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Cat. No. | Product Name | Target | Signaling Pathways |
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T20766 |
Sulfisoxazole acetyl
Gantrisin,Acetylsulfisoxazole,Gantrisin Pediatric,Lipo Gantrisin,乙酰磺胺异噁唑 |
Antibacterial | Microbiology/Virology |
Sulfisoxazole acetyl (Gantrisin) 是 Sulfisoxazole 的一种衍生物,是口服有效的二氢蝶酸合酶抑制剂。Sulfisoxazole acetyl 显示出抗菌作用。 | |||
T11007L |
Levofloxacin Hydrochloride Impurity A
Levofloxacin Hydrochloride Impurity A(117707-40-1 Free base),左氧氟沙星杂质A(盐酸盐) |
Antibacterial | Microbiology/Virology |
Levofloxacin Hydrochloride Impurity A 是一种喹诺酮类药物,具有广谱抗菌作用。 | |||
T0500 |
Chloroxine
Capitrol,氯喔星 |
Antibacterial; Antibiotic | Microbiology/Virology |
Chloroxine (Capitrol) 是重要的 8-羟基喹啉衍生物之一,有抗细菌,抗真菌,抗原生动物和抗阿米巴虫活性,可研究肠道阿米巴病,还可研究头皮屑和头皮脂溢性皮炎。 | |||
T1482 |
Ciclopirox
环吡酮,HOE296b,环吡酮胺 |
ATPase; Ferroptosis; Antibacterial; Autophagy; Antifungal | Apoptosis; Autophagy; Membrane transporter/Ion channel; Microbiology/Virology |
Ciclopirox (HOE296b) 是一种合成的抗真菌剂,可研究浅表真菌病。 | |||
T28574 |
Ro 24-4383
Ro 244383 |
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Ro 24-4383 is a carbamate-linked dual-action antibacterial agent. | |||
T61284 |
Antibacterial agent 94
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Antibacterial agent 94 (compound 5b) is a highly effective antibacterial agent that demonstrates strong activity against various bacterial strains. Notably, Antibacterial Agent 94 is capable of eradicating MRSA persisters, highlighting its potential as a therapeutic solution. Its mechanism of action involves interference with the bacterial membrane and disruption of the phosphatidylglycerol (PG) synthesis pathway [1]. | |||
T28598 |
Ro-23-9424
Ro 239424,Ro23-9424 |
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Ro-23-9424 is a dual-action cephalosporin with a fleroxacin esterified at the 3' position and aminothiazolylmethoxyimino-type side chain at the 7 position. Ro-23-9424 has broad and potent antibacterial activity in vitro and in vivo. | |||
T62740 | Antibacterial agent 110 | ||
Antibacterial agent 110 (Compound 4e) 是一种有效的抗细菌 (antibacterial) 剂,作用于 P. aeruginosa (MIC: 1 μg/ml)。Antibacterial agent 110 可以使代谢停滞和细胞内氧化应激,并阻碍 DNA 复制。Antibacterial agent 110 可以破坏细胞膜,具有良好的抗菌膜作用。 | |||
T68998 |
Parconazole Free Base
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Parconazole Free Base is used in veterinary as an oral fungicide with a broad-spectrum activity against dermatophytes, yeasts, and others fungi. This compound does not have any antibacterial effect. The mechanism of action involves inhibition of the fungal cytochrome P450 dependent 14alpha-dimethylation of lanosterol to ergosterol. | |||
T14359 |
AVX 13616
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Others | Others |
AVX 13616 shows the potent in vivo antibacterial activity of Avexa’s lead antibacterial candidate; particularly against drug-resistant Staphylococcus pathogens. IC50 value: 2-4 ug/ml (MICs) Target: antibacterial agent AVX13616 was as active as mupirocin i | |||
T82343 |
Gamma-Glutamyl Transferase-IN-1
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Gamma-Glutamyl Transferase-IN-1 (compound 4de) 是一种 β-羰基酰肼类抑制剂,靶向谷氨酰转移酶,具有抗真菌和抗菌活性。它通过促进活性氧积累、破坏细胞膜和失调组蛋白乙酰化来发挥作用。 | |||
