All ProductsDisplaying Products by Catalog Number (3800 - 3899)
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| Cat. No. | 产品名称/活性 |
|---|---|
| 3800 | CD 2665 |
| Selective RARβ/γ antagonist | |
| 3803 | VER 155008 |
| Hsp70 inhibitor | |
| 3804 | NS 1619 |
| KCa1.1 (BK) channel activator | |
| 3805 | Repaglinide |
| Kir6 (KATP) channel blocker | |
| 3806 | MCH (human, mouse, rat) |
| Potent endogenous MCH agonist | |
| 3807 | Disulfiram |
| Reversibly stimulates SERCA Ca2+-ATPase; displays a range of other activities | |
| 3812 | Cl-4AS-1 |
| Steroidal androgen receptor agonist | |
| 3813 | TFM-4AS-1 |
| Selective androgen receptor modulator (SARM) | |
| 3815 | R 568 hydrochloride |
| Positive allosteric modulator of human calcium-sensing receptor (CaSR) | |
| 3817 | MRK 016 |
| α5-selective GABAA inverse agonist | |
| 3818 | TCS 1102 |
| Potent, dual orexin receptor antagonist | |
| 3822 | MM 11253 |
| RARγ-selective antagonist | |
| 3823 | ER 50891 |
| Selective RARα antagonist | |
| 3824 | CD 2314 |
| Selective RARβ agonist | |
| 3826 | 7,8-Dihydroxyflavone |
| TrkB agonist | |
| 3828 | Rufinamide |
| Prolongs inactivation of sodium channels; anticonvulsant | |
| 3829 | UK 78282 hydrochloride |
| Blocker of KV1.3 and KV1.4 channels | |
| 3834 | KH 7 |
| Selective soluble adenylyl cyclase inhibitor | |
| 3836 | JZL 184 |
| Potent MAGL inhibitor | |
| 3837 | CCMI |
| Positive allosteric modulator of α7 nAChRs | |
| 3842 | 5-Azacytidine |
| DNA methyltransferase inhibitor | |
| 3843 | Cyclic Pifithrin-α hydrobromide |
| p53 inhibitor | |
| 3845 | Thiazovivin |
| ROCK inhibitor; improves the efficiency of fibroblast reprogramming and induction of iPSCs | |
| 3850 | Sodium butyrate |
| Histone deacetylase inhibitor | |
| 3852 | Tranylcypromine hydrochloride |
| Irreversible inhibitor of LSD1; also inhibits MAO | |
| 3854 | 1-Oleoyl lysophosphatidic acid sodium salt |
| Endogenous agonist of LPA1 and LPA2 | |
| 3857 | Dexrazoxane hydrochloride |
| Topoisomerase II inhibitor | |
| 3858 | CH 223191 |
| Potent aryl hydrocarbon receptor (AhR) antagonist | |
| 3861 | UNC 0224 |
| Potent G9a and GLP inhibitor | |
| 3863 | Trovafloxacin mesylate |
| Antibiotic; inhibits bacterial DNA synthesis | |
| 3864 | Oxcarbazepine |
| Anticonvulsant; inhibits Na+ channel activity | |
| 3865 | Licarbazepine |
| Active metabolite of oxcarbazepine (Cat. No. 3864) | |
| 3866 | SKF 86466 hydrochloride |
| Potent and selective α2 antagonist | |
| 3869 | TCS 2002 |
| Potent GSK-3β inhibitor | |
| 3870 | (±)-PPCC oxalate |
| Selective sigma (σ) agonist (σ1> σ2) | |
| 3872 | EHT 1864 |
| Potent Rac family inhibitor | |
| 3873 | MeBIO |
| Inactive analog of BIO (Cat. No. 3194) | |
| 3875 | BCTC |
| TRPV1 antagonist | |
| 3881 | Kisspeptin 234 |
| Kisspeptin receptor antagonist; kisspeptin 10 (Cat. No. 2570) analog | |
| 3884 | MRS 2768 tetrasodium salt |
| Selective P2Y2 agonist | |
| 3887 | PG 01037 dihydrochloride |
| Selective D3 antagonist | |
| 3892 | NF 546 |
| Selective P2Y11 agonist | |
| 3894 | PP 121 |
| Dual kinase inhibitor; inhibits PI 3-K family kinases | |
| 3895 | NS 309 |
| Positive modulator of KCa2 (SK) and KCa3.1 (IK) channels | |
| 3896 | Rotigotine hydrochloride |
| D2 and D3 agonist | |
| 3898 | SF 11 |
| NPY Y2 receptor antagonist | |
| 3899 | JNJ 303 |
| Potent and selective IKs blocker |