121
31
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T15573 |
Inarigivir soproxil
SB9200 |
HCV Protease | Microbiology/Virology; Proteases/Proteasome |
Inarigivir soproxil (SB9200) 是一种先天免疫激动剂。 它还显示出针对耐药丙型肝炎病毒 (HCV) 变体的有效抗病毒活性。在基因型 1 HCV 复制子系统细胞中, HCV 1a/1b 的 EC50 为 2.2 和 1.0 μM。 | |||
T40276 |
GS-621763
|
SARS-CoV | Microbiology/Virology |
GS-621763 是具有口服活性的 GS-441524 前药,在小鼠体内具有抗SARS-CoV-2病毒活性。 | |||
T1649 |
Tenofovir
替诺福韦,泰诺福韦,PMPA,TDF,GS 1278 |
HBV; HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Tenofovir (GS 1278) 是一种核苷酸逆转录酶抑制剂,可研究 HIV 和慢性乙型肝炎。 | |||
T60440 |
Antiviral agent 17
|
||
Antiviral agent 17 (Compound 4) 是一种抗感染剂,在人类复制子试验中显著保留其抗病毒作用,EC50值为0.015 μM。Antiviral agent 17 对小鼠诺如病毒(MNV)表现出良好的抗病毒活性。Antiviral agent 17 在研究传染性和恶性疾病方面具有潜力。 | |||
T16702 |
QL47
|
Virus Protease; BTK | Angiogenesis; Microbiology/Virology; Tyrosine Kinase/Adaptors |
QL47 是一种宿主靶向的小分子抗病毒剂,具有抗病毒活性,对登革热病毒和其他 RNA 病毒有抑制作用。QL47 可作为病毒翻译的抑制抑制剂和 BTK 的共价抑制剂,可用于研究淋巴瘤。 | |||
T16911 |
Sorivudine
BV-araU,索立夫定 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Sorivudine (BV-araU) 是口服有效的,嘧啶核苷抗代谢药物。它的抗病毒活性来自某些 DNA 病毒中存在的特定胸苷激酶选择性转化为核苷酸,从而反过来会干扰病毒 DNA 合成。 | |||
T8328 |
STING agonist-1
G10 |
Virus Protease; STING | Immunology/Inflammation; Microbiology/Virology |
STING agonist-1 (G10)是一种人类特异性 STING 激动剂,可引发针对新兴甲病毒的抗病毒活性。它抑制甲病毒属 VEEV 复制,IC90值为 24.57 μM。 | |||
T0220 |
Foscarnet sodium
Phosphonoformate,膦甲酸钠 |
Virus Protease; Reverse Transcriptase; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Foscarnet sodium (Phosphonoformate) 是一种病毒 DNA 聚合酶活性抑制剂,可逆地抑制病毒复制。它是一种用于治疗巨细胞病毒性视网膜炎的抗病毒剂。 | |||
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。 | |||
T9249 |
ITMN4077
|
Antiviral | Immunology/Inflammation |
ITMN4077 对感染人类 HuH7 细胞的丙型肝炎病毒具有抗病毒活性,评估为抑制 HCV 亚基因组复制子复制,EC50 为 2.131μM。 | |||
T22337 |
Ganciclovir sodium
RS-21592 sodium,Cytovene IV sodium,2'-Nor-2'-deoxyguanosine sodium,BW 759 sodium,更昔洛韦钠 |
Nucleoside Antimetabolite/Analog; Others; Antifection; HSV | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
Ganciclovir sodium (Cytovene IV sodium) 是核苷类似物和口服抗病毒药物,具有抗病毒活性,尤其是针对巨细胞病毒和单纯疱疹病毒 1 型。 | |||
T77555 |
3-Methoxycatechol
1,2-Dihydroxy-3-methoxybenzene |
Antiviral | Immunology/Inflammation |
3-Methoxycatechol 是一种木质素衍生的可再生化学品,可促进食管发生癌变。1,2-Dihydroxy-3-methoxybenzen 对脑脊髓炎病毒(EMCV)表现出很强的抗病毒活性. | |||
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。 | |||
T9672 |
GRL-0496
|
SARS-CoV | Microbiology/Virology |
GRL-0496 是氯吡啶酯衍生物,是有效的 SARS-CoV 3CLpro 抑制剂,IC50为 30 nM。GRL-0496显示出抗 SARS-CoV 病毒活性,EC50为 6.9 μM。 | |||
T1454 |
Acyclovir
Aciclovir,Acycloguanosine,阿昔洛韦 |
Apoptosis; DNA/RNA Synthesis; Antibacterial; Antibiotic; HSV | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Acyclovir (Aciclovir) 是鸟嘌呤类似物和具有口服活性的抗病毒剂。它对HSV-1(IC50为 0.85 μM),HSV-2(IC50为 0.86 μM) 和水痘带状疱疹病毒有活性。 | |||
T11760 |
KIN101
