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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCY-175 | Icarisid II |
>98%,Standard References
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| DCG-023 | Epimeredinoside A |
>98%,Standard References
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| DCJ-068 | Sanguinarine citrate |
>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-047 | 25-OCH3-Protopanaxtiol |
>98%,Standard References
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| DCY-090 | beta-boswellic acid,3-acetyl,11-keto |
>98%,Standard References
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| DCY-089 | alpha-boswellic acid,3-acetyl |
>98%,Standard References
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| DCS-085 | R-Notoginsenoside R2 |
>98%,Standard References
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| DCY-134 | O-diacetyldaurisoline |
>98%,Standard References
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| DCZ-251 | Sanguinarine Sulfate |
>98%,Standard References
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| DCF-013 | 3,′6-d isinapoyl sucrose |
>98%,Standard References
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| DCQ-066 | 13-Dehydroxyindaconintine |
>98%,Standard References
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| DCX-046 | Sipeimine-3β-D-glucoside |
>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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| DCQ-082 | 25-OH-PPD |
>98%,Standard References
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| DCY-121 | 20(R)Protopanaxdiol |
>98%,Standard References
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| DCX-035 | Dihydrocucurbitacin F |
>98%,Standard References
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| DCY-150 | Icarisid I |
>98%,Standard References
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| DCY-135 | Bullatine G |
>98%,Standard References
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| DCY-159 | Isosinensetin；3’,4’ ,5,7,8-pentamethoxyflavone |
>98%,Standard References
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| DCD-075 | 6-O-Caffeoylerigeroside |
>98%,Standard References
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| DCJ-026 | Worenine chloride |
>98%,Standard References
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| DCJ-052 | 7-O-Methylchrysin |
>98%,Standard References
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| DCM-065 | 3-O-galloylmucic acid |
>98%,Standard References
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| DCZ-121 | Vitamin B6 |
>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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| DC39094 | JHU395 |
JHU395 is a novel orally bioavailable GA (glutamine antagonists) prodrug designed to circulate inert in plasma, but permeate and release active GA within target tissues. JHU395 delivers active GA to malignant peripheral nerve sheath tumor (MPNST), and significantly inhibits tumor growth without observed toxicity.
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| DC39081 | BCH |
BCH (LAT1-IN-1) is a selective and competitive inhibitor of system L amino acid transporter 1 (LAT1). BCH (LAT1-IN-1) induces apoptosis in cancer cells.
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