103
35
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T62577 | Anti-MRSA agent 5 | ||
Anti-MRSA agent 是一种 MRSA 的有效拮抗剂 (MIC50: 0.38 μg/mL),hERG 活性较低 (IC50: 40 μM)。Anti-MRSA agent 对哺乳动物细胞的毒性也很低,几乎不可能获得细菌的耐药性。 | |||
T60546 | Anti-MRSA agent 6 | ||
Anti-MRSA agent 6 (compound 3q6) 是一种有效的抗耐甲氧西林金黄色酿脓葡萄球菌(anti-MRSA)剂,对 MCF-7、A549 细胞具有低细胞毒性。 | |||
T79778 |
Anti-MRSA agent 8
|
||
Anti-MRSA agent 8(Compound 7g)为DAPG衍生物,展现出显著的抗菌活性,主要通过作用于细菌细胞膜以发挥效能。此化合物可应用于耐甲氧西林Staphylococcus aureus(MRSA)的研究领域。 | |||
T63775 | Anti-MRSA agent 1 | ||
Anti-MRSA agent 1 是 MRSA 抑制剂,其 MIC 值为 0.5 μg/mL,能够有效的缓解 MRSA 抵抗作用。 | |||
T63632 | Anti-MRSA agent 3 | ||
Anti-MRSA agent 3 能够明显的抑制耐甲氧西林金黄色葡萄球菌 (MRSA) 的活性 (MIC: 0.098 μg/ml),并且对正常细胞毒性较低。Anti-MRSA agent 3 对细菌基因组 DNA 具有较高的结合亲和力,对细菌细胞壁和细胞膜具有较强的破坏能力。 | |||
T62383 | Anti-MRSA agent 2 | ||
Anti-MRSA agent 2 (compound 14) 能够较好的抑制耐甲氧西林金黄色葡萄球菌 (MRSA) (MIC: 0.098 μg/ml),对正常细胞的毒性相对较低。Anti-MRSA agent 2 能够较强的破坏细菌膜,并具有较好的与细菌基因组DNA 结合的能力。 | |||
T74527 | Anti-MRSA agent 4 | ||
Anti-MRSA agent 4 (compound 7a) 为针对耐甲氧西林金黄色葡萄球菌 (MRSA) 的革兰氏阳性菌强效选择性生长抑制剂,具有MIC≤ 0.26 µM的显著效力。此外,该化合物在HEK293细胞中未显示细胞毒性和溶血活性。 | |||
T74810 | Anti-MRSA agent 7 | ||
Anti-MRSA agent 7 (Compound 12)作为一种抗菌剂,具有针对S. aureus DNA gyrase、E. coli DNA gyrase、S. aureus topo IV和E. coli topo IV的显著抑制效果,其IC50值分别为0.185 μM、0.365 μM、0.341 μM和0.059 μM。 | |||
T7897 |
PK150
|
Others; Antibacterial | Microbiology/Virology; Others |
PK150 是一种 Sorafenib 类似物,具有抗菌活性。它抑制甲氧西林敏感金黄色葡萄球菌,耐甲氧西林金黄色葡萄球菌,万古霉素中介金黄色葡萄球菌的 MIC 分别为 0.3,0.3-1,0.3 µM。 | |||
T22269 |
Benzyldodecyldimethylammonium Chloride Dihydrate
|
Antibacterial | Microbiology/Virology |
Benzyldodecyldimethylammonium chloride dihydrate 可以用作杀虫试剂,可以靶向耐药性细菌,如耐甲氧西林金黄色葡萄球菌、耐多药铜绿假单胞菌等,且具有浓度依赖性。 | |||
T8507 |
MAC-545496
|
Antibacterial | Microbiology/Virology |
MAC-545496 是一种抗毒剂,可逆转耐甲氧西林的菌株中的 β-内酰胺耐药性。它是糖肽抗性相关蛋白 R 的纳摩尔抑制剂,对全长 GraR 蛋白具有很强的结合亲和力。 | |||
T40475 |
Ceftobiprole medocaril
BAL5788,头孢比普酯 |
Antibacterial | Microbiology/Virology |
Ceftobiprole medocaril (BAL5788) 是 Ceftobiprole 的前药。Ceftobiprole 是一种广谱的头孢菌素,对耐甲氧西林金黄色葡萄球菌具有活性。 | |||
TQ0077 |
Ceftobiprole
Ro 63-9141,BAL 9141,头孢吡普 |
Antibacterial | Microbiology/Virology |
Ceftobiprole (Ro 63-9141) 是一种广谱头孢菌素,对甲氧西林耐受的金黄色葡萄球菌的MIC90值为 2 μg/mL。 | |||
T7387 |
Ceftaroline fosamil
TAK-599,头孢罗林酯,PPI0903 |
Antibacterial; Antibiotic | Microbiology/Virology |
Ceftaroline fosamil (TAK-599) 是一种头孢菌素衍生物,是抗甲氧西林金黄色葡萄球菌 (MRSA) T-91825 的 N-膦酰基前药,可研究 MRSA 感染。 | |||
