49
12
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8972 |
FIT-039
|
Others; DNA/RNA Synthesis; CDK; HSV | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
FIT-039 是一种选择性和 ATP 竞争性的口服活性 CDK9 抑制剂,对CKD9/cyclin T1的IC50为 5.8 μM。它抑制HSV-1(IC50为 0.69 μM),HSV-2,人腺病毒和人CMV 的复制。它可抑制耐药性HSV 和其他 DNA 病毒,是有前途的抗病毒药物。 | |||
T2504 |
Pritelivir
普瑞利韦,BAY 57-1293,AIC316 |
DNA/RNA Synthesis; HSV | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Pritelivir (BAY 57-1293) 是一种病毒解旋酶-引物酶复合物抑制剂,有抗病毒活性。它对 HSV-1 和 HSV-2 具有活性,IC50值为 20 nM。 | |||
T0355 |
Valpromide
Depamide,Valpramide,丙戊酰胺,Dipropylacetamide,2-propylpentanamide |
Epoxide Hydrolase; HSV | Metabolism; Microbiology/Virology |
Valpromide (Dipropylacetamide) 是丙戊酸的羧酰胺衍生物,用于治疗癫痫和一些情感障碍。 | |||
TP1534 |
HSV-gB2 (498-505)
HSV-gB2 498-505 |
||
This is the immunodominant epitope gB-8p from herpes simplex virus (HSV) glycoprotein B (gB), amino acids 498 to 505. | |||
T0688 |
Ganciclovir
BW 759,更昔洛韦,RS-21592,2'-Nor-2'-deoxyguanosine |
Nucleoside Antimetabolite/Analog; Others; Antibiotic; Antifection; HSV | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
Ganciclovir (2'-Nor-2'-deoxyguanosine) 是核苷类似物和口服抗病毒药物,对CMV 具有抗病毒活性。它用于治疗与艾滋病相关的巨细胞病毒感染的并发症。 | |||
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。 | |||
T61563 |
HSV-1/HSV-2-IN-2
|
||
HSV-1/HSV-2-IN-2是一种 HSV-1、HSV-2和 VV 抑制剂,EC50值为6.8、8.9和8.9 μM,并显示出抗病毒活性。 | |||
T0929 |
Docusate sodium
Aerosol OT,多库脂钠,Dioctyl sulfosuccinate sodium salt,Bis(2-ethylhexyl) sulfosuccinate sodium salt,Constonate |
Opioid Receptor; HSV | Endocrinology/Hormones; GPCR/G Protein; Microbiology/Virology; Neuroscience |
Docusate sodium (Aerosol OT) 是一种口服的非处方泻药和大便软化剂,可用于研究便秘。 | |||
T0964 |
Floxuridine
氟尿苷,5-Fluorouracil 2'-deoxyriboside,FUDR,Deoxyfluorouridine,NSC 27640 |
Apoptosis; Nucleoside Antimetabolite/Analog; Others; DNA/RNA Synthesis; Antibacterial; HSV | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology; Others |
Floxuridine (FUDR) 是一种嘧啶类似物,也是一种抗肿瘤代谢物。它抑制胸苷酸合成酶,导致 DNA 合成中断和细胞毒性。它是一种可诱导细胞凋亡的金黄色葡萄球菌感染抑制剂 ,具有抗HSV 和CMV 病毒的作用。 | |||
T62075 |
HSV-1/HSV-2-IN-1
|
||
HSV-1/HSV-2-IN-1 是一种 HSV-1 和 HSV-2 抑制剂,能够作用于 HSV-1 (KOS) (EC50: 7.6 μM),HSV-2 (G) (EC50: 7.6 μM),HSV-1 TK-KOS ACVr (EC50: 4 μM) 和牛痘病毒 (EC50: 12 μM)。 | |||
T10445 |
B220
|
HSV | Microbiology/Virology |
B220 是一种能抑制 HSV-1,HSV-2 和人巨细胞病毒 (CMV) 生长的抗病毒剂。 | |||
T74809 |
STING agonist-30
|
STING; Antifection | Immunology/Inflammation; Microbiology/Virology |
