13
1
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T21588 |
Olomoucine
|
ERK; CDK | Cell Cycle/Checkpoint; MAPK |
Olomoucine 是 Cdk2/cyclin A、Cdc2/CyclinB、CDK2/CyclinE、CDK5/p35 和 ERK1/p44 MAP 激酶的 ATP 竞争性抑制剂,IC50 分别为 7、7、7、3 和 25 µM。 Olomoucine 调节细胞周期并表现出抗黑色素肿瘤活性。 | |||
T22409 |
Proguanil
氯胍,chloroguanide,chlorguanide |
Others | Others |
Proguanil, a prophylactic antimalarial drug, inhibits the dihydrofolate reductase of plasmodia and thereby blocks the biosynthesis of pyrimidines and purines, which are essential for DNA synthesis and cell multiplication. | |||
TNU1134 |
7-benzyl-3-methylxanthine
|
||
7-benzyl-3-methylxanthine belongs to Heterocyclic Compounds - Purines. | |||
TNU1262 |
1H-Imidazo[4,5-d]pyridazin-7-amine
|
||
1H-Imidazo[4,5-d]pyridazin-7-amine belongs to Heterocyclic Compounds - Purines; Intermediates and Building Blocks - Nucleoside bases. | |||
TNU0909 |
1,9-Dihydro-9-methyl-6H-purin-6-one
|
||
1,9-Dihydro-9-methyl-6H-purin-6-one belongs to Heterocyclic Compounds - Purines. | |||
TNU1133 |
1,7-Dibenzyl-3-methylxanthine
|
||
1,7-Dibenzyl-3-methylxanthine belongs to Heterocyclic Compounds - Purines. | |||
TNU0907 | 6-Chloro-9-methyl-9H-purine | ||
Heterocyclic Compounds - Purines; Intermediates and Building Blocks - Electrophiles | |||
TNU0908 | 9-Methyladenine | ||
Heterocyclic Compounds - Purines; Intermediates and Building Blocks - Nucleophiles | |||
TNU0900 |
2-Amino-6-ethoxypurine
|
||
Heterocyclic Compounds –Purines; Intermediates and Building Blocks - Nucleoside bases | |||
TNU1104 |
6-Chloro-2-(trifluoromethyl)-9H-purine
|
||
Heterocyclic Compounds - Purines; Intermediates and Building Blocks - Nucleoside bases; Multi-functional; Scaffolds and Templates | |||
TNU0611 |
4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidine
|
||
Heterocyclic compound –purines, intermediate and building block; Used for modified nucleosides and nucleic acids | |||
T35413 |
(6R,S)-5,6,7,8-Tetrahydrofolic Acid (hydrochloride)
|
||
(6R,S)-5,6,7,8-Tetrahydrofolic acid (THFA), the reduced form of folic acid, serves as a cofactor in methyltransferase reactions and is the major one-carbon carrier in one carbon metabolism. Its metabolites participate in the synthesis of thymidine for incorporation into DNA or the synthesis of purines, as well as in the formation of methionine, which can be converted to the ubiquitous methyl donor, S-adenosylmethionine . THFA has also been used to study the activation of metabolite-binding ribos... | |||
T63240 | Lometrexol disodium | ||
Lometrexol (DDATHF) disodium 是人丝氨酸羟甲基转移酶 1/2 (hSHMT1/2) 的有效抑制剂,也是抗嘌呤类抗叶酸 (antifolate) 药,能够降低甘氨酰胺核糖核苷酸甲酰基转移酶 (GARFT) 的活性,但不引起可检测水平的 DNA 链断裂。Lometrexol disodium 对嘌呤从头合成具有抑制作用,可造成异常的细胞增殖,凋亡 (apoptosis) 和细胞周期停滞,表现出抗癌效果。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4746 |
Purine
7H-Imidazo(4,5-d)pyrimidine,嘌呤 |
Others; Endogenous Metabolite | Metabolism; Others |
Purine (7H-Imidazo(4,5-d)pyrimidine) 是内源性代谢产物的一种。 |