All ProductsDisplaying Products by Catalog Number (4300 - 4399)
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| Cat. No. | 产品名称/活性 |
|---|---|
| 4300 | TC 14012 |
| CXCR4 antagonist; ACKR3 (CXCR7) agonist | |
| 4301 | TC-DAPK 6 |
| Potent and selective inhibitor of DAPK1 | |
| 4305 | ICA 069673 |
| KV7.2/KV7.3 channel opener | |
| 4306 | INCB 3284 dimesylate |
| Selective CCR2 antagonist | |
| 4307 | YC 1 |
| Soluble guanylyl cyclase (sGC) activator; induces G1 cell cycle arrest | |
| 4308 | Rasagiline mesylate |
| Selective and irreversible MAO-B inhibitor | |
| 4309 | TPEN |
| Cell-permeable Zn2+ chelator; also inhibits RNA binding protein Lin28 | |
| 4310 | ML 7 hydrochloride |
| Selective inhibitor of myosin light chain kinase | |
| 4311 | GW 542573X |
| Selective KCa2.1 (SK) channel activator | |
| 4312 | Nigericin sodium salt |
| Selective K+ ionophore | |
| 4316 | Bropirimine |
| Immunomodulatory and antitumor compound | |
| 4317 | JNJ 10397049 |
| Selective OX2 antagonist | |
| 4318 | BX 795 |
| PDPK1 (PDK1) inhibitor | |
| 4319 | A 784168 |
| Potent and selective TRPV1 antagonist | |
| 4322 | JH 295 |
| Irreversible Nek2 inhibitor | |
| 4323 | VU 0360172 hydrochloride |
| Positive allosteric modulator of mGlu5 receptors | |
| 4324 | KC7F2 |
| HIF-1α inhibitor; down-regulates HIF-1α protein synthesis | |
| 4325 | Phosphocreatine disodium salt |
| Phosphate reservoir | |
| 4327 | JW 480 |
| Potent and selective inhibitor of serine hydrolase KIAA1363 (AADACL1) | |
| 4330 | AMG 21629 |
| Potent and selective TRPV1 antagonist | |
| 4333 | PSB 1114 |
| Potent, selective P2Y2 agonist | |
| 4334 | PSB 0777 ammonium salt |
| Potent adenosine A2A agonist | |
| 4336 | TG 003 |
| Potent inhibitor of Clk-family kinases; also inhibits DYRK1A/B | |
| 4340 | TAK 779 |
| Potent and selective CCR5 and CCR2 chemokine receptor antagonist | |
| 4341 | A 582941 |
| α7 nAChR partial agonist | |
| 4343 | UNC 0638 |
| Selective G9a and GLP inhibitor | |
| 4346 | Ro 67-7476 |
| Positive allosteric modulator of mGlu1 receptors | |
| 4347 | Ro 67-4853 |
| Positive allosteric modulator of group I mGlu receptors | |
| 4349 | Olanzapine |
| 5-HT2A antagonist; also D2 antagonist; atypical antipsychotic | |
| 4350 | Axitinib |
| Potent VEGFR-1, -2 and -3 inhibitor | |
| 4351 | JHW 007 hydrochloride |
| High affinity dopamine uptake inhibitor | |
| 4353 | TC-G 24 |
| Potent and selective GSK-3β inhibitor | |
| 4355 | TC-F 2 |
| Potent, reversible and selective FAAH inhibitor | |
| 4359 | Lomeguatrib |
| MGMT inhibitor | |
| 4361 | Bosutinib |
| Dual Src-Abl inhibitor; antiproliferative | |
| 4365 | TC-MCH 7c |
| Selective melanin-concentrating hormone receptor 1 (MCH1R) antagonist | |
| 4366 | SAG |
| Potent Smoothened receptor agonist; activates the Hedgehog signaling pathway | |
| 4367 | Psora 4 |
| Potent KV1.3 channel blocker | |
| 4368 | Crizotinib |
| Potent c-MET/ALK inhibitor | |
| 4372 | BC 11 hydrobromide |
| Selective urokinase (uPA) inhibitor | |
| 4374 | BIMU 8 |
| Potent 5-HT4 agonist | |
| 4375 | SMER 3 |
| Selective inhibitor of E3 ubiquitin ligase | |
| 4379 | (S)-(+)-Ketamine hydrochloride |
| NMDA receptor antagonist; enantiomer of ketamine hydrochloride (Cat. No. 3131); neuroprotective | |
| 4380 | WAY 100635 maleate |
| Potent 5-HT1A antagonist; also D4 agonist | |
| 4382 | Letrozole |
| Potent, reversible non-steroidal aromatase inhibitor | |
| 4385 | Donepezil hydrochloride |
| Potent AChE inhibitor | |
| 4387 | Calhex 231 hydrochloride |
| Negative allosteric modulator of calcium-sensing receptor (CaSR) | |
| 4388 | MNI 137 |
| Selective negative allosteric modulator of group II mGlu receptors | |
| 4390 | Thiamet G |
| Potent O-GlcNAcase inhibitor | |
| 4392 | 680C91 |
| Potent and selective tryptophan 2,3-dioxygenase (TDO) inhibitor | |
| 4395 | Moclobemide |
| Reversible MAO-A inhibitor |