STING agonist-30 是一种高效的 STING 激动剂,能激发STING依赖的免疫激活。STING agonist-30 对包括HSV(单纯疱疹病毒)、轮状病毒及SARS-CoV-2(严重急性呼吸系统综合症冠状病毒2)在内的多种病毒显示出广谱抑制效果。 | |||
T50026 |
Aquacycline
|
HSV | Microbiology/Virology |
Aquacycline 是一种广谱抗生素,通过抑制细菌中的蛋白质合成起作用。它可防止氨酰-tRNA 与复杂的 m-核糖体 RNA 结合。它还具有抗 HSV-1 活性。 | |||
T60272 |
Isatin-β-thiosemicarbazone
IBT |
HSV | Microbiology/Virology |
Isatin-β-thiosemicarbazone 是一种有效的单纯疱疹病毒 (HSV) 抑制剂。Isatin-β-thiosemicarbazone 在对 HSV-1 和 HSV-2 都具有抑制作用,表现出抗病毒活性。Isatin-β-thiosemicarbazone 是一种有效的抗痘病毒剂 (anti-poxvirus)可用用于治疗猴痘病毒、正痘病毒和牛痘病毒。 | |||
T7055 |
Bz-RS-ISer(3-Ph)-Ome
Methyl (2R,3S)-3-(benzoylamino)-2-hydroxy-3-phenylpropanoate |
Others; HIV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
Bz-RS-ISer(3-Ph)-Ome (Methyl (2R,3S)-3-(benzoylamino)-2-hydroxy-3-phenylpropanoate) 是紫杉醇衍生物,在低细胞毒性下抑制 HSV 复制周期,阻断 Vero 细胞的有丝分裂,影响 M-MSV 诱导的肿瘤大小,并通过抑制 PHA 诱导的 T 淋巴细胞增殖而影响免疫应答。 | |||
T3045 |
Salubrinal
|
Apoptosis; Phosphatase; PERK; Autophagy; HSV | Apoptosis; Autophagy; Metabolism; Microbiology/Virology |
Salubrinal 是一种磷酸酶抑制剂 ,对真核翻译起始因子 2 亚基 (eIF2α) 发挥作用。它作为双特异性磷酸酶 2 抑制剂,抑制抗胶原蛋白抗体诱导的关节炎。它具有抗HSV-1病毒的活性,并抑制由HSV-1蛋白 ICP34.5 介导的eIF2α的去磷酸化。 | |||
T1643 |
Penciclovir
喷昔洛韦,BRL 39123,VSA 671 |
HCV Protease; Antifection; HSV | Microbiology/Virology; Proteases/Proteasome |
Penciclovir (BRL 39123) 是一种疱疹病毒核苷类似物 DNA 聚合酶抑制剂。它作用于HSV1 和 2,IC50分别为 0.04-1.8 μg/mL 和 0.06-4.4 μg/mL。 | |||
T67836 |
AT-533
|
HSP; HSV | Cytoskeletal Signaling; Metabolism; Microbiology/Virology |
AT-533 是有效的 HSV 和 Hsp90 抑制剂。AT-533 可以阻断 HIF-1α/VEGF/VEGFR-2 信号通路,从而抑制血管生成和肿瘤生长。AT-533 也抑制下游通路的激活,包括 Erk1/2, FAK, Akt/mTOR/p70S6K。AT-533 抑制人脐静脉内皮细胞 (HUVEC) 的细胞迁移、侵袭和管形成。 | |||
T11449L |
Golotimod
Gamma-D-glutamyl-L-tryptophan,SCV 07 |
Antibiotic | Microbiology/Virology |
Golotimod (SCV 07) 是一种具有抗菌活性的二肽,具有免疫调节活性,能显著提高抗结核治疗的疗效,诱导胸腺和脾脏细胞增殖,调节巨噬细胞功能,抑制 STAT3 信号传导。Golotimod 可用于研究复发性生殖器单纯疱疹病毒 2 (HSV-2)感染和口腔黏膜炎。 | |||
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。 | |||
T13209L | Tromantadine hydrochloride | HSV | Microbiology/Virology |
Tromantadine hydrochloride is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication). | |||
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。 | |||
T76336 |
Astodrimer
|
||
Astodrimer (SPL7013 free base) 是一种体积较大(3-4 nm, ~ 16.5 kDa)、带负电荷、高度分支化的树状高分子,有效抑制并杀灭多种病毒,包括 SARS-CoV-2、HIV-1、HSV-1、HSV-2、HPV 等,具有广谱的抗病毒和杀病毒活性,同时展现出抗菌特性。 | |||
T73983 | Cidofovir diphosphate tri(triethylamine) | ||
