| DC44551 |
Wistin
|
Wistin, isolated from Caragana sinica roots, is a PPARα and PPARγ agonist. |
| DC44550 |
2′-Deoxy-2′-fluoroadenosine
|
2′-Deoxy-2′-fluoroadenosine can be used for the synthesis of 2′-Deoxy-2′-fluoro-modified oligonucleotides hybridized with RNA. 2′-Deoxy-2′-fluoroadenosine can be cleaved efficiently by E. coli purine nucleoside phosphorylase (PNP) to the toxic agent 2-flu |
| DC44549 |
Purine riboside triphosphate
|
Purine riboside triphosphate is a triphosphate derivative of purine riboside. Purine riboside is a naturally occurring base analog which closely resembles adenosine. Purine riboside inhibits carcinogenic growth. Purine riboside strongly inhibits RNA and D |
| DC44548 |
Mps1-IN-1 dihydrochloride
|
Mps1-IN-1 dihydrochloride is a potent, selective and ATP-competitive Mps1 kinase inhibitor, with an IC50 and a Kd of 367 nM and 27 nM. |
| DC44546 |
Ac-rC Phosphoramidite
|
Ac-rC Phosphoramidite is used for the oligoribonucleotide phosphorodithioate modification (PS2-RNA). |
| DC44545 |
Bz-rA Phosphoramidite
|
Bz-rA Phosphoramidite is used for ribonucleotides modification. |
| DC44544 |
1-Hydroxyanthraquinone
|
1-Hydroxyanthraquinone, a naturally occurring compound with oral activity from some plants like Tabebuia avellanedae, exhibits carcinogenic effect. |
| DC44543 |
CCT241533 dihydrochloride
|
CCT241533 dihydrochloride is a potent and selective ATP competitive inhibitor of CHK2 with an IC50 of 3 nM and Ki of 1.16 nM. |
