Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T67737 |
gp120-α4β7 binding inhibitor 11
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
gp120-α4β7 binding inhibitor 11是一种抗HIV 药物。gp120-α4β7 binding inhibitor 11干扰HIV 相关糖蛋白gp12G 与整合素α4β7的结合(IC50=1.64nM)。 | |||
T60871 |
gp120-IN-1
|
||
gp120-IN-1 (compound 4e) 是 HIV-1 gp120蛋白的有效抑制剂,CC50值为 100.90 μM,IC50值为 2.2 μM。gp120-IN-1 抑制 gp120 蛋白介导的病毒进入细胞。gp120-IN-1 具有抗 HIV-1 活性。gp120-IN-1 在 SUP-T1 细胞中具有剂量依赖性细胞毒性。 | |||
T60714 |
gp120-IN-2
|
||
gp120-IN-2 (compound 4i) 显示出抗 HIV-1 活性。它是 HIV-1 gp120的有效抑制剂,IC50值为 7.5 μM,CC50值为 112.93 μM。gp120-IN-2 在癌细胞 SUP-T1 中表现出剂量依赖性的细胞毒性。 | |||
T16276 |
NBD-556
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
NBD-556是一种 CD4 模拟物,识别 HIV-1 包膜蛋白 gp120 并诱导 gp120 重组,类似于 CD4 结合,可阻断 gp120-CD4 的相互作用。 | |||
T76537 |
GP120, HIV-1 MN
|
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GP120,HIV-1MN 是一种肽。GP120,HIV-1MN 可用于 HIV 感染的研究。 | |||
T6418 |
BMS-378806
BMS378806,BMS-806,1-[(2R)-4-苯甲酰基-2-甲基-1-哌嗪基]-2-(4-甲氧基-1H-吡咯并[2,3-B]吡啶-3-基)-1,2-乙二酮 |
gp120/CD4; HIV Protease | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
BMS-378806 (BMS-806) 是一种 HIV-1 抑制剂,可选择性抑制 HIV-1 gp120 结合到 CD4 受体,EC50为 0.85-26.5 nM。 | |||
TP1785L |
Peptide T acetate(106362-32-7 free base)
|
Others; HIV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
Peptide T acetate(106362-32-7 free base) 是一种来自 HIV-1 gp120 V2 区域的八肽。它是一种合成八肽,其可能的作用机制是 gp120 对 CD4 受体的竞争性抑制以及与血管肠肽受体的结合和抑制细胞因子作用。 | |||
T4665 |
Temsavir
BMS626529 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Temsavir (BMS626529) 是一种新型附着抑制剂,靶向 HIV-1 gp120 并阻止其与 CD4+ T 细胞结合。 | |||
T71665 |
INCB-9471
|
HIV Protease; CCR | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
INCB-9471 是一种 CCR5 拮抗剂,具有抗HIV活性,抑制 HIV-1 gp120 之间的相互作用。 | |||
T10570 |
Fostemsavir Tris
BMS-663068 Tris |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Fostemsavir Tris (BMS-663068 Tris) 是一种 HIV-1附着抑制剂。 | |||
T3523 |
Fostemsavir
BMS-663068,磷坦姆沙韦 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Fostemsavir (BMS-663068) 是 BMS-626529 的原药,可抑制 HIV-1 与细胞 CD4 受体的结合,能结合gp120。 | |||
T23108 |
Ophiobolin C
|
Others | Others |
inhibitor of human CCR5 binding to HIV-1 gp120 | |||
T80580 |
Zinlirvimab
10-1074 |
||
Zinlirvimab是一种IgG1-λ2类人源化HIV中和抗体,专一性靶向HIV-1 gp120包膜糖蛋白(IIIB gp120 V3环)。 | |||
T30532 |
BMS-585248
CHEMBL236995,CIO2TZZ9H1,BMS 585248,UNII-CIO2TZZ9H1 |
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BMS-585248 is a highly effective HIV-1 adhesion inhibitor that targets the viral envelope protein gp120. | |||
TP2401 |
Peptide T amide
D-Ala(1)-peptide T amide |
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Peptide T amide is an octapeptide segment of HIV envelope gp120 and is used in AIDS therapy. | |||
T72099 |
Carbomethoxycarbonyl-D-Pro-D-Phe-OBzl
|
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Carbomethoxycarbonyl-D-Pro-D-Phe-OBzl (化合物 (CPF(LL)) 是一种 HIV-1抑制剂。Carbomethoxycarbonyl-D-Pro-D-Phe-OBzl 能与 gp120相互作用以阻断 gp120与 CD4的结合,并保留 CD4依赖的 T 细胞功能。 | |||
T69371 |
BMS 378806
|
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BMS-378806 is an orally bioavailable HIV-1 inhibitor that interferes with gp120-CD4 interaction. | |||
T62340 |
NBD-14189
|
||
NBD-14189 是一种有效的 HIV-1 进入拮抗剂,能够作用于 HIV-1HXB2 假病毒 (IC50: 89 nM)。NBD-14189 能够结合 HIV-1 gp120,并具有显著的抗病毒作用 (EC50<200 nM)。 | |||
T71094 |
CD4 (81-92)
|
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CD4 (81-92) is a peptide that was previously found to inhibit gp120 binding, HIV-1 infectivity, and syncytium formation. | |||
TP1785 |
Peptide T
|
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Peptide T is an octapeptide from the V2 region of HIV-1 gp120. Peptide T is a synthetic octapeptide whose possible mechanism of action is the competitive inhibition of gp120 to the CD4 receptor as well as binding to vasointestinal peptide receptors and in | |||
T81295 |
Retrocyclin-1
|
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Retrocyclin-1是一种θ防御素,具有识别并结合含碳水化合物表面分子的能力,能够保护细胞抵御HIV-1感染。该化合物对胎球蛋白、gp120(Kd=35.4 nM)、CD4(Kd=31 nM)以及半乳糖神经酰胺(Kd=24.1 nM)展现出高度亲和性。 | |||
T62299 |
NBD-14270
|
||
NBD-14270 是一种有效的 HIV-1 进入拮抗剂,能够作用于 50 株 HIV-1 假型病毒 (IC50: 89 nM)。NBD-14270 是一种吡啶类似物,细胞毒性低 (CC50>100 μM)。NBD-14270 能够结合 HIV-1 gp120 并表现出显著的抗病毒活性 (EC50<200 nM)。 | |||
