45
4
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37792 |
A2A receptor antagonist 1
CPI-444 analog,A2A receptor antagonist 1 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
A2A receptor antagonist 1 (CPI-444 analog)是腺苷 A2A 和 A1受体的拮抗剂,Ki 值分别为4和264 nM。 | |||
T2578 |
Didanosine
ddI,去羟肌苷,2',3'-Dideoxyinosine |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Didanosine (ddI) 是一种逆转录酶抑制剂,IC50为490nM。 | |||
T16325 |
NITD008
7-Deaza-2'-C-acetylene-adenosine |
Others | Others |
NITD008 (7-Deaza-2'-C-acetylene-adenosine) 是一种有效的和选择性的腺苷核苷抑制剂,是一种腺苷核苷类似物,具有广谱的抗病毒活性,抑制登革热病毒、动物杯状病毒和寨卡病毒。 | |||
T34914 |
Trabodenoson
INNO-8875,INO-8875,PJ875,PJ-875,INNO 8875,INNO8875,PJ 875 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Trabodenoson (INO-8875) 是一种具有选择性和有效性的的腺苷 A1 受体激动剂,是一种腺苷类似物,可用于研究原发性开角型青光眼。 | |||
TNU0178 |
2'-O-(2-Azidoethyl)adenosine
|
Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
2'-O-(2-Azidoethyl)adenosine 是一种嘌呤核苷类似物,具有潜在的抗肿瘤活性。2’-O-(2-Azidoethyl)adenosine 的活性与抑制DNA合成和凋亡有关。 | |||
T20048 |
Vidarabine phosphate
|
Antiviral | Immunology/Inflammation |
Vidarabine phosphate 是一种单磷酸腺苷类似物。它是 VIDARABINE 的单磷酸酯。它还具有抗病毒和可能的抗肿瘤特性。 | |||
T7736 |
2-Chloroadenosine
|
Adenosine Receptor | GPCR/G Protein; Neuroscience |
2-Chloroadenosine 是腺苷类似物,可防止大鼠海马缺血细胞长期丢失。它是尿苷内流 (Ki:33 μM) 的竞争性抑制剂,高亲和力与硝基苄基硫肌苷结合 (Ki:0.18 mM)。它是一种人红细胞核苷转运体的转运渗透剂。 | |||
T2409L |
Tenofovir Disoproxil Fumarate
GS-1278 Disoproxil Fumarate,Tenofovir DF,富马酸替诺福韦酯 |
HBV; HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Tenofovir Disoproxil Fumarate (GS-1278 Disoproxil Fumarate) 是一种核苷酸逆转录酶抑制剂,有潜力研究艾滋病和慢性乙型肝炎。 | |||
T1675 |
Adefovir dipivoxil
Hepsera,GS 0840,阿德福韦酯,Preveon |
Others; HBV; Reverse Transcriptase | Microbiology/Virology; Others |
Adefovir dipivoxil (GS 0840) 是一种腺苷类似物,是核苷逆转录酶抑制剂 Adefovir 的口服前药,具有抗乙型肝炎病毒、疱疹病毒和人类免疫缺陷病毒的活性。 | |||
T10491 |
Galidesivir
BCX4430,Immucillin-A |
Others | Others |
Galidesivir (BCX4430) 是一种广谱抗病毒化合物,是一种腺苷类似物,能抑制病毒 RNA 依赖的 RNA 聚合酶 (RdRp) 活性。Galidesivir 在体外对多种 RNA 病毒病原体有抑制作用,可减少受感染动物的肺部感染。 | |||
T6360 |
3-deazaneplanocin A HCl
|
Others; Histone Methyltransferase | Chromatin/Epigenetic; Others |
3-deazaneplanocin A HCl 是组蛋白甲基转移酶 (EZH2) 和 S-腺苷同型半胱氨酸水解酶 (AHCY) 抑制剂。 | |||
T13256 |
UP202-56
|
AChR | Neuroscience |
