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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC1349 | Cg500354 |
Novel inducer of neural differentiation and growth arrest in human primary GBM-derived cells, playing a tumor-suppressive role via cAMP/CREB signaling pathway
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| DCC1348 | Cg0009 |
Novel GSK3 inhibitor, inducing cell death through cyclin D1 depletion in breast cancer cells
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| DCC1347 | Cfi-402257 Hcl |
Novel Highly Potent, Selective, Bioavailable TTK (threonine tyrosine kinase) Inhibitor
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| DCC1346 | Cfi-400936 |
Potent inhibitor of TTK kinase
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| DCC1345 | Cfg920 |
Novel non-steroid reversible dual inhibitor of CYP17 and CYP11B2 against prostate cancer with fewer cardiac side effects
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| DCC1344 | Cf-ahx-lflv-dpp |
Novel Probe for the High Temperature Requirement A (HTRA) Serine Proteases
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| DCC1343 | Cestrin |
Novel probe for cellulose synthase trafficking, inhibiting cellulose deposition and interferes with the trafficking of cellulose synthase complexes and their associated proteins KORRIGAN1 and POM2/CSI1
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| DCC1342 | Ceph-ams |
Novel small molecule prodrug for use with SEAKER cells, exhibiting enhanced anticancer activity
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| DCC1341 | Cephaeline |
Natural disrupter of RNA G-quadruplexes, inhibiting G-quadruplex-dependent alternative splicing, stimulting the stomach lining and inducing vomiting
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| DCC1340 | Cep-8983 |
Novel selective inhibitor of the nuclear enzymes poly(ADP-ribose) polymerase (PARP) 1 and 2
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| DCC1339 | Cep-32215 |
Novel potent, selective, and orally bioavailable inverse agonist of the histamine H 3 receptor (H 3 R)
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| DCC1338 | Cep-2563 |
Prodrug of CEP-751 (KT-6587) as antitumor agent, inhibiting protein kinases
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| DCC1337 | Cep-14513 |
Novel potent ALK inhibitor
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| DCC1336 | Cep-14083 |
Novel potent ALK inhibitor. also inhibiting the insulin receptor
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| DCC1335 | Cemmec13 |
Novel highly selective TAF1 inhibitor
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| DCC1334 | Cell Death Modulator Dn1 |
Novel modulator of cell death signal transduction pathways, reducing the cytotoxicity of anthrax lethal toxin (LT)
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| DCC1333 | Ceftolozane |
Broad-spectrum, fifth-generation cephalosporin antibiotic, inactivating penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall
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| DCC1332 | Ceftiofur |
beta-Lactamase-stable, broad-spectrum, third-generation cephalosporin antibiotic with antibacterial activity
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| DCC1331 | Cefquinome Sulfate |
Broad-spectrum fourth-generation cephalosporin antibiotic
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| DCC1330 | Cefozopran Hydrochloride |
Fourth-generation cephalosporin
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| DCC1329 | Cefotiam |
Third-generation broad spectrum antibiotic against both gram-positive and gram-negative microorganisms
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| DCC1328 | Cefotetan |
Broad-spectrum, beta-lactamase-resistant, second-generation cephalosporin antibiotic, inhibiting bacterial cell wall synthesis via inhibition of cross-linking of peptidoglycans
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| DCC1327 | Cefonicid |
Second-generation, semi-synthetic, beta-lactam cephalosporin antibiotic with antibacterial activity
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| DCC1326 | Cefmenoxime |
Third-generation, semi-synthetic, beta-lactam cephalosporin antibiotic with antibacterial activity
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| DCC1325 | Cefazolin |
First-generation cephalosporin antibiotic and interleukin 15 inhibitor, specifically interacting with interleukin 15 (IL-15) receptor subunit α (IL-15Rα) and to inhibit IL-15-dependent TNF-α and IL-17 synthesis, showing inhibitory activity against all of
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| DCC1324 | Ceefourin-2 |
Novel highly selective inhibitor of multidrug resistance protein 4 (MRP4)
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| DCC1323 | ceb-52 |
Potent Antagonist for the Human Thyrotropin Receptor (TSHR)
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| DCC1322 | Ce-157119 |
Highly permeable non-Pglycoprotein substrate
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| DCC1321 | Cdm-3032 |
Novel anti-hepatitis B virus (HBV) agent
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| DCC1320 | Cdk-probe-p12 |
Novel photoaffinity probe for cyclin-dependent kinase (CDK) family
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