94
1
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9103 |
BVDV-IN-1
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
BVDV-IN-1 是一种牛病毒性腹泻病毒 (BVDV) 的非核苷抑制剂 (NNI),EC50 为 1.8 μM。它直接与 BVDV RdRp 的疏水口袋结合,对耐 NNI 氨基硫脲 (TSC) 的 BVDV 具有抗病毒活性。 | |||
T6729 |
Lomibuvir
VX-222,VCH-222 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Lomibuvir (VCH-222) (VX-222) 是丙型肝炎病毒 NS5B 聚合酶的一种非核苷变构抑制剂,Kd 值为 17 nM,已证明具有临床疗效。Lomibuvir 抑制 1b/Con1 型 HCV 亚基因组复制子,EC50为 5.2 nM。Lomibuvir 优先抑制延长的 RNA 合成,而非从头合成的 RNA。 | |||
T2330 |
Rilpivirine
TMC278,R278474,利匹韦林,DB08864 |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Rilpivirine (R278474) 是一种二芳基嘧啶衍生物和非核苷逆转录酶抑制剂,具有抗 HIV-1 的抗病毒活性,用于治疗 HIV 感染。 | |||
T7700 |
Lersivirine
3-氰基-5-[[3,5-二乙基-1-(2-羟基乙基)-1H-吡唑-4-基]氧基]苯腈,Lersivirine(UK 453061),UK-453061 |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Lersivirine (UK-453061) 是非核苷逆转录的抑制剂 (NNRTI),有效抑制 NNRTI 耐药病毒。它对野生型人类免疫缺陷病毒和临床相关 NNRTI 耐药菌株显示出强大的抗逆转录病毒活性。 | |||
T2393 |
Efavirenz
EFV,依非韦伦,DMP 266,依法韦仑,Sustiva,Stocrin,L-743726 |
HIV Protease; Reverse Transcriptase; Autophagy | Autophagy; Microbiology/Virology; Proteases/Proteasome |
Efavirenz (DMP 266) 是一种人类免疫缺陷病毒 1 非核苷类似物逆转录酶抑制剂。它也是一种野生型HIV-1 RT 抑制剂,Ki 为 2.93 nM,有效抑制 HIV-1 复制,IC95为 1.5 nM。 | |||
T3172 |
Trovirdine
曲韦定,LY300046 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Trovirdine (LY300046) 是一种硫脲类非核苷类逆转录酶抑制剂。 | |||
T1815 |
Dapivirine
R147681,达匹维林,TMC120 |
Apoptosis; HIV Protease; Reverse Transcriptase; Autophagy | Apoptosis; Autophagy; Microbiology/Virology; Proteases/Proteasome |
Dapivirine (R147681) 是一种二芳基嘧啶非核苷类逆转录酶抑制剂。 | |||
T31860 |
Fosdevirine
GSK-2248761A,IDX 899,GSK 2248761A,GSK 2248761,GSK-2248761,IDX-12899,GSK2248761,FDV,GSK2248761A |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Fosdevirine (GSK2248761) 是一种具有选择性和高效性的非核苷类逆转录酶 (NNRTI) 抑制剂 ,具有抗 HIV 活性,可用于研究迟发性癫痫等神经系统相关疾病。 | |||
T68103L |
Mk-6186 HCl
Mk-6186 HCl(1034474-19-5 Free base) |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
MK-6186 HCl,一种新型非核苷类逆转录酶抑制剂,具有抗病毒活性,可用于研究HIV。 | |||
T67788 |
BAY-43-9695
|
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
BAY-43-9695是具有抗人巨细胞病毒(HCMV)活性的非核苷类化合物,是BAY-38-4766的主要代谢产物。 | |||
T68103 |
MK-6186
|
Reverse Transcriptase | Microbiology/Virology |
MK-6186 是一种新型非核苷类逆转录酶抑制剂,具有抗病毒活性,可用于研究病毒感染。 | |||
T3632 |
Doravirine
多拉维林,多拉韦林,MK-1439 |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Doravirine (MK-1439) 是一种高度特异性的HIV-1非核苷逆转录酶抑制剂,对野生型以及K103N 和Y181C 逆转录酶突变体的IC50值分别为 4.5 nM,5.5 nM 和 6.1 nM。 | |||
T67804 |
KM-023
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
KM-023是一种新的第二代非核苷类逆转录酶抑制剂,可用于研究人类免疫缺陷病毒(HIV)1型感染。 | |||
T3489 |
Dasabuvir
ABT-333,达塞布韦 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Dasabuvir (ABT-333) 是丙型肝炎病毒非结构蛋白 5B 的非核苷抑制剂,是一种 RNA 依赖性 RNA 聚合酶,具有抗 HCV 的潜在活性。 | |||
T7212 |
Delavirdine mesylate
U 90152 (mesylate),BHAP-U 90152 (mesylate),Delavirdine (mesylate) |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Delavirdine mesylate (BHAP-U 90152(mesylate)) 是一种口服活性非核苷逆转录酶抑制剂。它抑制 HIV-1 病毒复制,可以用于艾滋病的相关研究。它选择性地抑制 HIV-1 逆转录酶,其选择性超过 DNA 聚合酶 α 和 DNA 聚合酶 δ 。 | |||
