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24

抑制剂 & 化合物

2

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T9614	MERS-CoV-IN-1	SARS-CoV	Microbiology/Virology
	MERS-CoV-IN-1 对冠状病毒的活性具有优异的抑制作用，可用作预防冠状病毒引起疾病的药物组合物。
T7766	Remdesivir 瑞德西韦,GS-5734	SARS-CoV; DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology
	Remdesivir (GS-5734) 是一种核苷类似物，一种广谱的抗病毒化合物，通过抑制病毒的 RNA 依赖性 RNA 聚合酶发挥活性。Remdesivir 对埃博拉病毒、SARS 病毒、MERS病毒等均有活性，对 COVID-19 有潜在治疗价值。
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。
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。
T60951	Molnupiravir EIDD-2801,Lagevrio,MK-4482	SARS-CoV; Influenza Virus	Microbiology/Virology
	Molnupiravir (MK-4482) (EIDD-2801) 是核糖核苷类似物 EIDD-1931 的异丙酯前体药物，具有口服生物利用度。Molnupiravir 可用于 COVID-19 ，季节性和流行性流感的研究，对多种冠状病毒和流感病毒具有广谱的抗病毒活性，例如，SARS-CoV-2，MERS-CoV，SARS-CoV。
T60085	MM3122 GTPL11533,MM-3122,Ac-GQFR-kbt	SARS-CoV	Microbiology/Virology
	MM3122 (MM-3122) 是一种选择性的 II 型跨膜丝氨酸蛋白酶 (TMPRSS2) 抑制剂，IC50为 0.34 nM。MM3122 可以有效阻断 TMPRSS2，从而抑制 SARS-CoV-2 和 MERS-CoV 进入人类细胞。
T8498	EIDD-1931 Beta-d-N4-hydroxycytidine	Virus Protease; HCV Protease; SARS-CoV; Topoisomerase	DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome
	EIDD-1931 (Beta-d-N4-hydroxycytidine) 是一种核苷类抗病毒试剂，可抑制丙型肝炎病毒、基孔肯亚病毒和委内瑞拉马脑炎病毒的复制活性。
T6573	E 64c 阿洛司他丁酸,NSC 694279,EP 475,Loxistatin Acid	SARS-CoV; Cysteine Protease	Microbiology/Virology; Proteases/Proteasome
	E 64c (EP 475) 是一种不可逆且可透过膜的半胱氨酸蛋白酶抑制剂，是 E-64 的衍生物。它也是钙离子激活中性蛋白酶抑制剂和组织蛋白酶 C 弱不可逆抑制剂，可抑制 MERS-CoV。
T36652	Anti-MERS-3A1 mAb Anti-MERS-3A1 mAb
	Anti-MERS-3A1 mAb (MERS-3A1) is a high-affinity human monoclonal IgG1 antibody derived from CHO cells. It effectively inhibits the interaction between the MERS-CoV spike protein and the DPP4 receptor[1].
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).
T68674	Vincapusine
	Vincapusine is a natural inhibitor of 3C-like protease (3CLpro), targeting SARS-CoV-2 3CLpro, SARS-CoV 3CLpro and MERS-CoV 3CLpro.
T39334	Remdesivir nucleoside monophosphate
	Remdesivir nucleoside monophosphate, a metabolite of Remdesivir, is a potent antiviral compound with nucleoside analogue characteristics. It exhibits effective antiviral activity against both SARS-CoV and MERS-CoV.
T70451	Blancoxanthone
	Blancoxanthone is a molecule isolated from plants could also be potential drug candidates against COVID-19. Moreover, these could also show promising inhibitory effects against influenza-parainfluenza viruses, respiratory syncytial virus, severe acute respiratory syndrome (SARS), and Middle East respiratory syndrome coronavirus (MERS-CoV).
T72312	SARS-CoV-2 3CLpro-IN-10
	SARS-CoV-2 3CLpro-IN-10(5d)为一种有效的抗 SARS-CoV-2 3CL 蛋白酶抑制剂，其IC50值仅为190 nM，同时对SARS-CoV-1的IC50值为790 nM，对MERS-CoV的IC50值则为70 nM，显示出广谱的抗病毒活性。
T78867	WU-04	SARS-CoV	Microbiology/Virology
	WU-04为针对SARS-CoV-2的3CLpro蛋白的非共价抑制剂，对包括Alpha、Beta、Gamma、Delta、Lambda和Omicron在内的6种SARS-CoV-2变体及SARS-CoV与MERS-CoV的3CLpro蛋白展现出高效的抑制作用。
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...
T76669	Anti-MERS-D12 mAb
	Anti-MERS-D12 mAb (MERS-D12; MERS Antibody-D12) 是一种IgG1类人源单克隆抗体，与MERS-CoV Spike蛋白的二聚体结构中的受体结合域(RBD)上的DPP4相互作用区直接结合，实现通过阻断受体结合的方式达到中和效果。
T72313	SARS-CoV-2 3CLpro-IN-11
	SARS-CoV-2 3CLpro-IN-11(11d)为一种针对SARS-CoV-2 3CL蛋白酶的有效抑制剂，具备IC50值140 nM，并对SARS-CoV-1和MERS-CoV分别展现出IC50值240 nM与70 nM的抑制活性，显示出其广谱的抗病毒能力。
T79339	NSC89641	SARS-CoV	Microbiology/Virology
	NSC89641对MERS-CoV Mpro和SARS-CoV-2 Mpro均显示出显著的抑制作用，其IC50值分别小于3.5 μM和为3.05 μM，表明NSC89641对这两种冠状病毒主要蛋白酶具有较高的选择性抑制效力。
T69547	UAWJ9-36-3
	UAWJ9-36-3 is a SARS-CoV-2 Protease inhibitor (IC50 = 54 nM). UAWJ9-36-3 showed potent binding and enzymatic inhibition against the Mpro's from SARS-CoV-2, SARS-CoV, MERS-CoV, HCoV-OC43, HCoV-NL63, HCoV-229E, and HCoV-HKU1. UAWJ9-36-3 is a promising candidate to be further developed as a broad-spectrum coronavirus antiviral.
T69548	UAWJ9-36-1
	UAWJ9-36-1 is a SARS-CoV-2 Protease inhibitor (IC50 = 51 nM). UAWJ9-36-1 showed potent binding and enzymatic inhibition against the Mpro's from SARS-CoV-2, SARS-CoV, MERS-CoV, HCoV-OC43, HCoV-NL63, HCoV-229E, and HCoV-HKU1. UAWJ9-36-1 is a promising candidate to be further developed as a broad-spectrum coronavirus antiviral.
T73973	Imatinib Impurity E
	Imatinib Impurity E 是 Imatinib 的杂质。Imatinib 是一种口服生物可用的酪氨酸激酶抑制剂，可选择性抑制 BCR/ABL，v-Abl，PDGFR，c-kit 激酶活性。Imatinib (STI571) 靠近 ATP 结合位点结合，将其锁定在封闭或自我抑制的构象中，因此半竞争性抑制蛋白质的酶活性。Imatinib 还抑制 SARS-CoV 和MERS-CoV。
T74467	Remdesivir de(ethylbutyl 2-aminopropanoate)
	Remdesivir de(ethylbutyl 2-aminopropanoate) 是 Remdesivir 的一种杂质，后者为一种具有抗病毒活性的核苷类似物。在 HAE 细胞针对 SARS-CoV 和 MERS-CoV 的实验中，Remdesivir 的 EC50 值为 74 nM；在针对鼠肝炎病毒的延迟脑肿瘤细胞实验中，其 EC50 值为 30 nM。此外，Remdesivir 亦被认为具有针对 2019-nCoV (COVID-19) 的研究潜力。
T68485	Apilimod HCl
	Apilimod dimesylate is a potent and selective PIKfyve inhibitor. It exhibits no significant activity at other lipid kinases and protein kinases, including PIP4K, PIP5K, mTOR, PI3K and PI4K. Apilimod dimesylate inhibits cellular entry by SARS-CoV-2, MERS-CoV and MHV S pseudovirions. It reduces the number of SARS-CoV-2-infected hiPSC-derived pneumocyte-like cells by 85% and inhibits SARS-CoV-2 replication in donor lung tissue. It also exhibits selective cytotoxicity in B-cell non-Hodgkin lymphoma ...