TP1873 |
Peptide T TFA
|
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Peptide T (TFA) is an octapeptide derived from the V2 region of HIV-1 gp120. It serves as a ligand for the CD4 receptor, effectively inhibiting the binding of HIV to the CD4 receptor. | |||
T68789 | N-(3-Phenyl-2-propenyl)-1-deoxynojirimycin | ||
The effect of N-(3-phenyl-2-propenyl)-1-deoxynojirimycin (ppDNM) on the lectin binding to HIV-1 glycoprotein was analyzed by using biotinylated lectins of various sugar specificities as probes. ppDNM potentially inhibited HIV-1-induced syncytium formation and viral infectivity of HIV-1 without cytotoxicity. The lectin binding assay showed that ppDNM treatment reduced Con A binding to gp120 of HIV-1. | |||
TP1910 |
CALP1
|
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Cell-permeable calmodulin (CaM) agonist that binds to the EF-hand/Ca2+-binding site; produces CaM-dependent activation of phosphodiesterase. Also binds to cytoplasmic sites on other Ca2+ channels, including NMDA and HIV-1 gp120-activated channels, inhibit | |||
T68842 |
Complestatin
|
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Complestatin is a compound extracted from Streptomyces lavendulae mycelia; on acid hydrolysis yields D-4-hydroxyphenylglycine & D-3,5-dichloro-4-hydroxyphenylglycine & acidic chromophore; inhibits gp120-CD4 binding. It is isolated from the culture broth of Streptomyces and has anti-HIV-1 activity. It has a role as a metabolite, an antimicrobial agent and an anti-HIV-1 agent. | |||
T7624 |
DAPTA
DAPTA(TFA),D-Ala-peptide T-amide,Adaptavir |
HIV Protease; CCR | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
DAPTA (Adaptavir) 是一种合成肽,是 CCR5抑制剂,有抗 HIV 的活性。 | |||
T77792 |
HIV Peptide T
|
||
HIV Peptide T(Peptide T),这种合成的八肽是HIV感染治疗中的一种抗病毒药物,其主要通过竞争性抑制gp120(HIV表面蛋白)与CD4受体的相互作用,同时与血管肠肽(vasointestinal peptide, VIP)受体同源结合并且阻断细胞因子的产生与作用来发挥功效。 | |||
T36185 | Globotriaosylceramides (hydroxy) (porcine) | ||
Globotriaosycleramides are glycosphingolipids found in mammalian cell membranes that are synthesized from lactosylceramides . They act as receptors for Shiga and Shiga-like toxins in vitro and in vivo. Globotriaosylceramides accumulate in endothelial cells, pericytes, vascular smooth muscle cells, renal epithelial cells, dorsal ganglia neuronal cells, and myocardial cells in patients with Fabry disease, a lysosomal storage disorder characterized by a deficiency in the enzyme α-galactosidase A. G... | |||
T36186 |
Globotriaosylceramides (porcine)
|
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Globotriaosycleramides are glycosphingolipids found in mammalian cell membranes that are synthesized from lactosylceramides . They act as receptors for Shiga and Shiga-like toxins in vitro and in vivo. Globotriaosylceramides accumulate in endothelial cells, pericytes, vascular smooth muscle cells, renal epithelial cells, dorsal ganglia neuronal cells, and myocardial cells in patients with Fabry disease, a lysosomal storage disorder characterized by a deficiency in the enzyme α-galactosidase A. G... | |||
T37874 |
Feglymycin
|
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Feglymycin is a 13-amino acid peptide originally isolated from Streptomyces that has antibacterial and antiviral activities. It is active against Gram-positive bacteria (MICs = 32-64 μg/ml) and inhibits HIV viral replication in H9 cells (IC50 = ~5 μM). Feglymycin is also active against clinical isolates of HIV-1 from clades A-D, A/E, and G (EC50s = 0.5-6.7 μM). It interacts with gp120 and inhibits HIV-1 NL4.3 binding to human soluble CD4 (EC50 = 4.4 μM) and to CD4+ SupT1 T cells by 74.5% when us... | |||
T38103 |
Defensin HNP-3 (human) (trifluoroacetate salt)
|
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Defensin HNP-3 is a peptide secreted by human polymorphonuclear leukocytes (PMNs) that has antimicrobial properties. It induces lysis of mammalian cells when used at a concentration of 25 μg/mL. It also inhibits growth of E. faecalis (ED50 = 100 nM) and clinical isolates of P. aeruginosa (MIC90 = 4 μM). HNP-3 binds to recombinant HIV-1 envelope glycoprotein (gp120) and human CD4 (Kds = 52.8 and 34.9 nM, respectively). It also binds to recombinant, immobilized human surfactant protein D (SP-D; Kd... |