Cat. No. | Product name | CAS No. |
DC23342 |
S-Trityl-L-cysteine
S-Trityl-L-cysteine (NSC 83265) is a potent, cell-permeable, selective inhibitor of mitotic kinesin Eg5, inhibits basal ATPase activity (IC50=1 mM) and microtubule-activated ATPase activity of Eg5 (IC50=140 nM). |
2799-07-7 |
DC21709 |
SU 16f
Featured
SU 16f is a potent and selective PDGFRβ inhibitor with IC50 of 10 nM, displays >14-fold, >229-fold and >10,000-fold selectivity over VEGFR2, FGFR1 and EGFR respectively. |
251356-45-3 |
DC9794 |
SU-10994
SU-10994 is a novel VEGFR inhibitor. |
|
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.. |
688036-19-3 |
DC7302 |
SU14813
Featured
SU14813 is an oral, multitargeted tyrosine kinase inhibitor (TKI) targeting vascular endothelial growth factor receptors (VEGFR), platelet-derived growth factor receptors (PDGFR), Kit, and fms-like tyrosine kinase 3 (FLT-3). |
627908-92-3 |
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. |
2126749-48-0 |
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. |
38937-66-5 |
DC12232 |
Suberylglycine
Suberylglycine is an acyl glycine, which is a normally minor metabolite of fatty acid. |
60317-54-6 |
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. |
108392-27-4 |
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 |
54182-58-0 |
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. |
1197054-49-1 |
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. |
2071636-70-7 |
DC9732 |
Sufugolix(TAK-013)
Featured
Sufugolix(TAK-013) is a non-peptide, orally-active, selective antagonist of the gonadotropin-releasing hormone receptor (GnRHR) (IC50 = 0.1 and 0.06 nM for affinity and in vitro inhibition, respectively). |
308831-61-0 |
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 |
127-71-9 |
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. |
1308672-74-3 |
DC10268 |
(+/-)-Sulfinpyrazone
Sulfinpyrazone is one of the most studied platelet COX inhibitors, also a uricosuric agent that competitively inhibits uric acid reabsorption in kidney proximal tubules. |
57-96-5 |
DC10246 |
Sulisobenzone
Sulisobenzone is an ingredient in some sunscreens which protects the skin from damage |
4065-45-6 |
DC10349 |
Sumanirole maleate
Featured
Sumanirole maleate(PNU 95666E; U95666E) is a highly selective D2 receptor full agonist with an ED50 of about 46 nM. |
179386-44-8 |
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. |
314728-85-3 |
DC20205 |
Super-TDU
Featured
Super-TDU is an inhibitory peptide targeting YAP-TEADs interaction. |
1599441-71-0 |
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. |
5424-37-3 |
DC20559 |
Surfen
Surfen is a small molecule antagonist of heparan sulfate, binds to heparin, low molecular weight heparins, and to HS and other GAGs. |
3811-56-1 |