T21358 |
Dalbavancin
BI 397,BI-397,VER 001,A-A 1,BI397,VER-001,Dalbavancin HCl,达巴万星 |
Antibacterial; Antibiotic | Microbiology/Virology |
Dalbavancin (BI-397) HCl 是一种半合成的脂糖肽抗生素,对革兰氏阳性细菌有杀菌活性。Dalbavancin 抑制金黄色葡萄球菌和炭疽芽孢杆菌的 MIC90分别为 0.06 μg/mL 和 0.25 μg/mL。 | |||
T4208 |
Targocil
|
Antibacterial | Microbiology/Virology |
Targocil 是一种磷壁酸生物合成的抑菌抑制剂,可抑制甲氧西林敏感金黄色葡萄球菌 (MSSA) 和耐甲氧西林金黄色葡萄球菌 (MRSA) 的生长,对于 MRSA 和 MSSA 的MIC90值都为 2 μg/mL。 | |||
T2549 |
Robenidine hydrochloride
Rasexinium,Dexium,氯苯胍盐酸盐,Robenidine Hydrochoride,Toraxine,盐酸氯苯胍,Nugatex |
Antibacterial; Antibiotic; Parasite | Microbiology/Virology |
Robenidine hydrochloride (Robenidine Hydrochoride) 是一种主要用于家禽的抗球虫剂, 对 MRSA 和 VRE 有抑制活性,其 MIC50值分别为 8.1 和 4.7 μM。 | |||
T3114 |
Povidone iodine
Betadine,聚乙烯吡酮磺,Povidone-iodine,聚乙烯吡咯烷酮碘,Isodine,PVP iodine,iodopovidone,PVP-I |
Antibacterial; Antibiotic | Microbiology/Virology |
Povidone iodine (Povidone-iodine) 有很强的抗细菌活性, 可杀死 MRSA 和 MSSA 菌株,其 MICs 值分别为 31.25 mg/L 和7.82 mg/L。 | |||
T61037 |
Glycosyltransferase-IN-1
|
Others | Others |
Glycosyltransferase-IN-1 是一种糖基转移酶 (glycosyltransferase) 抑制剂,具有抑菌活性,抑制 MSSA、MRSA 、枯草杆菌和肠杆菌。 | |||
T36033 |
DETA NONOate
NOC-18,Diethylamine NONOate |
NO Synthase | Immunology/Inflammation |
DETA NONOate (NOC 18)是外源性一氧化氮 (NO) 供体,具有血管舒张和抗抑郁活性。DETA NONOate 可用于激活神经元中的内向电流,可加速MRSA感染伤口的愈合。 | |||
T64316 |
VP-4604
1-((4-Nitrophenyl)sulfonyl)piperidine |
||
VP-4604是一种有效的抗耐甲氧西林金黄色葡萄球菌(MRSA)化合物。VP-4604对金黄色葡萄球菌展现出显著的抑制微生物生长的作用,MIC 为4-8μg/mL。VP-4604抑制耐甲氧西林金黄色葡萄球菌的生长,其生长抑制率达到95%以上。 | |||
T67826 |
Alalevonadifloxacin
|
DNA gyrase; Topoisomerase; Antibacterial | DNA Damage/DNA Repair; Microbiology/Virology |
Alalevonadifloxacin 是一种DNA 回旋酶和DNA 拓扑异构酶抑制剂,是一种喹诺酮类针对Mrsa 的新型抗菌化合物。Alalevonadifloxacin 对治疗细菌性革兰氏阳性、革兰氏阴性和厌氧性感染有潜在作用。 | |||
T0391 |
Linezolid
PNU-100766,雷奈佐利 |
MAO; Antibacterial; Antibiotic | Metabolism; Microbiology/Virology; Neuroscience |
Linezolid (PNU-100766) 是恶唑烷酮类合成抗生素,抑制细菌蛋白质合成的起始阶段,具有抗感染作用。 | |||
T4165 |
Delpazolid
LCB01-0371 |
Antibacterial; Antibiotic | Microbiology/Virology |
Delpazolid (LCB01-0371) 是一种恶唑烷酮类新型抗生素,能抑制MSSA 和MRSA 的生长,对它们的MIC90值都为 2 μg/mL。 | |||
T31064 |
CP-5484
CP 5484,UNII-A53TMV6VUN,CP5484 |
||
Cp-5484 is a new kind of Quaternary carbapenem with strong anti MRSA activity and low acute toxicity. | |||
T39816 |
Ceftaroline fosamil inner salt
TAK-599 free acid,PPI0903freeacid |
||
