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Cat. No. | Product Name | Target | Signaling Pathways |
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T13865 |
Resorcinolnaphthalein
|
RAAS | Endocrinology/Hormones |
Resorcinolnaphthalein 是一种特异性的血管紧张素转换酶 2 激活剂,EC50=19.5 μM。Resorcinolnaphthalein 能够用于高血压和肾纤维化的研究 | |||
T9109 |
SSAA09E2
|
RAAS; SARS-CoV | Endocrinology/Hormones; Microbiology/Virology |
SSAA09E2 是一种新型的SARS-CoV 复制抑制剂,通过阻断SARS-S 与SARS-CoV 受体血管紧张素转换酶-2 的早期相互作用发挥作用。 | |||
T20033 |
Direct Violet 1
NSC75778,NSC 75778,Airedale Violet ND,NSC-75778,直接青莲N,Direct Violet N,CCRIS 2413 |
SARS-CoV | Microbiology/Virology |
Direct Violet 1 (CCRIS 2413) 是一种偶氮染料,是纺织品染料,也是 SARS-CoV-2 刺突蛋白和 ACE2 抑制剂之间的蛋白质相互作用 ,IC50为 1.47-2.63 µM。 | |||
T73098 |
BACE2-IN-1
|
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BACE2-IN-1 是一种高选择性 BACE2抑制剂, 抑制常数 Ki 为 1.6 nM。BACE2抑制剂可用于 Ⅱ 型糖尿病的研究。 | |||
T16116 |
MLN-4760
|
RAAS | Endocrinology/Hormones |
MLN-4760 是选择性的人ACE2抑制剂,IC50=0.44 nM,对人ACE2的选择性是其他相关蛋白的 5000 多倍,包括人睾丸 ACE (IC50,>100 μM) 和牛 carboxypeptidase A (IC50,27 μM)。 | |||
TP1622 |
DX600 TFA
|
RAAS | Endocrinology/Hormones |
DX600 TFA 是 ACE2 的特异性抑制剂,不会与 ACE 发生交叉反应。 | |||
T10850 |
CMP-5
|
Antiviral; Histone Methyltransferase | Chromatin/Epigenetic; Immunology/Inflammation |
CMP-5 是一种具有选择性的 PRMT5 抑制剂,是刺突蛋白、神经纤毛蛋白受体和 ACE2 的强结合剂,抑制 PRMT5 甲基转移酶活性。CMP-5 具有抗病毒活性,可用于研究SARS病毒感染。 | |||
T35324 |
DX600
|
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DX600 是一种angiotensin-converting enzyme 2 (ACE2)的特异抑制剂,不会与ACE 发生交叉反应。 | |||
T37695 |
NMNNAGDKWSAFLKEQSTLAQMYPLQEIQNLTVKLQLQALQQ
|
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NMNNAGDKWSAFLKEQSTLAQMYPLQEIQNLTVKLQLQALQQ, an ACE2-related peptide, serves as a valuable research tool for comprehending ACE2 functions. | |||
T40384 |
Mca-Ala-Pro-Lys(Dnp)-OH
|
||
Mca-Ala-Pro-Lys(Dnp)-OH, a specific quenched fluorogenic substrate for ACE2, enables the detection of ACE2 activity in various tissues including urinary, heart, and lung. | |||
T76200 |
STIEEQAKTFLDKFNHEAEDLFYQSSLASWN
|
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STIEEQAKTFLDKFNHEAEDLFYQSSLASWN 是与血管紧张素转换酶 2 (ACE2) 相关的肽,适用于研究 ACE2 功能。 | |||
T70986 |
GL-1001 sodium salt
|
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GL-1001 sodium salt is an ACE2 inhibitor. | |||
T81849 | MAT-POS-e194df51-1 | SARS-CoV | Microbiology/Virology |
MAT-POS-e194df51-1 是一种非共价、非肽类、口服活性的SARS-CoV-2主蛋白酶 (Mpro) 抑制剂,IC50 值达 37nM。该化合物展现细胞毒性,其在 A549-ACE2-TMPRSS2 和 HeLa-ACE2 细胞线上的 EC50 值分别为 64 nM 和 126 nM。 | |||
T70985 |
GL-1001 disodium tetrahydrate
|
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GL-1001 disodium tetrahydrate is an ACE2 inhibitor. | |||
T76605 |
Abz-Ser-Pro-3-nitro-Tyr
|
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Abz-Ser-Pro-3-nitro-Tyr 是 ACE2 (angiotensin-converting enzyme-2) 的底物。 | |||
T80048 |
Mca-YVADAP-Lys(Dnp)-OH TFA
|
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Mca-YVADAP-Lys(Dnp)-OH TFA为Caspase-1及血管紧张素转换酶2(ACE2)特异性的荧光底物。 | |||
T76090 |
Mca-YVADAP-Lys(Dnp)-OH
|
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Mca-YVADAP-Lys(Dnp)-OH 是caspase-1和血管紧张素转换酶 2 (ACE2) 的荧光底物。 | |||
T78770 |
Garcinone B
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Angiotensin-converting Enzyme (ACE) | Metabolism |
Garcinone B,一种氧杂蒽酮衍生物,为山竹果皮中分离的天然产物,有效抑制ACE2和Mpro,适用于COVID-19研究。 | |||
T72913 | (R)-MLN-4760 | ||
(R)-MLN-4760 是 MLN-4760 的活性较低的 R 型异构体,是一种ACE2抑制剂,IC50值为 8.4 μM。 | |||
T80587 |
Alunacedase alfa
HrsACE2,GSK 2586881 |
SARS-CoV | Microbiology/Virology |