Cidofovir diphosphate tri triethylamine 是西多福韦的细胞内活性代谢物。diphosphate tri triethylamine 是病毒 DNA 聚合酶的选择性抑制剂,对 HCMV,HSV-1和 HSV-2的 Ki 值分别为 6.6,0.86 和 1.4 μM。 | |||
T76581 |
HHV-2 Envelope Glycoprotein G (552-574)
|
||
HHV-2 包膜糖蛋白 G (552-574) 是 gG-2 的免疫显性区域,能够与所有单纯疱疹 (HSV-2) 血清产生反应。 | |||
T70933 |
Weinbersterol disulfate A
|
||
Weinbersterol disulfate A is a derivatives of 2beta,3alpha-dihydroxy-5alpha-cholestane. It has shown inhibitory action against HSV-2. and proved to be active against DEN-2 and JV. | |||
T68619 |
FR-48217
|
||
FR-48217 is an immunoactive peptide that inhibits multiplication of HSV-1 and HSV-2. | |||
T75518 | Galactofucan | ||
Galactofucan (Fucogalactan) 是一种硫酸多糖。Galactofucan 可以从棕色海藻 Saccharina longicruris 中提取,具有抗凝血、抗肿瘤、抗血栓形成、抗炎、抗病毒等特性。Galactofucan 对 HSV-1和 HSV-2具有抗病毒活性,IC50值分别为 0.76 和 1.34 µg/mL 。Galactofucan 可用于癌症和炎症的研究。 | |||
TP1536 |
Histone H4 (2-21)
|
||
Histone H4 (2-21) is a pivotal core histone involved in the process of chromatinization specific to the genomes of herpes simplex virus 1 (HSV-1). | |||
T80374 |
HBA(111–142)
|
HSV | Microbiology/Virology |
HBA(111-142) 是一种源于 α-血红蛋白 C 端的32-聚体抗菌肽片段,对 ESKAPE 病原体展示出了抗菌效果。它能形成淀粉样原纤维结构,并表现出针对多种病毒,包括麻疹病毒和疱疹病毒(HSV-1、HSV-2、HCMV)的抗病毒活性。 | |||
T13209 |
Tromantadine
|
HSV | Microbiology/Virology |
Tromantadine is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication). | |||
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). | |||
T81293 |
Retrocyclin-2
|
||
Retrocyclin-2是一种具有针对HIV、Influenza A和HSV的抗微生物活性的肽类化合物。 | |||
T72864 |
Perillic acid
紫苏酸 |
||
Perillic acid 是 Perillyl alcohol 的代谢物。Perillic acid 诱导肺癌细胞周期阻滞和凋亡 (apoptosis)。Perillic acid 具有抗HSV-1和免疫调节活性。 | |||
T75444 | Peniterphenyl A | ||
Peniterphenyl A,一种源于深海青霉属植物的天然产物,能够抑制HSV-1/2病毒的细胞内入侵。它可能通过与HSV-1/2病毒的糖蛋白D直接相互作用,干扰病毒的吸附和膜融合过程,进而有效阻断病毒感染。因此,Peniterphenyl A是抗HSV-1/2研究领域中一个极具潜力的先导化合物。 | |||
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 | |||
T35701 |
FSL-1 TFA
|
||
FSL-1 TFA, a bacterial-derived toll-like receptor 2/6 (TLR2/6) agonist, enhances resistance to experimental HSV-2 infection[1]. FSL-1 TFA induces MMP-9 production through TLR2 and NF-κB/AP-1 signaling pathways in monocytic THP-1 cells[2]. FSL-1 significantly reduces HSV-2 replication in human vaginal epithelial cells (EC)[1].FSL-1 induces significant resistance to experimental genital HSV-2 infection through elaboration of a specific cytokine response profile[1].FSL-1 (50 ng/mL, 24 hours) induce... | |||
T36073 |