T1595 |
Nevirapine
NSC 641530,奈韦拉平,BI-RG 587,奈伟拉平,NVP |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Nevirapine (NVP) 是一种 HIV-1逆转录酶非核苷抑制剂,Ki 值为 270 μM,可用于研究 HIV/AIDS。 | |||
T31860L |
(Iso)-Fosdevirine
(Iso)-Fosdevirine(Iso-1018450-26-4),(Iso)-GSK2248761 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
(Iso)-Fosdevirine ( (Iso)-GSK2248761) 是一种具有选择性和高效性的非核苷类逆转录酶 (NNRTI) 抑制剂 ,具有抗 HIV 活性,可用于研究迟发性癫痫等神经系统相关疾病。 | |||
T2551 |
Etravirine
TMC125,依曲韦林,R165335 |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Etravirine (R165335) 是一种非核苷逆转录酶抑制剂,具有抗 HIV 的作用。 | |||
T29037 |
UC-781
NSC 675186,UC781,UC 781 |
Antiviral; HIV Protease | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
UC-781 (NSC-675186) 是一种高效且具有选择性的人类免疫缺陷病毒 HIV-1 非核苷类逆转录酶(NNRTI)I抑制剂 ,C50 值为 5 nM。UC-781 具有抗病毒活性和耐药性。UC-781状态稳定,较低的 PH 或不同温度对其影响较小。 | |||
T8655 |
SR-717
|
STING | Immunology/Inflammation |
SR-717 是一种 cGAMP 的类似物,一种非核苷类 STING 激动剂,可以诱导 STING 形成“封闭”的激活构象。SR-717 具有抗肿瘤活性,可以促进免疫细胞的激活以及抗原的交叉提呈。 | |||
T28762 |
Setrobuvir
RO-5466731,ANA-598,RG7790,ANA598,RG-7790 |
HCV Protease; SARS-CoV; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
Setrobuvir (ANA-598) 是一种口服活性非核苷类HCV NS5B 聚合酶抑制剂,对新的RNA 合成和引物延伸具有抑制作用,IC50s 在4到5nM 之间。Setrobuvir 对SARS-CoV-2 RdRp 显示出很好的结合亲和力,能诱导RdRp 受到抑制。 | |||
T38237 |
2′-O-Methylcytidine
|
Nucleoside Antimetabolite/Analog; HCV Protease | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
2'-O-Methylcytidine 是 2'-代核苷,可抑制 HCV 复制。 它在体外抑制 NS5B 催化的 RNA 合成,其抑制方式是与底物核苷三磷酸竞争。 | |||
T27625 |
IQP-0528
SJ-3991,SJ3991,IQP0528 |
Antiviral; HIV Protease; Reverse Transcriptase | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
IQP-0528是一种高效的非核苷类逆转录酶抑制剂(NNRTI),通过阻断病毒进入,有可能用于治疗HIV 感染,并且作为杀微生物凝胶显示出抗病毒活性。IQP-0528对HIV-1和HIV-2都显示出抑制作用,对HIV-1的EC50为0.2 nM,对HIV-2的EC50为100 nM。 | |||
T21537L |
TMC647055 Choline Hydroxide Salt
TMC647055 Choline Hydroxide Salt (1204416-97-6 free base) |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
TMC647055 Choline Hydroxide Salt 是一种新型有效的 HCV NS5B 聚合酶非核苷抑制剂,可用于治疗 HCV 感染。它具有纳摩尔级细胞效力(EC(50) 为 82 nM),相关细胞毒性较小(CC(50)>20 μM),在大鼠和狗中具有良好的药代动力学特征。 TMC647055 显示出有体外生化、动力学和病毒学特征的前景。 | |||
T28204 |
NSC-176377
NSC 176377 |
||
NSC-176377 is a non-nucleoside reverse transcriptase inhibitor. | |||
T2330L |
Rilpivirine HCl
Rilpivirine hydrochloride,TMC278,Rilpivirine,TMC-278,TMC 278. trade name Edurant |
||
Rilpivirine is a potent non-nucleoside reverse transcriptase inhibitor. | |||
T23968 |
DC_501
DC 501,DC501 |
||
DC_501 is a selective non-nucleoside DNA methyltransferase 1 inhibitor. | |||
T24354 |
L 738372
L-738,372,L 738,372,L738372,L738,372,L-738372 |
||
L 738372 is a non-nucleoside inhibitor of HIV-1 reverse transcriptase. | |||
T25493 |
HEPT
|
||
HEPT is a non-nucleoside inhibitor of HIV-1 reverse transcription. | |||
T27542 |
HI-207
HI207,HI 207 |
||
HI-207 is an inhibitor of non-nucleoside reverse transcriptase. | |||
T24087 |
GCA-186
I-EBU-dM,IEBUdM,I EBU dM,GCA 186 |
