Penicillin X Sodium

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Penicillin X Sodium
Category Antibiotics
Catalog number BBF-02675
CAS 5985-13-7
Molecular Weight 372.37
Molecular Formula C16H17N2O5SNa
Purity > 95%

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BBF-02675 1 g $3148 In stock

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Description

It is produced by the strain of Penicillium notatum NRRL 1209, Pen. chrysogenum NRRL 1951. It is an antibiotic.

Specification

Synonyms (2S,5β)-6α-[[(4-Hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2β-carboxylic acid sodium salt; 6α-[(4-Hydroxyphenylacetyl)amino]penicillani cacid sodium salt; Penicillin III sodium; p-Hydroxybenzylpenicillin sodium; Benzylpenicillin Impurity C
IUPAC Name sodium;4-[2-[[(2S,5R,6R)-2-carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptan-6-yl]amino]-2-oxoethyl]phenolate
Canonical SMILES CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=C(C=C3)[O-])C(=O)O)C.[Na+]
InChI InChI=1S/C16H18N2O5S.Na/c1-16(2)12(15(22)23)18-13(21)11(14(18)24-16)17-10(20)7-8-3-5-9(19)6-4-8;/h3-6,11-12,14,19H,7H2,1-2H3,(H,17,20)(H,22,23);/q;+1/p-1/t11-,12+,14-;/m1./s1
InChI Key VLUNNMCSPBQUDX-LQDWTQKMSA-M

Properties

Appearance Colorless Amorphous Powder
Melting Point 228-235°C
Solubility Soluble in Water

Reference Reading

1. Enzymatic dimerization of penicillin X
T Shin, T Yoshioka, N Shibamoto, S Murao, T Tsuchida, H Agematu, K Kominato, R Okamoto, H Nishida J Antibiot (Tokyo) . 1993 Jan;46(1):141-8. doi: 10.7164/antibiotics.46.141.
Penicillin X methyl ester was transformed into three types of dimer by laccase from Coriolus versicolor. The dimers are considered to be formed by free-radical addition of phenoxy radicals produced by laccase. The enzyme reaction with the ester as substrate was more suitable for forming dimers than that with the sodium salt as substrate. Penicillin X pivaloyloxymethyl ester was also transformed into a dimer, which had antibacterial activity in the presence of esterase.

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* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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