Sulfamoxole - analytical standard,Moligand™ , CAS No.729-99-7

CAS: 729-99-7 Cat. No.: S114300 Peso molecular: 267.3 Beilstein Registry Number: 248434 Número EC: 211-982-7 PubChem CID: 12894

GRADE & PURITY Analytical standard, Moligand™

Synonyms

Sulfamoxolum | Tardamid | 4-Amino-N-(4,5-dimethyl-1,3-oxazol-2-yl)benzenesulfonamide | DTXSID5023617 | Justamil | Sulfanilamide, N1-(4,5-dimethyl-2-oxazolyl)- | Sulfono | 2-(p-Aminobenzolsulfonamido)-4,5-dimethyloxazol | 4-amino-N-(4,5-dimethyl-1,3-oxazol

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Descripción general

Sulfamoxole is a broad- spectrum chemotherapeutic antimicrobial agent. Sulfamoxole can be used for the study of pediatric infections.

Specifications

Sinónimos

Sulfamoxolum | Tardamid | 4-Amino-N-(4, 5-dimethyl-1, 3-oxazol-2-yl)benzenesulfonamide | DTXSID5023617 | Justamil | Sulfanilamide, N1-(4, 5-dimethyl-2-oxazolyl)- | Sulfono | 2-(p-Aminobenzolsulfonamido)-4, 5-dimethyloxazol | 4-amino-N-(4, 5-dimethyl-1, 3-oxazol

Especificaciones y pureza

analytical standard, Moligand™

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Protected from light

Enviado en

Wet ice

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

Grado

Analytical standard, Moligand™

Tipo de acción

INHIBITOR

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Nombres e identificadores

• Sonrisas canónicas: CC1=C(OC(=N1)NS(=O)(=O)C2=CC=C(C=C2)N)C
• IUPAC Name: 4-amino-N-(4,5-dimethyl-1,3-oxazol-2-yl)benzenesulfonamide
• InChIKey: CYFLXLSBHQBMFT-UHFFFAOYSA-N
• INCHI: 1S/C11H13N3O3S/c1-7-8(2)17-11(13-7)14-18(15,16)10-5-3-9(12)4-6-10/h3-6H,12H2,1-2H3,(H,13,14)
• Isómeros SMILES: CC1=C(OC(=N1)NS(=O)(=O)C2=CC=C(C=C2)N)C
• PubChem CID: 12894
• Peso molecular: 267.3
• Beilstein: 248434

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: Aminobenzenesulfonamides
• Alternative Parents: Benzenesulfonyl compounds Aniline and substituted anilines 2,4,5-trisubstituted oxazoles Organosulfonamides Heteroaromatic compounds Aminosulfonyl compounds Oxacyclic compounds Azacyclic compounds Primary amines Organopnictogen compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aminobenzenesulfonamide - Benzenesulfonyl group - 2,4,5-trisubstituted 1,3-oxazole - Aniline or substituted anilines - Organosulfonic acid amide - Azole - Oxazole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Heteroaromatic compound - Organoheterocyclic compound - Azacycle - Oxacycle - Organic nitrogen compound - Organopnictogen compound - Organic oxygen compound - Primary amine - Amine - Organosulfur compound - Organonitrogen compound - Organic oxide - Organooxygen compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as aminobenzenesulfonamides. These are organic compounds containing a benzenesulfonamide moiety with an amine group attached to the benzene ring.
• External Descriptors: sulfonamide - sulfonamide antibiotic - oxazole

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)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: light sensitive
• Peso molecular: 267.310 g/mol
• XLogP3: 1.300
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 267.068 Da
• Monoisotopic Mass: 267.068 Da
• Topological Polar Surface Area: 107.000 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 373.000
• 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