Cat. No. | Product Name | Target | Signaling Pathways |
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T35427 |
β-Lactamase-IN-2
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Antibacterial | Microbiology/Virology |
β-Lactamase-IN-2 是 β-内酰胺酶的有效抑制剂。β-Lactamase-IN-2显示出抗菌活性。 | |||
T19206 |
β-Lactamase-IN-1
4-(1,3-dihydroxypropan-2-yl)-6-methoxypyrido[2,3-b]pyrazin-3-one,beta-lactamase-IN-1 |
Antibacterial | Microbiology/Virology |
β-Lactamase-IN-1 (4-(1,3-dihydroxypropan-2-yl)-6-methoxypyrido[2,3-b]pyrazin-3-one) 是一种 β-Lactamase 抑制剂,针对淋病奈瑟菌的感染。 | |||
T60370 |
Metallo-β-lactamase-IN-2
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Metallo-β-lactamase-IN-4 (compound 40) 是一种有效的金属 -β- 内酰胺酶 (MBL) 抑制剂,其对于 VIM-1、NDM-1和 IMP-7的 IC50值分别为 0.1 μM, 1.3 μM 和 5.0 μM。 | |||
T60050 |
ANT3310
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Antibacterial | Microbiology/Virology |
ANT3310 是一种广谱共价丝氨酸 β-内酰胺酶抑制剂,对 AmpC、CTX-M-15、TEM-1、OXA-48、OXA-23 和 KPC-2 的 IC50 范围为 1 nM 至 175 nM。 ANT3310 可用于细菌感染研究。 | |||
T11125 |
Durlobactam sodium salt
杜巴坦,ETX2514 sodium salt,杜洛巴坦 |
Antibacterial | Microbiology/Virology |
Durlobactam sodium salt (ETX2514 sodium salt)是一种 β-内酰胺酶抑制剂,针对 A 类 KPC-2、C 类 AmpC 和 D 类 OXA-24,IC50 值分别为 4 nM、14 nM 和 190 nM。 Durlobactam sodium salt 可用于对包括鲍曼不动杆菌在内的耐药革兰氏阴性菌的研究。 | |||
T16028 |
IMB-XH1
Mcl1-IN-2,7-[(2-吡啶基氨基)-2-噻吩基甲基]-8-喹啉醇 |
BCL; Antibacterial | Apoptosis; Microbiology/Virology |
IMB-XH1 (Mcl1-IN-2) 是一种骨髓细胞因子 1 抑制剂。它也是非竞争性的 Delhi metallo-β-lactamase(NDM-1) 抑制剂。它对金属 β-内酰胺酶 NDM-1,IMP-4,ImiS 和 L1 的 IC50值分别为 0.4637 μM,3.980 μM,0.2287 μM 和 1.158 μM。 | |||
T60914 | Metallo-β-lactamase-IN-8 | ||
Metallo-β-lactamase-IN-8 (化合物 17) 是有效,可逆和竞争性的广谱金属-β-内酰胺酶 (MβLs)抑制剂,具有抗菌活性。Metallo-β-lactamase-IN-8 对L1,ImiS,IMP-1和VIM-2的IC50值分别为 1.3 μM,5.7 μM,9.8 μM。 | |||
T60494 |
Metallo-β-lactamase-IN-7
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Metallo-β-lactamase-IN-7 是VIM 型金属 β-内酰胺酶的有效抑制剂,其对VIM-2、VIM-1和VIM-5 的IC50值分别为 0.019 μM、13.64 μM 和 0.38 μM。它还可以增强 Meropenem 对革兰氏阴性菌的抗菌活性。 | |||
T60239 | Metallo-β-lactamase-IN-6 | ||
Metallo-β-lactamase-IN-6 is a highly effective inhibitor of VIM-Type metallo-β-lactamase, demonstrating IC 50 values of 0.56 μM, 29.50 μM, and 5.78 μM for VIM-2, VIM-1, and VIM-5, respectively. In addition, Metallo-β-lactamase-IN-6 exhibits potent synergistic antibacterial properties when combined with Meropenem, particularly against engineered Escherichia coli strains and clinically isolated Pseudomonas aeruginosa carrying the VIM-2 MBL gene [1]. | |||
T69482 |
MßL-IN-2I
|
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MßL-IN-2I is a potent broad-spectrum metallo-β-lactamase (MβL) inhibitor which inhibits the MβLs NDM-1, VIM-2, ImiS, and L1. | |||
T62486 |
VIM-2-IN-1
|
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VIM-2-IN-1 (compound 1dj) 是一种 β-内酰胺酶 (β-lactamase) 抑制剂,具有抗菌作用。VIM-2-IN-1 能够作用于 Verona 整合子编码的金属-β-内酰胺酶 (VIM-2) (IC50: 23 μM)、德国亚胺培内酶-1 (GIM-1) (IC50: 48 μM) 和新德里金属 (NDM-1) (IC50: 231 μM)。 | |||
T38020 |
O-Benzylhydroxylamine (hydrochloride)
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O-Benzylhydroxylamine is a building block.1,2It has been used in the synthesis of β-lactam inhibitor precursors and fluoroquinolone derivatives with antibiotic activity. 1.Bellettini, J.R., and Miller, M.J.A short synthesis of an important precursor to a new class of bicyclic β-lactamase inhibitorsTetrahedron Lett.38(2)167-168(1997) 2.Asadipour, A., Moshafi, M.H., Khosravani, L., et al.N-substituted piperazinyl sarafloxacin derivatives: synthesis and in vitro antibacterial evaluationDaru.26(2)19... | |||
T69266 |
Cefcanel free acid
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Cefcanel is a semisynthetic third-generation cephalosporin with antibacterial activity. Cefcanel is active against the species E. coli, K. aerogenes and Proteus mirabilis; H. influenzae and M. catarrhalis has reasonable susceptibility. Cefcanel inhibits 90% of S. aureus strains at 2 µg/ml, irrespective of the presence of a β-lactamase. Cefcanel binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall. PBPs are enzymes involved in the te... |