Ceftaroline fosamil (TAK-599) inner salt, a cephalosporin derivative, is an N-phosphono prodrug of anti-methicillin-resistant Staphylococcus aureus (MRSA) T-91825. Ceftaroline fosamil inner salt can be used for the research of MRSA infection. | |||
T74269 |
Antibacterial agent 83
|
||
Antibacterial agent 83 (compound 17h) 对各种耐万古霉素 Enterococcus faecalis(VRE) 和耐甲氧西林 Staphylococcus aureus(MRSA) 显示出有效的抗菌活性。Antibacterial agent 83 可以显着减少 MRSA 的生物膜形成,并表现出良好的选择性。Antibacterial agent 83 在人肝微粒体中代谢稳定。 | |||
T30767 |
CB-181963
CB 181963,CB181963,UNII-6784994L0W,CAB 175 |
||
CB-181963, a new cephalosporin, is an effective antistaphylococcal drug, showing excellent activity against the resistance of MRSA strains to other cephalosporins in planktonic and biofilm cultures. | |||
T40301 |
Antibacterial agent 28
|
||
Antibacterial agent 28, with a minimum inhibitory concentration (MIC) range of 0.5-2 μg/mL, exhibits promising potential as an antibacterial candidate targeting MRSA infections. | |||
T80390 |
HG4
|
||
HG4为快速作用的抗菌多肽,具有抗生物膜和抗炎活性。特别是针对MRSA菌株(MIC: 32-64 μg/mL),它对革兰氏阳性病原体表现出显著活性。此外,HG4能够与细菌脂质结合,并能减少S. aureus MRSA USA300细菌的ATP浓度。 | |||
T35064 |
Viquidacin
NXL101,NXL-101,NXL 101 |
||
Viquidacin ( NXL-101) is an oral/intravenous antibiotic that targets Gram-positive bacteria such as MRSA. In 2008, Novexel announced it had discontinued the development of Viquidacin (NXL 101). | |||
T61121 | NusB-IN-1 | ||
NusB-IN-1 (Compound 22r) is a highly effective bacterial rRNA synthesis inhibitor, administered orally. It exhibits potent antimicrobial activity against MRSA and VRSA [1]. | |||
T82761 |
CDFI
|
||
CDFI为MurJ(脂质II翻转酶)的抑制剂,能够提升β-内酰胺类对抗MRSA的活性。 | |||
T83097 | Antibacterial agent 165 | ||
Antibacterialagent 165 (compound 3) 是一种有效针对细菌 (bacterial) 的羟基喹啉衍生物抑制剂,具备抗耐甲氧西林金黄色葡萄球菌 (MRSA) 的能力。 | |||
T39230 |
Contezolid acefosamil
MRX-4,Contezolid acefosamil |
||
Contezolid acefosamil (MRX-4), an orally active prodrug, is metabolized into Contezolid (MRX-I), an oxazolidinone derivative with potent in vitro efficacy against multidrug-resistant Gram-positive bacteria, including MRSA. | |||
T73127 | C16-K-cBB1 | ||
C16-K-cBB1 是一种对 MRSA(甲氧西林耐药金黄色葡萄球菌)有效且选择性的抗菌剂,其 MIC 为 1 μg/mL。C16-K-cBB1 具有很好的选择性,由于其溶血活性较弱。在 12.5 μg/mL 浓度下,C16-K-cBB1 能够在 120 分钟内杀死 MRSA 细胞。 | |||
T80387 |
HG2
|
||
HG2 是一種具有快速抗菌效能的肽類化合物,展現了顯著的抗生物膜及抗炎特性。該化合物對革兰氏阳性病原体有效,特別是對 MRSA (最小抑菌浓度:16-32μg/mL) 有良好活性。HG2 能夠結合至细菌脂質,并且有效降低 S. aureus MRSA USA300株中的 ATP 濃度。 | |||
T74715 | Antibacterial agent 136 | ||
