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

CAS: 326886-05-9 Cat. No.: S287579 Formula: C₁₃H₁₁BrN₂O₃S Peso molecolare: 355.21 Numero EC: 806-202-2 PubChem CID: 135446537

QUALITÀ & PUREZZA ≥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

Panoramica

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.

Specifiche

Sinonimi

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

Specifiche e purezza

≥98%(HPLC)

Meccanismi biochimici e fisiologici

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

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

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

Purezza

≥98%(HPLC)

Nomi e identificatori

Pubchem Sid

488202918

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488202918

Sorrisi canonici

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+

Isomeri SMILES

C1=CC=C(C=C1)S(=O)(=O)N/N=C/C2=C(C=CC(=C2)Br)O

PubChem CID

135446537

Peso molecolare

355.21

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: 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
• Descrizione: 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

Obiettivi associati (non umani)

Candida albicans (78123 Activities)

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: 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 molecolare: 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

Domande frequenti

What is the purity of this product, and how is it determined?

This product is supplied at ≥98% purity, determined by HPLC. Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at ?20 °C. Freezer storage is required to maintain the specified shelf life.

How is this product shipped?

This product ships in an insulated container with ice pads. Unpack on arrival and transfer it to the storage condition stated above.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 326886-05-9, the molecular formula is C13H11BrN2O3S, and the molecular weight is 355.21 g/mol. InChIKey OEMCLQLAWYKPRK-OQLLNIDSSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.