Syringaldazine - ≥99% , CAS No.14414-32-5

CAS: 14414-32-5 Cat. No.: S133231 Formule: [HOC₆H₂(OCH₃)₂CH=N-]₂ Poids moléculaire: 360.36 Numéro CE: 238-390-1 PubChem CID: 135401234

GRADE & PURITY ≥99%

Synonyms

A808179 | S-9900 | Benzaldéhyde, 4-hydroxy-3,5-diméthoxy-, [(4-hydroxy-3,5-diméthoxyphényl)méthylène]hydrazone | Benzaldéhyde, 4-hydroxy-3,5-diméthoxy-, 2-[(4-hydroxy-3,5-diméthoxyphényl)méthylène]hydrazone | 4-[(1E)-[(E)-2-[(4-hydroxy-3,5-diméthoxyphényl

Storage

A conserver entre 2 et 8°C

Shipped In

Glace humide

Vue d’ensemble

La syringaldazine est un agent réducteur utilisé dans les études sur l'activité de la laccase et de la peroxydase.
Agent réducteur utilisé dans les études sur l'activité de la laccase et de la peroxydase.

Specifications

Synonymes

A808179 | S-9900 | Benzaldéhyde, 4-hydroxy-3,5-diméthoxy-, [(4-hydroxy-3,5-diméthoxyphényl)méthylène]hydrazone | Benzaldéhyde, 4-hydroxy-3,5-diméthoxy-, 2-[(4-hydroxy-3,5-diméthoxyphényl)méthylène]hydrazone | 4-[(1E)-[(E)-2-[(4-hydroxy-3,5-diméthoxyphényl

Spécifications et pureté

≥99%

Mécanismes biochimiques et physiologiques

L'aldéhyde Azo (3,5-diméthoxy-P-Hydroxybenzaldéhyde) du clou de girofle est un composé spécifique de la laccase qui ne peut pas être auto-oxydé. Il peut servir de substrat à la laccase et à la peroxydase en présence de peroxyde d'hydrogène (H2O2). Les ald

Conditions de stockage de stockage

A conserver entre 2 et 8°C

Expédié en

Glace humide

Pureté

≥99%

Noms et identifiants

• Pubchem Sid: 504773257
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504773257
• Sourires canoniques: COC1=CC(=CC(=C1O)OC)C=NN=CC2=CC(=C(C(=C2)OC)O)OC
• IUPAC Name: 4-[(E)-[(E)-(4-hydroxy-3,5-dimethoxyphenyl)methylidenehydrazinylidene]methyl]-2,6-dimethoxyphenol
• InChIKey: YARKTHNUMGKMGS-LQGKIZFRSA-N
• INCHI: 1S/C18H20N2O6/c1-23-13-5-11(6-14(24-2)17(13)21)9-19-20-10-12-7-15(25-3)18(22)16(8-12)26-4/h5-10,21-22H,1-4H3/b19-9+,20-10+
• Isomères SMILES: COC1=CC(=CC(=C1O)OC)/C=N/N=C/C2=CC(=C(C(=C2)OC)O)OC
• WGK Allemagne: 3
• PubChem CID: 135401234
• Poids moléculaire: 360.36

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Phenols
      • Subclass Methoxyphenols

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Phenols
• Subclass: Methoxyphenols
• Intermediate Tree Nodes: Not available
• Direct Parent: Methoxyphenols
• Alternative Parents: Dimethoxybenzenes Phenoxy compounds Anisoles Alkyl aryl ethers Aldazines Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Methoxyphenol - M-dimethoxybenzene - Dimethoxybenzene - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Aldazine - Azine - Monocyclic benzene moiety - Ether - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as methoxyphenols. These are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.
• External Descriptors: Not available

Data sources

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

Cibles associées (humaines)

GAA Tclin Lysosomal alpha-glucosidase (35701 Activities)

Discover Target: GAA

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PIN1 Tchem Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (36611 Activities)

Discover Target: PIN1

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GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

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KMT2A Tchem Histone-lysine N-methyltransferase MLL (17327 Activities)

Discover Target: KMT2A

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

MBNL1 Tbio Muscleblind-like protein 1 (34431 Activities)

Discover Target: MBNL1

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WRN Tbio Werner syndrome ATP-dependent helicase (8824 Activities)

Discover Target: WRN

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Cibles associées (non humaines)

Plasmodium falciparum (966862 Activities)

Explore this target

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Luciferin 4-monooxygenase (66902 Activities)

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Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

Discover Target: Txnrd1

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TGR Thioredoxin glutathione reductase (28579 Activities)

Discover Target: TGR

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Mapt Microtubule-associated protein tau (6 Activities)

Discover Target: Mapt

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in water (partly), and DMF (c = 5%).
• Point de fusion (°C): 209-210°C
• Poids moléculaire: 360.400 g/mol
• XLogP3: 2.500
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 7
• Exact Mass: 360.132 Da
• Monoisotopic Mass: 360.132 Da
• Topological Polar Surface Area: 102.000 Ų
• Heavy Atom Count: 26
• Formal Charge: 0
• Complexity: 405.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 2
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 2
• Covalently-Bonded Unit Count: 1

Références

1. Rui Wang, Yao Cheng, Yanan Xie, Jie Li, Yinliang Zhang, Zemin Fang, Wei Fang, Xuecheng Zhang, Yazhong Xiao.  (2019)  Statistical coupling analysis uncovers sites crucial for the proton transfer in laccase Lac15.  BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,      [PMID:31563321] [10.1016/j.bbrc.2019.09.088]

2. Kaifeng Xu, Ying Huo, Shiming Tang, Shuangyan Han, Ying Lin, Suiping Zheng.  (2024)  A novel laccase for alkaline medium temperature environments in the textile industry.  Biotechnology Journal,  19  (9): (2400383).  [PMID:39295545] [10.1002/biot.202400383]