3-(4-Bromophenyl)-7-[(methylsulfonyl)oxy]-4-oxo-4H-chromene,3-(4-溴苯基)-4-氧代-7-[(甲磺酰基)氧基]-4H-色烯 |
HCV Protease; Influenza Virus; RSV; Antifection | Microbiology/Virology; Proteases/Proteasome |
KIN101 (3-(4-Bromophenyl)-7-[(methylsulfonyl)oxy]-4-oxo-4H-chromene) 是 IRF-3 依赖性信号传导的异黄酮激动剂,可诱导 IRF-3 核易位。 它对 RNA 病毒、HCV 和 RSV 具有抗病毒活性。 | |||
T9394 |
CHIKV-IN-2
|
Dehydrogenase | Metabolism |
CHIKV-IN-2 基孔肯雅病毒的选择性抑制剂,具有强大的细胞抗病毒活性 (EC90=270 nM) 以及能够改善肝微粒体稳定性。它能够抑制细胞靶二氢乳清酸脱氢酶的活性。 | |||
TNU0060 |
3’-O-Methyladenosine
|
Antiviral; Adenosine deaminase | Immunology/Inflammation; Metabolism |
3’-O-Methyladenosine 是一种抗病毒化合物,对西尼罗河病毒具有抑制作用,可用于治疗病毒感染。3’-O-Methyladenosine 对腺苷脱氨酶VII型具有抑制作用,Ki 值为 493 µM。 | |||
T8591 |
RNase L-IN-2
5-(3-hydroxyphenyl)-8-thia-4,6-diazatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),5-trien-3-one |
Others | Others |
RNase L-IN-2 是 RNase L 的激活剂,EC50 为 22 uM;对多种类型的 RNA 病毒(包括人类病原体人类副流感病毒 3 型)具有广谱抗病毒活性,在有效浓度下没有细胞毒性。 | |||
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。 | |||
T26873 |
BMY-27709
BMY 27709,BMY27709 |
Influenza Virus | Microbiology/Virology |
BMY-27709 是一种流感病毒生长抑制剂,对 A/WSN/33 病毒生长的 IC50 值为 3-8 μM,对流感病毒的部分亚型也展现出抑制活性。BMY-27709 对 H1 和 H2 病毒感染的早期起作用,通过抑制血凝素蛋白展现其抗病毒活性。然而,BMY-27709 对 H3 亚型病毒以及 B 型/Lee/40 流感病毒没有作用。 | |||
T36433 |
A2ti-2
A2ti-2 |
Virus Protease; Antiviral | Immunology/Inflammation; Microbiology/Virology |
A2ti-2 是一种亲和力较低且具有选择性的膜联蛋白 A2/S100A10 异四聚体 (A2t) 抑制剂(IC50 : 230 μM)。A2ti-2 具有抗病毒活性,可选择性破坏 A2 和 S100A10 之间的蛋白质相互作用,可防止人乳头瘤病毒 16 型 (HPV16) 感染。 | |||
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。 | |||
T8501 |
3-Phenyl-N-[1-(phenylmethyl)-4-piperidinyl]-tricyclo[3.3.1.13,7]decane-1-carboxamide
|
Influenza Virus | Microbiology/Virology |
3-Phenyl-N-[1-(phenylmethyl)-4-piperidinyl]-tricyclo[3.3.1.13,7]decane-1-carboxamide 具有抗埃博拉病毒的抗病毒活性靶向表面暴露的糖蛋白并抑制病毒进入宿主细胞。 Vero 细胞的体外研究表明,该化合物抑制病毒复制,EC50 为 0.38 μM。 | |||
T60095 |
CCF0058981
|
SARS-CoV | Microbiology/Virology |
CCF0058981 (CCF981) 是3-氯苯基类似物,是一种非共价 SARS-CoV-2 3CLpro(SC2)抑制剂,IC50为 68 nM。CCF0058981 抑制 SC1 (SARS-CoV-1 3CLpro),IC50为 19 nM。CCF0058981 具有抗病毒功效,具有用于 COVID-19 研究的潜力。 | |||
T3614 |
Inosine pranobex
Groprinosin,Isoprinosine,异丙肌苷,Immunovir,Delimmun |
IL Receptor; HIV Protease | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
Inosine pranobex (Delimmun) 是一种免疫增强剂,它是一种广谱抗病毒剂,用于 HIV 感染。 | |||
T17026 |
Tecovirimat
ST-246,特考韦瑞 |
Cysteine Protease | Proteases/Proteasome |
Tecovirimat 是一种核心蛋白半胱氨酸蛋白酶抑制剂,可能用于治疗天花感染。Tecovirimat 是一种新型抗病毒药物,对多种正痘病毒具有有效和选择性的活性(EC50:约 10 nM)。通过靶向病毒 p37 蛋白直系同源物来抑制正痘病毒的排出。迄今为止,Tecovirimat 已在所有小动物和非人类灵长类动物预防和治疗痘病毒引起的疾病模型中显示出功效。 | |||
T24234 |
JX040
JX 040,JX-040 |
||
JX040 is an enterovirus replication inhibitor. JX040 has strong antiviral activity against non-polio enteroviruses and it has weak antiviral activity against polioviruses. | |||
T24385 |
L-Acosamine nucleoside
