Cat. No. | Product Name | Target | Signaling Pathways |
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T72203 |
Reverse transcriptase-IN-3
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Reverse transcriptase-IN-3, 作为一种嘧啶-5-羧酰胺衍生物,主要用于抑制HIV-1。它对HIV-1野生型及其突变型病毒株均展示出高效的抑制活性。 | |||
T0682 |
Lamivudine
GR109714X,BCH-189,拉米夫定 |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Lamivudine (BCH-189) 是一种核苷逆转录酶抑制剂,可抑制HIV 逆转录酶1和2 以及乙型肝炎病毒的逆转录酶。 | |||
T14313 |
Apricitabine
AVX754,SPD754 |
HIV Protease; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
Apricitabine (SPD754) 是一种具有高选择性和口服活性的HIV-1逆转录酶抑制剂(Ki=0.08μM),是2′-脱氧-3′-氧-4′-硫代胞苷(dOTC)的(-)对映体 。 Apricitabine 对DNA 聚合酶α、β和γ具有抑制作用,Ki 值分别为300μM、12μM 和112.25μM。Apricitabine 在抗逆转录病毒HIV 感染者中显示出良好的抗逆转录病毒治疗效果,具有良好的耐受性和较低的选择性抗性。 | |||
T61679 |
Abacavir monosulfate
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Abacavir monosulfate is an orally active, competitive nucleoside reverse transcriptase inhibitor that effectively inhibits HIV replication. Additionally, it exhibits anticancer properties in prostate cancer cell lines, and has the ability to penetrate the blood-brain-barrier and suppress telomerase activity [1] [2] [3]. | |||
FL0097 |
beta-L-D4A
2'3'-didehydro-2'3'-dideoxyadenosine |
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beta-L-D4A 是一种核苷类型的HIV-1逆转录酶抑制剂。 | |||
T78737 |
NNRTIs-IN-3
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HIV Protease | Microbiology/Virology; Proteases/Proteasome |
NNRTIs-IN-3(化合物8)作为一种HIV-1非核苷逆转录酶抑制剂,表现出较高的效力(EC50=0.01 µM)。 | |||
T35428 |
β-Rubromycin
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β-Rubromycin is a bacterial metabolite originally isolated from Streptomyces that has diverse biological activities.1 It inhibits the growth of HMO2, KATO-III, and MCF-7 cells with GI50 values of 0.5, 0.84, and <0.1 μM, respectively. β-rubromycin inhibits HIV-1 reverse transcriptase activity by 39.7% when used at a concentration of 10 μM. It also has antibacterial activity against Gram-positive bacteria. The structure of β-rubromycin was originally described as containing an ortho-quinone group,... |