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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T38175 |
MPro N3
|
||
Coronavirus main protease (Mpro) inhibitor (respective IC50 values are 2.7, 4 and 8.8 μM for MHV-A29, HCoV-229E and FOPV replication in vitro). Inhibits viral cell infection in an MHV plaque reduction assay. Also inhibits SARS-CoV-2 viral cell entry in a plaque reduction assay (IC50 = 16.8 μM). | |||
T37173 |
MPro Inhibitor 11a
|
||
MProinhibitor 11a is an inhibitor of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (MPro; IC50= 0.053 μM in a TR-FRET assay).1It reduces viral yield in the culture supernatant of SARS-CoV-2-infected Vero E6 cells (EC50= 0.53 μM). MProinhibitor 11a also reduces viral RNA copy numbers in the same model when used at concentrations ranging from 1.85 to 50 μM. 1.Dai, W., Zhang, B., Jiang, X.-M., et al.Structure-based design of antiviral drug candidates targeting the SARS-... | |||
T38174 | Mpro inhibitor N3 hemihydrate | ||
Mpro inhibitor N3 hemihydrate is a potent inhibitor of SARS-CoV-2 Mpro with an EC50 of 16.77 μM for SARS-CoV-2. Mpro inhibitor N3 hemihydrate specifically inhibits Mpro from multiple coronaviruses, including SARS-CoV and MERS-CoV. Mpro inhibitor N3 hemihydrate displays inhibition against HCoV-229E, FIPV, and MHV-A59 with individual IC50 of 4.0 μM, 8.8 μM, and 2.7 μM, respectively[1][2]. Mpro inhibitor N3 hemihydrate (0-0.64 μM) is able to penetrate cells to inhibit the replication of IBV viruses... | |||
T37174 |
SARS-CoV MPro-IN-1
|
||
MProinhibitor 11b is an inhibitor of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) main protease (MPro; IC50= 0.04 μM in a TR-FRET assay).1It reduces viral yield in the culture supernatant of SARS-CoV-2-infected Vero E6 cells (EC50= 0.72 μM). MProinhibitor 11b also reduces viral RNA copy numbers in the same model when used at concentrations ranging from 1.85 to 50 μM. 1.Dai, W., Zhang, B., Jiang, X.-M., et al.Structure-based design of antiviral drug candidates targeting the SARS-C... | |||
T63098 |
SARS-CoV-2 Mpro-IN-2
|
||
SARS-CoV-2 Mpro-IN-2 是一种选择性的、低细胞毒性的、非共价 Mpro 抑制剂,其 IC50 值为 0.40 μM。SARS-CoV-2 Mpro-IN-2 表现出良好的抗 SARS-CoV-2 作用,其 EC50 值为 1.1 μM。SARS-CoV-2 Mpro-IN-2 能够用于研究 COVID-19。 | |||
T69545 |
Mpro 61
|
||
Mpro 61 is a potent non-covalent inhibitor of SARS-CoV-2 main protease. | |||
T62991 | Mpro/PLpro-IN-1 | ||
Mpro/PLpro-IN-1 (Compound 29) 是一种双重作用的 SARS-CoV-2 蛋白酶抑制剂。Mpro/PLpro-IN-1 也是一种 Mpro/PLpro 的有效抑制剂,对 M pro 具有微摩尔抑制作用(IC50:1.72 μM),对 PL pro 具有亚微摩尔抑制作用(IC50:0.67 μM)。 | |||
T72447 |
SARS-CoV-2 Mpro-IN-5
|
||
SARS-CoV-2 Mpro-IN-5是一种针对主要蛋白酶(MPro)和组织蛋白酶L(CatL)的双重抑制剂,具备IC50s分别为1800 nM和145 nM。该化合物在对抗SARS-CoV2方面显示出显著的抗病毒活性,并能在表达hACE2的A549细胞中阻断SARS-CoV2复制,IC50值达14.7 nM。 | |||
