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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4620 | Sb-7720770 Dihydrochloride |
Novel Rho kinase inhibitor
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| DCC4619 | Sb-744941 |
Novel inhibitor of mitogen and Stress-Activated Kinases 1 (MSK1)
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| DCC4618 | Sb-656933 |
Novel CXCR2 selective antagonist, inhibiting ex vivo neutrophil activation and ozone-induced airway inflammation in humans
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| DCC4617 | sb-649915 |
Novel 5-HT1A/B autoreceptor antagonist and serotonin reuptake inhibitor
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| DCC4616 | Sb-414796 |
Potent and selective dopamine D3 receptor antagonist
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| DCC4615 | Sb-390570 |
Novel TRPV4 blocker
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| DCC4614 | Sb-354364 |
AntiMycobacterium tuberculosis agent
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| DCC4613 | Sb-284851-bt |
Selective p38a kinase inhibitor, inhibiting Brd4
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| DCC4612 | Sb-277011a Dihydrochloride |
Selective dopamine D3 receptor antagonist
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| DCC4611 | Sb-267268 |
Nonpeptidic antagonist of alpha(v)beta3 and alpha(v)beta5 integrins, reducing angiogenesis and VEGF expression
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| DCC4610 | Sb2602 |
Novel selective mTOR inhibitor
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| DCC4609 | sb-258719 Hydrochloride |
Selective 5-HT7 receptor antagonist
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| DCC4608 | Sb-243213 Dihydrochloride |
Selective 5-HT2C_receptor>5-HT2C inverse agonist
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| DCC4607 | Sb-239272 |
Inhibitor of p38 MAPK
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| DCC4606 | Sb-226552 |
Potent and selective agonist for the human ß3-adrenoceptor
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| DCC4605 | Sb-220025 Trihydrochloride |
Potent, specific inhibitor of human p38 mitogen-activated protein (MAP) kinase
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| DCC4604 | Sb-209670 |
Dual ETA and ETB receptor antagonist
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| DCC4603 | Sb-203347 |
Selective, active-site-directed 14 kDa PLA2 inhibitor, totally inhibiting LT and PAF formation, while prostanoid formation was not altered
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| DCC4602 | Sb1617 |
Novel neuroprotective agent, suppressing abnormal tau protein aggregation
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| DCC4601 | Sb1495 |
Novel reversible covalent inhibitor of the cyclin-dependent kinase 5 (Cdk5)-mediated phosphorylation of PPARγ at Ser245, a key factor in the insulin-sensitizing effect of PPARγ-targeted drugs
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| DCC4600 | Sb1404 |
PPARγ covalent ligand
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| DCC4599 | Sazetidine-a Dihydrochloride |
Subtype-selective α4β2 nicotinic acetylcholine receptor partial agonist
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| DCC4598 | Saussureamine C |
Inhibitor of H274Y and N294S mutants
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| DCC4597 | Sat-in-3 |
Novel inhibitor of salmonella serine acetyltransferase (SAT), the enzyme that catalyzes the rate-limiting step of L-cysteine biosynthesis
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| DCC4596 | Satavaptan Fumarate |
Selective non-peptide vasopressin V2 receptor antagonist
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| DCC4595 | Satavaptan |
Selective non-peptide vasopressin V2 receptor antagonist
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| DCC4594 | Sars-cov-2 Nsp14/16 Inhibitor 2a |
Novel potent SARS-CoV-2 MTase Nsp14 and Nsp16 inhibitor
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| DCC4593 | Sars-cov-2 Nsp14 Mtase Inhibitor 16 |
Novel SARS-CoV-2 nsp14 Methyltransferase inhibitor
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| DCC4592 | Sars-cov-2 Mpro Inhibitor E24 |
Novel SARS-CoV-2 Main Protease (Mpro) Inhibitor, inhibiting viral replication with a nanomolar EC 50 value (844 nM) in SARS-CoV-2-infected Vero E6 cells, impairing SARS-CoV-2 replication in human lung epithelial cells and human-induced pluripotent stem ce
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| DCC4591 | Sars-cov 3clpro-in-7d |
Novel potent SARS-CoV-2 3CLpro inhibitor with IC 50 value of 73 nM
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