vulgaris

AZD-0284 是核受体 (RORγ) 的选择性反向激动剂。它对呼吸道疾病及斑块型寻常型银屑病具有潜在的应用价值。

Phaseolus vulgaris leucoagglutinin (PHA-L) 是从红芸豆 (Phaseolus vulgaris) 中提取的一种凝集素。它在神经解剖学领域有重要应用，特别是作为顺行轴突示踪剂，用于探索神经系统中的神经元、轴突及其末梢结构的形态学特征。

Phaseolus Vulgaris Erythroagglutinin (Fluorescein)是一种应用于生命科学研究的生物材料或有机化合物。

Phaseolus Vulgaris Leucoagglutinin (PHA-L) Fluorescein作为一种植物源性凝集素，它能与多糖、多肽等生物分子产生特异性相互作用，进而被用作生物分析中的探针工具。Phaseolus Vulgaris Leucoagglutinin (PHA-L) Fluorescein也是一种在生命科学研究中可作为生物材料或有机化合物使用的物质。

Phaseolus Vulgaris Erythroagglutinin (Biotinylated)是一种用于生命科学研究的生物材料或有机化合物。

Phaseolus Vulgaris Leucoagglutinin (Biotinylated)作为一种植物源性凝集素，它能与多糖、多肽等生物分子产生特异性相互作用，进而被用作生物分析中的探针工具。Phaseolus Vulgaris Leucoagglutinin (Biotinylated) Biotinylated也是一种在生命科学研究中可作为生物材料或有机化合物使用的物质。

Phaseolus Vulgaris Erythroagglutinin (PHA-E)作为一种植物源性凝集素，它能与多糖、多肽等生物分子产生特异性相互作用，进而被用作生物分析中的探针工具。Phaseolus Vulgaris Erythroagglutinin (PHA-E)也是一种在生命科学研究中可作为生物材料或有机化合物使用的物质。

Phaseolus Vulgaris Leucoagglutinin (Rhodamine)作为一种植物源性凝集素，它能与多糖、多肽等生物分子产生特异性相互作用，进而被用作生物分析中的探针工具。Phaseolus Vulgaris Leucoagglutinin (Rhodamine)也是一种在生命科学研究中可作为生物材料或有机化合物使用的物质。

Lipopolysaccharides, fromProteus vulgaris是普通变形杆菌 (Proteus vulgaris) 提取的脂多糖内毒素和TLR-4激活剂，属于S型LPS，能够激活免疫系统的致病相关分子模式 (PAMP) 并诱导细胞分泌迁移体。其典型结构由O抗原、核心寡糖和脂质A组成。该化合物具有独特的分子结构及对壳聚糖的优良亲和力 (Kb=2.72 μM)，优于假结核耶尔森菌 (Kb=6.06 μM) 和大肠杆菌 (Kb=79.50 μM)。

Methyl Aminolevulinate Hydrochloride (5-Aminolevulinic acid methyl ester) 是增敏剂，可用于光动力疗法。Methyl aminolevulinate 是一种前药，可代谢为原卟啉 IX。

Hellebrigenol 是从越南蟾蜍毒液中提取的丁二烯内酯 ，具有抗肿瘤活性。

Salnacedin (G-201) 是一种小分子化合物，可用于治疗免疫系统疾病、皮肤和肌肉骨骼疾病，可用于研究寻常痤疮、皮炎和银屑病。

Nadifloxacin (OPC7251) 是一种对粉刺有效的广谱氟喹诺酮类抗生素。

2-Hydroxy-4-methoxybenzaldehyde (4-Methoxysalicylaldehyde) 是一种来自三种东非药用植物，Mondia whitei、Rhus vulgaris Meikle 和Sclerocarya caffra Sond 的酪氨酸酶抑制剂。它是香兰素的异构体，可用于合成尿苷M7。

Prolyl-4-hydroxylase Inhibitor 11 是一种新型脯氨酸4-羟化酶抑制剂，对普通小球藻(Chlorella vulgaris)氧化应激和 Cu(II)毒性的保护作用。

Sandosaponin A, an olean-12-ene-type triterpene oligoglycoside, is isolated from kidney bean, the seed of Phaseolus vulgaris L.

