All ProductsDisplaying Products by Catalog Number (3300 - 3399)
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| Cat. No. | Product Name / Activity |
|---|---|
| 3300 | SU 5402 |
| Potent FGFR and VEGFR inhibitor | |
| 3301 | NU 6140 |
| Cdk2 inhibitor; also potent inhibitor of aurora kinase A and B | |
| 3302 | CD 3254 |
| Potent and selective RXRα agonist | |
| 3304 | SU 16f |
| Potent and selective PDGFRβ inhibitor | |
| 3308 | Zileuton |
| 5-LOX inhibitor; orally bioavailable | |
| 3309 | Fluvastatin sodium |
| Potent HMG-CoA reductase inhibitor | |
| 3312 | BzATP triethylammonium salt |
| Photoaffinity label for ATPase; also P2X7 agonist and P2X1/P2Y1 partial agonist | |
| 3313 | rac BHFF |
| Potent and selective postitive allosteric modulator of GABAB receptors | |
| 3314 | BI 78D3 |
| Selective, competitive JNK inhibitor | |
| 3316 | PF 670462 |
| Potent and selective CK1ε and CK1δ inhibitor | |
| 3317 | AZ 11645373 |
| Potent and selective human P2X7 antagonist | |
| 3319 | ARL 17477 dihydrochloride |
| Selective nNOS inhibitor | |
| 3323 | AZ 10606120 dihydrochloride |
| Potent P2X7 antagonist | |
| 3324 | QS 11 |
| ARFGAP1 inhibitor; modulates Wnt/β-catenin signaling | |
| 3326 | BGC 20-761 |
| High affinity 5-HT6 antagonist | |
| 3327 | CID 755673 |
| Selective protein kinase D inhibitor | |
| 3328 | Desformylflustrabromine hydrochloride |
| Positive allosteric modulator of α4β2 nAChRs; also muscle-type nAChR inhibitor | |
| 3333 | NDT 9513727 |
| Potent, selective human C5a receptor negative allosteric modulator (NAM) | |
| 3336 | A 769662 |
| Potent AMPK activator | |
| 3337 | CART (55-102) (rat) |
| Neuromodulatory neuropeptide fragment; satiety factor | |
| 3342 | L-798,106 |
| Potent and highly selective EP3 antagonist | |
| 3345 | MLN 4760 |
| Potent and selective angiotensin-converting enzyme 2 (ACE2) inhibitor | |
| 3347 | SNAP 94847 hydrochloride |
| Potent and selective MCH1 antagonist | |
| 3348 | 10Panx |
| Panx-1 mimetic inhibitory peptide; blocks pannexin-1 gap junctions | |
| 3349 | Biocytin |
| Versatile marker for neuroanatomical investigations | |
| 3352 | JNJ 28871063 hydrochloride |
| Potent ErbB receptor family inhibitor | |
| 3354 | PF 429242 dihydrochloride |
| Competitive inhibitor of SREBP site 1 protease | |
| 3356 | WR 1065 dihydrochloride |
| p53 activator. Also ROS scavenger | |
| 3361 | JNJ 17203212 |
| Reversible, competitive and potent TRPV1 antagonist | |
| 3362 | MIRA-1 |
| Restores mutant p53 activity; proapoptotic | |
| 3364 | BIX 01294 |
| GLP and G9a inhibitor | |
| 3367 | AT 101 |
| Downregulates Bcl-2 and Mcl-1; pro-apoptotic | |
| 3368 | SB 271046 hydrochloride |
| Selective 5-HT6 antagonist; orally active | |
| 3369 | AC 55541 |
| Potent and selective PAR2 agonist | |
| 3370 | AC 264613 |
| PAR2 receptor agonist | |
| 3371 | TCS OX2 29 |
| Potent and selective OX2 antagonist | |
| 3373 | Valinomycin |
| Selective K+ ionophore | |
| 3374 | Cortistatin 14 |
| Endogenous neuropeptide; binds sst1 - sst5, ghrelin receptor and MRGPRX2 | |
| 3377 | (d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin |
| Selective vasopressin V1A antagonist | |
| 3378 | EIPA |
| Inhibits TRPP3-mediated currents; also inhibits the Na+/H+ exchanger (NHE) | |
| 3379 | Phenamil |
| Inhibits TRPP3-mediated currents; also inhibits epithelial Na+ channels | |
| 3380 | Benzamil |
| NCX inhibitor, Deg/ENaC channel blocker; amiloride (Cat. No. 0890) derivative | |
| 3383 | VU 152100 |
| Positive allosteric modulator of M4 receptors | |
| 3384 | (Z)-Pugnac |
| O-GlcNAcase and β-hexosaminidase inhibitor | |
| 3387 | Gedunin |
| Hsp90 inhibitor; exhibits anticancer and antimalarial activity | |
| 3392 | VKGILS-NH2 |
| Control peptide for SLIGKV-NH2 (Cat. No. 3010) | |
| 3394 | LRGILS-NH2 |
| Control peptide for SLIGRL-NH2 (Cat. No. 1468) | |
| 3395 | Lestaurtinib |
| JAK2, FLT3 and TrkA inhibitor; also inhibits AurA and AurB | |
| 3396 | Desmopressin |
| Synthetic vasopressin analog; V1B and V2 agonist | |
| 3397 | LY 2365109 hydrochloride |
| Potent and selective GlyT1 inhibitor |