T75500 | Batzelladine D | ||
Batzelladine D (Compound 1) 是一种 Pdr5p 转运蛋白催化活性和功能活性的抑制剂。Batzelladine D 抑制 Pdr5p ATPase 活性,IC50值为 7.1 µM。Batzelladine D 具有抗真菌 (antifungal)、抗寄生虫 (antiparasitic)、抗病毒 (antiviral)、抗细菌 (antibacterial) 和抗肿瘤活性。 | |||
T69350 |
Ethionamide HCl
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Ethionamide HCl is the salt form of Ethionamide, a second-line antitubercular agent that inhibits mycolic acid synthesis. Ethionamide is a nicotinamide derivative, with antibacterial activity, used to treat tuberculosis. Although the exact mechanism of action of ethionamide is unknown, it may inhibit the synthesis of mycolic acid, a saturated fatty acid found in the bacterial cell wall, thereby inhibiting bacterial cell wall synthesis. This eventually leads to bacterial cell wall disruption and ... | |||
T83703 |
BLP-3 TFA
Bombin-like Peptide 3 |
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BLP-3是一种在X. laevis皮肤中表达的内源性多肽,具有抗菌特性。在20 µg/ml的浓度下对N. meningitidis、N. gonorrhoeae、N. lactamica和N. cinerea有效。BLP-3折叠成α-螺旋结构,能插入并破坏类细菌膜。 | |||
T82342 |
Gamma-Glutamyl Transferase-IN-2
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Gamma-Glutamyl Transferase-IN-2 (compound 4dq),一种β-羰基酰肼类抑制剂,针对谷氨酰转移酶 (gamma-glutamyl transferase),展现其抗真菌与抗菌活性。该化合物通过诱导活性氧积累、破坏细胞膜以及干扰组蛋白乙酰化来发挥其生物学效应。 | |||
T75296 |
Pazufloxacin
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Pazufloxacin (T-3761)是氟喹诺酮类广谱抗生素。 | |||
T74790 | FtsZ-IN-7 | ||
FtsZ-IN-7 是一种有效的FtsZ 抑制剂,可促进 FtsZ 聚合并抑制 FtsZ 的 GTPase 活性。因此,FtsZ-IN-7 抑制细菌分裂导致细菌细胞死亡。FtsZ-IN-7 显示出杀菌活性,没有明显的引发细菌耐药性的趋势以及快速杀菌特性。并且 FtsZ-IN-7 对哺乳动物细胞表现出低溶血活性和细胞毒性。 | |||
T36021 |
Flumequine-13C3
Flumequine-13C3 |
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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, fl... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T1262 |
Tazobactam
Tazobactamum,Tazobactam acid,他唑巴坦酸,YTR-830H,CL-298741,他唑巴坦 |
Antibacterial; Antibiotic | Microbiology/Virology |
Tazobactam (YTR-830H) acid 是一种具有抗菌活性的β-内酰胺酶抑制剂。 | |||
T5707 |
3-O-Methylgalangin
3-Methylgalangin,GALANGIN-3-METHYLETHER,高良姜素 3-O-甲醚,高良姜素-3-甲醚 |
Antibacterial | Microbiology/Virology |
3-O-Methylgalangin (GALANGIN-3-METHYLETHER) 是一种来源于高良姜根茎的天然黄酮,具有抗菌活性,抑制胰腺脂肪酶。 | |||
T1165 |
Ethionamide
Bayer 5312,乙硫异烟胺,2-ethylthioisonicotinamide,Ethinamide |
Dehydrogenase; CAT; Antibacterial; Antibiotic | Metabolism; Microbiology/Virology; oxidation-reduction |
Ethionamide (2-ethylthioisonicotinamide) 是一种抗结核抗生素。 | |||
T1153 |
Trimethoprim
NIH 204,BW 56-72,甲氧苄啶,NSC-106568 |
DHFR; DNA/RNA Synthesis; Antifolate; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Trimethoprim (NSC-106568) 是抑菌抗生素,也是具有口服活性的二氢叶酸还原酶抑制剂。它对多种革兰氏阳性和革兰氏阴性需氧细菌具有活性,可用于尿路感染,肺孢子菌肺炎和志贺氏菌病的研究。 | |||
T1235L |
Lincomycin
U 10149,U10149,U-10149 |
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Lincomycin is a lincosamide antibiotic that comes from the actinomycete Streptomyces lincolnensis. Although similar in structure, antibacterial spectrum, and mechanism of action to macrolides, lincomycin is also effective against other organisms including | |||
T81080 |
Strictinin
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Strictinin 是从普洱茶 (Pu'er teas) 分离得到的酚类化合物,展现出潜在的抗病毒、抗菌和通便活性。这些活性是由于它加速小肠转运所致,并非因增强胃排空、增加食物摄入或诱导大鼠腹泻而发挥作用。 |