Cefixime trihydrate - Moligand™,≥98% , CAS No.125110-14-7

CAS: 125110-14-7 Cat. No.: Y333700 Fórmula: C₁₆H₂₁N₅O₁₀S₂ Peso molecular: 507.5 Número CE: 635-033-5

GRADE & PURITY Moligand™, ≥98%

Synonyms

CCG-208807 | CEFIXIME [USP MONOGRAPH] | CEFIXIME [VANDF] | CNV9DH4SXQ | (E)-cefixime trihydrate | Q27259597 | D07640 | DS-6675 | CEFIXIME [ORANGE BOOK] | Cefixime [USAN] | CEFIXIME TRIHYDRATE [WHO-DD] | CEFIXIME TRIHYDRATE [MI] | Cefixime (USP) | 2H-Benzi

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

CCG-208807 | CEFIXIME [USP MONOGRAPH] | CEFIXIME [VANDF] | CNV9DH4SXQ | (E)-cefixime trihydrate | Q27259597 | D07640 | DS-6675 | CEFIXIME [ORANGE BOOK] | Cefixime [USAN] | CEFIXIME TRIHYDRATE [WHO-DD] | CEFIXIME TRIHYDRATE [MI] | Cefixime (USP) | 2H-Benzi

Especificações e pureza

Moligand™,≥98%

Mecanismos bioquímicos e fisiológicos

Cefixime trihydrate (FR-17027 trihydrate) is an antibiotic and a third generation cephalosporin antibiotic, useful for the treatment of a number of bacterial infections

Condições de armazenamento de armazenamento

Store at 2-8°C,Argon charged

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Grau

Moligand™

Tipo de ação

INHIBITOR

Pureza

≥98%

Nomes e identificadores

• Pubchem Sid: 504763892
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504763892
• Sorrisos canónicos: C=CC1=C(N2C(C(C2=O)NC(=O)C(=NOCC(=O)O)C3=CSC(=N3)N)SC1)C(=O)O.O.O.O
• IUPAC Name: (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;trihydrate
• InChIKey: IPYWNMVPZOAFOQ-NABDTECSSA-N
• INCHI: 1S/C16H15N5O7S2.3H2O/c1-2-6-4-29-14-10(13(25)21(14)11(6)15(26)27)19-12(24)9(20-28-3-8(22)23)7-5-30-16(17)18-7;;;/h2,5,10,14H,1,3-4H2,(H2,17,18)(H,19,24)(H,22,23)(H,26,27);3*1H2/b20-9-;;;/t10-,14-;;;/m1.../s1
• SMILES isoméricas: C=CC1=C(N2[C@@H]([C@@H](C2=O)NC(=O)/C(=N\OCC(=O)O)/C3=CSC(=N3)N)SC1)C(=O)O.O.O.O
• CAS alternativo: 79350-37-1
• Peso molecular: 507.5

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Lactams
      • Subclass Beta lactams
        • Level5 Cephems
          • Level6 Cephalosporins

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Lactams
• Subclass: Beta lactams
• Intermediate Tree Nodes: Cephems
• Direct Parent: Cephalosporins
• Alternative Parents: N-acyl-alpha amino acids and derivatives 2,4-disubstituted thiazoles 1,3-thiazines 2-amino-1,3-thiazoles Dicarboxylic acids and derivatives Tertiary carboxylic acid amides Heteroaromatic compounds Secondary carboxylic acid amides Amino acids Azetidines Thiohemiaminal derivatives Azacyclic compounds Dialkylthioethers Carboxylic acids Primary amines Organic oxides Carbonyl compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Cephalosporin - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - 2,4-disubstituted 1,3-thiazole - Meta-thiazine - Dicarboxylic acid or derivatives - 1,3-thiazol-2-amine - Heteroaromatic compound - Azole - Tertiary carboxylic acid amide - Thiazole - Amino acid - Amino acid or derivatives - Carboxamide group - Azetidine - Secondary carboxylic acid amide - Carboxylic acid derivative - Dialkylthioether - Carboxylic acid - Azacycle - Hemithioaminal - Thioether - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Primary amine - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Aromatic heteropolycyclic compound
• Descrição: This compound belongs to the class of organic compounds known as cephalosporins. These are compounds containing a 1,2-thiazine fused to a 2-azetidinone to for a oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid moiety or a derivative thereof.
• 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

Propriedades químicas e físicas

• Sensibilidade: Air sensitive
• Peso molecular: 507.500 g/mol
• Hydrogen Bond Donor Count: 7
• Hydrogen Bond Acceptor Count: 15
• Rotatable Bond Count: 8
• Exact Mass: 507.073 Da
• Monoisotopic Mass: 507.073 Da
• Topological Polar Surface Area: 241.000 Ų
• Heavy Atom Count: 33
• Formal Charge: 0
• Complexity: 861.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• 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: 4

XLogP3

Referências

1. Guanxiong Liu, Yihan Li, Hui Wang, Hongchen Zhu, Junli Fan, Chunyu Wan, Minghao Wang, Yan Chen, Changqian Zhou, Qun Wang, Hongxia Zhao, Xin Li, Lijuan Gui, Lei Zhang, Shuang Jiang, Yingping Li, Yuqi Wang, Zonglin Liu, Peizhi Zhu, Yu Zhu.  (2026)  High-yield synthesis of antibiotic-derived carbon dots for enhanced Achyranthes bidentata growth and in vitro bone bonding.  Materials Today Advances,      [PMID:] [10.1016/j.mtadv.2026.100754]