All ProductsDisplaying Products by Catalog Number (4200 - 4299)
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| Cat. No. | Product Name / Activity |
|---|---|
| 4202 | Adenine |
| Adenine receptor agonist | |
| 4204 | BTZO 1 |
| MIF binder | |
| 4206 | Valdecoxib |
| Selective and potent COX-2 inhibitor | |
| 4207 | SB 277011A dihydrochloride |
| Selective D3 antagonist | |
| 4213 | SB 297006 |
| Potent and selective CCR3 antagonist | |
| 4214 | Prostaglandin F2α |
| Naturally-occurring prostanoid; potent vasoconstrictor | |
| 4216 | Valsartan |
| High affinity, selective AT1 antagonist | |
| 4219 | Banoxantrone dihydrochloride |
| Prodrug topoisomerase II inhibitor | |
| 4220 | XCC |
| Adenosine receptor antagonist | |
| 4221 | TCS 21311 |
| Potent JAK3 inhibitor. Also inhibits GSK-3β and PKC | |
| 4222 | Dynole 34-2 |
| Dynamin I inhibitor | |
| 4228 | A 286982 |
| Potent inhibitor of the LFA-1/ICAM-1 interaction | |
| 4231 | Nateglinide |
| Kir6 (KATP) blocker; displays high affinity for SUR1/Kir6.2 channels | |
| 4236 | CP 945598 hydrochloride |
| CB1 antagonist | |
| 4237 | PD 184352 |
| Selective MEK inhibitor | |
| 4238 | PF 184 |
| Potent and selective IKKβ inhibitor | |
| 4239 | PF 04217903 mesylate |
| Highly selective MET inhibitor | |
| 4241 | Olopatadine hydrochloride |
| H1 antagonist; ocular antiallergic agent | |
| 4242 | GW 803430 |
| MCH1 antagonist | |
| 4243 | Kisspeptin 10 (rat) |
| Endogenous ligand for kisspeptin receptor | |
| 4245 | Meclizine dihydrochloride |
| Human pregnane X receptor agonist; H1 antagonist | |
| 4247 | Torin 1 |
| Potent and selective mTOR inhibitor | |
| 4248 | Torin 2 |
| Potent and selective mTOR inhibitor | |
| 4249 | A 887826 |
| Potent voltage-dependent NaV1.8 channel blocker | |
| 4253 | TMPyP4 tosylate |
| Inhibitor of human telomerase | |
| 4254 | TAK 715 |
| Potent p38 MAPK inhibitor; anti-inflammatory | |
| 4256 | Tiagabine hydrochloride |
| Selective GAT-1 inhibitor; anticonvulsant | |
| 4257 | PP 242 |
| Dual mTORC1/mTORC2 inhibitor | |
| 4261 | MRS 4062 triethylammonium salt |
| Selective P2Y4 receptor agonist | |
| 4265 | AS 1842856 |
| Potent and selective Foxo1 inhibitor; orally bioavailable | |
| 4266 | ML 141 |
| Selective Cdc42 Rho family inhibitor | |
| 4273 | LRRK2-IN-1 |
| Potent and selective LRRK2 inhibitor | |
| 4274 | AP 24534 |
| Potent multi-kinase and pan-Bcr-Abl inhibitor | |
| 4276 | ERB 041 |
| Potent ERβ agonist | |
| 4277 | PF 477736 |
| Selective Chk1 inhibitor | |
| 4278 | PF 431396 |
| Dual FAK/PYK2 inhibitor | |
| 4279 | PF 3644022 |
| Potent MK2 inhibitor | |
| 4281 | PF 4800567 hydrochloride |
| Selective casein kinase 1ε inhibitor | |
| 4282 | WYE 687 dihydrochloride |
| Potent and selective mTOR inhibitor | |
| 4285 | HBX 41108 |
| Selective USP7 inhibitor | |
| 4287 | Poly(I:C) |
| TLR3 agonist | |
| 4288 | ISO 1 |
| Macrophage migration inhibitory factor (MIF) inhibitor | |
| 4289 | RP 001 hydrochloride |
| Potent S1P1 agonist | |
| 4293 | CID 2745687 |
| GPR35 antagonist | |
| 4295 | VU 0357017 hydrochloride |
| Positive allosteric modulator of M1 receptors | |
| 4297 | SMER 28 |
| Positive regulator of autophagy | |
| 4299 | iCRT 14 |
| Inhibits β-catenin-responsive transcription (CRT) |