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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2352 | Gsk1379767a |
Novel dual inhibitor of BPTF and Brd4
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| DCC2351 | Gsk1370319a |
Novel specific P2X(7) receptor antagonist
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| DCC2350 | (BrMT)2 |
Non-peptidic snail toxin; Activator of the Kv1.1 potassium ion channel
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| DCC2349 | Gsk-1264 |
Novel allosteric inhibitor of human immunodeficiency virus (HIV) integrase, blocking viral replication and abnormal multimerization involving specific protein domains
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| DCC2348 | Gsk1180781a |
Novel selective inhibitor of MmpL3 mutation
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| DCC2347 | Gsk1104252a |
Potent and selective GPR119 agonist
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| DCC2346 | Gsk1030058a |
Novel inhibitor of polo-like kinase
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| DCC2345 | Gsk1023156a |
Novel inhibitor of polo-like kinase
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| DCC2344 | Gsk1007102b Tfa Salt |
Potent inhibitor of AKT kinase, showing activity against auxotrophic M. tuberculosis and being potentiated with meropenem
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| DCC2343 | Gsk-1004723 |
Novel dual H1 and H3 receptor antagonist with a long duration of action
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| DCC2342 | Gsk1000163a |
Potent inhibitor of AKT kinase
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| DCC2341 | Gsk059a |
Novel potent EchA6 inhibitor
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| DCC2340 | Gsk002 |
Novel allosteric HIV-1 integrase (IN) inhibitor, disrupting formation of mature HIV particles
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| DCC2339 | gsh-mem |
Glutamate receptor antagonist and radical scavenging agent
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| DCC2338 | Gsa-0902 |
Novel high potent and selective stabilizer of the MYC G-quadruplex (G4)
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| DCC2337 | Gs-8374 |
Potent and selective inhibitor of HIV-1 protease, effectively inhibiting protease mutants with amino acid insertions, also inhibiting major aspartyl peptidase 1 (May1), a secreted Cryptococcus neoformans protease
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| DCC2336 | Gs-621763 |
Novel oral prodrug of GS-441524, inhibiting SARS-CoV-2, including variants of concern (VOC) in cell culture and human airway epithelium organoids
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| DCC2335 | Gs-563253 |
Novel Inhibitor of Hepatitis C Viral Infectivity
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| DCC2334 | Gs-441524 Triphosphate (gs-443902 Sodium) |
Novel potent inhibitor of feline infectious peritonitis (FIP) virus in tissue culture and experimental cat infection studies
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| DCC2333 | Grp-156784 |
Novel allosteric inhibitor of respiratory syncytial virus (RSV)
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| DCC2332 | Grl-8234 |
Novel β-Secretase BACE1 Inhibitor, reversing memory impairments and rescuing age-related cognitive decline
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| DCC2331 | Grl-117c |
Novel CCR5 inhibitor, inhibiting the replication of wild-type R5-HIV-1
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| DCC2330 | Grk6-in-18 |
Novel, potent, and selective G protein-coupled receptor kinase 6 (GRK6) inhibitor with an IC50 value of 6 nM against GRK6 and selectivity against a panel of 85 kinases
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| DCC2329 | Grk5-in-2 |
Novel potent G-protein-coupled receptor kinase 5 (GRK5) inhibitor
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| DCC2328 | Grincamycin B |
Natural Potent Inhibitor for Glioblastoma Stem Cell via Targeting RHOA and PI3K/AKT
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| DCC2327 | Grc-6211 |
Novel oral specific TRPV1 antagonist, decreasing bladder overactivity and noxious bladder input in cystitis animal models
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| DCC2326 | Grc-17536 |
Novel orally available, potent and selective inhibitor of Transient Receptor Potential Ankyrin 1 (TRPA1) with IC50 value less than 10 nM
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| DCC2325 | Grayanotoxin Iii |
Natural blocker of the voltage-gated sodium channels located in the cell membrane of neurons
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| DCC2324 | Grassypeptolide A |
Novel Nrf2 modulator via a thus far uncharacterized mechanism
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| DCC2323 | Granisetron |
Potent 5HT3 antagonist
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