discover Target: PMP22

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

Discover Target: CBX1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MPHOSPH8 Tbio M-phase phosphoprotein 8 (656 Activities)

Discover Target: MPHOSPH8

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ATG4B Tchem Cysteine protease ATG4B (985 Activities)

Discover Target: ATG4B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)

Discover Target: RGS4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADH1A Tclin Alcohol dehydrogenase (35 Activities)

Discover Target: ADH1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Obiettivi associati (non umani)

Saccharomyces cerevisiae (19171 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Rattus norvegicus (775804 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GCN5 Histone acetyltransferase GCN5 (89 Activities)

Discover Target: GCN5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Trpa1 Transient receptor potential cation channel subfamily A member 1 (1003 Activities)

Discover Target: Trpa1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

pfk 6-phospho-1-fructokinase (7870 Activities)

Discover Target: pfk

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

Discover Target: Txnrd1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)

Discover Target: fba

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FTL Ferritin light chain (43324 Activities)

Discover Target: FTL

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

crtY Lycopene cyclase (9 Activities)

Discover Target: crtY

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Certificati (CoA, COO, BSE/TSE e tabella di analisi)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

61 results found

Lot Number	Certificate Type	Data	Oggetto
H2612705	Certificate of Analysis	Jun 22, 2026	I105563
H2612706	Certificate of Analysis	Jun 22, 2026	I105563
H2612707	Certificate of Analysis	Jun 22, 2026	I105563
H2612708	Certificate of Analysis	Jun 22, 2026	I105563
G2607018	Certificate of Analysis	May 06, 2026	I105563
H2605006	Certificate of Analysis	May 06, 2026	I105563
D2630375	Certificate of Analysis	May 06, 2026	I105563
D2630424	Certificate of Analysis	May 06, 2026	I105563
D2630425	Certificate of Analysis	May 06, 2026	I105563
D2630426	Certificate of Analysis	May 06, 2026	I105563
D2630427	Certificate of Analysis	May 06, 2026	I105563
H2613018	Certificate of Analysis	May 06, 2026	I105563
J2531444	Certificate of Analysis	Nov 03, 2025	I105563
J2531370	Certificate of Analysis	Nov 03, 2025	I105563
J2531420	Certificate of Analysis	Nov 03, 2025	I105563
J2531441	Certificate of Analysis	Nov 03, 2025	I105563
I2506008	Certificate of Analysis	Jun 24, 2025	I105563
F2518411	Certificate of Analysis	Jun 24, 2025	I105563
F2518410	Certificate of Analysis	Jun 24, 2025	I105563
F2518409	Certificate of Analysis	Jun 24, 2025	I105563
F2518408	Certificate of Analysis	Jun 24, 2025	I105563
F2518379	Certificate of Analysis	Jun 24, 2025	I105563
F2518380	Certificate of Analysis	Jun 24, 2025	I105563
L2406530	Certificate of Analysis	Oct 22, 2024	I105563
L2406462	Certificate of Analysis	Oct 22, 2024	I105563
L2406463	Certificate of Analysis	Oct 22, 2024	I105563
L2406464	Certificate of Analysis	Oct 22, 2024	I105563
F2411238	Certificate of Analysis	May 16, 2024	I105563
F2411237	Certificate of Analysis	May 16, 2024	I105563
F2411236	Certificate of Analysis	May 16, 2024	I105563
I2406219	Certificate of Analysis	May 16, 2024	I105563
F2411239	Certificate of Analysis	May 16, 2024	I105563
E2408061	Certificate of Analysis	Nov 17, 2023	I105563
K2330108	Certificate of Analysis	Nov 17, 2023	I105563
K2330110	Certificate of Analysis	Nov 17, 2023	I105563
K2330112	Certificate of Analysis	Nov 17, 2023	I105563
K2330114	Certificate of Analysis	Nov 17, 2023	I105563
I2304340	Certificate of Analysis	Aug 18, 2023	I105563
I2304350	Certificate of Analysis	Aug 18, 2023	I105563
I2304385	Certificate of Analysis	Aug 18, 2023	I105563
F2305295	Certificate of Analysis	May 24, 2023	I105563
F2305294	Certificate of Analysis	May 24, 2023	I105563
F2305296	Certificate of Analysis	May 24, 2023	I105563
D2418049	Certificate of Analysis	May 24, 2023	I105563
F2305292	Certificate of Analysis	May 10, 2023	I105563
F2305285	Certificate of Analysis	May 10, 2023	I105563
F2305293	Certificate of Analysis	May 10, 2023	I105563
G2311061	Certificate of Analysis	May 10, 2023	I105563
D2320040	Certificate of Analysis	Nov 21, 2022	I105563
K2224520	Certificate of Analysis	Nov 21, 2022	I105563
K2224518	Certificate of Analysis	Nov 21, 2022	I105563
K2224517	Certificate of Analysis	Nov 21, 2022	I105563
K2224516	Certificate of Analysis	Nov 21, 2022	I105563
E2310060	Certificate of Analysis	Nov 21, 2022	I105563
H2215147	Certificate of Analysis	Jun 05, 2022	I105563
H2215146	Certificate of Analysis	Jun 05, 2022	I105563
H2215145	Certificate of Analysis	Jun 05, 2022	I105563
H2215144	Certificate of Analysis	Jun 05, 2022	I105563
F2201266	Certificate of Analysis	May 24, 2022	I105563
E2220212	Certificate of Analysis	May 24, 2022	I105563
C2208137	Certificate of Analysis	Mar 15, 2022	I105563

