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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19179 |
Adenosine deaminase
|
Others | Others |
Adenosine deaminase is an enzyme that catalyzes the irreversible deamination of 2'-deoxyadenosine and adenosine to 2'-deoxyinosine and inosine, respectively. | |||
T60800 |
Deaminase inhibitor-1
|
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Deaminase inhibitor-1 是一种 APOBEC3G DNA 脱氨酶的抑制剂,IC50值为 18.9 μM。 | |||
T9111 |
8-Azaadenosine
|
Adenosine deaminase | Metabolism |
8-Azaadenosine 是 ADAR1抑制剂和是 A-to-I 编辑抑制剂。它可阻断 RNA 编辑并抑制甲状腺癌细胞的增殖、3D 生长、侵袭和迁移。 | |||
T4006 |
Pentostatin
Nipent,CI-825,Covidarabine,喷司他丁,Deoxycoformycin |
Adenosine deaminase; Adenosine Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Pentostatin (CI-825) 是一种高亲和力的,不可逆的腺苷脱氨酶抑制剂,Ki 为 2.5 pM。 | |||
T2558 |
Cladribine
2-chlorodeoxyadenosine,克拉屈滨,2-Chloro-2′-deoxyadenosine,CldAdo,2CdA |
Apoptosis; Adenosine deaminase | Apoptosis; Metabolism |
Cladribine (2CdA) 是一种嘌呤核苷类似物,是具有口服活性的腺苷脱氨酶抑制剂。它能作为 DNA 合成的抑制剂,可阻断受损 DNA 的修复。它可抑制 DNA 甲基化,具有抗淋巴瘤活性,可研究血液恶性肿瘤和多发性硬化。 | |||
T2169 |
Zebularine
NSC309132,4-Deoxyuridine |
DNA Methyltransferase; Autophagy | Autophagy; Chromatin/Epigenetic |
Zebularine (4-Deoxyuridine) 是一种 DNA 甲基化抑制剂,还抑制胞苷脱氨酶。它通过以共价水合物的形式与活性大小结合,充当胞苷脱氨酶的过渡态类似物抑制剂。 | |||
T26972 |
Cedazuridine
西达尿苷,(4R)-2'-Deoxy-2',2'-difluoro-3,4,5,6-tetrahydrouridine |
DNA Methyltransferase | Chromatin/Epigenetic |
Cedazuridine ((4R)-2'-Deoxy-2',2'-difluoro-3,4,5,6-tetrahydrouridine) 是一种口服的胞苷脱氨酶抑制剂,具有抗肿瘤特性。 | |||
T6987 |
β-Chloro-L-alanine
3-Chloro-L-alanine,3-氯-L-丙氨酸,L-β-Chloroalanine |
Antibacterial | Microbiology/Virology |
β-Chloro-L-alanine (L-β-Chloroalanine) 是一种抑菌氨基酸类似物,可抑制多种酶,包括苏氨酸脱氨酶和丙氨酸消旋酶。 | |||
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。 | |||
T50029 |
2-((2,2-Dibenzylhydrazineylidene)methyl)pyridine
2-[(1E)-(dibenzylhydrazin-1-ylidene)methyl]pyridine |
Others | Others |
2-((2,2-Dibenzylhydrazineylidene)methyl)pyridine (2-[(1E)-(dibenzylhydrazin-1-ylidene)methyl]pyridine) 是一种杂环化合物。它可以抑制单胺氧化酶,导致体内单胺水平升高;也可以抑制腺苷脱氨酶,导致体内腺苷水平升高;还可以可以增加某些神经递质的活性,包括血清素和多巴胺。 | |||
T23634 |
Adecypenol
OM-3223,OM3223,OM 3223,Antibiotic OM 3223 |
||
Adecypenol is a unique adenosine deaminase inhibitor. It shows effective inhibitory activity against calf intestinal adenosine deaminase. | |||
T70255 | Elapegademase | ||
Elapegademase is an Adenosine Deaminase Inhibitor | |||
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. | |||
T27384 |
FR-234938
