| Cat.No. | Name | Information |
|---|---|---|
| M4531 | Rosiridin | Rosiridin inhibits MAO A and MAO B and has A potential role in depression and alzheimer's disease. The inhibition rate of Rosiridin against MAO B at 10 μM was 83.8% (pIC50=5.38). |
| M4530 | Rosin | Isolated from pine or pine piles, Rosin is a frequent contact allergen that causes allergic contact dermatitis. |
| M4529 | Rosavin | Rosavin comes from R. Rosea. Rosavin has shown antidepressant, adaptogenic and antianxiety - like effects in mouse models. |
| M4528 | Rosarin | Rosarin is a cinnamyl glycoside isolated from rhodiola rosea. Rosarin has anti-inflammatory and neuroprotective effects. Rosarin inhibited the expression of iNOS, IL-1β and TNF-α in the kidney and prefrontal cortex of mice. |
| M4527 | Oxypaeoniflorin | Oxypaeoniflorin, a monoterpene glycoside isolated from Paeoniae, is an antioxidant. Oxypaeoniflorin has neuroprotective and anti-inflammatory effects. |
| M4526 | Benzoylpaeoniflorin | Benzoylpaeoniflorin, a natural compound extracted from paeonia lactiflora, has the potential to be used in the study of coronary heart disease by reducing apoptosis. |
| M4525 | Alibiflorin | Albiflorin, a monoterpenoid glycoside with neuroprotective effects, is the main component of peony root. Albiflorin also has anti-inflammatory, antioxidant and pain relieving effects. |
| M4524 | Ligustroflavone | Ligustroflavone, which can be extracted from Ligustrum lucidum, is a potential calcium sensitive receptor (CaSR) antagonist. Ligustroflavone has protective effect on diabetic osteoporosis mice. |
| M4523 | Specnuezhenide | Specnuezhenide ((8E)-Nuezhenide) was separated from the fruit of the ligustrum lucidum. Specnuezhenide ((8E)-Nuezhenide) inhibited IL-1β -induced chondrocyte inflammation by inhibiting NF-κB and WNT /β-catenin signaling. Specnuezhenide ((8E)-Nuezhenide) showed anti-inflammatory effects in rat models of osteoarthritis (OA). |
| M4522 | Ursolic acid | Ursolic acid (Prunol) is a natural triterpenoid carboxylic acid compound with preventive and anticancer activities. Ursolic acid also has proteasome agonist activity, EC50=14 μmol/L. |
| M4521 | Dehydrocorydaline | Dehydrocorydaline is an alkaloid, it can regulate protein expression of Bax, Bcl-2. Dehydrocorydaline elevates p38 MAPK activation. Dehydrocorydaline elevates p38 MAPK activation. Anti-inflammatory and anti-cancer activities. Dehydrocorydaline shows strong anti-malarial effects, and low cytotoxicity. |
| M4520 | (+)-Corydaline | Corydaline ((+) -corydaline) is an isoquinoline alkaloid extracted from Corydalis Yanhusuo. It is an inhibitor of AChE with IC50 of 226 µM. Corydaline is a μ-opioid receptor agonist (Ki = 1.23 µM) that inhibits the replication of enterovirus 71 (EV71) (IC50 = 25.23 µM). Corydaline has anti-angiogenesis, anti-allergy, gastric emptying and anti-nociception effects. |
| M4519 | Procyanidin-B1 | Procyanidin B1 is a polyphenolic flavonoid that exists in common fruits and can bind to TLR4/MD-2 complex, showing anti-inflammatory activity. |
| M4518 | Procyanidin-B2 | Procyanidin B2 is a natural flavonoid with anti-tumor and anti-oxidation effects. Procyanidin B2 inhibited NLRP3 inflammasome activation via suppression of AP-1 pathway. |
| M4517 | Proanthocyanidins | Proanthocyanidins can be used as antioxidant and anti-cancers agent. Proanthocyanidin also exhibit anti-inflammatory, cardioprotective, antibacterial and antifungal properties. |
| M4516 | Sinomenine-Hydrochloride | Sinomenine hydrochloride (Cucoline hydrochloride), an alkaloid derived from Sinomenium Acutum, is a blocker of NF-κB activation. Sinomenine is also a μ-opioid receptor activator. |
| M4515 | Fangchinoline | Fangchinoline, a bisbenzylisoquinoline alkaloid, is a novel HIV-1 inhibitor with pain-relieving, blood pressure-depressing, and antibiotic activities. |
| M4514 | Tetrandrine | Tetrandrine (NSC-77037; D-tetrandrine) is a diphenylisoquinoline alkaloid that inhibits voltage-gated calcium channels (ICa) and Ca2+ -activated potassium channels. |
| M4513 | Dihydrocapsaicin | Dihydrocapsaicin is a natural capsaicin that is a selective TRPV1 agonist and increases P-Akt levels. Dihydrocapsaicin can enhance hypothermic induced neuroprotection. |
| M4512 | Tectoridin | Tectoridin is an isoflavone isolated from Maackia Amurensis. Tectoridin is a phytoestrogen that activates estrogen and thyroid hormone receptors. Tectoridin exerts estrogenic effects through the ER dependent genomic pathway and the GPR30 dependent non-genomic pathway. |
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