Antibacterial agent 136 (compound 3) 是恶二唑酮类抗生素。Antibacterial agent 136 对 Staphylococcus aureus(MRSA) 具有很高的抗菌效力,MIC50值为 0.8 μM。 | |||
T64054 |
Antibacterial agent 88
|
||
Antibacterial agent 88 是一种有效的抗细菌剂,能够作用于 B. subtilis (MIC: 4 μg/ml),对 MRSA、MRSE 和 S. aureus 的 MIC 值均为 ≤0.0156 μg/mL。 | |||
T83098 | Antibacterial agent 163 | ||
Antibacterialagent 163 (compound 1) 是一种羟基喹啉衍生物,能有效抑制细菌 (bacterial)。该化合物特别针对耐甲氧西林金黄色葡萄球菌 (MRSA) 表现出抑制作用。 | |||
T63224 |
Antibacterial agent 104
|
||
Antibacterial agent 104 是有效的抗细菌 (antibacterial) 剂,体外具有显著的抗细菌作用,体内表现出良好的抗 MRSA 效果。 | |||
T64069 | Antibacterial agent 87 | ||
Antibacterial agent 87 是一种有效的抗细菌剂,能够作用于 MRSA (MIC: 0.125 μg/ml)、MRSE (MIC: 0.0625 μg/ml) 和 S. aureus (MIC: 0.0625 μg/ml)。 | |||
T74502 | Antibacterial agent 108 | ||
Antibacterial agent 108 (Compound 1h) 是一种有效的抗细菌剂,对 MRSA 和一些抗生素抗性菌的 MIC 值均为 3 μM。 | |||
T64315 |
VP-4509
|
||
VP-4509 是一种抗耐甲氧西林金黄色葡萄球菌 (MRSA) 剂 (MIC: 49.3 μM)。VP-4509 对革兰氏阴性细菌铜绿假单胞菌 (ATCC9027) 表现出高抗菌效果。 | |||
T80391 |
LCI peptide
|
||
LCI peptide为具备抗细菌特性的抗菌肽。该肽对多种细菌株显示活性,包括植物病原体、黄单胞菌、假单胞菌,以及大肠杆菌、Gentamicin抗性 MRSA和Xoo。 | |||
T74776 | Antibacterial agent 139 | ||
Antibacterial agent 139 对革兰氏阳性菌具有抗菌活性。Antibacterial agent 139 具有抗 MRSA、抗 VISA 和抗 LRSE 活性。Antibacterial agent 139 去极化细菌细胞膜。 | |||
T37464 |
CAY10711
|
||
CAY10711 is a substituted diamine that produces rapid bactericidal activity against both Gram-positive and Gram-negative bacteria, including methicillin-resistant S. aureus (MRSA) and stationary-phase bacteria. It displays MIC99 values of 2.9, 11.5, 2.9, and 2.9 μM against S. aureus RN4220, P. aeruginosa PAO1, E. coli ANS1, and MRSA 10082B, respectively. CAY10711 reduces biofilm formation and promotes biofilm dispersal in P. aeruginosa. It is synergistic with kanamycin and has limited adverse ef... | |||
T80414 |
ASP-1
|
||
ASP-1是一种活性强的抗葡萄球菌肽,其对金黄色葡萄球菌及耐甲氧西林金黄色葡萄球菌(MRSA)的最低抑制浓度(mic)范围为2μg/mL至64μg/mL。 | |||
T80275 |
Lynronne-2
|
||
Lynronne-2是抗菌肽,对革兰氏阳性细菌,包含MDR菌株具有活性(耐甲氧西林MRSA菌株MIC: 32-256 μg/mL)。该化合物亦对P. aeruginosa感染展现效用。 | |||
T74803 | Levonadifloxacin | ||
Levonadifloxacin ((S)-(-)-Nadifloxacin; WCK 771),作为一种宽谱抗葡萄球菌药物,对甲氧西林敏感金黄色葡萄球菌(MSSA)及对甲氧西林耐药金黄色葡萄球菌(MRSA)显示出显著的抗菌活性,并能有效减少THP-1单核细胞对MRSA和MSSA菌株的吞噬。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5724 |
Neogambogic acid
neo-gambogic acid,新藤黄酸 |
Apoptosis; Others; Antibacterial | Apoptosis; Microbiology/Virology; Others |
