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Other Targets

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Cat. No. Product Name Field of Application Chemical Structure
DC8102 SU6656 Featured SU 6656 is a selective inhibitor of Src kinases, Including Src, Yes, Lyn, and Fyn (IC50 = 280, 20, 130, 170 nM, respectively).
DC21708 SU-11752 SU-11752 is a potent, selective inhibitor of DNA-PK, >500-fold selectivity over PI3Kγ, inhibits DNA double-strand break repair in cells and sensitizs ionizing radiation in cancer cells..
DC9950 SU5614 Featured SU5614 is a potent and selective FLT3 inhibitor.
DC21710 SU-909 Featured SU-909 (SU909, IKKα-IN-48) is a potent, selective IKKα inhibitor with Ki of 0.08±0.07 uM, 10-20-fold selectivity over IKKβ (IC50=1.0±0.28 uM); inhibits FCS-stimulated phosphorylation of p100 in U2OS cells with IC50 of 8.8 uM, inhibits the noncanonical NF-kB pathway without affecting IKKβ-dependent IKappa-Bα loss in the canonical pathway.
DC20177 Suberohydroxamic acid;suberic bishydroxamic acid Suberohydroxamic acid is a competitive HDAC inhibitor with IC50 values of 0.25 and 0.3 μM for HDAC1 and HDAC3 respectively.
DC12232 Suberylglycine Suberylglycine is an acyl glycine, which is a normally minor metabolite of fatty acid.
DC11334 Suc-Ala-Ala-Pro-Abu-pNA trifluoroacetate salt Featured Suc-AAP-Abu-pNA is a chromogenic peptide substrate for pancreatic elastase.It is cleaved by elastase to release p-nitroalinide (p-NA), which can be quantified by colorimetric detection at 405 nm as a measure of enzyme activity.
DC10581 Succinobucol(AGI 1067) Featured Succinobucol is a phenolic antioxidant with anti-inflammatory and antiplatelet effects.
DC10230 Sucralfate Sucralfate is a sucrose sulfate-aluminium complex that binds to the ulcer, creating a physical barrier that protects the gastrointestinal tract from stomach acid and prevents the degradation of mucus
DCAPI1548 Sucralose Sucralose is a low-calorie artificial sweetener.
DC26055 Caspase-1/4 Chromogenic Substrate(Suc-YVAD-pNA) Featured Suc-YVAD-pNA is a colorimetric substrate for caspase-1/interleukin-1β-converting enzyme (ICE) and caspase-4.
DC23770 Sudemycin E Sudemycin E is an alternative splicing inhibitor that binds to the U2 small nuclear ribonucleoprotein (snRNP) component SF3B1, causes a rapid change in alternative pre-messenger RNA splicing.
DC23769 Sudemycin K Sudemycin K is a synthetic antitumor splicing inhibitor with IC50 of 15 nM (MCL1 alternative splicing regulation), shows cytotoxicity in HeLa cells with IC50 of 2.3 nM.
DCAPI1303 Sulbactam Sulbactam
DCAPI1308 Sulbactam sodium (Unasyn) Sulbactam sodium (Unasyn)
DC10264 Sulfabenzamide Sulfabenzamide is an antibacterial/antimicrobial which also exhibit their antitumor effects through multiple mechanisms including inhibition of membrane bound carbonic anhydrases, prevention of microtubule assembly, cell cycle arrest, and inhibition of an
DCAPI1128 Sulfadoxine (Sulphadoxine) Sulfadoxine (Sulphadoxine)
DCAPI1294 Sulfameter (Bayrena) Sulfameter (Bayrena)
DCAPI1071 Sulfamethizole (Proklar) Sulfamethizole (Proklar)
DC9115 Salicylazosulfapyridine Sulfasalazine, a sulfa agent and a derivative of mesalazine, is used primarily as an anti-inflammatory agent.
DCAPI1320 Sulfathiazole Sulfathiazole is an organosulfur compound that has been used as a short-acting sulfa drug.
DC22567 Sulfatinib Featured Sulfatinib (HMPL-012) is a potent, multi-targeted tyrosine kinase inhibitor of VEGFR-1/2/3, FGFR1, CSF1R with IC50 of 2/24/1 nM, 15 nM, 4 nM, respectively.
DCAPI1171 Sulindac (Clinoril) Sulindac (Clinoril)
DC10246 Sulisobenzone Sulisobenzone is an ingredient in some sunscreens which protects the skin from damage
DC10349 Sumanirole maleate Featured Sumanirole maleate(PNU 95666E; U95666E) is a highly selective D2 receptor full agonist with an ED50 of about 46 nM.
DC9550 Sunifiram Sunifiram (DM-235) is a piperazine derived ampakine-like drug which has nootropic effects in animal studies with significantly higher potency than piracetam.
DC20205 Super-TDU Featured Super-TDU is an inhibitory peptide targeting YAP-TEADs interaction.
DCAPI1179 Suprofen (Profenal) Suprofen (Profenal)
DC20560 Surfen hydrate Surfen hydrate is a small molecule antagonist of heparan sulfate, binds to heparin, low molecular weight heparins, and to HS and other GAGs.
DC20559 Surfen Surfen is a small molecule antagonist of heparan sulfate, binds to heparin, low molecular weight heparins, and to HS and other GAGs.

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