Alda 1 - 10mM in DMSO , CAS No.349438-38-6

CAS: 349438-38-6 Cat. No.: A423552 Formula: C15H11Cl2NO3 Peso molecolare: 324.16 Numero EC: 803-635-9
Disponibile su ordine
GRADE & PURITY 10mM in DMSO
Synonyms
CHEBI:94988 | SCHEMBL503808 | Alda 1 | Benzamide, N-(1,3-benzodioxol-5-ylmethyl)-2,6-dichloro- | N-(1,3-benzodioxol-5-ylmethyl)-2,6-dichlorobenzamide | DTXSID801324445 | C74792 | HMS2847P05 | ALDH2 Agonist, Alda-1 | SMR000518092 | Alda1 | Alda-1 | Q271667
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
Germania (EU)
USA*
Price
Qty
1ml
A423552-1ml
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1 Disponibile

51,11€

60,65€
Salva 9,55 € (15.74%)
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinonimi
CHEBI:94988 | SCHEMBL503808 | Alda 1 | Benzamide, N-(1,3-benzodioxol-5-ylmethyl)-2,6-dichloro- | N-(1,3-benzodioxol-5-ylmethyl)-2,6-dichlorobenzamide | DTXSID801324445 | C74792 | HMS2847P05 | ALDH2 Agonist, Alda-1 | SMR000518092 | Alda1 | Alda-1 | Q271667
Specifiche e purezza
10mM in DMSO
Meccanismi biochimici e fisiologici
Activator of aldehyde dehydrogenase 2 (ALDH2). Increases activity of wild-type ALDH2*1 and variant ALDH2*2 (by ~2-fold and 11-fold respectively). Capable of partly restoring mutant ALDH2*2 activity; protective against cardiac ischemia.
Condizioni di conservazione di stoccaggio
Store at -80°C
Spedito in
Dry ice packs + Cold packs
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Tipo di azione
AGONIST
Nomi e identificatori
Pubchem Sid528763276
Sorrisi canoniciC1OC2=C(O1)C=C(C=C2)CNC(=O)C3=C(C=CC=C3Cl)Cl
IUPAC NameN-(1,3-benzodioxol-5-ylmethyl)-2,6-dichlorobenzamide
InChIKeyNMKJFZCBCIUYHI-UHFFFAOYSA-N
INCHI1S/C15H11Cl2NO3/c16-10-2-1-3-11(17)14(10)15(19)18-7-9-4-5-12-13(6-9)21-8-20-12/h1-6H,7-8H2,(H,18,19)
Isomeri SMILES C1OC2=C(O1)C=C(C=C2)CNC(=O)C3=C(C=CC=C3Cl)Cl
WGK Germania 3
Peso molecolare 324.16
Reaxy-Rn 18465242
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=18465242&ln=

Documentazione

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree Nodes Halobenzoic acids and derivatives
Direct Parent2-halobenzoic acids and derivatives
Alternative Parents Benzodioxoles  Benzamides  Dichlorobenzenes  Benzoyl derivatives  Aryl chlorides  Vinylogous halides  Secondary carboxylic acid amides  Oxacyclic compounds  Acetals  Organopnictogen compounds  Organonitrogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 2-halobenzoic acid or derivatives - Benzamide - Benzodioxole - Benzoyl - 1,3-dichlorobenzene - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Vinylogous halide - Carboxamide group - Secondary carboxylic acid amide - Acetal - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organohalogen compound - Organochloride - Aromatic heteropolycyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as 2-halobenzoic acids and derivatives. These are benzoic acids or derivatives carrying a halogen atom at the 2-position of the benzene ring.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
Peso molecolare324.200 g/mol
XLogP34.000
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count3
Exact Mass323.012 Da
Monoisotopic Mass323.012 Da
Topological Polar Surface Area47.600 Ų
Heavy Atom Count21
Formal Charge0
Complexity372.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Riferimenti
1. Jing Zhang, Yan Zhao.  (2025)  Deficiency of Aldehyde Dehydrogenase 2 Sensitizes cells to Glutamate-Induced Cytotoxicity via Elevation of GluN1 Expression.  TOXICOLOGY,      [PMID:40592419] [10.1016/j.tox.2025.154226]
Calcolatori di soluzioni
Recensioni

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