Neogambogic acid 是藤黄的有效成分,可诱导细胞凋亡并具有抗癌作用。它有效抑制耐甲氧西林的金黄色葡萄球菌。 | |||
T1465 |
Mupirocin
Pseudomonic acid,莫匹罗星,BRL-4910A |
DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Mupirocin (BRL-4910A) 是从Pseudomonas fluorescens 中分离得到的一种有口服活性的抗生素。它可逆地抑制异亮氨酸转移RNA,并抑制细菌蛋白和RNA 的合成起抗菌作用。 | |||
T8148 |
Mupirocin calcium hydrate
莫匹罗星钙,Mupirocin calcium |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Mupirocin calcium hydrate 是从Pseudomonas fluorescens 中分离得到的,一种有口服活性的抗生素。它可逆地抑制异亮氨酸转移RNA,并抑制细菌蛋白和RNA 的合成起到抗菌作用。 | |||
TN4943 |
Sanguisorbigenin
地榆皂苷元,Tomentosolic acid,3β-Hydroxyurs-12,19-dien-28-oic acid,19-Dehydroursolic acid,Ursa-12,19-dien-28-oic acid |
Antibacterial | Microbiology/Virology |
Sanguisorbigenin (Tomentosolic acid) 抑制耐甲氧西林金黄色葡萄球菌,是一种天然抗菌剂。 | |||
TN2281 |
Sinapaldehyde
trans-3,5-Dimethoxy-4-hydroxy cinnamaldehyde,TRANS-3,5-二甲氧基-4-羟基肉桂醛,芥子醛 |
Antibacterial | Microbiology/Virology |
Sinapaldehyde (trans-3,5-Dimethoxy-4-hydroxy cinnamaldehyde) 对耐甲氧西林的金黄色葡萄球菌和大肠杆菌有抗菌作用,MIC 值都为 128 μg/mL。 | |||
T8724 |
6-Methoxydihydrosanguinarine
|
Others | Others |
6-Methoxydihydrosanguinarine 是一种从M. cordata 果实中分离出的生物碱,它对 MCF-7 细胞系(IC50:0.61 μM)和 SF-268 细胞系(IC50:0.54 μM)具有强的细胞毒性。 | |||
TN1524 |
Continentalic acid
|
NOS; COX; Antibacterial; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Continentalic acid 是来自 Aralia continentalis 的,对金黄色葡萄球菌的 MIC 约为 8-16 µg/mL,包括对甲氧西林敏感的金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌标准菌株。 | |||
T3S0153 |
Xanthatin
苍耳亭,叶黄制菌素 |
Apoptosis; VEGFR; Lipoxygenase; Wnt/beta-catenin; Antibacterial | Angiogenesis; Apoptosis; Cytoskeletal Signaling; Metabolism; Microbiology/Virology; Stem Cells; Tyrosine Kinase/Adaptors |
Xanthatin 是一种从Xanthium strumarium 叶子中提取的天然产物,可诱导细胞凋亡。它抑制布鲁氏菌的IC50值为 2.63 μg/ mL,对寄生虫特异性锥虫硫磷还原酶具有不可逆的弱抑制作用。它通过抑制PGE2的合成和 5-脂氧合酶的活性而显示出抗炎活性。 | |||
TJS1779 |
Protosappanin A
原苏木素A,PTA |
NADPH-oxidase; IL Receptor; IκB/IKK; TNF; NF-κB; TLR; ROS; COX; HIV Protease; JAK; NO Synthase; STAT | Angiogenesis; Apoptosis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Microbiology/Virology; Neuroscience; NF-κB; Proteases/Proteasome; Stem Cells |
Protosappanin A (PTA) 是从苏木中分离得到的免疫抑制成分和主要联苯化合物,通过下调 JAK2和 STAT3的磷酸化,抑制 JAK2/STAT3依赖的炎症通路。 | |||
T10838 |
Closthioamide
|
Antibacterial | Microbiology/Virology |
Closthioamide is a potent inhibitor of bacterial DNA gyrase and highly active against MRSA, Ec, VRE, and Mv (MICs: 0.58 μM, 9.00 μM, 0.58 μM and 72.03 μM). | |||
T74200 |