||
GCA-186 is an effective non-nucleoside HIV-1 reverse transcriptase inhibitor. | |||
T27384 |
FR-234938
FR 234938 |
||
FR-234938 is a non-nucleoside adenosine deaminase inhibitor with anti-inflammatory activity. | |||
T25501 |
HI-236
HI 236,D-PBT,D PBT,DPBT |
||
HI-236 is used as a non-nucleoside HIV-1 reverse-transcriptase inhibitor. | |||
T33435 | MK-4965 | ||
MK-4965 is a new type of non-nucleoside reverse transcriptase inhibitor with antiviral activity. | |||
T70851 |
U 88204
|
||
U 88204 is a non-nucleoside HIV-1 reverse transcriptase inhibitor. | |||
T28507 |
RDEA-427
RDEA 427 |
||
RDEA-427, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection. | |||
T26940 |
Calanolide A
NSC 675451,NSC675451,NSC-675451 |
||
Calanolide A, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection. | |||
T70794 | Nevirapine dimer | ||
Nevirapine dimer is a non-nucleoside reverse transcriptase inhibitor (NNRTI). | |||
T68450 |
IDX-989
|
||
IDX-989 is an HIV-1 non-nucleoside reverse transcriptase inhibitor. | |||
T69435 |
GW-4511
|
||
GW-4511 is a benzophenone non-nucleoside HIV-1 reverse transcriptase inhibitor. | |||
T26946 |
Capravirine
S-1153,AG1549,S1153,AG-1549,AG 549 |
||
Capravirine, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection. | |||
T71566 |
MK-7445
|
||
MK-7445 is a conformationally constrained inhibitor of non-nucleoside reverse transcriptase. | |||
T27512 |
GW-695634
GW5634,GW695634,GW-5634G,GW-5634 |
||
GW-695634, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection. | |||
T70156 |
K-5a2
|
||
K-5a2 is a novel human immunodeficiency virus type 1 (HIV-1) non-nucleoside reverse transcriptase inhibitor (NNRTI). | |||
T31369 |
Deleobuvir
BI207127,BI-207127,BI 207127,BI-207127NA |
||
Deleobuvir(BI207127) is an inhibitor of non-nucleoside hepatitis C virus NS5B polymerase for the treatment of hepatitis C. | |||
T70545 | HI-253 | ||
HI-253 is a potent non-nucleoside inhibitor of drug-resistant human immunodeficiency virus (HIV). | |||
T71517 | Nevirapine quinone methide | ||
Nevirapine quinone methide is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used to treat HIV-1 infection and AIDS. | |||
T27383 |
FR-221647
|
||
FR-221647 is a non-nucleoside adenosine deaminase inhibitor, it has moderate activity and good pharmacokinetics compared with the known inhibitors EHNA and pentostatin. | |||
T70627 |
U 89674
|
||
U 89674 is a non-nucleoside reverse transcriptase inhibitor used for the prevention of the spread of HIV-1 infection. | |||
T24839 |
Stampidine
HI-113,HI 113,HI113 |
||
Stampidine can prevent the sexual transmission of HIV-1. It exhibited remarkable subnanomolar to low nanomolar in vitro antiretroviral potency against nucleoside reverse transcriptase inhibitor-resistant primary clinical HIV isolates, non-nucleoside RT-re |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T16674 |
Pseudouridine
|
Endogenous Metabolite | Metabolism |
Pseudouridine 是非编码 RNA 中丰富的修饰核苷,通过稳定 RNA 结构增强核糖体 RNA 和的转移 RNA 功能。 |