Cat. No. | Product name | CAS No. |
DC12413 |
cIAP1 E3 ligase inhibitor D19-14
cIAP1 E3 ligase inhibitor D19-14 (cIAP1 inhibitor D19-14) is an improved analog of D19, demonstrates significantly increased ability to inhibit cIAP1 autoubiquitination and reduce protein levels of c-MYC in vitro. |
|
DC12285 |
CID 1375606
Featured
CID 1375606 is a surrogate agonist of orphan G protein-coupled receptor GPR27. |
313493-80-0 |
DC22056 |
CID 9998128
CID 9998128 is a potential multi-target drug for the Alzheimer's disease (AD), inhibits the Aβ42 amyloid fibrillization and is capable to clear Aβ42 fibrils. |
733807-13-1 |
DC12243 |
CID-1067700
CID-1067700 is a pan GTPase inhibitor, and competitively inhibits Ras-related in brain 7 (Rab7) with a Ki of 13 nM. |
314042-01-8 |
DC20895 |
CID3528206
CID3528206 is a potent, small molecule yeast TORC1 inhibitor that inhibits TORC1 activity both in vitro and in vivo with IC50 of 150 nM and 3.9 uM, respectively. |
674359-78-5 |
DC7385 |
CID-755673
Featured
CID755673 is a potent and selective cell-active small molecule inhibitor for PKD with an IC50 of 182 nM; exhibits selective PKD1 inhibition when compared with AKT, PLK1, CAK, CAMKIIα, and PKC isoforms. |
521937-07-5 |
DC23753 |
CID888706
CID888706 is a small molecule, pan activator of Rho-family GTPases.. |
496775-95-2 |
DC20904 |
CIDD 0067106
CIDD 0067106 is a novel natural product-based diaryloxazole that potent and selective antiproliferative activities against androgen receptor-positive breast cancer cells (MDA-MB-453 cell GI50=0.8 uM). |
2151865-39-1 |
DC11374 |
Cilastatin
Cilastatin is an inhibitor of dipeptidase (dehydropeptidase I), a renal dipeptidase. |
82009-34-5 |
DC9325 |
Cilazapril (monohydrate)
Featured
Cilazapril Monohydrate is a angiotensin-converting enzyme (ACE) inhibitor used for the treatment of hypertension and congestive heart failure. |
92077-78-6 |
DC20341 |
Ciliobrevin D
Featured
Ciliobrevin D is a cell-permeable, reversible, specific inhibitor of cytoplasmic dynein, blocks dynein-dependent microtubule gliding and ATPase activity while sparing kinesin dependent cellular trafficking. |
1370554-01-0 |
DC9582 |
Cilomilast
Cilomilast(SB 207499; Ariflo) is a potent PDE4 inhibitor with IC50 of about 110 nM, has anti-inflammatory activity and low central nervous system activity. |
153259-65-5 |
DC22028 |
Ciluprevir
Ciluprevir (BILN2061) is a potent HCV NS3/4A protease inhibitor with Ki of 0.66 and 0.30 nM for NS3-NS4A protease of HCV 1b and HCV 1a, respectively. |
300832-84-2 |
DC12134 |
Cimiside B
Cimiside B, a glycoside alkaloid, isolated from the rhizome of Cimicifuga dahurica. |
152685-91-1 |
DC20093 |
Cinchonine ((8R,9S)-Cinchonine; LA40221)
Featured
Cinchonine is a natural compound present in Cinchona bark. Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells. |
118-10-5 |
DC9896 |
Cinnarizine
Featured
Cinnarizine is a medication derivative of piperazine, and characterized as an antihistamine and a calcium channel blocker. |
298-57-7 |
DC21572 |
Cipemastat
Cipemastat (Ro 32-3555) is a potent, second-generation, orally active MMP inhibitor, preferentially inhibits collagenases (MMP-1, -8, and -13) and gelatinase B (MMP-9). |
174265-38-4 |
DC9603 |
Ciprofibrate
Ciprofibrate is a peroxisome proliferator-activated receptor agonist. |
52214-84-3 |
DCAPI1372 |
Ciprofloxacin (Cipro)
Featured
Ciprofloxacin (Bay-09867) is a fluoroquinolone antibiotic, exhibiting potent antibacterial activity. |
85721-33-1 |
DC9466 |
Ciproxifan (maleate)
Featured
Ciproxifan maleate(FUB-359 maleate) is a highly potent and selective histamin H3-receptor antagonist with IC50 of 9.2 nM, with low apparent affinity at other receptor subtypes. |
184025-19-2 |
DC12100 |
Cirsimaritin
Cirsimaritin binds weakly to the benzodiazepine site on GABAA receptors, with antidepressant, anxiolytic and antinociceptive activities. |
6601-62-3 |
DC20342 |
cis Ned-19
cis Ned-19 is the stereoisomer of trans Ned-19, a chemical probe for the Ca(2+)-releasing second messenger NAADP. |
1137264-00-6 |