Glicophenone
|
||
Glicophenone 作为一种抗细菌(antibacterial)剂,对MRSA OM481、MRSA OM505、MRSA OM584、MRSA OM623 以及MSSA 209P的MIC值均为32 μg/mL。 | |||
TN4308 |
Isolupalbigenin
|
Antifection | Microbiology/Virology |
Isolupalbigenin shows promising cytotoxic effects toward HL-60 cells (IC50 4.3 ± 0.7 to 18.0 ± 1.7 uM), it also shows in vitro inhibitory activity toward human glyoxalase I. Isolupalbigenin shows two different antibacterial activities against MRSA: direct growth inhibition and intensification of methicillin sensitivity, it could lead to the development of compounds for new approaches against MRSA infection. | |||
TN3216 |
(3R)-7,4’-Dihydrohomoisoflavanone
7,4'-Dihydroxyhomoisoflavanone |
Antibacterial | Microbiology/Virology |
(3R)-7,4’-Dihydrohomoisoflavanone 是一种天然化合物,对金黄色葡萄球菌和耐甲氧西林金黄色葡萄菌(MRSA)都具有强大的抗菌性能。 | |||
TN4097 | Gancaonin G | Antifection | Microbiology/Virology |
Gancaonin G shows antibacterial effects on the MRSA strains with MIC values of 16 microg/ml, it also shows more moderate antibacterial activity against Streptococcus mutans. | |||
T2S0058 |
6-Ethoxychelerythrine
乙氧基白屈菜红碱,Ethoxychelerythrin |
Antibacterial | Microbiology/Virology |
6-Ethoxychelerythrine (Ethoxychelerythrin) 具有抗菌活性,对烟曲霉和耐甲氧西林金黄色葡萄球菌 (MRSA) 表现出很强的活性。 | |||
TN3450 |
Artanin
|
Antifection | Microbiology/Virology |
Artanin displays promising inhibition against both MSSA and MRSA with minimal inhibitory concentrations (MICs) of 8-64 ug/ml, but very weak against Gram-negative pathogen and yeast with MICs of 256 to ≥1024 ug/ml. | |||
T38349 |
Talaromycesone A
|
||
Talaromycesone A is a fungal metabolite originally isolated fromTalaromyces.1It is active againstS. epidermidisand methicillin-resistantS. aureus(MRSA) bacteria (IC50s = 3.70 and 5.48 μM, respectively). Talaromycesone A inhibits acetylcholinesterase (AChE) in a cell-free assay (IC50= 7.49 μM for the human enzyme). 1.Wu, B., Ohlendorf, B., Oesker, V., et al.Acetylcholinesterase inhibitors from a marine fungus Talaromyces sp. strain LF458Mar. Biotechnol. (NY)17(1)110-119(2015) | |||
TN2524 |
1-Acetyl-β-carboline
1-Acetyl-beta-carboline |
Antifection | Microbiology/Virology |
Combination of 1-acetyl-beta-carboline with ampicillin exhibits synergistic antibacterial activity against MRSA. | |||
T73207 |
Laburnetin
|
||
Laburnetin 是一种异黄酮类抗菌剂 (antibacterial agent)。Laburnetin 对真菌、S. vesicarium 具有抗菌活性。Laburnetin 增强了耐甲氧西林 (Methicillin) 金黄色葡萄球菌 (MRSA) 菌株对甲氧西林的敏感性。Laburnetin 可用于控制栽培物种的虫害。 | |||
