| DC8550 |
MCB-613
Featured
|
MCB-613 is a novel and potent stimulator of p160 steroid receptor coactivators (SRCs). It is a Pan-SRCs stimulator. |
|
| DC23706 |
Netoglitazone(MCC 555)
Featured
|
Netoglitazone, also known as isaglitazone and MCC-555, is an agent belonging to the glitazone class of antidiabetic agents with antihyperglycemic activity. Netoglitazone exerts both peroxisome proliferator-activated receptor (PPAR) alpha and gamma agonist activity. Netoglitazone decreases bone formation and increases marrow adipocyte formation in vivo.MCC 555 (Isaglitazone. |
|
| DC26109 |
MCL0129 tetrahydrochloride
Featured
|
MCL0129 is a selective, potent melanocortin-4 receptor (MC4R) antagonist with Ki of 7.9 nM, without affinity for MC1 and MC3. |
|
| DC26085 |
MCL0129 |
MCL0129 is a selective, potent melanocortin-4 receptor (MC4R) antagonist with Ki of 7.9 nM, without affinity for MC1 and MC3. |
|
| DC22643 |
Mcl1-IN-2 |
Mcl1-IN-2 is an Mcl-1 inhibitor without a reported IC50 value.. |
|
| DC20444 |
Mcl-1-Puma inhibitor 8 |
Mcl-1-Puma inhibitor 8 is a small-molecule dual-acting compound that targets the apoptotic Mcl-1-PUMA interface with Ki of 0.3 uM (Mcl-1, FPA), reduces multiple cancer cells and inhibits PUMA-mediated apoptosis. |
|
| DC10353 |
MCOPPB triHydrochloride |
MCOPPB 3Hcl is a nociceptin receptor agonist with pKi of 10.07; weaker activity at other opioid receptors. |
|
| DC23820 |
MCP110
Featured
|
MCP110 is a potent Ras/Raf-1 interaction inhibitor. |
|
| DC23644 |
MCT1-IN-4a |
MCT1-IN-4a is a potent, selective monocarboxylate transporter 1 (MCT1) inhibitor with IC50 of 90 nM. |
|
| DC7841 |
MDA 19 |
MDA 19 is a selective human CB2 receptor agonist with Ki of 43.3 nM. |
|
| DC12581 |
MDI-2268
Featured
|
MDI-2268 (MDI2268) is a small-molecule, in vivo-active inhibitor of plasminogen activator inhibitor type-1 (PAI-1), demonstrates excellent pharmacokinetics, potent activity against vitronectin-bound PAI-1 in vivo, and efficacy in murine model of venous thrombosis. |
|
| DC7743 |
Mdivi-1
Featured
|
Mdivi-1 is a selective cell-permeable inhibitor of mitochondrial division DRP1 (dynamin-related GTPase) and mitochondrial division Dynamin I (Dnm1) with IC50 of 1-10 μM. |
|
| DC10569 |
MDK1088（T.cruzi Inhibitor）
Featured
|
MDK-1088, also known as T.cruzi Inhibitor, is a Trypanosoma cruzi inhibitor. MDK-1088 has CAS#1350920-22-7 . The last 4 digit f CAS# was used in its name. |
|
| DC10573 |
MDK34597 (PI3K inhibitor)
Featured
|
MDK34597 is a PI3K inhibitor.MDK34597 is an analog of PI-103 and acts as a dual PI3K/mTOR Inhibitor. |
|
| DC10572 |
MDK35833（Oct3/4-inducer-1）
Featured
|
MDK35833, also known as Oct3/4-inducer-1, is a potent Oct3/4-inducer. |
|
| DC24209 |
MDK7229(MD2-IN-1)
Featured
|
MDK7229, also known as MD2-IN-1 is a MD2 (Myeloid differentiation protein 2) inhibitor. |
|
| DC10570 |
MDK74978（Multi-kinase inhibitor）
Featured
|
MDK74978, also known as Multi-kinase inhibitor I, is a Multi-kinase inhibitor. MDK74978 has CAS#778274-97-8. The last 5 digit was used in its name. |
|
| DC10571 |
MDK-8582（Hnps-PLA Inhibitor）
Featured
|
MDK-8582, also known as Hnps-PLA Inhibitor, is an nhibitor of human nonpancreatic secretory Phospholipase A (hnps-PLA). |
|
| DC10650 |
MDVN1003
Featured
|
MDVN1003 is a potent inhibitor of BTK amd PI3K delta. |
|
| DC23739 |
Meayamycin |
Meayamycin is an analogue of FR901464 that binds to the splicing factor 3b (SF3b) complex and inhibits pre-mRNA splicing, shows picomolar antiproliferative activity against various cancer cell lines and multidrug-resistant cells.. |
|
| DCAPI1081 |
Mecarbinate |
Mecarbinate |
|
| DC9035 |
Meclofenoxate HCl |
Meclofenoxate hydrochloride, an ester of dimethylethanolamine (DMAE) and 4-chlorophenoxyacetic acid (pCPA), has been shown to improve memory, have a mentally stimulating effect, and improve general cognition. |
|
| DC20446 |
Mefuparib hydrochloride(CVL218)
Featured
|
Mefuparib(CVL218) hydrochloride is a potent, highly selective, competitive PARP1/2 inhibitor with IC50 of 3.2/1.9 nM, respectively.CVL218 was more potent than Remdesivir in blocking Coronavirus infection of cells and equally as potent as Remdesivir in blocking replication of virus once it has entered the cells. |
|
| DC7461 |
Meisoindigo
Featured
|
Meisoindigo(Natura-α; N-Methylisoindigotin; Dian III), a derivative of Indigo naturalis, might induce apoptosis and myeloid differentiation of acute myeloid leukemia (AML). |
|
| DC26032 |
Melagatran |
Melagatran is a synthetic, small-peptide direct thrombin inhibitor with anticoagulant activity. |
|
| DC11353 |
MIF-1 |
Melanocyte-stimulating hormone release-inhibiting factor (MSH-R-IF) is a hypothalamic tripeptide that binds to rat striatum (Kd = 4.69 nM) and has diverse biological activities. |
|
| DC8311 |
Meleagrin |
Meleagrin is an antibiotic derived from a deep ocean, penicillin-producingP. chrysogenum. |
|
| DC21274 |
Melflufen |
Melflufen (Melphalan flufenamide, J1) is a novel dipeptide and alkylating prodrug of melphalan, inhibits angiogenesis in vitro and in vivo. |
|
| DC21917 |
MELK inhibitor 17 |
MELK inhibitor 17 is a potent, selective MELK inhibitor with Ki/IC50 of 0.39/3 nM, >100-fold selectivity over CHK1, CAMKK2, NUAK1 and ERK2. |
|
| DCAPI1316 |
Meloxicam (Mobic) |
Meloxicam (Mobic) |
|