Phaseolin, a protein from red kidney bean (Phaseolus vulgaris L.), plays a pivotal role in hypersensitivity induction.

Phaseollidin, an antimicrobial phytoalexin, is produced by Phaseolus vulgaris (French bean).

Jatrorrhizine hydrochloride 是从小檗的根中提取的化合物，具有具有神经保护、抗菌、抗疟原虫和抗氧化活性。Jatrorrhizine hydrochloride 是一种具有口服活性和选择性的乙酰胆碱酯酶 (AChE)抑制剂，抑制去甲肾上腺素 (NE) 的摄取。

Sandosaponin B is a olean-12-ene-type triterpene oligoglycoside isolated from kidney bean, the seed of Phaseolus vulgaris L.

Olumacostat glasaretil 是乙酰辅酶A 羧化酶的有效抑制剂。

10'-Desmethoxystreptonigrin is an antibiotic originally isolated from Streptomyces and a derivative of the antibiotic streptonigrin. It is active against a variety of bacteria, including S. aureus, S. faecalis, E. coli, K. pneumoniae, and P. vulgaris (MICs = 0.4, 1.6, 3.1, 3.1 and 0.4 μg/ml, respectively). 10'-Desmethoxystreptonigrin is cytotoxic to HCT116 colon and A2780 ovarian cancer cells (IC50s = 0.004 and 0.001 μg/ml, respectively), as well as HCT116 cells resistant to etoposide and teniposide and cisplatin-resistant A2780 cells (IC50s = 0.003, 0.001, and 0.01 μg/ml, respectively). 10'-Desmethoxystreptonigrin is also an inhibitor of p21ras farnesylation (IC50 = 21 nM).

Flumequine-13C3is intended for use as an internal standard for the quantification of flumequine by GC- or LC-MS. Flumequine is a fluoroquinolone antibiotic.1It is active againstS. aureus, S. pyogenes, B. subtilis, E. coli, P. aeruginosa, S. faecalis, andK. pneumoniae(MICs = 1-100 μg ml). Flumequine is also active against field isolates of B. hyodysenteriae (MICs = 6.25-200 μg ml).2It inhibits DNA gyrase, disrupting supercoiling of bacterial DNA to block transcription and replication.3In vivo, flumequine (50 mg kg) increases survival in rat models ofP. vulgaris-induced urinary tract infection andP. mirabilis-induced prostatitis.1Formulations containing flumequine have been used in the treatment of urinary tract infections in veterinary medicine. 1.Rohlfing, S.R., Gerster, J.R., and Kvam, D.C.Bioevaluation of the antibacterial flumequine for urinary tract useAntimicrob. Agents Chemother.10(1)20-24(1976) 2.Aller-Morán, L.M., Martínez-Lobo, F.J., Rubio, P., et al.Evaluation of the in vitro activity of flumequine against field isolates of Brachyspira hyodysenteriaeRes. Vet. Sci.10351-53(2015) 3.Smith, J.T.The mode of action of 4-quinolones and possible mechanisms of resistanceJ. Antimicrob. Chemother.18 (Suppl. D)21-29(1986)

Halometasone is a synthetic corticosteroid.1,2Formulations containing halometasone have been used in the treatment of psoriasis vulgaris and eczematous dermatoses. 1.de la Brassine, M., Kint, A., Lachapelle, J.M., et al.Halomethasone (C 48.401-Ba) for the topical treatment of common dermatosesJ. Int. Med. Res.12(5)307-309(1984) 2.Zhu, J.-W., Wu, X.-J., Lu, Z.-F., et al.Role of VEGF receptors in normal and psoriatic human keratinocytes: Evidence from irradiation with different UV sourcesPLoS One8(1)e55463(2013)