UP202-56 is an adenosinergic agonist and is an adenosine analog. | |||
T38449 |
Guanosine 5'-triphosphate-5'-adenosine
GpppA,Guanosine 5'-triphosphate-5'-adenosine |
||
Guanosine 5'-triphosphate-5'-adenosine, the 5′ cap analog, is a fluorescent substrate analog. | |||
T40721 |
N7-Methyl-guanosine-5'-triphosphate-5'-adenosine
N7-Methyl-guanosine-5'-triphosphate-5'-adenosine,m7GpppA |
||
N7-Methylguanosine-5'-triphosphate-5'-adenosine (m7GpppA) is a dinucleotide cap analog employed in the process of in vitro RNA transcription. | |||
T74135 | N7-Methyl-guanosine-5'-triphosphate-5'-adenosine diammonium | ||
N7-Methyl-guanosine-5'-triphosphate-5'-adenosine (m7GpppA) diammonium 是体外 RNA 转录中使用的二核苷酸帽类似物。 | |||
T75046 | 3’-Beta-C-Methyl-N6-isopentenyl adenosine | ||
3’-Beta-C-Methyl-N6-isopentenyl adenosine 是一种腺嘌呤核苷类似物。腺苷类似物大多可作为平滑肌血管扩张剂,也被证明能够抑制癌症进展。它的热门产品有 Adenosine phosphate,Acadesine ,Clofarabine ,Fludarabine phosphate 和 Vidarabine 。 | |||
T75048 | 3’-Beta-C-ethynyl-N6-(m-trifluoromethyl benzyl)adenosine | ||
3’-Beta-C-ethynyl-N6-(m-trifluoromethyl benzyl)adenosine 是一种腺嘌呤核苷类似物。腺苷类似物大多可作为平滑肌血管扩张剂,也被证明能够抑制癌症进展。它的热门产品有 Adenosine phosphate,Acadesine ,Clofarabine ,Fludarabine phosphate 和 Vidarabine 。 | |||
T75196 | 2’-O-Methyladenosine 5’-monophosphate triethyl ammonium | ||
2’-O-Methyladenosine 5’-monophosphate triethyl ammonium 是一种腺嘌呤核苷类似物。腺苷类似物大多可作为平滑肌血管扩张剂,也被证明能够抑制癌症进展。它的热门产品有 Adenosine phosphate,Acadesine ,Clofarabine ,Fludarabine phosphate 和 Vidarabine 。 | |||
T75208 | 2-Diethoxymethyl adenosine | ||
2-Diethoxymethyl adenosine 是一种腺嘌呤核苷类似物。腺苷类似物大多可作为平滑肌血管扩张剂,也被证明能够抑制癌症进展。它的热门产品有 Adenosine phosphate,Acadesine ,Clofarabine ,Fludarabine phosphate 和 Vidarabine 。 | |||
T75043 | 1-(β-D-Xylofuranosyl)-N6-Isopentenyladenine | ||
1-(β-D-Xylofuranosyl)-N6-Isopentenyladenine 是一种腺嘌呤核苷类似物。腺苷类似物大多可作为平滑肌血管扩张剂,也被证明能够抑制癌症进展。它的热门产品有 Adenosine phosphate,Acadesine ,Clofarabine ,Fludarabine phosphate 和 Vidarabine 。 | |||
T75049 | 3’-Beta-C-ethynyl-N6-iso-pentenyl adenosine | ||
3’-Beta-C-ethynyl-N6-iso-pentenyl adenosine 是一种腺嘌呤核苷类似物。腺苷类似物大多可作为平滑肌血管扩张剂,也被证明能够抑制癌症进展。它的热门产品有 Adenosine phosphate,Acadesine ,Clofarabine ,Fludarabine phosphate 和 Vidarabine 。 | |||
T75227 | 2-Amino-3’,5’-di-O-acetyl-N6,N6-dimethyl-2’-O-methyladenosine | ||
