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Cat. No. | Product Name | Target | Signaling Pathways |
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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。 | |||
T20406 |
Acyclovir L-isoleucinate
Acyclovir isoleucinate |
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Acyclovir L-isoleucinate is an acyclovir impurity. It also is an Acyclovir amino acid ester prodrug. | |||
T23626 |
Acyclovir alaninate
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Acyclovir alanine is a pro-drug of Acyclovir. Acyclovir works by decreasing the production of DNA of the virus and it shows very low cytotoxicity. | |||
T1454L |
Acyclovir sodium
Aciclovir sodium |
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Acyclovir sodium is an antimetabolite. Acyclovir sodium inhibits HSV-specified DNA polymerases and prevents further viral DNA synthesis. | |||
T29628 |
Acyclovir mixture with hydrocortisone
Xerese,ME 609,ME609,ME-609,Lipsovir |
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Acyclovir mixture with hydrocortisone is used for Herpes simplex labialis. | |||
T60709 |
Acyclovir monophosphate
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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。 | |||
T22304 |
Desciclovir
BW A515U,地昔洛韦,6-Deoxyacyclovir,DCV |
Antifection | Microbiology/Virology |
Desciclovir (DCV) 是抗疱疹药物阿昔洛韦的前药,口服有活性,在体内被黄嘌呤氧化酶转化成为阿昔洛韦。 | |||
T1087 |
Valacyclovir hydrochloride
Valaciclovir hydrochloride,盐酸伐昔洛韦,盐酸万乃洛韦,Valaciclovir HCl |
DNA/RNA Synthesis; Antibiotic; HSV | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Valacyclovir hydrochloride (Valaciclovir hydrochloride) 是一种口服有效的抗病毒药物,能抑制疱疹 B,单纯疱疹和带状疱疹。它抑制 HSV-1W,IC50为2.9 μg/ml。它是 Aciclovir 的前药。 | |||
T64299 | Valacyclovir hydrochloride hydrate | ||
Valacyclovir hydrochloride hydrate 是一种有效的抗病毒剂,是一种前药,在体内可快速转化为阿昔洛韦。Valacyclovir hydrochloride hydrate 能够用于配制治疗眼部疱疹的眼部插入物。Valacyclovir hydrochloride hydrate 能够用于单纯疱疹、带状疱疹和乙型疱疹的治疗。 | |||
T20927 |
Benzyloxycarbonyl valacyclovir
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Benzyloxycarbonyl valacyclovir is a biochemical. | |||
T35010 |
Valacyclovir Related Compound D
N-Ethyl valacyclovir |
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Valacyclovir Related Compound D is a bioactive chemical. | |||
T65324 |
Diacetylacyclovir
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Diacetylacyclovir 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 T65324,CAS号为 75128-73-3。 | |||
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。 | |||
T31659 |
Eprociclovir
AV10,AV-10,A-5021,A 5021,A5021,AV 10 |
Antifection | Microbiology/Virology |
Eprociclovir (A-5021) 是一种新型阿昔洛韦类似物,是 EHV1 复制的强效抑制剂,可能用于治疗和/或预防该病毒感染。Eprociclovir 对大多数人类疱疹病毒都有很强的抗疱疹活性。 | |||
T70027 | Eprociclovir potassium | ||
Eprociclovir potassium is a new acyclovir analogue and a potent inhibitor of EHV1 replication and may have potential for the treatment and/or prophylaxis of infections with this virus. Eprociclovir possess potent anti-herpetic activity against most human herpesviruses. A-5021 proved to be about 15-fold more potent than acyclovir in inhibiting viral replication. Eprociclovir inhibits murine herpetic keratitis. A-5021 eyedrops, which are easily applied onto the affected cornea, ameliorated clinica... | |||
T69817 |
Eprociclovir Na
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Eprociclovir Na is the salt form of Eprociclovir, also known as A-5021, a new acyclovir analogue and a potent inhibitor of EHV1 replication and may have potential for the treatment and/or prophylaxis of infections with this virus. Eprociclovir possess potent anti-herpetic activity against most human herpesviruses. A-5021 proved to be about 15-fold more potent than acyclovir in inhibiting viral replication. Eprociclovir inhibits murine herpetic keratitis. A-5021 eyedrops, which are easily applie... | |||
T40911 | 9-Carboxymethoxymethylguanine | ||
9-Carboxymethoxymethylguanine is the primary metabolite derived from Aciclovir, a guanosine analogue with potent antiviral properties. Aciclovir, also known as Acyclovir, acts as an orally active antiviral agent. | |||
T68957 |
Eprociclovir dihydrate
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Eprociclovir dihydrate is a new acyclovir analogue and a potent inhibitor of EHV1 replication and may have potential for the treatment and/or prophylaxis of infections with this virus. Eprociclovir possess potent anti-herpetic activity against most human herpesviruses. A-5021 proved to be about 15-fold more potent than acyclovir in inhibiting viral replication. Eprociclovir inhibits murine herpetic keratitis. A-5021 eyedrops, which are easily applied onto the affected cornea, ameliorated clinica... | |||
T36490 | AZT triphosphate TEA | ||
AZT triphosphate TFA (3'-Azido-3'-deoxythymidine-5'-triphosphate TFA) is a active triphosphate metabolite of Zidovudine (AZT). AZT triphosphate TFA exhibits antiretroviral activity and inhibits replication of HIV. AZT triphosphate TFA also inhibits the DNA polymerase of HBV. AZT triphosphate TFA activates the mitochondria-mediated apoptosis pathway[1][2][3]. Treatment with 100 μM Zidovudine (AZT) for 48h disrupts the mitochondrial tubular network via accumulation of AZT triphosphate (AZT-TP) in ... |
Cat. No. | Product Name | Target | Signaling Pathways |
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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). |