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| Catalog | name | Description | price |
|---|---|---|---|
| R-CG-133 | Glycyrrhetinic acid(GA)-peg-N3 | Glycyrrhetinic acid(GA)-peg-N3,Glycyrrhetinic acid-polyethylene glycol-Azide ,GA-PEG-N3 from ruixi.The main functional components of Glycyrrhiza are glycyrrhizic acid. The molecular structure of glycyrrhizic acid contains 1 molecule glycyrrhetinic acid and 2 molecule glucuronic acid. Glycyrrhetinic acid has anti-inflammatory, anti-oxidation, anti-tumor, antibacterial, anti-virus and other functions. | price> |
| R-M-1038 | DABCYL-γ-Abu-Pro-Gln-Gly-Leu-Glu(EDANS)-Ala-Lys-NH₂ | DABCYL-γ-Abu-Pro-Gln-Gly-Leu-Glu(EDANS)-Ala-Lys-NH₂ is a Highly soluble fluorogenic (FRET) matrix metalloproteinase (MMP) substrate . The fluorescence increase is measured using an excitation wavelength of 340 nm and an emission wavelength of 485 nm. Due to the relatively high emission wavelength of EDANS the substrate allows convenient measurement of MMP activity in complex biological media like synovial fluid and culture medium. | price> |
| R-R-1968 | Aloesin CAS No.30861-27-9 | Aloesin (Aloeresin)/CAS No.30861-27-9 is a tyrosinase inhibitor, and shows anti-inflammatory activity, ultraviolet protection, and antibacterium effects. Aloesin can induce apoptosis and be used in ovarian cancer research. | price> |
| R-CG-134 | Glycyrrhetinic acid(GA)-peg-Alkyne | Glycyrrhetinic acid(GA)-peg-Alkyne,Glycyrrhetinic acid-polyethylene glycol-Alkyne ,GA-PEG-Alkyne from ruixi.The main functional components of Glycyrrhiza are glycyrrhizic acid. The molecular structure of glycyrrhizic acid contains 1 molecule glycyrrhetinic acid and 2 molecule glucuronic acid. Glycyrrhetinic acid has anti-inflammatory, anti-oxidation, anti-tumor, antibacterial, anti-virus and other functions. | price> |
| R-M-819 | DABCYL-γ-Abu-Ser-Gln-Asn-Tyr-Pro-Ile-Val-Gln-EDANS trifluoroacetate salt | The fluorogenic HIV-1 protease substrate DABCYL-Gaba-SQNYPIVQ-EDANS consists of an octapeptide with a fluorescent donor (EDANS) and a quenching acceptor (DABCYL), attached at the COOH- and NH₂-termini. The γ-Abu spacer was inserted to avoid potential steric hindrance of substrate binding by the bulky acceptor. This FRET substrate is cleaved by the HIV-1 protease at the Tyr-Pro bond which results in a time-dependent increase in fluorescence intensity; excitation at 340 nm, emission at 490 nm. | price> |
| R-R-1969 | ACA-28 CAS No.948044-25-5 | ACA-28 (compound 2a)/CAS No.948044-25-5 is a potent ERK MAPK signaling modulator. ACA-28 selectively inhibits cancer cell growth by inducing apoptosis with ERK hyperactivation ACA-28 inhibits cell growth of melanoma cells (SK-MEL-28) and normal melanocytes (NHEM), with IC50 values of 5.3 and 10.1 μM, respectively. | price> |
| R-HF-016 | Hyaluronate(HA)-SS-Diacerein,MW:100K | Hyaluronate(HA)-SS-Diacerein MW:100K,Hyaluronate-S-S-Diacerein,MW:100K , Hyaluronate(HA)100k-SS-1,8-Diacetoxy-3-carboxyanthraquinone ,Hyaluronate((HA)100k-SS-Diacerein from ruixi.Disulfide bond has the Glutathione (GSH) reduction response.Ruixi biotech provides high-quality products, which are customized by Ruixi. | price> |
| R-M-820 | Defensin 5 (human) trifluoroacetate salt | Human defensin-5 (HD 5) is a key regulator of gut microbiota homeostasis. HD 5 exhibits microbicidal activity against bacteria, fungi, and viruses and is released by Paneth cells in the small intestine.As a biomarker, HD 5 might be used to distinguish between ulcerative colitis (low levels of HD 5) or Crohn colitis (high levels of HD 5). | price> |
| R-R-1970 | DIM-C-pPhOH CAS No.151358-47-3 | DIM-C-pPhOH/CAS No.151358-47-3 is a nuclear receptor 4A1 (NR4A1) antagonist. DIM-C-pPhOH inhibits cancer cell growth and mTOR signaling, induce apoptosis and cellular stress. DIM-C-pPhOH reduces cell proliferation with IC50 values of 13.6 μM and 13.0 μM for ACHN cells and 786-O cells, respectively. | price> |
