All ProductsDisplaying Products by Catalog Number (2400 - 2499)
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| Cat. No. | Product Name / Activity |
|---|---|
| 2400 | FK 888 |
| High affinity NK1 antagonist | |
| 2402 | MRS 2211 |
| Competitive P2Y13 antagonist | |
| 2408 | Ro 90-7501 |
| Inhibitor of Aβ42 fibril formation | |
| 2410 | L-371,257 |
| Potent and selective oxytocin receptor antagonist | |
| 2411 | A-71623 |
| Potent and selective CCK1 agonist; suppresses feeding | |
| 2412 | BIBO 3304 trifluoroacetate |
| Highly selective NPY Y1 receptor antagonist | |
| 2414 | H 1152 dihydrochloride |
| Selective Rho-kinase (ROCK) inhibitor | |
| 2420 | [Pyr1]-Apelin-13 |
| Potent peptide apelin agonist | |
| 2426 | Apelin-36 (human) |
| Endogenous apelin agonist | |
| 2430 | GGTI 298 |
| Geranylgeranyltransferase I (GGTase I) inhibitor | |
| 2435 | CCT 018159 |
| Hsp90 inhibitor | |
| 2440 | NNC 26-9100 |
| Selective sst4 agonist | |
| 2441 | JNJ 10191584 maleate |
| Selective H4 antagonist; orally active | |
| 2442 | CGP 53353 |
| Selective inhibitor of PKCβII | |
| 2443 | RITA |
| MDM2-p53 interaction inhibitor | |
| 2450 | NF 157 |
| Selective P2Y11 and P2X1 antagonist | |
| 2451 | LY 344864 hydrochloride |
| Potent and selective 5-HT1F agonist | |
| 2453 | LY 379268 |
| Highly selective group II mGlu agonist | |
| 2456 | Co 101244 hydrochloride |
| GluN2B-selective NMDA antagonist | |
| 2458 | ZM 447439 |
| Inhibits Aurora kinase B | |
| 2459 | Tropisetron hydrochloride |
| Potent 5-HT3 antagonist; also α7 nAChR partial agonist | |
| 2460 | Lazabemide hydrochloride |
| Selective MAO-B inhibitor | |
| 2463 | SCH 442416 |
| Very selective, high affinity A2A antagonist | |
| 2464 | TNP-ATP triethylammonium salt |
| Potent and selective P2X antagonist | |
| 2465 | SDZ WAG 994 |
| Potent and selective A1 agonist | |
| 2466 | UK 14,304 tartrate |
| α2 agonist. Water-soluble form of UK 14,304 (Cat. No. 0425) | |
| 2471 | ER 27319 maleate |
| Selective Syk kinase inhibitor | |
| 2472 | Triacsin C |
| Inhibitor of acyl-CoA synthetase | |
| 2473 | GW 4064 |
| Selective farnesoid X receptor (FXR) agonist | |
| 2474 | GW 3965 hydrochloride |
| Orally active liver X receptor (LXR) agonist | |
| 2475 | ZM 323881 hydrochloride |
| Potent, selective inhibitor of VEGFR-2 | |
| 2476 | SR 11302 |
| AP-1 inhibitor; antitumor agent | |
| 2478 | 2-Pyridylethylamine dihydrochloride |
| H1 agonist | |
| 2479 | JTE 907 |
| Selective CB2 receptor inverse agonist | |
| 2481 | JTC 801 |
| Selective NOP antagonist | |
| 2485 | Glycyl-H 1152 dihydrochloride |
| Selective Rho-kinase (ROCK) inhibitor. More selective analog of H 1152 dihydrochloride (Cat. No. 2414) | |
| 2489 | C 75 |
| Potent fatty acid synthase inhibitor; proapoptotic | |
| 2490 | (±)-Clopidogrel hydrochloride |
| Selective P2Y12 antagonist | |
| 2494 | VUF 8430 dihydrobromide |
| Potent and high affinity H4 agonist | |
| 2498 | PNU 120596 |
| Positive allosteric modulator of α7 nAChRs; active in vivo |