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| Catalog | name | Description | price |
|---|---|---|---|
| R-R-3277 | Spiroxatrine CAS No.1054-88-2 | Spiroxatrine (R 5188)/CAS No.1054-88-2 is a selective, dual antagonist of 5-HT1α and α2-adrenergic, with the Ki values of 3.94, 224000, 118.5 nM for 5-HT1α, 5-HT1β and 5-HT2, respectively. Spiroxatrine (R 5188) has a sedative effect. | price> |
| R-C-1578 | JK184 CAS:315703-52-7 | JK-184 is a potent downstream hedgehog(Hh)signaling inhibitor that prevents Gli-dependent transcriptional activity(IC50=30nM).JK184 can specially inhibit Gli in the Hedgehog(Hh)pathway,which showed great promise for cancer therapeutics. | price> |
| R-R-3278 | LY-272015 hydrochloride CAS No.172895-15-7 | LY-272015 hydrochloride/CAS No.172895-15-7 is an orally active, specific 5-HT2B receptor antagonist. LY-272015 hydrochloride completely inhibits the phosphorylation of ERK2 induced by 5-HT or BW723C86. LY-272015 hydrochloride is antihypertensive in Deoxycorticosterone Acetate (DOCA)-salt-hypertensive rats. | price> |
| R-C-1579 | VU0364770 CAS:61350-00-3 | VU 0364770 is a positive allosteric modulator(PAM)of mGlu4 with EC50 of 1.1 μM,exhibits insignificant activity at 68 other receptors,including other mGlu subtypes. | price> |
| R-R-3279 | (E)-3,4,5-Trimethoxycinnamic acid CAS No.20329-98-0 | (E)-3,4,5-Trimethoxycinnamic acid (TMCA)/CAS No.20329-98-0 is a cinnamic acid substituted by multi-methoxy groups. (E)-3,4,5-Trimethoxycinnamic acid is an orally active and potent GABAA/BZ receptor agonist. (E)-3,4,5-Trimethoxycinnamic exhibits favourable binding affinity to 5-HT2C and 5-HT1A receptor, with IC50 values of 2.5 and 7.6 μM, respectively. (E)-3,4,5-Trimethoxycinnamic acid shows anticonvulsant and sedative activity. (E)-3,4,5-Trimethoxycinnamic acid can be used for the research of insomnia, headache and epilepsy. | price> |
| R-C-1580 | VU0361737 CAS:1161205-04-4 | VU 0361737 is a selective positive allosteric modulator(PAM) for mGlu4 receptor with EC50 of 240 nM and 110 nM at human and rat receptors,respectively,displays weak activity at mGlu5 and mGlu8 receptors,is inactive at mGlu1,mGlu2,mGlu3,mGlu6 and mGlu7 receptors,can penetrate into CNS. | price> |
| R-R-3280 | YM348 CAS No.372163-84-3 | YM348/CAS No.372163-84-3 is a potent and orally active 5-HT2C receptor agonist, which shows a high affinity for cloned human 5-HT2C receptor (Ki: 0.89 nM). | price> |
| R-R-3281 | ST1936 CAS No.1210-81-7 | ST1936/CAS No.1210-81-7 is a selective, nanomolar affinity 5-HT6 receptor agonist with Ki values of 13 nM, 168 nM and 245 nM for human 5-HT6, 5-HT7 and 5-HT2B receptors, respectively. ST1936 also shows moderate affinity (Ki of 300 nM) for human and rat α2 adrenergic receptor. | price> |
| R-C-1581 | NU7026 CAS:154447-35-5 | NU7026(LY293646)is a potent DNA-PK inhibitor with IC50 of 0.23 μM in cell-free assays,60-fold selective for DNA-PK than PI3K and inactive against both ATM and ATR.NU7026 enhances G2/M cell arrest and apoptosis. | price> |
| R-C-1582 | Motolimod (VTX-2337) CAS:926927-61-9 | Motolimod(VTX-2337)is a selective and potent Toll-like receptor 8(TLR8)agonist with EC50 of 100 nM,>50-fold selectivity over TLR7. | price> |
| R-R-3282 | (S)-Mirtazapine CAS No.61337-87-9 | (S)-Mirtazapine ((S)-Org3770)/CAS No.61337-87-9 is a S(+)-enantiomer of Mirtazapine with pronociceptive properties in an animal model of acute thermal nociception. (S)-Mirtazapine is a stereoselective 5-HT2 receptor antagonist. (S)-Mirtazapine is metabolized by CYP2D6 and CYP1A2. | price> |
| R-C-1583 | Alvespimycin | Alvespimycin is a heat shock protein 90(Hsp90)inhibitor and promising therapeutic agent for cancer. | price> |
| R-R-3283 | Repinotan hydrochloride CAS No.144980-77-8 | Repinotan hydrochloride (BAY x 3702)/CAS No.144980-77-8 is a potent, selective, brain-penetrant and orally active 5-HT1A receptor agonist, with Ki values of 0.19 nM (calf hippocampus), 0.25 nM (rat and human cortex), and 0.59 nM (rat hippocampus Repinotan hydrochloride has a weak affinity for other related receptors. Repinotan hydrochloride has pronounced neuroprotective effects. | price> |
| R-C-1584 | GRT6005(Cebranopadol) CAS:863513-91-1 | Stop production. | price> |
| R-R-3284 | Clothiapine CAS No.2058-52-8 | Clothiapine/CAS No.2058-52-8, an atypical antipsychotic agent, shares with clozapine its strong antiserotonergic properties. | price> |
| R-C-1585 | VR23 CAS : 1624602-30-7 | VR23 is a small molecule that potently inhibited the activities of trypsin-like proteasomes(IC50=1nM),chymotrypsin-like proteasomes(IC50=50-100nM),and caspase-like proteasomes(IC50=3uM). | price> |
| R-R-3285 | Renzapride CAS No.112727-80-7 | Renzapride (BRL 24924)/CAS No.112727-80-7, a substituted benzamide, is a full 5-HT4 receptor agonist with a Ki value of 115 nM. Renzapride (BRL 24924) is also a 5HT2b and 5HT3 receptor antagonist. Renzapride could be used for constipation predominant irritable bowel syndrome (C-IBS) study. | price> |
| R-C-1586 | TGX-221 CAS:663619-89-4 | TGX-221 is a potent,selective,and cell membrane permeable inhibitor of the PI3K p110β catalytic subunit,used for cancer treatment. | price> |
| R-R-3286 | Dolasetron Mesylate hydrate CAS No.878143-33-0 | Dolasetron Mesylate hydrate (MDL-73147EF hydrate)/CAS No.878143-33-0 is a serotonin 5-HT3 receptor antagonist used to treat nausea and vomiting following chemotherapy. | price> |
| R-C-1587 | T-5224 CAS:530141-72-1 | T-5224 is a selective inhibitor of transcription factor c-Fos/activator protein (AP)-1 with anti-inflammatory effects.T-5224 specifically inhibits the DNA binding activity of c-Fos/c-Jun and the IL-1β-induced up-regulation of Mmp-3,Mmp-13 and Adamts-5 transcription. | price> |

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