| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC22584 | Mavorixafor(AMD-070) Featured | A potent and selective antagonist of CXCR4 with IC50 of 13 nM in a CXCR4 125I-SDF inhibition binding assay. |
|
| DC11667 | PF-592379 | A potent, selective, orally active agonist of dopamine D3 receptor with EC50 of 21 nM. |
|
| DC5083 | Cinacalcet (AMG-073) HCl Featured | AMG-073 HCl (Cinacalcet HCl) represents a new class of compounds for the treatment of hyperparathyroidism. |
|
| DC7357 | Anamorelin Featured | Anamorelin(RC1291; ONO-7643) is a synthetic orally active ghrelin receptor agonist which is under development for the management of non-small lung cancer associated cachexia/anorexia. |
|
| DC11095 | ATR-101 free base | ATR-101 (PD-132301, Nevanimibe) is a selective and potent inhibitor of ACAT1 with IC50 of 52 nM. |
|
| DC8799 | Avanafil(TA-1790) Featured | Avanafil(TA-1790) is a potent and highly selective phosphodiesterase-5(PDE-5) inhibitor(IC50=5.2 nM) for erectile dysfunction; lower selectivity against PDE1, PDE6, and PDE11. |
|
| DC8801 | Cinacalcet (AMG-073) Featured | Cinacalcet(AMG-073) is an orally active, second-generation calcimimetic compound; AMG 073 represents a new class of compounds for the treatment of hyperparathyroidism. |
|
| DCAPI1241 | Doxercalciferol (Hectorol) Featured | Doxercalciferol is a synthetic vitamin D2 analog, suppressing parathyroid synthesis and secretion, used to treat secondary hyperparathyroidism and metabolic bone disease. |
|
| DC8177 | Enclomiphene citrate Featured | Enclomiphene is a non-steroidal estrogen receptor antagonist that promotes gonadotropin-dependent testosterone secretion by the testes. |
|
| DC7020 | Ibutamoren mesylate Featured | Ibutamoren mesylate (MK-0677) is an orally active nonpeptide growth hormone (GH) secretagogue. |
|
| DC6577 | Paricalcitol | Paricalcitol |
|
| DC10531 | PCO371 Featured | PCO371 is a novel, orally active small molecule that acts as a full agonist of PTHR1. |
|
| DC11664 | PF-00446687 hydrochloride | PF-00446687 hydrochloride (PF-446687) is a potent, selective melanocortin-4 receptor (MC4R) agonist with EC50 of 12 nM. |
|
| DC11665 | PF-00446687 | PF-00446687(PF-446687) is a potent, selective melanocortin-4 receptor (MC4R) agonist with EC50 of 12 nM. |
|
| DC7480 | PF-3274167（cligosiban） Featured | PF-3274167 is a high-affinity nonpeptide oxytocin receptor (OTR) antagonist, with Ki of 9.5 nM. |
|
| DC5901 | Tadalafil Featured | Tadalafil is a potent and selective inhibitor of Phosphodiesterase-5 (PDE5) This compound prevents the breakdown of phosphodiesterases, many of which are used as secondary messengers. By preventing the breakdown of these messenger molecules, tadalafil can |
|
| DC4133 | Udenafil | Udenafil is a new phosphodiesterase type 5 (PDE5) inhibitor used to treat erectile dysfunction (ED) |
|