S-Acetyl-L-glutathione
|
||
S-Acetyl-L-glutathione is a derivative of glutathione .1 It increases intracellular GSH levels in primary fibroblasts derived from patients with glutathione synthetase deficiency when used at a concentration of 50 μM. S-Acetyl-L-glutathione (5 mM) induces apoptosis in Daudi, Raji, and Jurkat lymphoma cells.2 It inhibits the replication of herpes simplex virus 1 (HSV-1) in human foreskin fibroblasts when used at concentrations of 5 and 10 mM.3 S-Acetyl-L-glutathione (6.25 μg/g per day) increases ... | |||
T35696 |
Olomoucine II
|
||
Olomoucine II is an inhibitor of cyclin-dependent kinases (CDKs; IC50s = 7.6, 0.1, 19.8, 0.45, and 0.06 μM for Cdk1, -2, -4, -7, and -9, respectively).1It is selective for CDKs over 10 additional kinases (IC50s = >100 μM for all) but does inhibit ERK2 (IC50= 32 μM) and the ATP-binding cassette transporter B1 (ABCB1; IC50= 6.4 μM).1,2Olomoucine II inhibits proliferation of a variety of cancer cells, including those expressing wild-type p53 or mutant p53 (mean IC50s = 7.4 and 10.1 μM, respectively... | |||
T80120 |
FITC-εAhx-HHV-2 Envelope Glycoprotein G (561-578)
|
HSV | Microbiology/Virology |
FITC-εAhx-HHV-2 EnvelopeGlycoproteinG (561-578) 是带有FITC标记的糖蛋白G (gG-2)的免疫原性片段,涵盖了其氨基酸序列的561至578位点。此段具有广泛的与单纯疱疹病毒2型(HSV-2)血清呈现交叉反应的特性。 | |||
T1087L |
Valaciclovir
|
||
Valacyclovir (Valaciclovir) 是一种具有口服活性的抗病毒药物,用于抑制单纯疱疹,带状疱疹和疱疹 B。Valacyclovir 抑制 HSV-1W (50=2.9 μg/ml)。Valacyclovir 是 Aciclovir 的前药。 | |||
T60709 |
Acyclovir monophosphate
|
||
Acyclovir monophosphate 是抗单纯疱疹病毒 (HSV)剂,并且具有抗肿瘤活性。Acyclovir monophosphate 通过抑制病毒 DNA 聚合酶从而阻断 DNA 合成,同时能终止病毒 DNA 的链延伸。 | |||
T11449L2 |
Golotimod (TFA) (229305-39-9 free base)
SCV 07 (TFA),Gamma-D-glutamyl-L-tryptophan (TFA),Golotimod (TFA) |
STAT | JAK/STAT signaling; Stem Cells |
Golotimod TFA (SCV 07 TFA) 一种免疫调节肽,具有抗菌作用,能够明显增加抗结核研究的效果,刺激胸腺和脾细胞增殖,改善巨噬细胞功能。Golotimod TFA 能够抑制 STAT3 信号传导,调节接受放疗或放疗与顺铂联合用药的动物模型中口腔粘膜炎的持续时间和严重程度。Golotimod TFA 具有潜力进复发性生殖器单纯疱疹病毒 2 型 (HSV-2) 的研究。 | |||
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 | |||
T75282 | Oxytetracycline calcium | ||
Oxytetracycline calcium 是一种属于四环素类的抗生素。Oxytetracycline calcium 强力抑制革兰氏阴性和革兰氏阳性细菌。Oxytetracycline calcium 是一种蛋白质合成抑制剂,可阻止 aminoacil-tRNA 与复杂的核糖体 RNA 结合。Oxytetracycline calcium 还具有抗HSV-1的活性。 | |||
T78119 |
Z-L(D-Val)G-CHN2
|
HSV | Microbiology/Virology |
Z-L(D-Val)G-CHN2(即Z-LVG-CHN2)是半胱氨酸蛋白酶抑制剂的异构体,作为一种三肽衍生物,模仿了人体半胱氨酸蛋白酶结合中心的部分结构。它可以抑制HSV,并且能有效阻断SARS-COV-2的3CL pro蛋白酶,从而抑制病毒活性(EC50=190 nM),但对脊髓灰质炎病毒复制无显著作用。 | |||