| R-CG-135 | Hyaluronate(HA)-Hyd-DOX | Hyaluronate-Hydrazone-Doxorubicin,Hyaluronate(HA)-Hyd-DOX,HA-Hyd-DOX from ruixi.Hydrazone bond has pH response effect. Ha-hyd-dox is used for the acid triggered release of adriamycin via hydrazone bond. The product is a amphiphilic polymer precursor drug, and the prepared nanoparticles have a spherical core-shell structure. Ha hyd DOX nanoparticles have good stability in vitro. The drug release curve shows that DOX release is obviously regulated by pH gradient. | price> |
| R-M-821 | Defensin HNP-1 (human) trifluoroacetate salt,CAS : 148093-65-6 | Defensin HNP-1 (human) trifluoroacetate salt,CAS : 148093-65-6 from ruixi. It is a kind of Antimicrobial peptide. It can be applied to Antimicrobial & Antiviral Peptides. | price> |
| R-R-1971 | 3,6-Dihydroxyflavone CAS No.108238-41-1 | 3,6-Dihydroxyflavone/CAS No.108238-41-1 is an anti-cancer agent. 3,6-Dihydroxyflavone dose- and time-dependently decreases cell viability and induces apoptosis by activating caspase cascade, cleaving poly (ADP-ribose) polymerase (PARP). 3,6-Dihydroxyflavone increases intracellular oxidative stress and lipid peroxidation. | price> |
| R-CG-136 | Hyaluronate(HA)-Hyd-Paclitaxel(PTX) | Hyaluronate-Hydrazone-Doxorubicin,Hyaluronate(HA)-Hyd-DOX,HA-Hyd-DOX from ruixi.Hydrazone bond has pH response effect. Ha-hyd-dox is used for the acid triggered release of adriamycin via hydrazone bond. The product is a amphiphilic polymer precursor drug, and the prepared nanoparticles have a spherical core-shell structure. Ha hyd DOX nanoparticles have good stability in vitro. The drug release curve shows that DOX release is obviously regulated by pH gradient. | price> |
| R-M-822 | Defensin HNP-2 (human) trifluoroacetate salt | Defensin HNP-2 (human) trifluoroacetate salt,CAS :120721-97-3 from ruixi.It is a kind of Antimicrobial peptide , it can be applied to antimicrobial & antiviral peptides. | price> |
| R-R-1972 | GK563 CAS No.2351820-19-2 | GK563/CAS No.2351820-19-2 is a selective Ca2+-independent phospholipase A2 (GVIA iPLA2) inhibitor with an IC50 value of 1 nM. GK563 is 22000 times more active against GVIA iPLA2 than GIVA cPLA2. GK563 reduces β-cell apoptosis induced by proinflammatory cytokines, raising the possibility that it can be beneficial in countering autoimmune diseases, such as type 1 diabetes. | price> |
| R-CG-137 | mPEG-PGA-g-PEI-g-DXMS(20%) | mPEG-PGA-g-PEI-g-DXMS,Methoxy-poly(ethylene glycol)-poly(L-glutamic acid)-graft-Polyethylenimine-graft-Dexamethasone from ruixi.MPEG copolymerized PGA, and then grafted to Pei. Thus, mpeg-pga-g-pei is formed. Then dexamethasone was grafted onto mpeg-pga-g-pei. Finally, the product was prepared into nanoparticles with positive charge for drug delivery system. | price> |
| R-M-823 | Endotrophin (mouse) trifluoroacetate salt,CAS:1678414-54-4 | Endotrophin is a carboxyl-terminal cleavage product of collagen 6 alpha-3 chain which is produced and released by adipocytes and massively upregulated in malignant tumors of breast, liver colon and pancreas. Endotrophin provides a link between obesity and aggressive tumor growth and may serve as sensitive diagnostic marker and valid therapeutic target for designing better strategies to treat cancer and ameliorate obesity-induced insulin resistance. | price> |
| R-R-1973 | Lobetyolin CAS No.129277-38-9 | Lobetyolin/CAS No.129277-38-9, a bioactive compound, is derived from Codonopsis pilosula. Lobetyolin has anti-inflammatory, anti-oxidative and xanthine oxidase inhibiting activities. Lobetyolin also induces the apoptosis via the inhibition of ASCT2-mediated glutamine metabolism. Lobetyolin is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. | price> |
| R-DZPE-001 | mPEG-PGA-g-PEI | Methoxy-poly(ethylene glycol)-poly(L-glutamic acid)-graft-Polyethylenimine,mPEG-PGA-g-PEI from ruixi.Mpeg-pga-g-pei was obtained by copolymerizing PGA with MPEG and grafting it to Pei.Finally, the product has a drug delivery system. | price> |
| R-M-824 | Endothelin (16-21) trifluoroacetate salt,CAS : 121377-67-1 | The endothelin C-terminal fragment HLDIIW was found to be a full agonist at ET-B receptors while being inactive or weakly active at ET-A receptors. The tryptophan in position 21 played a key role in the activity of ET (16-21) at the ET-B receptors. | price> |

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