Shz 1 - ≥98%(HPLC) , CAS No.326886-05-9

CAS: 326886-05-9 Cat. No.: S287579 Peso molecular: 355.21 Número EC: 806-202-2 PubChem CID: 135446537

GRADE & PURITY ≥98%(HPLC)

Synonyms

EN300-1212502 | MS-25546 | Z49626720 | E98660 | N'-(5-BROMO-2-HYDROXYBENZYLIDENE)BENZENESULFONOHYDRAZIDE | N-[(E)-(5-bromo-2-hydroxyphenyl)methylideneamino]benzenesulfonamide | HY-108440 | N'-[(E)-(5-bromo-2-hydroxyphenyl)methylidene]benzenesulfonohydrazi

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Descripción general

Product description

Shz-1, a small cardiogenic molecule, induces various cardiac-specific genes including sarcomeric tropomyosin in P19CL6 cells. Shz-1 induces Nkx2.5 expression in mouse. Shz-1 activates the axolotl TPM4 promoter-driven ectopic expression in C2C12 cells.

Specifications

Sinónimos

EN300-1212502 | MS-25546 | Z49626720 | E98660 | N'-(5-BROMO-2-HYDROXYBENZYLIDENE)BENZENESULFONOHYDRAZIDE | N-[(E)-(5-bromo-2-hydroxyphenyl)methylideneamino]benzenesulfonamide | HY-108440 | N'-[(E)-(5-bromo-2-hydroxyphenyl)methylidene]benzenesulfonohydrazi

Especificaciones y pureza

≥98%(HPLC)

Mecanismos bioquímicos y fisiológicos

Activator of early cardiac genes (includingNkx2.5) in pluripotent stem cells. Induces phenotypic differentiation in human mobilized peripheral blood mononuclear cells. Enhances myocardial regenerative repair by stem cells in a rat myocardial cryoinjury mo

Condiciones de almacenamiento de almacenamiento

Store at -20°C

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%(HPLC)

Nombres e identificadores

• Pubchem Sid: 488202918
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488202918
• Sonrisas canónicas: C1=CC=C(C=C1)S(=O)(=O)NN=CC2=C(C=CC(=C2)Br)O
• IUPAC Name: N-[(E)-(5-bromo-2-hydroxyphenyl)methylideneamino]benzenesulfonamide
• InChIKey: OEMCLQLAWYKPRK-OQLLNIDSSA-N
• INCHI: 1S/C13H11BrN2O3S/c14-11-6-7-13(17)10(8-11)9-15-16-20(18,19)12-4-2-1-3-5-12/h1-9,16-17H/b15-9+
• Isómeros SMILES: C1=CC=C(C=C1)S(=O)(=O)N/N=C/C2=C(C=CC(=C2)Br)O
• PubChem CID: 135446537
• Peso molecular: 355.21

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Benzenesulfonamides

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Benzenesulfonamides
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzenesulfonamides
• Alternative Parents: Benzenesulfonyl compounds P-bromophenols Bromobenzenes 1-hydroxy-2-unsubstituted benzenoids Sulfonohydrazides Hydrazinosulfonyl compounds Aryl bromides Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organobromides Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Benzenesulfonamide - Benzenesulfonyl group - 4-halophenol - 4-bromophenol - Bromobenzene - Halobenzene - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Sulfonohydrazide - Hydrazinosulfonyl compound - Aryl bromide - Aryl halide - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Organic oxide - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Organosulfur compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as benzenesulfonamides. These are organic compounds containing a sulfonamide group that is S-linked to a benzene ring.
• 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

Objetivos asociados (no humanos)

Candida albicans (78123 Activities)

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Solvent:DMSO, Max Conc. mg/mL: 35.52, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 17.76, Max Conc. mM: 50
• Peso molecular: 355.210 g/mol
• XLogP3: 2.900
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 353.967 Da
• Monoisotopic Mass: 353.967 Da
• Topological Polar Surface Area: 87.100 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 429.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1