Alunacedase alfa (HrsACE2; GSK 2586881) 是一种人源重组的可溶性血管紧张素转化酶 2(hrsACE2)。作为转基因可溶性形态的 ACE2,Alunacedase alfa 能够减少 SARS-CoV-2 与细胞膜结合 ACE2 的竞争性进入,因此具有研究 SARS-CoV-2 的可能性。 | |||
T76851 | Regdanvimab | ||
Regdanvimab (CT-P59),一种靶向SARS-CoV-2刺突蛋白受体结合域的人单克隆抗体,通过阻断与ACE2的相互作用来防止病毒进入,适用于COVID-19研究。 | |||
T81206 | SARS-CoV-2-IN-65 | SARS-CoV | Microbiology/Virology |
SARS-CoV-2-IN-65(compound 2f(81))是一种具有口服活性的有效可逆SARS-CoV-2进入抑制剂。它通过抑制Calu-3细胞中RBD:ACE2的相互作用和TMPRSS2的活性,阻断了假病毒通过ACE2依赖性途径的进入。 | |||
T36655 | Anti-Spike-RBD mAb | ||
Anti-Spike-RBD mAb is a CHO cell derived human monoclonal IgG1 antibody. Blocking the interaction of spike protein and ACE2 is a potential therapeutic approach for SARS-CoV-2 treatment[1]. [1]. Chunyan Wang, et al. A Human Monoclonal Antibody Blocking SARS-CoV-2 Infection. Nat Commun. 2020 May 4;11(1):2251. | |||
T36876 | SBP1 | ||
Human ACE2 receptor-derived 23-amino acid peptide. Binds receptor binding domain (RBD) of insect-derived SARS-CoV-2 spike protein (KD = 1.3 μM for N-terminal biotinylated, insect-derived spike protein RBD; see Zhang et al preprint publication). Please note - unpublished, in-house data suggests approximately 75-fold lower affinity for insect-derived SARS-CoV-2 RBD than reported by Zhang et al. | |||
T36435 |
SP 10
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Peptide originally derived from SARS-CoV Spike (S) protein; corresponds to amino acid residues 668 to 679. Highly potent inhibitor of SARS-CoV S protein and ACE2 interaction (IC50 = 1.88 nM in biochemical assay). Inhibits interaction of SARS-CoV S protein and Vero E6 cells in vitro. Please note, this peptide displays 80% sequence identity to homologous site on SARS-CoV-2 S-protein (residues 689-697). | |||
T36942 |
SSAA09E1
SSAA09E1 |
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SSAA09E1 is an inhibitor of severe acute respiratory syndrome coronavirus (SARS-CoV) viral entry.1It reduces infection of HEK293T cells transiently transfected with angiotensin-converting enzyme 2 (ACE2) by an HIV-based virus system pseudotyped with SARS-CoV surface glycoprotein (EC50= 6.7 μM). SSAA09E1 also inhibits the proteolytic activity of cathepsin L (IC50= 5.33 μM) but not cathepsin B when used at a concentration of 20 μM. 1.() | |||
T36877 |
SBP1-FITC
SBP1-FITC |
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Fluorescently labelled peptide derived from human ACE2 (SBP1, Cat. No. 7233). Composed of SBP1 conjugated to FITC (Fluorescein-5-isothiocyanate; Cat. No. 5440). SBP1 binds receptor binding domain (RBD) of insect-derived SARS-CoV-2 spike protein (KD = 1.3 μM for N-terminal biotinylated, insect-derived spike protein RBD; see Zhang et al preprint publication). Please note - unpublished, in-house data suggests SBP1 has approximately 75-fold lower affinity for insect-derived SARS-CoV-2 RBD than repo... | |||
T83742 |
SBP1 TFA
Spike Binding Peptide 1 |
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Spike binding peptide 1 (SBP1) 为对应于血管紧张素转换酶2 (ACE2) 的第21至43位氨基酸的肽。已将脂质纳米粒子 (LNPs) 包裹的抗病毒化合物奥司他韦磷酸盐与SBP1结合并通过体外研究评估其控制释放奥司他韦磷酸盐的长期潜力。SBP1 (2%) 固定于交联的羟基丙烯酸酯和乙基黄原酸乙酯网络,提高了对严重急性呼吸系统冠状病毒2(SARS-CoV-2)刺突糖蛋白,亦称表面糖蛋白,的网络捕获效率。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T2563 |
Acetyl-L-carnitine hydrochloride
Acetyl L-carnitine hydrochloride,O-Acetylcarnitine,乙酰-L-肉(毒)碱盐酸盐,O-acetyl-L-carnitine,O-Acetyl-L-carnitine hydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
Acetyl-L-carnitine hydrochloride (Acetyl L-carnitine hydrochloride) 是一种由内源性左旋肉碱的乙酰化形式的盐酸盐组成的营养补充剂,具有潜在的神经保护、认知增强、抗抑郁和免疫调节活性。还可缓解化疗、糖尿病或其他疾病引起的周围神经病变。此外,乙酰左旋肉碱可能通过增加T淋巴细胞成熟来调节免疫反应,并可能下调促炎细胞因子对病毒(如SARS-CoV-2)的反应。它还可能破坏ACE2信号通路并抑制活性氧(ROS)的产生。 |