化合物

MERS-CoV-IN-1

Cat.No: T9614

Target: SARS-CoV

Cat.No: T7766

Synonym: 瑞德西韦,GS-5734

Target: SARS-CoV, DNA/RNA Synthesis

SARS-CoV-2/MERS Mpro-IN-2

Cat.No: T72231

SARS-CoV-2/MERS Mpro-IN-1

Cat.No: T72230

Cat.No: T60951

Synonym: EIDD-2801,Lagevrio,MK-4482

Target: SARS-CoV, Influenza Virus

Cat.No: T60085

Synonym: GTPL11533,MM-3122,Ac-GQFR-kbt

Target: SARS-CoV

Cat.No: T8498

Synonym: Beta-d-N4-hydroxycytidine

Target: Virus Protease, HCV Protease, SARS-CoV, Topoisomerase

Cat.No: T6573

Synonym: 阿洛司他丁酸,NSC 694279,EP 475,Loxistatin Acid

Target: SARS-CoV, Cysteine Protease

Anti-MERS-3A1 mAb

Cat.No: T36652

Synonym: Anti-MERS-3A1 mAb

SARS-CoV-2-IN-1

Cat.No: T12836

Target: Others

Cat.No: T68674

Remdesivir nucleoside monophosphate

Cat.No: T39334

Cat.No: T70451

SARS-CoV-2 3CLpro-IN-10

Cat.No: T72312

Cat.No: T78867

Target: SARS-CoV

Mpro inhibitor N3 hemihydrate

Cat.No: T38174

Anti-MERS-D12 mAb

Cat.No: T76669

SARS-CoV-2 3CLpro-IN-11

Cat.No: T72313

Cat.No: T79339

Target: SARS-CoV

Cat.No: T69547

Cat.No: T69548

Imatinib Impurity E

Cat.No: T73973

Remdesivir de(ethylbutyl 2-aminopropanoate)

Cat.No: T74467

Cat.No: T68485

Cat. No.	Product Name	Target	Signaling Pathways
T3374	Dihydrotanshinone I DHTS,15,16-dihydrotanshinone I,二氢丹参酮I,二氢丹参酮 I	SARS-CoV; ROS	Immunology/Inflammation; Microbiology/Virology
	Dihydrotanshinone I (DHTS) 是从丹参中分离到的一种天然产物，可抑制 MERS-CoV，可研究心血管疾病。
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.

天然产物

Dihydrotanshinone I

Cat.No: T3374

Synonym: DHTS,15,16-dihydrotanshinone I,二氢丹参酮I,二氢丹参酮 I

Target: SARS-CoV, ROS

Cat.No: TN3528

Target: Antifection

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