TN3907 |
Pinosylvin monomethyl ether
(E)-3-Hydroxy-5-methoxystilbene |
Antifection | Microbiology/Virology |
(E)-3-Hydroxy-5-methoxystilbene possesses inhibitory activity against several Gram-positive bacteria, including isolates of methicillin-resistant Staphylococcus aureus (MRSA), Mycobacterium bovis BCG, and avirulent Bacillusanthracis (Sterne strain), among | |||
TN1444 |
Bis(dihydrochelerythrinyl)amine
bis[6-(5,6-dihydrochelerythrinyl)]amine |
Antifection | Microbiology/Virology |
BIS-[6-(5,6-dihydro-chelerythrinyl)] ether shows strong activity against Aspergillus fumigatus and methicillin-resistant Staphylococcus aureus (MRSA). | |||
T75273 | Teicoplanin sodium | ||
Teicoplanin sodium (Antibiotic MDL-507 sodium) 是一种有效的脂糖肽类抗生素。Teicoplanin sodium 对 HIV-1、SARS-CoV1 和 SARS-CoV2 显示出抗病毒活性。Teicoplanin sodium 具有抗 MRSA 活性。 | |||
TN4319 |
Isopimaric acid
|
Antifection | Microbiology/Virology |
Isopimaric acid is active against MDR and MRSA strains of S. aureus which are becoming increasingly resistant to antibiotics, the minimum inhibitory concentrations (MIC) are 32-64 microg/mL . Isopimaric acid is also possible that an antagonistic interacti | |||
T79943 |
6-C-Methylquercetin-3,4'-dimethyl ether
|
Antibiotic | Microbiology/Virology |
6-C-Methylquercetin-3,4'-dimethyl etheris 是一种黄酮醇衍生物,提取自Bauhinia thonningii Schum叶。本化合物对多重耐药的革兰氏阴性细菌及耐甲氧西林金黄色葡萄球菌(MRSA)表现出抗菌活性。 | |||
T75560 | 4(1H)-Quinolinone, 1-methyl-2-(5Z)-5-undecen-1-yl- | ||
4(1H)-Quinolinone, 1-methyl-2-(5Z)-5-undecen-1-yl- (化合物2) 是一种从蛇床子提取的喹诺酮类生物碱。该化合物对耐甲氧西林金黄色葡萄球菌(MRSA)表现出活性,其最小抑制浓度(MIC)值对ATCC 33591和ATCC 25923株分别为32 μg/mL和16 μM/mL。 | |||
T74206 |
Kalimantacin A
|
||
Kalimantacin A是具有针对葡萄球菌(包括耐甲氧西林金黄色葡萄球菌)抗菌活性的有效抗生素。 | |||
T73673 |
Thiomarinol A
|
||
Thiomarinol A (4-Hydroxythiomarinol C) 是一种有效的抗生素。Thiomarinol A 是二硫代吡咯酮和海藻酸的混合物。Thiomarinol A 显示出抗菌活性。Thiomarinol A 以剂量依赖性方式抑制 MRSA IleRS,Kiapp 值为 19 nM。 | |||
T75278 | Pristinamycin | ||
Pristinamycin, 一种 Streptomyces pristinaespiralis 产生的口服活性链霉素样抗生素,由化学上不相关的两部分组成:Pristinamycin I (PI) 与 Pristinamycin II (PII)。该药物对包括耐甲氧西林金黄色葡萄球菌 (MRSA)、万古霉素耐药金黄色葡萄球菌 (VRSA) 和粪肠球菌 (VREF) 在内的多种抗生素耐药革兰氏阳性菌表现出强大活性。 | |||
T75555 | (6E,12E)-Tetradecadiene-8,10-diyne-1,3-diol | ||
'(6E,12E)-Tetradecadiene-8,10-diyne-1,3-diol' 是从白术根中分离出的一种具有抗菌活性的化合物,对 MRSA 显示出 4 - 32 μg/mL 的最小抑菌浓度(MIC),表现出对抗性细菌感染研究的潜力。 | |||
TN1814 |
Juncusol
6-甲基灯心草二酚,灯心草酚 |