T60488 |
Ganciclovir hydrate
|
||
Ganciclovir (BW 759) hydrate 是一种核苷类似物,是具有口服活性的抗病毒剂,显示出抗巨细胞病毒活性。Ganciclovir hydrate 对疱疹病毒和其他一些 DNA 病毒也具有体外抗病毒活性。Ganciclovir hydrate 在体外抑制人类疱疹病毒 (HSV 1 型和 2 型,CMV) 和腺病毒血清型1、2、4、6、8、10、19、22 和 28 的复制。Ganciclovir hydrate 对猫疱疹病毒 1 型 (FHV-1) 的 IC50为 5.2 μM,可扩散到大脑。 | |||
T11449 |
Golotimod hydrochloride (229305-39-9 free base)
Golotimod hydrochloride,Gamma-D-glutamyl-L-tryptophan hydrochloride,SCV 07 hydrochloride |
STAT | JAK/STAT signaling; Stem Cells |
Golotimod (SCV 07) hydrochloride 是一种免疫调节肽,具抗菌活性,能显著提升抗结核疾病研究效果。该化合物通过刺激胸腺和脾细胞增殖、改善巨噬细胞功能,展现其生物调节能力。此外,Golotimod hydrochloride 通过抑制STAT3信号传导,有效调节接受放疗或与顺铂联用治疗动物模型中的口腔粘膜炎持续时间和严重程度。还显示出对研究复发性生殖器单纯疱疹病毒 2 型 (HSV-2) 具有潜在应用价值。 | |||
T83706 |
BMAP 28 (bovine) TFA
Cathelicidin-5 (132-158),Bovine Myeloid Antimicrobial Peptide 28 |
||
BMAP 28是一种合成抗菌肽,对应牛防御素-5的132-158氨基酸。对大肠杆菌(E. coli)、金黄色葡萄球菌(S. aureus)、耐甲氧西林金黄色葡萄球菌(MRSA)、表皮葡萄球菌(S. epidermidis)及白色念珠菌(C. albicans)具有活性(MICs分别为2、2、4、1和8 µM)。在200 nM浓度下,BMAP 28能够使大肠杆菌的内膜渗透。在5 µM浓度下,减少Vero 76细胞中单纯疱疹病毒1型(HSV-1)的复制。在30 µM浓度下,对分离的人类红细胞引起溶血,并对分离的人类嗜中性粒细胞具有细胞毒性。BMAP 28 (0.8 mg/kg)可提高大肠杆菌或MRSA感染的小鼠的生存率,但对铜绿假单胞菌(P. aeruginosa)感染的小鼠无效。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3S1068 |
Oxyresveratrol
trans-Oxyresveratrol,2,3',4,5'-tetrahydroxystilbene,氧化白藜芦醇,Tetrahydroxystilbene |
Tyrosinase; Autophagy; HSV | Autophagy; Microbiology/Virology; Proteases/Proteasome |
Oxyresveratrol (trans-Oxyresveratrol) 是非竞争性酪氨酸酶抑制剂,对蘑菇酪氨酸酶的 IC50值为 1.2 µM。它抑制HSV-1,HSV-2和水痘带状疱疹病毒,具有神经保护作用。它是天然抗氧化剂和自由基清除剂。 | |||
T6742 |
2-Deoxy-D-glucose
2-Deoxy-D-arabino-hexose,2-deoxyglucose,D-Arabino-2-deoxyhexose,Ba 2758,D-2-脱氧葡萄糖,NSC 15193,2-DG,2-脱氧-D-葡萄糖 |
Apoptosis; Hexokinase; HSV | Apoptosis; Metabolism; Microbiology/Virology |
2-Deoxy-D-glucose (2-DG) 是葡萄糖的类似物,是一种糖酵解抑制剂。2-Deoxy-D-glucose 具有抗病毒活性,还具有抑制细胞增殖、诱导细胞凋亡的活性。 | |||
T3813 |
20(R)-Ginsenoside Rh2
20(R)-人参皂苷 RH2,(20R)Ginsenoside Rh2,Ginsenoside Rh2,20(R)-人参皂苷Rh2 |
Apoptosis; MMP; HSV | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
20(R)-Ginsenoside Rh2 (Ginsenoside Rh2) 是人参皂苷 Rh2 的次要立体异构体,具有基质金属蛋白酶抑制作用。它有抗癌、抗炎和抗氧化活性。 | |||
T5429 |
Theaflavin 3,3'-digallate
茶黄素-3,3'-双没食子酸,8-Gingerol,TFDG |
Virus Protease; Antioxidant; HIV Protease; HSV | Microbiology/Virology; oxidation-reduction; Proteases/Proteasome |