FR 234938 |
||
FR-234938 is a non-nucleoside adenosine deaminase inhibitor with anti-inflammatory activity. | |||
T10015 |
1-Deazaadenosine
|
Others | Others |
1-Deazaadenosine is a potent Adenosine deaminase inhibitor (Ki: 0.66 μM). It exhibits anti-cancer activities in vitro and has the potential to be a chemotherapy agent for lymphoproliferative disorders. | |||
T10308 | AMPD2 inhibitor 1 | Others | Others |
AMPD2 inhibitor 1 is an inhibitor of adenosine monophosphate deaminase 2 (AMPD2), used in the research of salt craving, sugar craving, umami craving, and addictions including tobacco, drug, nicotine and alcohol addictions. | |||
T15343 |
Fosteabine
YNK 01,Cytarabine ocfosfate,阿糖胞苷烷磷酯 |
Others | Others |
Fosteabine is an oral and prodrug analog of cytarabine. It is resistant to deoxycytidine deaminase. | |||
T37106 | 2'-Deoxyadenosine-5'-triphosphate (sodium salt hydrate) | ||
2'-Deoxyadenosine-5'-triphosphate (dATP) is a purine nucleotide and derivative of the nucleic acid adenosine 5'-triphosphate .1dATP is a substrate for DNA polymerase in the synthesis of DNA.2It is a noncompetitive inhibitor of ribonucleotide reductases, which provides feedback inhibition during DNA synthesis.1dATP has commonly been used in DNA synthesis, sequencing, and labeling in research applications.3,4dATP accumulates in adenosine deaminase deficiency, a disorder characterized by mutations ... | |||
T60701 |
Fludarabine-Cl
|
||
Fludarabine-Cl 抑制 RNA 腺苷脱氨酶1 (ADAR1) ,它可用于预防和/或治疗与肿瘤或癌症相关的疾病。 | |||
T38346 | ABT 702 hydrochloride | ||
Potent non-nucleoside adenosine kinase inhibitor (IC50 = 1.7 nM), selective over other sites of adenosine interaction (A1, A2A and A3 receptors, adenosine transporter and adenosine deaminase). Displays oral activity in animal models of pain and inflammation. | |||
T77703 |
2,4-Dimethylpyrrole
|
Others | Others |
2,4-Dimethylpyrrole 是一种有效的卟啉原脱氨酶抑制剂,用于治疗和/或预防先天性红细胞生成性卟啉症(CEP)。 | |||
T60553 | Tetrahydrouridine dihydrate | ||
Tetrahydrouridine dihydrate (THU dihydrate) 是有效的胞苷脱氨酶抑制剂。Tetrahydrouridine dihydrate 比内在胞苷更有效地竞争性阻断酶的活性位点。 | |||
T40566 |
2′-O-(2-Methoxyethyl)guanosine
2′-O-(2-Methoxyethyl)guanosine,2'-O-MOE-rG |
||
2′-O-(2-Methoxyethyl)guanosine (2'-O-MOE-rG), a modified nucleoside, can be enzymatically converted from 2′-O-(2-methoxyethyl)-2,6-diaminopurine riboside by adenosine deaminase. However, this compound is not readily phosphorylated by cytosolic nucleoside kinases, and it cannot be incorporated into cellular DNA or RNA. | |||
