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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DCC1326 |
Cefmenoxime |
Third-generation, semi-synthetic, beta-lactam cephalosporin antibiotic with antibacterial activity |
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DCC1327 |
Cefonicid |
Second-generation, semi-synthetic, beta-lactam cephalosporin antibiotic with antibacterial activity |
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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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DCC1329 |
Cefotiam |
Third-generation broad spectrum antibiotic against both gram-positive and gram-negative microorganisms |
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DCC1330 |
Cefozopran Hydrochloride |
Fourth-generation cephalosporin |
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DCC1331 |
Cefquinome Sulfate |
Broad-spectrum fourth-generation cephalosporin antibiotic |
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DCC1332 |
Ceftiofur |
beta-Lactamase-stable, broad-spectrum, third-generation cephalosporin antibiotic with antibacterial activity |
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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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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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DCC1335 |
Cemmec13 |
Novel highly selective TAF1 inhibitor |
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DCC1336 |
Cep-14083 |
Novel potent ALK inhibitor. also inhibiting the insulin receptor |
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DCC1337 |
Cep-14513 |
Novel potent ALK inhibitor |
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DCC1338 |
Cep-2563 |
Prodrug of CEP-751 (KT-6587) as antitumor agent, inhibiting protein kinases |
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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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DCC1340 |
Cep-8983 |
Novel selective inhibitor of the nuclear enzymes poly(ADP-ribose) polymerase (PARP) 1 and 2 |
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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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DCC1342 |
Ceph-ams |
Novel small molecule prodrug for use with SEAKER cells, exhibiting enhanced anticancer activity |
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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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DCC1344 |
Cf-ahx-lflv-dpp |
Novel Probe for the High Temperature Requirement A (HTRA) Serine Proteases |
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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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DCC1346 |
Cfi-400936 |
Potent inhibitor of TTK kinase |
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DCC1347 |
Cfi-402257 Hcl |
Novel Highly Potent, Selective, Bioavailable TTK (threonine tyrosine kinase) Inhibitor |
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DCC1348 |
Cg0009 |
Novel GSK3 inhibitor, inducing cell death through cyclin D1 depletion in breast cancer cells |
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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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DCC1350 |
Cg-707 |
Novel PRL-3 inhibitor, blocking the migration and invasion of metastatic cancer cells |
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DCC1351 |
Cga-jk3
Featured
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CGA-JK3 is CGA-JK3 is an ATP-competitive inhibitor of IKKβ-catalyzed kinase activity. CGA-JK3 inhibits IκBα phosphorylation in LPS (HY-D1056) - induced RAW 264.7 cells. |
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DCC1352 |
C-gboxin |
Novel functional Gboxin analogue that is suitable for live-cell ultraviolet crosslink conjugation and click chemistry |
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DCC1353 |
Cgi-560 |
Novel Bruton's tyrosine kinase (BTK) inhibitor |
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DCC1354 |
Cgk062 |
Novel inhibitor of Wnt/β-catenin signaling; Anticancer agent promoting PKCα-mediated β-catenin phosphorylation/degradation |
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