T72451 |
SARS-CoV-2 Mpro-IN-6
|
||
SARS-CoV-2 Mpro-IN-6为共价、不可逆及选择性抑制剂,主要针对SARS-CoV-2 Mpro,IC50值为0.18 μM。该化合物对人组织蛋白酶B、F、K、L以及半胱天冬酶3无抑制作用。 | |||
T60686 | SARS-CoV-2 Mpro-IN-1 | ||
SARS-CoV-2 Mpro-IN-1 (化合物 16b-3) 是SARS-CoV-2主要蛋白酶 (Mpro) 的选择性不可逆抑制剂(IC50 = 116 nM)。 | |||
T79515 |
SARS-CoV-2 Mpro-IN-10
|
SARS-CoV | Microbiology/Virology |
SARS-CoV-2 Mpro-IN-10(27h)是Mpro抑制剂,具有IC50和EC50值分别为10.9 nM和43.6 nM,适用于SARS-CoV-2病毒的研究。 | |||
T72231 |
SARS-CoV-2/MERS Mpro-IN-2
|
||
SARS-CoV-2/MERS Mpro-IN-2 是一种有效的 SARS-CoV-2和MERS 主要蛋白酶抑制剂,IC50值分别为 0.21, 0.07 µM。 | |||
T81210 |
SARS-CoV-2 Mpro-IN-12
|
SARS-CoV | Microbiology/Virology |
SARS-CoV-2 Mpro-IN-12 (compound D026) 是一种抗SARS-CoV-2主要蛋白酶 (Mpro) 的抑制剂, 表现出抗病毒活性。 | |||
T79278 |
SARS-CoV-2 Mpro-IN-7
|
SARS-CoV | Microbiology/Virology |
Mpro-IN-7(化合物6g)是一种针对Mpro-SARS-CoV-2的高效抑制剂,具有IC50值为8.8 μM,CC50值为10 μM。 | |||
T79279 |
SARS-CoV-2 Mpro-IN-8
|
SARS-CoV | Microbiology/Virology |
SARS-CoV-2 Mpro-IN-8(compound 6b)是一抗SARS-CoV-2抗病毒化合物。 | |||
T79455 | SARS-CoV-2 Mpro-IN-9 | SARS-CoV | Microbiology/Virology |
SARS-CoV-2 Mpro-IN-9 (compound c7) 是非肽类、非共价型SARS-CoV-2 Mpro抑制剂,IC50值为0.085 μM,展现出改进的物化特性和药物代谢及药动学 (DMPK) 性质。在Vero E6 细胞中,对SARS-CoV-2感染显示抑制效果,EC50为1.10 μM,同时具备低细胞毒性(CC50>50 μM)。 | |||
T72446 |
SARS-CoV-2 Mpro-IN-4
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SARS-CoV-2 Mpro-IN-4是针对主要蛋白酶(MPro)和组织蛋白酶L(CatL)的双重抑制剂,其IC50s分别为900 nM和60 nM。此化合物对SARS-CoV2展现出抗病毒活性,在hACE2表达的A549细胞中可有效阻断SARS-CoV2复制,其IC50值为8.2 nM。 | |||
T72230 |
SARS-CoV-2/MERS Mpro-IN-1
|
||
SARS-CoV-2/MERS Mpro-IN-1 是一种有效的SARS-CoV-2和MERS 主要蛋白酶抑制剂,IC50值分别为 0.10、0.06 µM。 | |||
T1307 |
Carmofur
HCFU,卡莫氟 |
Nucleoside Antimetabolite/Analog; Virus Protease; SARS-CoV; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Carmofur (HCFU) 是 5-氟尿嘧啶的衍生物,是一种抗肿瘤药物。它是一种酸性神经酰胺酶抑制剂,用于治疗乳腺癌和结直肠癌。它抑制 SARS-CoV-2主要蛋白酶,还抑制 Vero E6 细胞 SARS-CoV-2,EC50为 24.3 μM。 | |||
T0825 |
Ebselen
SPI-1005,PZ-51,依布硒,CCG-39161 |
Phosphatase; Virus Protease; Calcium Channel; COX; HIV Protease | Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Ebselen (CCG-39161) 是一种谷胱甘肽过氧化物酶模拟物,是电压依赖性钙通道阻断剂。它抑制Mpro 和COVID-19病毒,是HIV-1衣壳 CTD 二聚化的抑制剂,具有抗炎、抗癌和抗氧化活性。 | |||
T1673 |
Acamprosate calcium
calcium acetylhomotaurinate,N-Acetylhomotaurine Calcium,Alcomed,阿坎酸钙,Sobriol,Campral EC,Calcium N-acetylhomotaurinate |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Acamprosate calcium (Campral EC) 是 GABA 受体激动剂和谷氨酸能系统调节剂,用于治疗酒精依赖。 | |||
T68921 |
Impromidine hydrochloride
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Impromidine hydrochloride 是一种非常有效和特异性的组胺H2受体激动剂,可用于进行心血管研究。 | |||
T0872L |
Amprolium Hydrochloride
