| Cat.No. | Name | Information |
|---|---|---|
| M4694 | Theobromine | Theobromine is a methylxanthine found in cocoa beans that inhibits adenosine receptor A1 (AR1) signaling. |
| M4693 | Biochanin-A | Biochanin A is A naturally occurring fatty acid amide hydrolase (FAAH) inhibitor that inhibits FAAH in mice, rats and humans with FAAH IC50 of 1.8, 1.4 and 2.4 μM, respectively. |
| M4692 | aurantio-obtusin | Aurantio-obtusin is an anthraquinone compound isolated from cassia seeds, which has anti-inflammatory, antioxidant, anticoagulant and antihypertensive effects. |
| M4690 | 2-O-galloylhyperin | 2-O-galloylhyperin |
| M4689 | Pectolinarin | Pectolinarin has anti-inflammatory activity. Pectolinarin inhibits il-6 and IL-8 secretion and PGE2 and NO production. Pectolinarin can inhibit cell proliferation and inflammatory response and induce apoptosis by inhibiting PI3K/Akt pathway. |
| M4688 | Momordin-Ic | Momordin-Ic is a SENP1 Inhibitor. Momordin Ic induces apoptosis through oxidative stress-regulated mitochondrial dysfunction. |
| M4687 | Secoisolariciresinol-Diglucoside | Secoisolariciresinol diglucoside ((S,S)-SDG), the main lignan in wholegrain flaxseed, is known for its beneficial effects including anti-inflammatory, antioxidant, anti-mutagenic, anti-microbial, anti-obesity, hypolipidemic, and neuroprotective effects. |
| M4686 | Eriodictyol | Eriodictyol is a flavonoid obtained from Chinese herbs, which has antioxidant and anti-inflammatory properties. Eriodictyol can induce Nrf2 signaling pathway. Eriodictyol is also an influenza dependent RNA polymerase inhibitor with an IC50 of 18 nM. |
| M4685 | Obtusifolin | Obtusifolin, a new coumarin from roots of Haplophyllum obtusifolium, regulates the gene expression and production of MUC5AC mucin in airway epithelial cells via inhibiting NF-kB pathway. |
| M4684 | Helicid | The Helicid (Helicide) is the main component of the Helicia nilgirica Bedd. It can be used to promote stability, sleep and pain relief research, it is used in psychoneurosis related research. |
| M4683 | Sclareol | Sclareol was isolated from Salvia sclarea and showed anticancer activity. Sclareol has strong cytotoxic activity against mouse leukemia (P-388), human epidermal carcinoma (KB), and human white blood cells. Sclareol can induce apoptosis. |
| M4682 | Monotropein | Monotropein comes from Morinda Officinalis. Monotropein inhibits the expression of inflammatory factors in a mouse model of colitis induced by sodium dextran sulfate. |
| M4681 | Clinodiside-A | Clinodiside A was isolated from the Chinese herbal medicine Clinopodium chinensis. |
| M4680 | Mollugin | Mollugin is Rubia Cordifolia L. Is a major bioactive ingredient in the. Mollugin has anticancer effects by inhibiting NF-κB activation induced by TNF-α. Mollugin can enhance the osteogenic effect of BMP-2 through the P38-Smad signaling pathway. |
| M4679 | Aloin | Aloin (Aloin-A) is a natural antitumor anthraquinone glycoside with iron chelating and non-atherogenic activities. |
| M4677 | Fargesin | Fargesin is an active new lignan isolated from the magnolia plant with antihypertensive and anti-inflammatory effects. |
| M4676 | Loureirin B | Loureirin B is a flavonoid isolated from The blood tree of Pterygophyllum SPP. It is an inhibitor of PAI-1 with IC50 value of 26.10 μM. Loureirin B can inhibit the phosphorylation of KATP, ERK and JNK at the same time, showing an anti-diabetes effect. |
| M4675 | Cimigenol-3-O-β-D-xylpyranoside | Cimigenoside is an active component of the genus Cohosh. |
| M4674 | Agrimol-B | Agrimol B is a polyphenol derivative isolated from Sepulchrum, which can inhibit fat formation, induce translocation and expression of SIRT1, and reduce the expression of PPARγ. |
| M4673 | Esculentoside-A | Esculentoside A (EsA), a triterpenoid saponin isolated from the root of Phytolacca esculenta. Esculentoside A (EsA) possesses anti-inflammatory activity in acute and chronic experimental models[2], has selective inhibitory activity towards cyclooxygenase-2 (COX-2). |
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