All ProductsDisplaying Products by Catalog Number (2200 - 2299)
01000200030004000500060007000800090010001100120013001400150016001700180019002000210022002300240025002600270028002900300031003200330034003500360037003800390040004100420043004400450046004700480049005000510052005300540055005600570058005900600061006200630064006500660067006800690070007100720073007400750076007700780079008000810082008300840085008600870088008900
| Cat. No. | 产品名称/活性 |
|---|---|
| 2202 | Zatebradine hydrochloride |
| Blocks hyperpolarization-activated current (If) | |
| 2208 | LY 255283 |
| Selective, competitive BLT2 receptor antagonist | |
| 2216 | des-His1-[Glu9]-Glucagon (1-29) amide |
| Glucagon receptor antagonist | |
| 2220 | FURA-2AM |
| Fluorescent Ca2+ indicator | |
| 2226 | Flutax 1 |
| Green-fluorescent taxol derivative; binds microtubules. Used for: imaging microtubules in live cells. Application: Fluorescent microscopy | |
| 2227 | CI 976 |
| Selective ACAT inhibitor | |
| 2229 | GW 0742 |
| Highly selective, potent PPARδ agonist | |
| 2237 | BRL 50481 |
| Selective PDE7 inhibitor | |
| 2238 | GW 441756 |
| Potent, selective TrkA inhibitor | |
| 2239 | GW 583340 dihydrochloride |
| Potent dual EGFR/ErbB2 inhibitor; orally active | |
| 2250 | SL 0101-1 |
| Selective ribosomal S6 kinase (RSK) inhibitor | |
| 2251 | Cisplatin |
| Potent pro-apoptotic anticancer agent; activates caspase-3 | |
| 2252 | Doxorubicin hydrochloride |
| Antitumor antibiotic agent. Inhibits DNA topoisomerase II | |
| 2253 | Go 6976 |
| Potent protein kinase C inhibitor; selective for α and β isozymes | |
| 2257 | GIP (1-39) |
| Highly potent insulinotropic peptide; GIP agonist | |
| 2258 | GLP-2 (human) |
| Endogenous hormone; displays intestinotrophic activity | |
| 2262 | WRW4 |
| Selective FPR2 antagonist | |
| 2266 | DY131 |
| Agonist selective for estrogen-related receptors ERRβ and ERRγ | |
| 2267 | Lactacystin |
| Cell-permeable, potent and selective proteasome inhibitor | |
| 2268 | NNC 55-0396 dihydrochloride |
| Highly selective CaV3.x blocker | |
| 2270 | SCH 58261 |
| Potent, highly selective A2A antagonist | |
| 2272 | Ro 08-2750 |
| Inhibits NGF binding to p75NTR and TrkA | |
| 2275 | TBB |
| Selective cell-permeable CK2 inhibitor | |
| 2280 | Raloxifene hydrochloride |
| Selective estrogen receptor modulator (SERM) | |
| 2281 | 2'-MeCCPA |
| Highly selective and potent A1 receptor agonist | |
| 2284 | SEW 2871 |
| Cell-permeable, selective S1P1 receptor agonist | |
| 2285 | Go 6983 |
| Broad spectrum PKC inhibitor | |
| 2289 | Lamotrigine isethionate |
| Inhibits glutamate release. Water-soluble salt of lamotrigine (Cat. No. 1611) | |
| 2292 | AQ-RA 741 |
| High affinity and selective M2 antagonist | |
| 2293 | Zebularine |
| DNA methyltransferase and cytidine deaminase inhibitor | |
| 2294 | Cordycepin |
| RNA synthesis inhibitor | |
| 2296 | Prostaglandin E2 |
| Promotes HSCs expansion; increases HSCs engraftment; also endogenous prostaglandin | |
| 2299 | SCH 39166 hydrobromide |
| High affinity D1-like antagonist |