|
||
L-Acosamine nucleoside has antiviral activity against HIV and HSV-1. | |||
T24103 |
GS-9148
|
||
GS-9148 is a dAMP analog. It also maintains its antiviral activity against drug-resistant HIV. | |||
T70710 |
M2WJ332
|
||
M2WJ332 is a novel M2-S31N inhibitor, showing antiviral activity against Influenza A virus. | |||
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. | |||
T70246 |
PD159206
|
||
PD-159206 is a nucleocapsid inhibitor. It exhibits good antiviral activity against HIV. | |||
T24773 |
SCH-43478
SCH 43478 |
||
SCH-43478 is a non-nucleoside agent of antiviral. It has an effective and selective activity against herpes simplex virus type 2 (HSV-2). | |||
T41013 |
Ganciclovir mono-O-acetate
|
||
Ganciclovir mono-O-acetate is a derivative of Ganciclovir, an orally active antiviral agent with activity against CMV. It belongs to the group of nucleoside analogues. | |||
T24563 |
Nummularine B
N-Demethylamphibine H,Daechuine S27 |
||
Nummularine B is a cyclopeptide alkaloid. It has antiviral activity against the porcine epidemic diarrhea virus. It also has potent inhibitory effects on PEDV replication. | |||
T41177 |
Galidesivir dihydrochloride
BCX 4430 |
||
Galidesivir is a viral RNA-dependent RNA polymerase (RdRP) inhibitor and broad spectrum antiviral nucleotide.In vitro, galidesivir displays antiviral activity against a range of RNA viruses, including bunyaviruses, arenaviruses, paramyxoviruses, coronaviruses, and flaviviruses (EC50values range from 3 μM to >100 μM). Galidesivir protects against Ebola and Marburg viral infection in animal models. | |||
T10677 | Carbodine | Others | Others |
Carbodine (Carbocyclic cytidine) is a broad-spectrum antiviral agent and targets CTP synthetase that converts UTP to CTP. It possesses significant antiviral activity against influenza virus types A0/PR-8/34 and A2/Aichi/2/68 in vitro. | |||
T16576 |
Pritelivir mesylate
BAY 57-1293 mesylate,AIC316 mesylate |
Others | Others |
Pritelivir mesylate is active against herpes simplex virus types 1 and 2 (IC50: 0.02 μM against HSV1-2). Pritelivir mesylate is an inhibitor of the viral helicase-primase complex. Pritelivir mesylate shows antiviral activity in vitro and in animal models | |||
T40120 |
FNC-TP
|
||
FNC-TP, the intracellular active form of FNC, is a potent nucleoside reverse transcriptase inhibitor (NRTI) with broad-spectrum antiviral activity against HIV, HBV, and HCV. | |||
T15028 |
Cyclopropavir
MBX-400,Filociclovir,ZSM-I-62 |
Others | Others |
Cyclopropavir (Filociclovir; MBX-400) is a compound of broad-spectrum anti-herpesvirus. It has good antiviral activity against cytomegalovirus (CMV), herpes simplex virus (HHV)-6 and HHV-8 (EC50s: 0.7 μM to 8 μM). | |||
T16439 |
PC786
|
Others | Others |