Proprietà chimiche e fisiche

Solubilità	Soluble in water; Soluble in Methanol
Sensibilità	Light & Moisture Sensitive
Punto di fusione (°C)	95°C
Peso molecolare	184.960 g/mol
XLogP3	-0.200
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	184.934 Da
Monoisotopic Mass	184.934 Da
Topological Polar Surface Area	43.100 Å²
Heavy Atom Count	5
Formal Charge	0
Complexity	44.900
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Domande frequenti e articoli

Common Reagents for Reducing Protein Disulfide Bonds

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Reducible protein Protein disulfide bond

A Practical Guide to Small-Molecule Chemical Probes: Concept Clarification, Causal Validation, and Experimental Selection (with Product Navigation and Tables A–D)

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Chemical probe Small-Molecule Chemical Probes

Endoproteinase Lys-C: Mechanism, Applications, and Method-Control Considerations for Lysine-Specific Digestion

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Peptide Mapping Serine protease Lys-C Endoproteinase Lys-C Lysine-specific cleavage Denaturing digestion LC–MS Sequence coverage Missed cleavage rate Critical peptide monitoring Method validation

Plant Omics Panorama: Workflow Frameworks and Multi-Omics Integration from Genomics to Transcriptomics, Proteomics, and Metabolomics

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

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Proteomics Plant omics Genomics Transcriptomics Metabolomics Multi-omics integration Phenomics Epigenomics

Bromelain: Enzymological Properties and Key Points for Food, Pharmaceutical, and Industrial Applications

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Cysteine protease bromelain proteolysis BAEE fibrin meat tenderization

Methionine: Biological Roles and Key Points for Research Application

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

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glutathione one-carbon metabolism SAM Redox homeostasis methionine SAH methylation homocysteine transsulfuration pathway

Review of Chymotrypsin: Enzymological Properties, Catalytic Mechanism, and Research Applications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Peptide Mapping Serine protease substrate specificity limited proteolysis catalytic triad Chymotrypsin Alpha-Chymotrypsin Oxyanion Hole Acyl-Enzyme Intermediate Methodological Quality Control

Clostridial Proteases: Classification, Molecular Mechanisms, and Research Applications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

clostridial proteases

Glycoprotein Hormone Family: Molecular Features, Signaling Bias, and In Vivo Pharmacokinetics

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Glycosylation Pharmacokinetics FSH LH hCG TSH Glycoprotein hormones Common α-subunit Specific β-subunit Signaling bias

Methodological Studies on Glycoprotein Structural Characterization and Quality Attribute Analysis

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Glycosylation Glycoprotein Quality Attributes Critical Quality Attributes Released Glycan Analysis Glycopeptide Analysis Intact Mass Spectrometry Higher-Order Structure Multi-Attribute Method Comparability Study

Research Framework for Multi-Enzyme Digestion Strategies and Optimization of Proteomic Coverage

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Proteomics Mass spectrometry Multi-Enzyme Digestion Coverage Optimization Proteolytic Strategy Peptide Detectability Sample Complexity Research Framework

Thiol and Disulfide Status in Biological Samples: Detection Methods and Applications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

glutathione disulfide bonds DTNB Thiol redox state Ellman assay protein thiol GSH/GSSG

Neuropathological Mechanisms of Cerebral Infarction

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

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Oxidative Stress neuroinflammation blood-brain barrier cerebral infarction ischemic stroke neuropathological mechanism ischemic penumbra excitotoxicity

Summary of Research Advances in Oxidative Stress

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

ROS Oxidative Stress Nrf2 ferroptosis non-coding RNA mitochondrial oxidative stress redox proteomic precision antioxidant therapy

Regulatory Mechanisms, Research Methods, and Modification-Omics Analysis of Protein Post-Translational Modifications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Glycosylation methylation SUMOylation Protein Post-Translational Modifications Ubiquitination Phosphorylation Acetylation Lactylation Modification Proteomics

Why Proximity to Cysteine Does Not Necessarily Lead to Covalent Bond Formation: Warhead Reactivity, Reaction Geometry, and Target-Site Microenvironment

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Cysteine Covalent Inhibition

Citations of This Product

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Recensioni

📚 Citazioni per applicazione

Other applications54

Controlled-release & nanoparticle carrier3

Drug / compound screening22

Cell viability9

Organic synthesis — reaction medium32

Nanoparticle / material biocompatibility1

Chromatography (HPLC / GC / TLC)20

Spectroscopy sample preparation13

Topical & ophthalmic formulation2

Extraction & workup solvent38

Industrial & non-pharma application2

Cytotoxicity screening8

Cell proliferation5

Polymer synthesis & polymerization1

Cancer cell line characterization1

Visualizza tutte le 112 citazioni →

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Iodoacetamide - Moligand™, ≥98% , Activator of TRPA1, CAS No.144-48-9, Activator of TRPA1

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