T60708 |
Cedazuridine hydrochloride
|
||
Cedazuridine (E7727) (Compound 7a) hydrochloride 是一种可用于研究癌症的,口服有效的胞苷脱氨酶 (CDA) 抑制剂 (IC 50 = 0.4 μM)。 | |||
T72635 |
AMPD2 inhibitor 2
|
||
AMPD2 inhibitor 2是一种针对AMP脱氨酶2 (AMPD2) 的高效抑制剂,具有针对hAMPD2和mAMPD2较低的IC50值,分别为0.1 μM 和 0.28 μM。该化合物可能对于探究AMPD2在高脂肪饮食小鼠模型中的生理功能具有重要意义。 | |||
T11168 | EHNA hydrochloride | Others | Others |
EHNA hydrochloride play roles in mediating diverse pharmacological responses, including antiviral, antitumour and antiarrhythmic effects. EHNA hydrochloride is a potent and selective dual inhibitor of cyclic nucleotide phosphodiesterase 2 (PDE2)(IC50=4 μM) and adenosine deaminase (ADA). EHNA hydrochloride exerts a concentration inhibition of the cGMP-stimulated PDE II (cGs-PDE)(IC50:0.8 μM (human), 2 μM (porcine myocardium)), but has smaller inhibitory effect on the unstimulated PDE2 activity. | |||
T17059 |
Tetrahydrouridine
NSC 112907,NSC112907,四氢尿苷,NSC-112907 |
DNA Methyltransferase | Chromatin/Epigenetic |
Tetrahydrouridine (NSC-112907; THU) 是一种多药耐药调节剂。它可用于癌症治疗,使肿瘤细胞对放射治疗更加敏感。 它是一种竞争性胞苷脱氨酶 (CDA) 抑制剂,可抑制 ara-C 和吉西他滨等细胞毒性脱氧胞苷类似物分解代谢中的脱氨作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1736 |
Hibifolin
棉皮素-8-O-Β-D-葡萄糖醛酸苷,棉花皮素-8-O-葡萄糖醛酸苷 |
Adenosine deaminase | Metabolism |
Hibifolin 是一种黄酮醇糖苷,是潜在的腺苷脱氨酶抑制剂。它可以保护神经元免受 beta-淀粉样蛋白诱导的毒性。 | |||
T13482 |
2'-O-Methyladenosine
|
Endogenous Metabolite | Metabolism |
2'-O-Methyladenosine 是甲基化腺嘌呤的残基,在正常人群和腺苷脱氨基酶缺乏病人的尿液中均可被检测到。它显示出独特的降血压活性。 | |||
T4901 |
5'-Guanylic acid disodium salt
Guanosine 5'-monophosphate disodium salt,5'-鸟苷酸二钠,鸟苷钠5'-单磷酸,GMP-5 |
Others; Endogenous Metabolite | Metabolism; Others |
5'-Guanylic acid disodium salt (GMP-5) 由鸟嘌呤,核糖和磷酸组成,是信使 RNA 中的一种核苷酸单体。 鸟苷衍生物参与细胞内信号转导,并已鉴定存在于端粒,核糖体 DNA,免疫球蛋白重链转换区和原癌基因的控制区中的重复基因组序列中。 | |||
T19146 |
5,6-Dihydrouridine
|
Endogenous Metabolite | Metabolism |
5,6-Dihydrouridine 是一种修饰碱基,存在于真核生物、细菌和某些古细菌tRNA D 环的保守位置。 | |||
T23905 |
Coformycin
NSC 277817 |
||
Coformycin is a ribonucleoside antibiotic synergist and adenosine deaminase inhibitor. | |||
T19346 |
5'-Guanylic acid
鸟苷酸,5'-guanosine monophosphate,5'-GMP |
Endogenous Metabolite | Metabolism |
5'-Guanylic acid (5'-guanosine monophosphate) 与几种代谢紊乱有关,包括腺苷脱氨酶缺乏症、 aica-核糖体途径、腺嘌呤磷酸转移酶缺乏症 (aprt) 以及 2-羟基葡糖酸盐途径。 | |||
T0665 |
Xanthine
2,6-Dihydroxypurine,海生丁(黄嘌呤),黄嘌呤,Isoxanthine |
Endogenous Metabolite; Adenosine Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Xanthine (Isoxanthine) 是一种植物生物碱,存在于茶、咖啡和可可中。Xanthine 是温和的中枢神经系统激活剂,也是嘌呤降解途径的中间产物。 |