PC786 shows effective antiviral activity against RSV-A (IC50 <0.09 to 0.71 nM) and RSV-B (IC50, 1.3 to 50.6 nM). PC786 is an inhaled respiratory syncytial virus L protein polymerase inhibitor. | |||
T37277 |
2-Amino-6-chloropurine
|
||
2-Amino-6-chloropurine is a precursor in the synthesis of nucleoside analogs with antiviral activity against Epstein-Barr virus (EBV) and human herpes virus 6 (HHV-6).1 1.Qiu, Y.-L., Ksebati, M.B., Ptak, R.G., et al.(Z)- and (E)-2-((hydroxymethyl)cyclopropylidene)methyladenine and -guanine. New nucleoside analogues with a broad-spectrum antiviral activityJ. Med. Chem.41(1)10-23(1998) | |||
T67784 |
6-fluorinated-aristeromycin2c
|
||
6-fluorinated-aristeromycin2c 具有抗病毒感染活性,对热病毒、寨卡病毒和Sars 冠状病毒具有抑制作用。 | |||
T70785 | Mefuparib Free Base | ||
Mefuparib Free Base is a potent, highly selective, competitive PARP1/2 inhibitor with IC50 of 3.2/1.9 nM, respectively. Mefuparib (CVL218), has been shown to have promising antiviral activity against the virus that causes COVID-19. | |||
T16575 |
Pritelivir mesylate hydrate
BAY 57-1293 mesylate hydrate,AIC316 mesylate hydrate |
Others | Others |
Pritelivir mesylate hydrate is active against herpes simplex virus types 1 and 2 (IC50: 0.02 μM against HSV1-2). Pritelivir mesylate hydrate is an inhibitor of the viral helicase-primase complex. Pritelivir mesylate hydrate shows antiviral activity in vit | |||
T80295 |
GLR-19
|
HSV | Microbiology/Virology |
GLR-19 为一种具有抗HIV功能的肽类化合物,亦展现出对HSV-2的抗病毒活性。 | |||
T21456 |
Grazoprevir hydrate
Grazoprevir,MK5172,MK 5172,MK-5172 |
||
Grazoprevir, a second generation hepatitis C virus protease inhibitor acting at the NS3/4a protease targets, has good activity against a range of hepatitis C virus genotype variants, including some that are resistant to most currently used antiviral medic | |||
T60673 |
Antiviral agent 18
|
||
Antiviral agent 18 (Compound 5) 对鼠诺如病毒显示出良好的抗病毒活性。Antiviral agent 18 是一种抗感染剂,具有用于传染性和恶性疾病的研究潜力。 | |||
T33282 |
Memotine HCl
UK-237101,UK-2371,UK 237101,UK 2371,UK2371 |
||
Memotine HCl has antiviral activity against respiratory tract infection and is used as a therapeutic agent for acute respiratory diseases. It is also a memo fracture in the form of hydrochloride, an isoquinoline, with anti-myxovirus and paramyxovirus acti |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7972 |
Gallic aldehyde
3,4,5-三羟基苯甲醛,五倍子醛 |
HSV | Microbiology/Virology |
Gallic aldehyde 对 HSV-1 显示出有效的抗病毒活性。 | |||
TN1693 |
Glabrone
|
Influenza Virus; PPAR | DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Glabrone 是从甘草根中分离的一种异黄酮,可与 PPAR-γ 配体结合,具有抗流感活性。 | |||
T8205 |
Norwogonin
5,7,8-Trihydroxyflavone,去甲汉黄芩素 |
Virus Protease | Microbiology/Virology |
Norwogonin (5,7,8-Trihydroxyflavone) 是从黄芩中分离出来的,对肠道病毒 71 具有抗病毒活性,IC50为 31.83 μg/ ml。 | |||
TN1453 |
Bruceantinol
|
Anti-infection | Microbiology/Virology |
Bruceantinol 是一种quassinol 化合物,分离自Brucea javanica 的 CH3OH 提取物。它能够将系统性寄主植物中灭活。有效的抑制浓度为 10 μM。 | |||