Amprovine,氨丙啉盐酸盐,Amprolio,Amprolium HCl,安普罗林盐酸盐 |
Parasite | Microbiology/Virology |
Amprolium Hydrochloride (Amprolium HCl) 是用于家禽的一种干扰硫胺素代谢的抗球虫药,通过抑制硫胺素吸收和碳水化合物合成而抑制球虫的硫胺转运。 | |||
T66151 | Dimethylethylammoniumpropane sulfonate | ||
Dimethylethylammoniumpropane sulfonate 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T66151。 | |||
T24162 |
Impromidine
Impromidina,Impromidinum |
||
Impromidine is a highly potent and specific agonist of the histamine H2 receptor. | |||
T0872 |
Amprolium
氨丙啉,安普罗林 |
Others; Parasite | Microbiology/Virology; Others |
Amprolium 是一种干扰硫胺素代谢的兽用球虫抑制剂。 | |||
T73059 |
Acamprosate
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Acamprosate 是一种口服活性原型神经调节剂。Acamprosate 可用于酒精依赖和酒精中毒的研究。 | |||
T32725 |
L-Flamprop-isopropyl
Effix,(+)-Flamprop-isopropyl |
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L-Flamprop-isopropyl is a bioactive chemical. | |||
T20594 |
Flamprop-methyl
WL-29761,Suffix plus,WL 29761,WL29761,Super-Suffix,Lancer |
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Flamprop-methyl is a post-emergence herbicide, it is usually used on wild oats. | |||
T8419 |
XP-59
|
SARS-CoV | Microbiology/Virology |
XP-59 是一种 SARS-CoV Mpro 抑制剂,其 Ki 值为 0.1 nM。 | |||
T8688 |
(Rac)-X77
CPD77,MUN91789 |
SARS-CoV | Microbiology/Virology |
(Rac)-X77 (MUN91789) 是一种 SARS-CoV-2 主要蛋白酶抑制剂。 | |||
T12836 |
SARS-CoV-2-IN-1
|
Others | Others |
SARS-CoV-2-IN-1 is a potent inhibitor of Mpro(SARS-CoV-2 Mpro, SARS-CoV Mpro and MERS-CoV Mpro with IC50s of 0.67, 0.90 and 0.58 μM, respectively). | |||
T68384 |
SCHEMBL12616233
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||
SCHEMBL12616233 is a novel inhibitor of SARS-CoV-2 main protease (MPro). | |||
T79344 |
CDD-1819
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SARS-CoV | Microbiology/Virology |
CDD-1819为非共价、非肽类SARS-CoV-2 Mpro有效抑制剂,其Ki值为5 nM。该化合物同样抑制ΔP168、A173V及ΔP168/A173V Mpro突变体。 | |||
T79345 |
CDD-1733
|
SARS-CoV | Microbiology/Virology |
CDD-1733是SARS-CoV-2 Mpro的非共价非肽抑制剂,具有12 nM的Ki值。该化合物也能够抑制ΔP168、A173V及ΔP168/A173V Mpro突变体。 | |||
T80636 | SARS-CoV-2-IN-59 | SARS-CoV | Microbiology/Virology |
SARS-CoV-2-IN-59(compound E07)为咪唑啉衍生物,其为一种针对SARS-CoV-2的非肽类小分子抑制剂,主要作用于冠状病毒的Mpro。SARS-CoV-2-IN-59于Mpro残基(Met 165, Gln 166,Met165, His 41, Gln 189)处展现出强烈的相互作用。 | |||
T82257 | GRL-1720 TFA | SARS-CoV | Microbiology/Virology |
GRL-1720 TFA,一种SARS-CoV-2 Mpro抑制剂,具有EC50值为15 μM的高效性能,表现出针对SARS-CoV-2的抗病毒活性。 | |||
T78895 | TKB245 | SARS-CoV | Microbiology/Virology |
TKB245为SARS-CoV-2 Mpro的高效抑制剂,能有效抑制VeroE6细胞内SARS-CoV-2的复制。 | |||
T69572 |
UAWJ248
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||
UAWJ248 is a SARS-CoV-2 Protease inhibitor. UAWJ248 provides new directions for the development of Mpro inhibitors as SARS-CoV-2 antivirals. | |||