2-Amino-3’,5’-di-O-acetyl-N6,N6-dimethyl-2’-O-methyladenosine 是一种腺嘌呤核苷类似物。腺苷类似物大多可作为平滑肌血管扩张剂,也被证明能够抑制癌症进展。它的热门产品有 Adenosine phosphate,Acadesine ,Clofarabine ,Fludarabine phosphate 和 Vidarabine 。 | |||
T39856 |
Purine riboside triphosphate
PTP,Purine riboside triphosphate |
||
Purine riboside triphosphate, a derivative of purine riboside, exhibits structural similarity to adenosine. This naturally occurring base analog possesses inhibitory effects on carcinogenic growth, particularly in cancer ascites cells, by strongly impeding RNA and DNA synthesis. | |||
T75042 | 1-(β-D-Xylofuranosyl)-N6-(m-trifluoromethylbenzyl)adenine | ||
1-(β-D-Xylofuranosyl)-N6-(m-trifluoromethylbenzyl)adenine 是一种腺嘌呤核苷类似物。腺苷类似物大多可作为平滑肌血管扩张剂,也被证明能够抑制癌症进展。它的热门产品有 Adenosine phosphate,Acadesine ,Clofarabine ,Fludarabine phosphate 和 Vidarabine 。 | |||
T75040 | 1-(β-D-Xylofuranosyl)-N6-(m-methoxybenzyl)adenine | ||
1-(β-D-Xylofuranosyl)-N6-(m-methoxybenzyl)adenine 是一种腺嘌呤核苷类似物。腺苷类似物大多可作为平滑肌血管扩张剂,也被证明能够抑制癌症进展。它的热门产品有 Adenosine phosphate,Acadesine ,Clofarabine ,Fludarabine phosphate 和 Vidarabine 。 | |||
T75209 | N6-Benzoyl-3'-O-DMT-2'-O-(2-methoxyethyl) adenosine | ||
N6-Benzoyl-3'-O-DMT-2'-O-(2-methoxyethyl) adenosine为嘌呤核苷类似物,其抗肿瘤活性广泛,特别是针对惰性淋巴系统的恶性肿瘤。该化合物通过抑制DNA合成和诱导细胞凋亡(apoptosis)等机制发挥抗癌作用。 | |||
T75202 | 2-(3-Methyln-propylidene hydrazino) adenosine | ||
2-(3-Methyln-propylidene hydrazino) adenosine 是一种广泛具有抗肿瘤活性的嘌呤核苷类似物,主要针对惰性淋巴系统恶性肿瘤。其抗癌机制包括抑制 DNA 合成和诱导细胞凋亡(apoptosis)。 | |||
T75070 | 8-Chloro-2’-deoxy-2’-fluoro-arabino adenosine | ||
8-Chloro-2’-deoxy-2’-fluoro-arabino adenosine 是嘌呤核苷类似物,广泛用于对抗肿瘤,特别是针对惰性淋巴系统恶性肿瘤。其抗癌机制主要通过抑制 DNA 合成和诱导细胞凋亡(apoptosis)实现。 | |||
T75056 | N1-Methyl-2’-beta-C-methyl adenosine | ||
N1-Methyl-2’-beta-C-methyl adenosine 是一种具有广泛抗肿瘤活性的嘌呤核苷类似物,主要靶向惰性淋巴系统恶性肿瘤。其抗癌机制主要通过抑制 DNA 合成和诱导细胞凋亡 (apoptosis) 实现。 | |||
T75061 | N1-Methyl-2’-O-(2-methoxyethyl) adenosine | ||
N1-Methyl-2’-O-(2-methoxyethyl) adenosine 是一种具有广泛抗肿瘤活性的嘌呤核苷类似物,主要靶向惰性淋巴系统恶性肿瘤。其机制主要依赖于抑制DNA合成及诱导细胞凋亡(apoptosis)。 | |||
T75050 | 3’-Deoxy-N6-(m-methoxy benzyl)adenosine | ||
3’-Deoxy-N6-(m-methoxy benzyl)adenosine 是一种具有广泛抗肿瘤活性的嘌呤核苷类似物,主要靶向惰性淋巴系统恶性肿瘤。其抗癌机制包括抑制DNA合成和诱导细胞凋亡(apoptosis)。 | |||
T74385 | Biotin-PEG7-C2-S-Vidarabine | ||
Biotin-PEG7-C2-S-Vidarabine 为一种含有 Vidarabine 的 PEG 类连接子,其中 Vidarabine 为对单纯疱疹病毒和水痘带状疱疹病毒有抗病毒效果的腺苷类似物。 | |||
