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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCY-121 | 20(R)Protopanaxdiol |
>98%,Standard References
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| DCQ-082 | 25-OH-PPD |
>98%,Standard References
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| DCH-060 | Quercetin-3-O-β-D-glucopyranosyl-7-O-β-D-gentiobiosid |
>98%,Standard References
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| DCX-046 | Sipeimine-3β-D-glucoside |
>98%,Standard References
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| DCQ-066 | 13-Dehydroxyindaconintine |
>98%,Standard References
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| DCF-013 | 3,′6-d isinapoyl sucrose |
>98%,Standard References
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| DCZ-251 | Sanguinarine Sulfate |
>98%,Standard References
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| DCY-134 | O-diacetyldaurisoline |
>98%,Standard References
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| DCS-085 | R-Notoginsenoside R2 |
>98%,Standard References
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| DCY-089 | alpha-boswellic acid,3-acetyl |
>98%,Standard References
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| DCY-090 | beta-boswellic acid,3-acetyl,11-keto |
>98%,Standard References
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| DCJ-047 | 25-OCH3-Protopanaxtiol |
>98%,Standard References
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| DCJ-060 | 3’-Methoxy apiin；Chrysoeiol-7-(2-O-apiosylglucoside) |
>98%,Standard References
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| DCJ-068 | Sanguinarine citrate |
>98%,Standard References
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| DCG-023 | Epimeredinoside A |
>98%,Standard References
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| DCY-175 | Icarisid II |
>98%,Standard References
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| DCS-097 | 1,3,5,8-Tetrahydroxylxanthone |
>98%,Standard References
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| DCS-112 | Ochnaflavone7-O-β-D-gluco-pyranoside |
>98%,Standard References
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| DCY-129 | Acetytastragaloside |
>98%,Standard References
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| DCF-009 | beta-rosasterol |
>98%,Standard References
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| DCY-141 | Yejunualactone |
>98%,Standard References
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| DCJ-050 | 3’-methoxy-5’-hydroxyisoflavone-7-O-β-D-glucoside |
>98%,Standard References
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| DCY-113 | Acevaltratum |
>98%,Standard References
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| DCY-142 | Ginkgolic acids |
>98%,Standard References
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| DCZ-129 | Panax notoginsenosides |
>98%,Standard References
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| DCZ-153 | paclitaxtide |
>98%,Standard References
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| DC12522 | MKK7-COV-3 Featured |
MKK7-COV-3 (MKK7 Covalen inhibitor 3) is a potent, selective, covalent MKK7 inhibitor with in vitro IC50 of 5 nM, displays >1,000-fold selectivity over MKK4 (IC50=7.81 uM), shows EC50 of 1.3 uM for reduction of p-JNK in ICW assays in Beas2B cell line, wit
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| DC22215 | RO 27-3225 Featured |
RO 27-3225 (RO27-3225, RO 273225) is a potent, selective melanocortin melanocortin receptor MC4R agonist with EC50 of 1 nM, >30-fold selectivity over MC3R.
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| DC21644 | SHP504 Featured |
SHP504 is a distinct, allosteric site 2 SHP2 inhibitor with IC50 of 21 uM (SHP2 1-525), and selective over the phosphatase domain (SHP2 PTP IC50>100 uM).downregulates DUSP6 mRNA, a downstream MAPK pathway marker, in KYSE-520 cancer cells.
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| DC33598 | GSK-805 Featured |
GSK805, also known as ROR gamma-t-IN-1, is a potent, orally bioavailable retinoid-related orphan receptor gamma t (RORγt) inverse agonist that interacts with the receptor's putative ligand binding domain without exerting significant effects on DNA binding.
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