Amoxicillin (trihydrate)

CAT: 0804-HY-B0467B-01Size: 500 mgDry Ice: NoHazardous: No
CAT#:0804-HY-B0467B-01Size:500 mg
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Description
Amoxicillin (Amoxycillin) trihydrateis an antibiotic with good oral absorption and broad spectrum antimicrobial activity. Amoxicillin trihydrateis inhibits the biosynthesis of polypeptides in the cell wall, thereby inhibiting cell growth[1][2][3].
CAS Number
[61336-70-7]
Product Name Alternative
Amoxycillin (trihydrate)
UNSPSC
12352005
Hazard Statement
H317, H334
Target
Antibiotic; Bacterial
Type
Reference compound
Related Pathways
Anti-infection
Applications
COVID-19-immunoregulation
Field of Research
Infection; Cancer
Assay Protocol
https://www.medchemexpress.com/Amoxicillin-trihydrate.html
Purity
99.80
Solubility
DMSO : 10 mg/mL (ultrasonic) |H2O : 2 mg/mL (ultrasonic)
Smiles
OC([C@@H]1N(C2=O)[C@]([C@@H]2NC([C@@H](C3=CC=C(O)C=C3)N)=O)([H])SC1(C)C)=O.[3H2O]
Molecular Formula
C16H25N3O8S
Molecular Weight
419.45
Precautions
H317, H334
References & Citations
[1]http://en.wikipedia.org/wiki/Amoxicillin|[2]Guo Y, et, al. Metabolic response of Lactobacillus acidophilus exposed to amoxicillin. J Antibiot (Tokyo) . 2022 May;75 (5) :268-281.|[3]Andes D, et, al. In vivo activities of amoxicillin and amoxicillin-clavulanate against Streptococcus pneumoniae: application to breakpoint determinations. Antimicrob Agents Chemother. 1998 Sep;42 (9) :2375-9. |[4]Kramer MJ, et, al. Activity of oral amoxicillin, ampicillin, and oxytetracycline against infection with chlamydia trachomatis in mice. J Infect Dis. 1979 Jun;139 (6) :717-9.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
Launched

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