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Cat. No. | Product Name | Target | Signaling Pathways |
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T76107 | Urease | ||
Urease 由多种类型细菌产生,是一些致病菌的有效毒力因子。Urease 还是幽门螺杆菌代谢和毒力的中心,帮助其在胃粘膜中定植。 | |||
T67827 |
Urease Inhibitor 07
|
Others | Others |
Urease Inhibitor 07 是一种异取代金属蛋白酶抑制剂 , 对结核分枝杆菌H37Rv 菌株的潜在活性。 | |||
T78237 |
Urease-IN-6
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Urease-IN-6为一种高效Urease抑制剂,IC50值为14.2 μM,适用于消化性溃疡和胃溃疡研究。 | |||
T62465 | Urease-IN-1 | ||
Urease-IN-1 是一种脲酶抑制剂 (IC50: 2.21±0.45 μM)。 | |||
T73047 |
Urease-IN-5
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Urease-IN-5, 作为一种尿素酶抑制剂,具有1.473 µM的IC50值。该化合物在细胞毒性方面表现较低,并对普通变形杆菌展现出17.78 µg/mL的IC50值的抑制活性。 | |||
T64121 | Urease-IN-2 | ||
Urease-IN-2 是一种脲酶 (urease) 非竞争性的抑制剂 (IC50: 0.94 μM,Ki: 1.6 μM),能够非竞争性的抑制 Jack bean 豆脲酶 (JBU)。 | |||
T80893 | Urease-IN-9 | ||
Urease-IN-9 (Compound 1e) 为脲酶抑制剂,具有IC50值为19.5 μM。 | |||
T79656 | Urease-IN-8 | ||
Urease-IN-8 (Compound 5e) 为一竞争性脲酶 (Urease) 抑制剂,具IC50值为3.51 μM,Ki值为3.11 μM,主要用于消化性溃疡与胃溃疡研究。 | |||
T73046 |
Urease-IN-4
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Urease-IN-4是一种尿素酶 (urease) 抑制剂,具有1.64 µM的IC50值。此化合物对细胞毒性低,能有效抑制普通变形杆菌,其IC50值为15.27 µg/mL。 | |||
T79652 | Urease-IN-7 | ||
Urease-IN-7 (Compound 5k),作为竞争性Urease抑制剂,具有IC50为3.33 μM和Ki值为3.62μM。该化合物可用于消化性溃疡和胃溃疡研究。 | |||
T3315 |
Benurestat
贝奴司他,EU-2826 |
Others; Antibacterial | Microbiology/Virology; Others |
Benurestat (EU-2826) 是有口服活性的脲酶抑制剂,可研究受感染的尿素分解。 | |||
T77348 |
Butylboronicacid
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Others | Others |
Butylboronicacid 是脲酶竞争性抑制剂,可作为单糖络合试剂。 | |||
T11305 |
Flurofamide
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Others | Others |
Flurofamide 是一种细菌尿素酶抑制剂,在感染性尿路结石方面有研究的价值。 | |||
T1592 |
Acetohydroxamic acid
Methylhydroxamic acid,Acetic acid,Lithostat,AHA,oxime,N-Hydroxyacetamide,乙酰氧肟酸 |
MMP; Antibacterial | Microbiology/Virology; Proteases/Proteasome |
Acetohydroxamic acid (N-Hydroxyacetamide) 是一种不可逆的细菌和植物尿素酶抑制剂,可研究慢性尿路感染。 | |||
T36962 |
MMP Inhibitor I (trifluoroacetate salt)
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MMP inhibitor I is a peptide inhibitor of matrix metalloproteinase-1 (MMP-1), MMP-2, and MMP-3 (IC50s = 1.3, 30, and 150 μM, respectively). It is selective for MMP-1, MMP-2, and MMP-3 over the proteases thermolysin, urease, trypsin, α-chymotrypsin, plasmin, and elastase at concentrations up to 4 mM. | |||
T78350 |
Glutamate dehydrogenase
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Glutamate dehydrogenase为存在于原核生物与真核生物线粒体中的酶类,适用于氨、α-酮戊二酸、L-谷氨酸及脲酶的酶促反应检测。 | |||
T79450 |
Enzyme-IN-2
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Enzyme-IN-2(化合物 15),作为ureases抑制剂,展现出了强效的抗尿素分解活性,其Ki值为2.36 μM,而IC50值为0.75 µM。 | |||
T36133 |
3,3'-((2-Chlorophenyl)methylene)bis(4-hydroxy-2H-chromen-2-one)
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3,3'-((2-Chlorophenyl)methylene)bis(4-hydroxy-2H-chromen-2-one) is a non-nucleotide inhibitor of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1; Ki = 50 μM).1,2 It also inhibits urease (IC50 = 84.53 μM for the Jack bean enzyme).3 |1. Choudhary, M.I., Fatima, N., Khan, K.M., et al. New biscoumarin derivatives-cytotoxicity and enzyme inhibitory activities. Bioorg. Med. Chem. 14(23), 8066-8072 (2006).|2. Onyedibe, K.I., Wang, M., and Sintim, H.O. ENPP1, an old enzyme with new functions, ... | |||
T37832 |
CAY10761
CAY10761 |
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CAY10761 is an inhibitor of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1; IC50s = 467 and 429 μM for the human and snake venom enzymes, respectively).1,2 It also inhibits mushroom tyrosinase (Ki = 1.9 μM) and urease from jack bean, P. mirabilis, and B. pasteurii (IC50s = 0.093, <0.125, and 0.089 mM, respectively, at pH 8.2).3,4 |1. Khan, K.M., Fatima, N., Rasheed, M., et al. 1,3,4-Oxadiazole-2(3H)-thione and its analogues: A new class of non-competitive nucleotide pyrophosphatases/p... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T4S0578 |
Guaijaverin
番石榴苷,Guajaverin,Quercetin-3-Arabinoside |
Others; Antioxidant; Antibacterial | Microbiology/Virology; Others; oxidation-reduction |
Guaijaverin (Quercetin-3-Arabinoside) 是一种尿素酶抑制剂,IC50值为 120 μM,有抗氧化和抗变形链球菌作用。 | |||
TN6604 |
4-Chlorocinnamic acid
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4-Chlorocinnamic acid is a photosensitive compound. 2-Chlorocinnamic acid and 4-chlorocinnamic acid show potent urease inhibitory activities with the respective IC50 values of 0.66 and 1.10 uM. | |||
TN3465 |
Atalantoflavone
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Antifection | Microbiology/Virology |
Atalantoflavone shows urease inhibitory potential. It displays weak cytotoxic activity against the human Caucasian prostate adenocarcinoma cell line PC-3. | |||
TN6659 |
2-Chlorocinnamic acid
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2-Chlorocinnamic acid is a photosensitive compound, it can inhibit tyrosinase activity. 2-Chlorocinnamic acid and 4-chlorocinnamic acid show potent urease inhibitory activities with the respective IC50 values of 0.66 and 1.10 uM. |