Theaflavin 3,3'-digallate (8-Gingerol) 是一种寨卡病毒蛋白酶抑制剂,IC50为 2.3 μM。它直接与 ZIKVpro 结合并抑制 ZIKV 复制,可抑制 gp41 和 NS2B-3 蛋白酶的活性,并具有抗 HSV 和 HIV-1病毒活性。它是红茶中的主要多酚,有抗肿瘤作用。 | |||
T6S1885 |
Benzoylmesaconine
Mesaconine 14-benzoate,苯甲酰新乌头原碱 |
Others | Others |
Benzoylmesaconine (Mesaconine 14-benzoate) 是乌头汤最丰富的组分。其中乌头汤可用于研究类风湿性关节炎。 | |||
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。 | |||
T0853L |
Adenosine 5'-monophosphate monohydrate
5'-AMP,腺苷-5'-单磷酸一水合物,5'-AMP monohydrate,5'-Adenylic acid |
AMPK; Adenosine Receptor; HSV | Chromatin/Epigenetic; GPCR/G Protein; Microbiology/Virology; Neuroscience; PI3K/Akt/mTOR signaling |
Adenosine 5'-monophosphate monohydrate (5'-AMP) 是一种核苷酸,用作 RNA 中的单体。它是一个腺苷 A1受体激动剂,对HSV-1和HSV-2具有显著的抗病毒活性。 | |||
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。 | |||
TN4587 | Mulberrofuran C | HSV | Microbiology/Virology |
Mulberrofuran C shows protective effects on t-BHP-induced oxidative stress with the EC50 value of 0.41 ± 0.48 uM ; it also shows protective effects on glutamate-induced cell death with the EC50 value of 16.50 ± 7.82 uM. Mulberrofuran C has antiviral effects against herpes simplex virus type 1 and 2 (HSV-1 and HSV-2). | |||
T83693 |
Magainin 2 TFA
MG2 |
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Magainin 2是一种从非洲爪蟾(X. laevis)皮肤中分离出的阳离子肽,具有宿主防御和抗菌活性。该化合物对细菌E. coli、K. pneumoniae、S. epidermidis、S. aureus及真菌C. albicans表现出活性(MICs分别为5、10、10、50和80 µg/ml)。Magainin 2(20 µM)能降低猕猴桃花粉的萌发率和平均管长。在被单纯疱疹病毒1型(HSV-1)或2型(HSV-2)感染的Vero细胞中,它可减少病毒复制(EC50s分别为22.16和19.8 µM),同时不影响细胞活性,其50%细胞毒性浓度值(CC50)大于100 µM。 | |||
TN6014 |
Norcepharadione B
鱼腥草 |
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Norcepharadione B shows good inhibitory activity against the replication of HSV-1, it also shows antimalarial activity with EC50 values of 7.5mug/ml. Norcepharadione B exhibits significant cytotoxicity against five human tumor cell lines (A-549, SK-OV-3, | |||
T35779 |
Oosporein
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Oosporein is a mycotoxin that has been found inBeauveriaand has diverse biological activities.1,2It is cytotoxic to Sf9 and Sf21 insect cells with 50% cytotoxic concentration (CC50) values of 4.23 and 10.43 μM, respectively.3Oosporin induces lethality in day-old cockerels (LD50= 6.12 mg/kg).4It inhibits Na+/K+-, Ca2+-, and Mg2+-ATPase activities by 27, 52, and 100%, respectively, in equine erythrocyte ghosts when used at a concentration of 200 μg/ml.2Oosporein inhibits herpes simplex 1 (HSV-1), ... |