Catalog |
name |
Description |
price |
R-C-577 |
VU 0364439 cas:1246086-78-1 |
VU 0364439 is a positive allosteric modulator(PAM)of mGlu4 receptors(EC50=19.8 nM in vitro for human mGlu4). |
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R-C-579 |
Anamorelin cas:249921-19-5 |
Anamorelin is currently under development for the management of non-small lung cancer associated cachexia/anorexia. |
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R-C-585 |
Linagliptin(BI-1356) cas:668270-12-0 |
Linagliptin (BI-1356) is a highly potent, selective DPP-4 inhibitor with IC50 of 1 nM and exhibits a 10,000-fold higher selectivity for DPP-4 than for other dipeptidyl peptidases such as DPP-2, DPP-8,and DPP-9.Linagliptin activates glomerular autophagy in a model of type 2 diabetes.DPP4 mediates ferroptosis in TP53-deficient CRC cells. |
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R-C-620 |
Vicriviroc Malate cas:541503-81-5 |
Vicriviroc maleate(SCH-417690 maleate;SCH-D maleate) is a potent,selective,oral bioavailable and CNS penetrated antagonist of CCR5,with a Ki of 2.5 nM,and also inhibits HIV-1 in PBMC cells,with IC90s of 3.3 nM (JrFL),2.8 nM (ADA-M), 1.8 nM (301657),4.9 nM (JV1083) and 10 nM (RU 570). |
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R-C-621 |
Maraviroc(Selzentry, UK-427857) cas:376348-65-1 |
Maraviroc (UK-427857) is a CCR5 antagonist for MIP-1α,MIP-1βand RANTES with IC50 of 3.3 nM,7.2 nM and 5.2 nM in cell-free assays,respectively.Maraviroc is used in the treatment of HIV infection. |
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R-C-631 |
MK4305 cas1030377-33-3 |
Suvorexant(MK-4305)is a potent,selective,and orally bioavailable antagonist of OX1R and OX2R currently under clinical investigation as a novel therapy for insomnia. |
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R-C-632 |
Aprepitant (MK-0869) cas:170729-80-3 |
Aprepitant is classified as an NK1 antagonist.Aprepitant has been shown to inhibit both the acute and delayed emesis induced by cytotoxic chemotherapeutic drugs by blocking substance P landing on receptors in the brains neurons.It has also been shown to increase the activity of the 5-HT3 receptor antagonists ondansetron and the corticosteroid dexamethasone,which are also used to prevent nausea and vomiting caused by chemotherapy. |
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R-C-645 |
CP945598(Otenabant ) cas:686344-29-6 |
Otenabant is a potent and selective cannabinoid receptor CB1 antagonist with Ki of 0.7 nM,exhibits 10,000-fold greater selectivity against human CB2 receptor. |
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R-C-720 |
CID-2011756 CAS:638156-11-3 |
CID 2011756 is an ATP competitive PKD inhibitor,with an IC50 of 3.2 µM for PKD1 in cell free assay,and also shows cellular pan-PKD inhibitory activity against PKD2 and PKD3 (IC50,0.6 and 0.7 µM,respectively).CID 2011756 also has antitumor activity. |
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R-C-725 |
tcs1102 CAS No. : 916141-36-1 |
TCS 1102 is a potent,dual orexin receptor antagonist(Ki values are 0.2 and 3 nM for OX2 and OX1 receptors respectively). |
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