Caspase; Antifection | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
Juncusol shows anxiolytic and sedative activities, it shows anxiolytic activity at dosages of 10 mg/kg; it can induce caspase-3-mediated cytotoxicity in HT22 cells. Juncusol has anti-microbial activity, it shows significant activity against MRSA strains. | |||
TN6010 |
Picrasidine S
|
||
Picrasidine S shows the potent cytotoxicity against human HeLa cervical, gastric MKN-28, and mouse melanoma B-16 cancer cells, it also shows the potent antibacterial activity against two strains of pathogenic bacteria methicillin-resistant Staphylococcus | |||
T38394 | PSMα3 | ||
PSMα3 is a peptide compound that can be utilized to induce tolerance in dendritic cells (DCs) for DC vaccination strategies. It effectively penetrates and modulates human monocyte-derived DCs by modifying the maturation process induced by TLR2 or TLR4. Additionally, PSMα3 inhibits the production of both pro- and anti-inflammatory cytokines and decreases antigen uptake. Notably, PSMα3 is a significant virulence factor released by the most pathogenic strains of methicillin-resistant Staphylococcus... | |||
T75700 | Longistyline A | ||
Longistyline A (Longistylin A) 是一种天然二苯乙烯,可从木豆中提取。Longistyline A 对耐甲氧西林金黄色葡萄球菌具有抑菌效应,MIC 值为 1.56 μg/mL。Longistyline A 具有神经保护作用,可用于感染和神经系统疾病的研究。 | |||
T36417 |
Nargenicin
Antibiotic 47444 |
||
Nargenicin is a macrolide antibiotic that selectively inhibits the growth of S. aureus, methicilin resistant S. aureus (MRSA), and M. luteus (MICs = 0.6, 0.3, and 2.5 μg/ml, respectively) over a panel of 11 Gram-positive and Gram-negative bacteria (MICs = >80 μg/ml). [1] It dose-dependently inhibits S. aureus DnaE in the presence of DNase I-activated DNA and E. coli DnaE when used at concentrations of 0.00001-0.1 and 0.01-100 μg/mL, respectively. [2] In murine BV-2 microglial cells, nargenicin (... | |||
T36000 |
3-Hydroxyterphenyllin
|
||
3-Hydroxyterphenyllin is a p-terphenyl fungal metabolite originally isolated from A. candidus that has diverse biological activities, including antioxidant, antiproliferative, antibacterial, and antiviral properties.1,2,3,4 It has a 96% scavenging effect on 2,2-diphenyl-1-picrylhydrazyl radicals when used at a concentration of 100 μg/ml.2 3-Hydroxyterphenyllin inhibits the growth of HeLa cervical, A549 lung, and HepG2 liver cancer cells (IC50s = 23, 36, and 32 μM, respectively), as well as methi... |