Cat. No. | Product name | CAS No. |
DC20328 |
C5-benzyl SAHA
C5-benzyl SAHA is a C5-modified SAHA analog that displays dual selectivity to HDAC6 (IC50=0.27 uM) and HDAC8 (IC50=0.38 uM) over HDAC 1, 2, and 3 (IC50=2.9-5.8 uM). |
2115700-64-4 |
DC10419 |
C 87
C87 is a novel small-molecule TNFα inhibitor; potently inhibits TNFα-induced cytotoxicity with an IC50 of 8.73 μM. |
332420-90-3 |
DC8704 |
Ca2+ channel agonist 1
Ca2+ channel agonist 1 is a N-type Ca2+ channel activity agonist, with EC50 of 14.23 uM, also inhibits cdk2 kinase activity with EC50 of 3.34 uM. |
1402821-24-2 |
DC4186 |
Cabazitaxel
Cabazitaxel (Jevtana, XRP6258) is a semi-synthetic derivative of a natural taxoid. |
183133-96-2 |
DC9423 |
Cabergoline
Cabergoline, an ergot derivative, is a potent dopamine receptor agonist on D2 receptors. |
81409-90-7 |
DC20856 |
CAD-031
Featured
CAD-031 (CAD31) is a novel brain penetrant, J147-derivative that has enhanced neurogenic activity over J147 in human neural precursor cells (NPCs). |
2071209-49-7 |
DC12253 |
Calcium polystyrene sulfonate (Poly(styrenesulfonic acid) calcium salt)
Calcium polystyrene sulfonate is an ion-exchange resin used for reducing blood levels of potassium. Calcium polystyrene sulfonate is used to treat hyperkalemia in patients with chronic kidney disease (CKD). |
37286-92-3 |
DC9386 |
Calcium-Sensing Receptor Antagonists I
Calcium-Sensing Receptor Antagonists I is an antagonist of calcium-sensing parathyroid hormone receptors. |
478963-79-0 |
DC20857 |
Calhex-231
Featured
Calhex-231 is a potent negative allosteric modulator of CaSR that blocks calcium-mediated activation with IC50 of 0.39 uM. |
652973-93-8 |
DC20329 |
Calindol hydrochloride
Calindol hydrochloride is a calcimimetic acting agent and positive allosteric modulator (agonist) of CaSR with EC50 of 0.31 uM (stimulated 3H IP accumulation in CHO cells at 2 mM Ca2+). |
729610-18-8 |
DC20021 |
Calmidazolium chloride (R 24571)
Featured
Calmidazolium chloride (R 24571) is a calmodulin (CaMK) antagonist, antagonizing CaM-dependent phosphodiesterase and calmodulin-induced activation of erythrocyte Ca2+-transporting ATPase with IC50s of 0.15 and 0.35 μM, respectively. Also in anti-cancer re |
57265-65-3 |
DC7095 |
W-7 hydrochloride
Featured
Calmodulin antagonist. Inhibits Ca2+-calmodulin-dependent phosphodiesterase (IC50 = 28 μM) and myosin light chain kinase (IC50 = 51 μM). |
61714-27-0 |
DC22045 |
CAM4066
CAM4066 (CAM-4066) is a potent and selective CK2α inhibitor with Kd of 0.32 uM and IC50 of 0.37 uM, shows significantly improved selectivity compared to other CK2α inhibitors. . |
2101206-81-7 |
DC22046 |
CAM4712
CAM4712 (CAM-4712) is a potent and selective CK2α inhibitor with IC50 of 7 uM, exhibits cell growth inhibition in HCT116 cell line with IC50 of 10 uM. |
|
DC20330 |
CAMKK2 inhibitor 4t
CAMKK2 inhibitor 4t is a potent, selective, orally available, brain-penetrant CAMKK2 inhibitor with pIC50 of 8.5. |
|
DC10377 |
Campesterol
Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects. |
474-62-4 |
DC6701 |
Camptothecine
Camptothecin (CPT) is a potent DNA enzyme topoisomerase I (topo I) inhibitor with an IC50 and IC70 of 50 nM and 0.225 μM for breast cancer cell line MDA-MB-231. |
7689-03-4 |
DC20859 |
CAN-508
Featured
CAN-508 is a potent, selective CDK9 inhibitor with IC50 of 0.35 uM (CDK9/cyclin T1), displays >35 fold selectivity over CDK1/2/4/7 (IC50=13.5-70 uM). |
140651-18-9 |
DC7825 |
Canagliflozin hemihydrate
Canagliflozin 0.5 H2O(JNJ 28431754; TA 7284) is a highly potent and selective SGLT2 inhibitor for hSGLT2 with IC50 of 2.2 nM, exhibits 413-fold selectivity over hSGLT1. |
928672-86-0 |
DC8553 |
Canertinib
Featured
Canertinib (CI-1033) is a pan-ErbB inhibitor for EGFR and ErbB2 with IC50 of 1.5 nM and 9.0 nM, no activity to PDGFR, FGFR, InsR, PKC, or CDK1/2/4. Phase 3. CI-1033 shows excellent potency for irreversible inhibition of erbB2 autophosphorylation in MDA-MB |
267243-28-7 |
DC4154 |
Capecitabine
Featured
Capecitabine is a tumor-selective fluoropyrimidine carbamate which achieves higher intratumoral 5-FU level with lower toxicity than 5-FU. |
154361-50-9 |
DC26044 |
Caprooyl-Tetrapeptide-3
Caprooyl tetrapeptide-3 is a derivative of tetrapeptide-3 that is linked to caproic acid. |
1012317-71-3 |