T83472 |
1,N6-Ethenoadenosine 5'-monophosphate sodium
1,N6-ε-AMP sodium,1,N6-Etheno-AMP sodium |
||
1,N6-Ethenoadenosine 5'-monophosphate (1,N6-Etheno-AMP) sodium 是一种针对adenosine 5'-monophosphate系统的荧光探针,具备低浓度检测能力。该化合物拥有较长的激发波长(250-300 nm)和415 nm的发射波长。 | |||
T75069 | N6-Methyl-2’-beta-C-ethynyl adenosine | ||
N6-Methyl-2’-beta-C-ethynyl adenosine 是一种嘌呤核苷类似物。嘌呤核苷类似物具有广泛的抗肿瘤活性,靶向惰性淋巴系统恶性肿瘤。这一过程中的抗癌机制依赖于抑制 DNA 合成,诱导细胞凋亡 (apoptosis) 等。 | |||
T75062 | N6-Methyl-2’-O-(2-methoxyethyl) adenosine | ||
N6-Methyl-2’-O-(2-methoxyethyl) adenosine 为嘌呤核苷类似物,具备广泛抗肿瘤活性,主要靶向惰性淋巴系统恶性肿瘤。其抗癌机制涉及抑制 DNA 合成及诱导细胞凋亡(apoptosis)。 | |||
T74384 | Biotin-PEG8-Vidarabine | ||
Biotin-PEG8-Vidarabine 是一款以 PEG 链为基础的连接物,其特征为包含抗病毒分子 Vidarabine。Vidarabine 对于单纯疱疹病毒及水痘带状疱疹病毒展现出明显的抑制作用。 | |||
T75203 | 2-(P-Cyanophenyl methylidene hydrazino) adenosine | ||
2-(P-Cyanophenyl methylidene hydrazino) adenosine 是一种具有广泛抗肿瘤活性的嘌呤核苷类似物,主要针对惰性淋巴系统恶性肿瘤。其抗癌机制包括抑制DNA合成和诱导细胞凋亡(apoptosis)。 | |||
T75063 | N1-Methyl-3’-O-(2-methoxyethyl) adenosine | ||
N1-Methyl-3’-O-(2-methoxyethyl) adenosine是一种具有广泛抗肿瘤活性的嘌呤核苷类似物,主要针对惰性淋巴系统恶性肿瘤。其抗癌机制包括抑制DNA合成和诱导细胞凋亡(apoptosis)等作用。 | |||
T37669 |
CAY10498
|
||
The A1, A2A, A2B, and A3 adenosine receptors (ARs) are ubiquitous G protein-coupled receptors. The four AR subtypes have been implicated in several areas of therapeutic interest such as stroke and other ischemic conditions, as well as inflammation, neurodegenerative diseases, diabetes, and sleep regulation. A3 AR antagonists are of interest as therapeutic agents in glaucoma agents and inflammation. CAY10498 is a potent and selective A3 AR antagonist exhibiting a Ki of 37 nM with 60 and 200-fold ... | |||
T75068 | N6-Ethyl-2’-beta-C-ethynyl adenosine | ||
N6-Ethyl-2’-beta-C-ethynyl adenosine 是一种嘌呤核苷类似物。嘌呤核苷类似物具有广泛的抗肿瘤活性,靶向惰性淋巴系统恶性肿瘤。这一过程中的抗癌机制依赖于抑制 DNA 合成,诱导细胞凋亡 (apoptosis) 等。 | |||
T75051 | 2-(n-Propylidene hydrazino) adenosine | ||
2-(n-Propylidene hydrazino) adenosine 是一种嘌呤核苷类似物。嘌呤核苷类似物具有广泛的抗肿瘤活性,靶向惰性淋巴系统恶性肿瘤。这一过程中的抗癌机制依赖于抑制 DNA 合成,诱导细胞凋亡 (apoptosis) 等。 | |||
T75035 | 2’-Chloro-N6-(3-trifluoromethyl)benzyl adenosine | ||
2’-Chloro-N6-(3-trifluoromethyl)benzyl adenosine是一种嘌呤核苷类似物,以其广泛的抗肿瘤活性而知名,特别是针对惰性淋巴系统的恶性肿瘤。其作用机制主要通过抑制DNA合成、诱导细胞凋亡(apoptosis)等方式发挥。 | |||
