Cat.No. | Name | Information |
---|---|---|
M39228 | FMoc-D-3-Thienylalanine | FMoc-D-3-Thienylalanine is an alanine derivative. |
M39227 | Fmoc-L-3-Cyanophenylalanine | Fmoc-L-3-Cyanophenylalanine is a phenylalanine derivative. |
M39226 | Fmoc-Asp-Oall | Fmoc-Asp-Oall is an aspartic acid derivative. |
M39225 | FMOC-D-4-Chlorophe | FMOC-D-4-Chlorophe is a phenylalanine derivative. |
M39224 | Fmoc-L-glutamic acid 5-tert-butyl ester | Fmoc-L-glutamic acid 5-tert-butyl ester is a glutamic acid derivative. |
M39223 | Fmoc-D-2-Trifluoromethylphenylalanine | Fmoc-D-2-Trifluoromethylphenylalanine is a phenylalanine derivative. |
M39222 | Echinulin | Echinulin (Echinuline) is a cyclic dipeptide carrying a triprenylated indole moiety. Echinulin contributes to the activation of T cell subsets, which leads to NF-κB activation.Echinulin exerts its immune roles by the NF-κB pathway.Echinulin has the potential to serve as a immunotherapeutic agent. |
M39221 | Sootepin D | Sootepin D (compound 6), a triterpene from the apical bud of Gardenia sootepensis, inhibits TNF-α-induced NF-κB activity with an IC50 of 8.3μM. Sootepin D has anti-inflammatory activity. |
M39220 | Dendrophenol | Dendrophenol (Moscatilin) acts as a NF-κB inhibitor. Antineoplastic activity. |
M39219 | Icariside F2 | Icariside F2 is a potent NF-κB inhibitor with an IC50 value of 16.25 μM. Icariside F2 is an aromatic glycoside isolated from the leaves of E. ulmoides Oliver. Icariside F2 has anti-inflammatory activity. |
M39217 | Laurotetanine | Laurotetanine ((+)-Laurotetanine) is an potent and orally active isoquinoline alkaloid, it exerts an anti-asthmatic effect by inhibition of IgE, histamine, and inflammatory reactions via down-regulating MUC5AC and NF-κB signaling pathways. |
M39216 | Cudraflavone B | Cudraflavone B is a prenylated flavonoid with anti-inflammatory and anti-tumor properties. Cudraflavone B is also a dual inhibitor of COX-1 and COX-2. Cudraflavone B blocks the translocation of nuclear factor κB (NF-κB) from the cytoplasm to the nucleus in macrophages. |
M39214 | Coronalolic acid | Coronalolic acid, extract from the apical bud of Gardenia sootepenesis Hutch, inhibits TNF-α-induced NF-κB activity and NO production. |
M39212 | Stipuleanoside R2 | Stipuleanoside R2 inhibits NF-κB activation stimulated by TNFα in a dose-dependent manner with IC50 value of 4.1 μM. |
M39211 | (Rac)-Myrislignan | (Rac)-Myrislignan is the racemate of Myrislignan. Myrislignan, a lignan isolated from Myristica fragrans Houtt, possesses anti-inflammatory activities. Myrislignan attenuates LPS-induced inflammation reaction in murine macrophage cells through inhibition of NF-kB signalling pathway activation. |
M39210 | 7,8-Didehydrocimigenol | 7,8-Didehydrocimigenol inhibits TNF-α-induced VCAM-1 expression, inhibits NF-kB activity and phosphorylation of ERK1/2 and Akt, increases PPAR-γ expression. 7,8-Didehydrocimigenol can be used for the research of cardiovascular disorders such as atherosclerosis. |
M39209 | Toralactone | Toralactone, isolated from Cassia obtusifolia, mediates hepatoprotection via an Nrf2-dependent anti-oxidative mechanism. |
M39207 | 4′-Hydroxywogonin | 4′-Hydroxywogonin has anti-inflammatory activity via TAK1/IKK/NF-κB, MAPKs and PI3/AKT signaling pathways. 4′-Hydroxywogonin inhibits angiogenesis by disrupting PI3K/AKT signaling. 4′-Hydroxywogonin inhibits cell proliferation and induces apoptosis. |
M39206 | Peucedanocoumarin III | Peucedanocoumarin III is an inhibitor of (alpha)-synuclein and Huntington protein aggregates that enhances the clearance of nuclear and cytoplasmic β23 aggregates and prevents cytotoxicity induced by disease-associated proteins. |
M39205 | Procyanidin B2 3,3'-di-O-gallate | Procyanidin B2, 3,3'-di-O-gallate is an active constituent. Procyanidin B2, 3,3'-di-O-gallate strongly suppresses the constitutive as well as Jagged1 (Notch1 ligand)-induced activated Notch1 pathway. |
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