T1506 |
Vidarabine
Adenine Arabinoside,阿糖腺苷,9-β-D-Arabinofuranosyladenine,Vira-A,Arabinosyladenine,Ara-A |
Nucleoside Antimetabolite/Analog; Tyrosine Kinases; DNA/RNA Synthesis; Antibiotic; HSV | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Tyrosine Kinase/Adaptors |
Vidarabine (Adenine Arabinoside) 是从链霉菌分离的核苷类抗生素,能抗单纯性疱疹和水痘-带状疱疹病毒。它对 HSV-1 和 HSV-2 的 IC50值分别为 9.3 μg/ml 和 11.3 μg/ml。 | |||
T10164 |
5,6-Dihydroxyindole
Dopamine lutine |
Endogenous Metabolite | Metabolism |
5,6-Dihydroxyindole (Dopamine lutine) 是黑色素的前体,显示出广谱的抗菌,抗真菌,抗病毒,抗寄生虫活性。5,6-Dihydroxyindole 也显示出细胞毒性作用。 | |||
T75643 |
Isoxanthohumol
|
HSV | Microbiology/Virology |
Isoxanthohumol 是一种从啤酒花和啤酒中提取的一种前黄酮类化合物,对几种人类癌细胞株具有抗增殖活性。Isoxanthohumol对肿瘤细胞肺转移灶的转移或侵袭有抑制作用。Isoxanthohumol具有抗病毒活性,对疱疹病毒(HSV1和HSV2)和牛病毒性腹泻病毒(BVDV)具有抑制作用。 | |||
T9715 |
Aplidine
|
SARS-CoV; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Aplidine 是有效的eEF1A2(KD=80 nM) 靶向的抗癌药物。Aplidine 具有抗病毒活性,抑制SARS-CoV-2的 IC90为 0.88 nM。Aplidine 在多发性骨髓瘤,晚期癌症及 COVID-19 领域有研究的价值。 | |||
TN2755 |
2-Desoxy-4-epi-pulchellin
|
Anti-infection | Microbiology/Virology |
2-Desoxy-4-epi-pulchellin 是分离自 Polygonum hydropiper 的二氯甲烷可溶部分的一种化合物。 | |||
T2S1865 |
Octyl gallate
Gallic acid octyl ester,n-Octylgallate,Octyl 3,4,5-trihydroxybenzoate,Progallin O,Stabilizer GA-8,没食子酸辛酯 |
Antioxidant; Influenza Virus; Reactive Oxygen Species; Antibacterial; Antifungal; HSV | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; oxidation-reduction |
Octyl gallate (Octyl 3,4,5-trihydroxybenzoate) 具有抗菌、抗氧化作用,有选择性和敏感性的荧光特性,广泛用作食品添加剂。它对 HSV-1,水泡性口炎病毒和脊髓灰质炎病毒有显著的抗病毒作用。 | |||
T3795 |
Corilagin
|
Apoptosis; TLR; Reverse Transcriptase; Antibacterial; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Microbiology/Virology |
Corilagin 是一种鞣酸,有抑制 RNA 肿瘤病毒逆转录酶的活性。它抑制金黄色葡萄球菌的生长,MIC 为 25 μg/mL。它有抗肿瘤活性,可用于肝癌和卵巢癌。 | |||
TN2395 | Epirengynic acid | Antiviral | Immunology/Inflammation |
Epirengynic acid has antiviral activity against RSV | |||
TN6420 |
Sikokianin A
|
||
Sikokianin A shows in vitro antiviral activity against HBsAg secretion. | |||
TN2220 |
Sophoranol
槐醇,(+)-Sophoranol |
HBV | Microbiology/Virology |
(+)-Sophoranol exhibits antiviral activity against the Coxsackie virus B3. It also shows potent anti-HBV activity with an inhibitory potency against HBsAg secretion and against HBeAg secretion. | |||
TN4932 |
Sageone
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PARP; Akt; Caspase; Antifection | Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Microbiology/Virology; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Sageone represents a promising anticancer agent against gastric cancer that warrants further study, it synergizes with cisplatin cytotoxicity in SNU-1 human gastric cancer cells.Sageone also shows antiviral activity. | |||
T25789 |
