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 Formule: C₂H₄INO Poids moléculaire: 184.96 Beilstein Registry Number: 1739080 Numéro CE: 205-630-1

112 Citations COA

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Iodoacetamide - Moligand™, ≥98% CAS No(144-48-9) I105563 by Aladdin Scientific

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DISPONIBLE À COMMANDE

QUALITÉ & PURETÉ Moligand™ ? ≥98%

Synonyms

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Fiche de spécifications

Vue d’ensemble Spécifications Noms et identifiants Documentation Données avancées Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques FAQ et articles Citations of This Product Calculateurs de solution Avis

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Pourquoi cette qualité

Moligand™, ≥98% Moligand™ pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Store at 2-8°C,Protected from light Expédition Wet ice. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 112 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Alkylating reagent for cysteine residues in peptide sequencing.

Spécifications

Synonymes

Spécifications et pureté

Moligand™, ≥98%

Mécanismes biochimiques et physiologiques

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

Conditions de stockage de stockage

Store at 2-8°C,Protected from light

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Moligand™

Type d'action

ACTIVATOR

Mécanisme d'action

Activator of TRPA1

Pureté

≥98%

Noms et identifiants

Pubchem Sid

508815490

Pubchem Sid Url

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

Sourires canoniques

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)

Isomères SMILES

C(C(=O)N)I

WGK Allemagne

RTECS

AC4200000

Numéro ONU

2811

Groupe d'emballage

III

Poids moléculaire

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=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

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Données avancées

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
Description	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

Structure 3D

Cibles associées (humaines)

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)

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

CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)

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

CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)

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

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

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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)

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

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

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

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

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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)

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

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

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

THPO Tbio Thrombopoietin (834 Activities)

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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

Cibles associées (non humaines)

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)

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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

Mécanismes d'action

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

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

Analytical Chart:

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61 results found

Lot Number	Certificate Type	Date	Article
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

Propriétés chimiques et physiques

Solubilité	Soluble in water; Soluble in Methanol
Sensibilité	Light & Moisture Sensitive
Point de fusion (°C)	95°C
Poids moléculaire	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

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

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Citations of This Product

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📚 Citations par application

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

Voir les 112 citations →

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Produits apparentés

Iodoacetamide - Moligand™, Ultra pure, ≥99%(NMR) , CAS No.144-48-9

Strontium Carbonate - ≥99.995% metals basis , CAS No.1633-05-2

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

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