T73555 | SPR41 | ||
SPR41 是一种有效的 SARS-CoV-2 主要蛋白酶抑制剂,对 SARS-CoV-2 Mpro, hCatL, hCatB 的 Ki 值分别为 0.184, 0.252, 14.4 µM。SPR41 具有抗病毒和细胞毒性。 | |||
T78770 |
Garcinone B
|
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。 | |||
T79884 |
D-4-77
|
SARS-CoV | Microbiology/Virology |
D-4-77是一种针对SARS-CoV-2 Mpro的有效抑制剂,显示出0.95 μM的IC50值。此外,D-4-77展现了抗病毒活性,具有0.49 μM的EC50值,并对SARS-CoV-2 Mpro诱发的宿主NF-κB先天免疫反应具有拮抗效应。 | |||
T73553 |
SPR39
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||
SPR39 是一种有效的 SARS-CoV-2 主要蛋白酶抑制剂,对 SARS-CoV-2 Mpro, hCatL, hCatB 的 Ki 值分别为 0.252、3.38、7.88 µM。SPR39 具有抗病毒和细胞毒性。 | |||
T83719 |
Mca-AVLQSGFR-K(Dnp)-K-NH2 TFA
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||
Mca-AVLQSGFR-K(Dnp)-K-NH2 是针对严重急性呼吸综合征冠状病毒(SARS-CoV)主蛋白酶(Mpro),也称为3C样蛋白酶(3CLpro)的荧光底物。SARS-CoV Mpro 切割后,会释放7-甲氧基香豆素-4-乙酰基(Mca),通过其荧光可以量化SARS-CoV Mpro 活性。Mca 的激发/发射波长最大值分别为328/420 nm。 | |||
T69508 | GRL-1720 | ||
GRL-1720 is a SARS-CoV-2 Protease inhibitor (IC50 = 320 nM). GRL-1720 contains an indoline which targets the SARS-CoV-2 main protease (Mpro) | |||
T70690 |
UAWJ246
|
||
UAWJ246 is a SARS-CoV-2 Protease inhibitor (IC50 = 45 nM). UAWJ246 provides new directions for the development of Mpro inhibitors as SARS-CoV-2 antivirals. | |||
T63483 |
INSCoV-614(1B)
|
||
INSCoV-614(1B) 是一种有效的 Mpro(3CLpro) 抑制剂。蛋白酶 (PLpro 和 3CLpro) 与病毒的转录和复制有关。INSCoV-614(1B) 对 SARS-CoV-2 感染表现出研究潜力。 | |||
T81203 |
SARS-CoV-2-IN-68
|
SARS-CoV | Microbiology/Virology |
SARS-CoV-2-IN-68(compound 6C)是共价SARS-CoV-2 PLpro/Mpro抑制剂,展现出有效抗病毒活性,并与PLpro的锌指结构域发生结合。 | |||
T63461 | INSCoV-600K(1) | ||
INSCoV-600K(1) 是一种有效的 Mpro(3CLpro) 抑制剂。蛋白酶 (PLpro 和 3CLpro) 与病毒的转录和复制有关。INSCoV-600K(1) 对 SARS-CoV-2 感染表现出研究潜力。 | |||
T63462 |
INSCoV-601I(1)
|
||
INSCoV-601I(1) 是一种有效的 Mpro(3CLpro) 抑制剂。蛋白酶 (PLpro 和 3CLpro) 与病毒的转录和复制有关。INSCoV-600I(1) 对 SARS-CoV-2 感染表现出研究潜力。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T72581 |
SARS-CoV MPro-IN-2
|
||
SARS-CoVMPro-IN-2 是一种有效的SARS-CoV-2 Mpro 抑制剂,IC50sub>值为 72.07 nM。病毒的主要蛋白酶 Mpro 作为加工病毒多蛋白的主要酶,有助于 SARS-CoV-2 在宿主细胞中的复制和转录,并已被定性为药物发现的有吸引力的靶点。SARS-CoVMPro-IN-2 具有研究 COVID-19 的潜力。 | |||
T32551 | Lamprolobine | ||
Lamprolobine is a bioactive chemical. | |||
T73900 | (±)-Alliin | ||
(±)-Alliin 是大蒜的主要活性成分。(±)-Alliin 被认为是SARS-CoV-2 (Mpro)的虚拟抑制剂。 | |||
T79947 |
10-Hydroxyaloin A
|
SARS-CoV | Microbiology/Virology |
10-Hydroxyaloin A有效抑制SARS-CoV-2,与SARS-CoV-2 Mpro活性位点显著结合。 | |||
TN3528 |
Bonducellpin D
|
Antifection | Microbiology/Virology |
Bonducellpin D may show inhibitory activities on the Para3 virus. It also exhibits moderate activity against four tested human cancer cell lines, HepG-2, K562, HeLa, and Du145. |