ampicillin

L-(+)-Ampicillin is an isomer of Ampicillin. Ampicillin is a β-lactam antibiotic used for treating bacterial infections.

Ampicillin Trihydrate (NCI-C56086) 是一种 β-内酰胺类广谱抗生素，可对抗多种革兰氏阳性和革兰氏阴性细菌。

Ampicillin sodium (Domicillin) 是Ampicillin 的钠盐形式，是Ampicillin 的广谱半合成衍生物。它通过与青霉素结合蛋白结合来抑制细菌细胞壁的合成，从而抑制肽聚糖的合成，肽聚糖是细菌细胞壁的关键成分。

Ampicillin (Aminobenzylpenicillin) 属于 β-内酰胺类抗生素，是一种半合成的青霉素。Ampicillin 具有杀菌活性，对各种革兰氏阳性细菌和革兰氏阴性细菌均有抑制活性。

Ampicillin-d5 是 2H 标记的 Ampicillin。Ampicillin 属于 β-内酰胺类抗生素，是一种半合成的青霉素。Ampicillin 具有杀菌活性，对各种革兰氏阳性细菌和革兰氏阴性细菌均有抑制活性。

Bacampicillin is an improved oral bioavailability penicillin antibiotic which is a prodrug of ampicillin.

Bacampicillin hydrochloride is an improved oral bioavailability penicillin antibiotic which is a prodrug of ampicillin.

Lenampicillin hydrochloride is an orally active prodrug of Ampicillin. Lenampicillin hydrochloride is an effective beta-lactam antibacterial agent that inhibits bacterial penicillin-binding proteins. It is applied in the investigation of suppurative skin

Pivampicillin, a pivalate ester analog of Ampicillin, is used to treat chronic obstructive pulmonary disease (COPD) in children and young adults.

Ampicillinoic acid is a hydrolysis (ring-open) product of ampicillin.

Piampicillin Hydrochloride is a Hydrochloride form of an oral active ampicillin new spray with antimicrobial activity.

Talampicillin is an ester of Ampicillin. It is hydrolyzed upon absorption to release ampicillin. It is well absorbed from the gastrointestinal tract resulting in a greater bioavailability of ampicillin than can be achieved with equivalent doses of ampicil

Lenampicillin is a Beta-lactam antibacterial agent.

Metampicillin is a semi-synthetic penicillin.

Talampicillin hydrochloride is a biochemical.

Piperacillin sodium salt(CL227193) )是一种β-内酰胺类广谱抗生素。

Sultamicillin 是一种具有口服活性的氨苄西林 舒巴坦双前药。它是一种半合成 β-内酰胺酶抑制剂。

Azlocillin is a semisynthetic ampicillin-derived penicillin belonging to acylureido.

Sultamicillin Tosylate (Unacim orale) 是一种口服活性 β-内酰胺酶抑制剂，具有抗菌活性。 它是舒巴坦与氨苄西林的双酯的甲苯磺酸盐。

Hetacillin 是一种β-内酰胺抗生素，属于氨基青霉素家族，通过酯酶转化为氨苄西林。氨苄西林是一种没有抗菌活性的前药。

1-Palmitoyl Lysophosphatidic Acid 是 LPA 的类似物，通过结合 Ca2+ 和 Mg2+ 提高氨苄西林、哌拉西林和头孢他啶对各种铜绿假单胞菌菌株的作用。

1-Palmitoyl lysophosphatidic acid (1-Palmitoyl LPA) is a LPA analog containing palmitic acid at the sn-1 position. LPA binds to one of five different G protein-coupled receptors (GPCRs) to mediate a variety of biological responses including cell proliferation, smooth muscle contraction, platelet aggregation, neurite retraction, and cell motility. In addition to playing a role in the aforementioned biological responses, 1-palmitoyl LPA enhances the action of β-lactam antibiotics (ampicillin, piperacillin, and ceftazidime) on various strains of Pseudomonas aeruginosa, a pathogen associated with pulmonary disease and pneumonia, via binding both Ca2+ and Mg2+.

Antibacterial agent 64 是一种强效YycG 抑制剂 (IC50=6.1 µM) 和抗菌剂。Antibacterial agent 64 与氨苄西林联合使用可协同根除生物膜内的活菌。

BING是一种来源于日本稻田鱼(O. laptipes)的抗菌肽，由液泡蛋白质分选相关蛋白13D样(Vps13D)衍生而来。对包括耐甲氧西林的金黄色葡萄球菌(MRSA; MICs = 4-64 µg/ml)在内的各种革兰氏阴性和革兰氏阳性细菌都有活性。与氨苄西林、阿莫西林和新霉素共同使用时，对抗铜绿假单胞菌(P. aeruginosa)表现出协同效应，并能抑制大肠杆菌(E. coli)对卡那霉素和氨苄西林的抗药性发展。在体内，BING提高了被鳗弧菌(E. tarda)感染的O. laptipes的生存率。