Melianone
NSC 302037,NSC-302037,NSC302037 |
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Melianone exhibits antiviral activity (EC50s: 3-11μM) against three important human pathogens, belonging to the Flaviviridae family, West Nile virus, Dengue virus, and Yellow Fever virus. | |||
T8263 |
3,4'-Dihydroxyflavone
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Influenza Virus | Microbiology/Virology |
3,4'-Dihydroxyflavone 是一种口服活性黄酮类化合物,具有抗甲型流感病毒的抗病毒活性。 | |||
TN4456 |
Lucidadiol
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AChR; HSV | Microbiology/Virology; Neuroscience |
Lucidadiol exhibits butyrylcholinesterase-inhibitory activity at concentrations up to 200 uM, it also possesses inhibitory activity against acetylcholinesterase (AChE) with the percentage inhibition at 100 uM. Lucidadiol shows antiviral activity against i | |||
TN3559 |
Cabraleahydroxylactone
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HSV | Microbiology/Virology |
Cabraleahydroxylactone displays antimycobacterial activity against Mycobacterium tuberculosis, it is weakly cytotoxic to a breast cancer (BC) cell line.It shows antiviral activity against herpes simplex virus type-1 with an IC50 value of 3.20 ug/mL, in comparison with the standard acyclovir (IC50=1.90ug/mL). | |||
T3930 |
Taraxerol acetate
醋酸蒲公英霜,Taraxeryl acetate |
Phosphatase; HSV | Metabolism; Microbiology/Virology |
Taraxeryl acetate shows the significant antiviral activity against herpes simplex virus (type II). It has less effect on cell cycle arrest and apoptosis of AGS cells than taraxerol. A. roxburghiana has antidiabetic activity, could be attributed due to PTP | |||
TN1632 |
Euparin
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Antifection | Microbiology/Virology |
Euparin exhibits a moderate antioxidant activity, it also exhibits antifungal activity against Trichophyton mentagrophytes. Euparin has antiviral activity, it exerts its effect during the early events of the replication cycle, from the virus adsorption to | |||
TN1843 |
Kushenol K
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PDE; HSV | Metabolism; Microbiology/Virology |
Kushenol K is a potent and Selective Inhibitor of cGMP Phosphodiesterase 5, it also has inhibitory effects on diacylglycerol acyltransferase (DGAT). Kushenol K shows weak antiviral activity against Herpes simplex virus types I and II. | |||
TN4696 | Odorinol | Antifection | Microbiology/Virology |
Odorine and odorinol inhibit both the initiation and promotion stages of two-stage skin carcinogenesis. (+)-Odorinol exhibits strong antiviral activity against Ranikhet disease virus (RVD) in chick embryo. | |||
TN3461 |
Asebotin
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Influenza Virus | Microbiology/Virology |
