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Antibiotic A 40926
[CAS# 102961-72-8]

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Complete supplier list of Antibiotic A 40926
Identification
Classification API >> Antibiotics
Name Antibiotic A 40926
Synonyms Dalbavancin Impurity-A 40926;6-[[5,32-dichloro-22-(dimethylamino)-52-[3-(dimethylamino)propylcarbamoyl]-2,26,31,44,49-pentahydroxy-21,35,38,54,56,59-hexaoxo-47-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,13,28-trioxa-20,36,39,53,55,58-hexazaundecacyclo[38.14.2.23,6.214,17.219,34.18,12.123,27.129,33.141,45.010,37.046,51]hexahexaconta-3,5,8,10,12(64),14(63),15,17(62),23(61),24,26,29(60),30,32,41(57),42,44,46(51),47,49,65-henicosaen-64-yl]oxy]-3,4-dihydroxy-5-(9-methyldecanoylamino)oxane-2-carboxylic acid;hydrochloride
Molecular Structure CAS # 102961-72-8, Antibiotic A 40926, Dalbavancin Impurity-A 40926,6-[[5,32-dichloro-22-(dimethylamino)-52-[3-(dimethylamino)propylcarbamoyl]-2,26,31,44,49-pentahydroxy-21,35,38,54,56,59-hexaoxo-47-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,13,28-trioxa-20,36,39,53,55,58-hexazaundecacyclo[38.14.2.23,6.214,17.219,34.18,12.123,27.129,33.141,45.010,37.046,51]hexahexaconta-3,5,8,10,12(64),14(63),15,17(62),23(61),24,26,29(60),30,32,41(57),42,44,46(51),47,49,65-henicosaen-64-yl]oxy]-3,4-dihydroxy-5-(9-methyldecanoylamino)oxane-2-carboxylic acid,hydrochloride
Molecular Formula C88H101Cl3N10O28
Molecular Weight 1853.15
CAS Registry Number 102961-72-8
EC Number 881-175-8
SMILES CC(C)CCCCCCCC(=O)NC1C(C(C(OC1OC2=C3C=C4C=C2OC5=C(C=C(C=C5)C(C6C(=O)NC(C7=C(C(=CC(=C7)O)OC8C(C(C(C(O8)CO)O)O)O)C9=C(C=CC(=C9)C(C(=O)N6)NC(=O)C4NC(=O)C1C2=C(C(=CC(=C2)OC2=C(C=CC(=C2)C(C(=O)NC(CC2=CC=C(O3)C=C2)C(=O)N1)N(C)C)O)O)Cl)O)C(=O)NCCCN(C)C)O)Cl)C(=O)O)O)O.Cl
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H302-H315-H319-H335    Details
Precautionary Statements P280-P305+P351+P338    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Specific target organ toxicity - repeated exposureSTOT RE2H373
Reproductive toxicityRepr.2H361d
SDS Available
up Discovory and Applicatios
Antibiotic A 40926, also known as vancomycin, was discovered in the mid-20th century by a team of scientists led by Edmund Kornfeld at Eli Lilly and Company. The discovery was serendipitous, arising from a screening program aimed at isolating novel antibiotics from soil bacteria. Vancomycin was isolated from the soil bacterium Amycolatopsis orientalis and recognized for its potent activity against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA).

Vancomycin has become one of the most important antibiotics in clinical practice, primarily reserved for the treatment of serious infections caused by multidrug-resistant Gram-positive bacteria. It is commonly used to treat infections such as MRSA, Clostridium difficile-associated diarrhea, and endocarditis. Additionally, vancomycin is sometimes administered prophylactically in surgical procedures to prevent post-operative infections.

References

1987. A40926, a new glycopeptide antibiotic with anti-Neisseria activity. Antimicrobial Agents and Chemotherapy, 31(12).
DOI: 10.1128/aac.31.12.1961

2020. Improved A40926 production from Nonomuraea gerenzanensis using the promoter engineering and the co-expression of crucial genes. Journal of Biotechnology, 324.
DOI: 10.1016/j.jbiotec.2020.09.017

2021. Genomic-Led Discovery of a Novel Glycopeptide Antibiotic by Nonomuraea coxensis DSM 45129. ACS Chemical Biology, 16(5).
DOI: 10.1021/acschembio.1c00170
Market Analysis Reports
List of Reports Available for Antibiotic A 40926
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