T74386 | Biotin-PEG7-C2-NH-Vidarabine-S-CH3 | ||
Biotin-PEG7-C2-NH-Vidarabine-S-CH3 是一种含 Vidarabine 的 PEG 类连接子。Vidarabine 为腺苷类似物,具抗病毒分子活性,有效针对单纯疱疹病毒及水痘带状疱疹病毒。 | |||
T37733 |
AMP-PNP tetralithium
|
||
Non-hydrolyzable AMP analog. Kir6 (KATP) channel blocker. Inhibits fast axonal transport and stabilizes the interaction of membranous organelles with microtubules. Brady (1985) A novel brain ATPase with properties expected for the fast axonal transport motor. Nature 317 73 PMID:2412134 |Yount et al (1971) Adenylyl imidodiphosphate, an adenosine triphosphate analog containing a P-N-P linkage. Biochemistry 10 2484 PMID:4326768 |Hehl and Neumcke (1994) KATP channels of mouse skeletal muscle: mechan... | |||
T36679 | Rp-cAMPS sodium salt | ||
Rp-cAMPS sodium salt, a cAMP analog, is a potent, competitive cAMP-induced activation of cAMP-dependent PKA I and II (Kis of 12.5 μM and 4.5 μM, respectively) antagonist. Rp-cAMPS sodium salt is resistant to hydrolysis by phosphodiesterases[1][2][3][4][5][6]. A membrane-permeable competitive cAMP antagonist (Rp-cAMPS) that blocks PKA activation by binding to the regulatory subunits without dissociating the kinase holoenzyme also inhibits synaptic plasticity but has no effect on normal synaptic t... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0853 |
Adenosine
腺苷,D-Adenosine,Adenine riboside |
Apoptosis; Nucleoside Antimetabolite/Analog; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
Adenosine (D-Adenosine) 是一种核糖核苷,由与核糖结合的腺嘌呤组成,具有血管扩张、抗心律失常和镇痛作用。 | |||
T17143 |
Toyocamycin
丰加霉素,Vengicide |
Apoptosis; Others; IRE1; Antibiotic; Antifungal | Apoptosis; Cell Cycle/Checkpoint; Microbiology/Virology; Others |
Toyocamycin (Vengicide) 是放线菌类产生的腺苷类似物,为 X 盒结合蛋白 1 (XBP1) 抑制剂,抑制 IRE1α 诱导的 ATP 依赖性 XBP1 mRNA 的断裂,IC50值为 80 nM。它还诱导凋亡。 | |||
T14149 |
AICAR phosphate
AICA Riboside phosphate,Acadesine phosphate |
Mitophagy; NOS; YAP; AMPK | Autophagy; Chromatin/Epigenetic; Immunology/Inflammation; PI3K/Akt/mTOR signaling; Stem Cells |
AICAR phosphate (Acadesine phosphate) 是 AMPK 激活剂且是自噬、YAP 和 mitophagy 抑制剂,也是一种腺苷类似物, 可调节糖代谢和脂代谢,抑制促炎细胞因子和 iNOS 的产生。 | |||
T10369 | Aristeromycin | Others | Others |
Aristeromycin is an adenosine analog and an antibiotic and. It is a potent S-adenosylhomocysteine hydrolase (AHCY) inhibitor. |