Asebotin shows anti-influenza A virus activity, it also possesses potent antiviral activity (100% inhibition at the concentration of 1 ug /mL) against highly pathogenic avian influenza strain H5N1. Asebotin can inhibit the proliferation of murine B cells. | |||
T75533 | Dihydromaniwamycin E | ||
Dihydromaniwamycin E 是一种热休克代谢物,对influenza 和SARS-CoV-2病毒具有抗病毒活性。 | |||
TN3925 |
Eichlerianic acid
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HSV | Microbiology/Virology |
Eichlerianic acid is a trypanocidal compound with an IC50 value of 10 mg/mL. Eichlerianic acid may have antiviral activity against Herpes simplex virus types I and II in vitro. Eichlerianic acid shows weak cytotoxicity (IC50 6.87 to >40 μM) against human cancer cell (HL-60, SMMC-7721, A-549, MCF-7 and SW480). | |||
TN5014 | Shoreic acid | Antifection; HSV | Microbiology/Virology |
Shoreic acid exhibits antibacterial activity against E. coli, P. aeruginosa, S. aureus, and B. subtilis with activity indices (AI) of 0.2, 0.3, 0.5 and 0.4, respectively, it also shows antifungal activity against C. albicans and T. mentagrophytes with AI | |||
T14368 |
Azadirachtin B
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Others | Others |
Azadirachtin B, a limonoid derived from the seed kernels of Azadirachta indica, exhibits a broad spectrum of biochemical activities, including insecticidal, nematocidal, anticancer, anti-inflammatory, antiviral, and osteogenic effects. It is effective against the Epstein-Barr virus early antigen (EBV-EA), enhances alkaline phosphatase (ALP) activity, and promotes osteoblast differentiation[1][2][3]. | |||
T37451 |
Stachybotrysin B
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Stachybotrysin B is a fungal metabolite originally isolated from S. chartarum and has antiviral and anticancer activities.1,2 It has antiviral activity against HIV in SupT1 cells (IC50 = 19.2 μM).1 Stachybotrysin B is cytotoxic to K562, HeLa, and HL-60 cells (IC50s = 21.72, 39.63, and 18.5 μM, respectively).2 |1. Zhao, J., Feng, J., Tan, Z., et al. Stachybotrysins A-G, phenylspirodrimane derivatives from the fungus Stachybotrys chartarum. J. Nat. Prod. 80(6), 1819-1826 (2017).|2. Ma, X.-h., Zhen... | |||
TN5463 |
Leachianone G
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Leachianone G exhibits significant antioxidant potentials in the ABTS, ONOO(-), and total ROS assays, it also shows inhibitory activities against pancreatic lipase, it may be used as drug candidate to control obesity. Leachianone G shows potent antiviral | |||
TN4402 | Labd-13-ene-8,15-diol | Antifection | Microbiology/Virology |
13(E)-Labd-13-ene-8alpha,15-diol shows antiviral and anticancer activity, it shows strong anti-HRV2 and HRV3 activity with a 50% inhibitory concentration (IC50) of 2.68 and 0.87 microg/mL,respectively; it also exhibits antilung and antilaryngeal cancer ac |