产品编号 | 产品名称 | CAS No. |
DC9577 |
Olprinone (Hydrochloride)
Olprinone Hcl(Loprinone Hcl) is a selective phosphodiesterase 3 (PDE3) inhibitor. |
119615-63-3 |
DC9600 |
Senicapoc
Senicapoc(ICA17043) is a potent and selective Gardos channel blocker; blocked Ca(2+)-induced rubidium flux from human RBCs/ inhibited RBC dehydration with IC50s of 11 nM/30 nM, respectively. IC50 value: 11/30 nM [1] Target: Gardos channel in vitro: I |
289656-45-7 |
DC9604 |
Desogestrel
Desogestrel(Org-2969) is a third-generation 19-nortestosterone derivative progestogen; is contained in many oral contraceptive preparations, both combined (COCs) to ethinyl-estradiol (EE) or alone in a progestin-only pill (POP). |
54024-22-5 |
DC9611 |
PI-1840
PI-1840 is a potent and selective inhibitor for chymotrypsin-like (CT-L) (IC50 value = 27 ± 0.14 nM) over trypsin-like and peptidylglutamyl peptide hydrolyzing (IC50 values >100 μM) activities of the proteasome. |
1401223-22-0 |
DC9635 |
SB-705498
SB-705498 is a potent, selective and orally bioavailable transient receptor potential vanilloid 1 (TRPV1) receptor antagonist with a pIC50 of 7.1. |
501951-42-4 |
DC9679 |
BAY1217389
BAY1217389 is an orally bioavailable, selective inhibitor of the serine/threonine kinase monopolar spindle 1 (Mps1, TTK), with potential antineoplastic activity. |
1554458-53-5 |
DC9692 |
Volitinib(Savolitinib)
Savolitinib(Volitinib; AZD-6094; Volitinib) is an orally bioavailable inhibitor of the c-Met receptor tyrosine kinase(IC50= 5 nM) with potential antineoplastic activity. |
1313725-88-0 |
DC9710 |
SRT3025
SRT3025 is a sirt1 activator. |
1231952-55-8 |
DC9859 |
GAL-021
GAL-021 is a new intravenous BKCa-channel blocker. |
1380341-99-0 |
DC9879 |
AZD8835
AZD8835 ia a novel mixed inhibitor of PI3Kα and PI3Kδ with IC50 of 6.2 nM and 5.7 nM, respectively, also with selectivity against PI3Kβ (IC50=431 nM) and PI3Kγ (IC50=90 nM). |
1620576-64-8 |
DC9948 |
SNX-5422(PF04929113)
PF-04929113 (SNX-5422) is a potent and selective Hsp90 inhibitor (Kd of 41 nM). PF-04929113 also inhibits Her-2 degradation (IC50 of 37 nM). |
908115-27-5 |
DCAPI1014 |
Eplerenone
Eplerenone |
107724-20-9 |
DCAPI1021 |
Cidofovir(Vistide)
Cidofovir(Vistide) |
113852-37-2 |
DCAPI1022 |
Dofetilide (Tikosyn)
Dofetilide (Tikosyn) |
115256-11-6 |
DCAPI1025 |
Dexamethasone
Dexamethasone is a potent synthetic member of the glucocorticoid class of steroid drugs used as an anti-inflammatory and immunosuppressant. |
1950-2-2 |
DCAPI1032 |
Dichlorphenamide (Diclofenamide)
Dichlorphenamide (Diclofenamide) |
120-97-8 |
DCAPI1056 |
Nattokinase
Nattokinase |
133876-92-3 |
DCAPI1064 |
Gentamycin sulfate (Gentacycol)
Gentamycin sulfate (Gentacycol) |
1405-41-0 |
DCAPI1080 |
Istradefylline (KW-6002)
Istradefylline(KW6002) is a very potent, selective and orally active adenosine A2A receptor antagonist(Ki=2.2 nM) in experimental models of Parkinson's disease. |
155270-99-8 |
DCAPI1084 |
Ezetimibe (Zetia)
Ezetimibe (Zetia) |
163222-33-1 |
DCAPI1177 |
Salubrinal
Salubrinal is a selective inhibitor of eIF2α dephosphorylation and inhibits ER stress-mediated apoptosis with EC50 of ~15 μM. |
405060-95-9 |
DCAPI1196 |
Eltrombopag (SB-497115-GR)
Eltrombopag (SB-497115-GR) |
496775-61-2 |