escin

Escin (Aescin) is biosynthesized from protoaescigenin and barringtogenol, occurring in the seeds of Aesculus.

Isoescin IB is a natural product from Aesculus hippocastanum L.

beta-Escin is a natural mixture of triterpenoid saponins isolated from horse chestnut (Aesculus hippocastanum) seeds, can be used as a vasoprotective anti-inflammatory, anti-edematous and anti-nociceptive agent.

Escin IV is a useful organic compound for research related to life sciences. The catalog number is T125324 and the CAS number is 219944-22-6.

Escin Ie, a derivative of Aescine found in Aesculi Semen extract, is characterized by its anti-inflammatory properties and potential therapeutic applications in treating chronic venous insufficiency and edema.

Escin IA (Escin IA;Aescin IA) is a triterpene saponin isolated from horse chestnut, which inhibits HIV-1 protease with IC50 values of 35 μM. Escin IA has anti-TNBC metastasis activity, and its action mechanisms involved inhibition of epithelial-mesenchymal transition process by down-regulating LOXL2 expression[1][2].

Escin Ib inhibits gastric emptying, at least in part, mediated by capsaicin-sensitive sensory nerves, to stimulate the synthesis and/or release of dopamine, to act through central dopamine2 receptor, which in turn causes the release of PGs.

Escin (Standard) is a reference standard for research and analysis in studies involving Escin. Escin (Aescin) is biosynthesized from protoaescigenin and barringtogenol, occurring in the seeds of Aesculus.

Escin IA (Standard) is a reference standard for research and analysis in studies involving Escin IA. Escin IA (Escin IA;Aescin IA) is a triterpene saponin isolated from horse chestnut, which inhibits HIV-1 protease with IC50 values of 35 μM. Escin IA has anti-TNBC metastasis activity, and its action mechanisms involved inhibition of epithelial-mesenchymal transition process by down-regulating LOXL2 expression[1][2].

Escin IB (Standard) is a reference standard for research and analysis in studies involving Escin IB. Escin Ib inhibits gastric emptying, at least in part, mediated by capsaicin-sensitive sensory nerves, to stimulate the synthesis and/or release of dopamine, to act through central dopamine2 receptor, which in turn causes the release of PGs.

Escin IIA, a naturally derived saponin isolated from the seeds of horse chestnut (Aesculus hippocastanum L.), has been shown to exert beneficial effects in acute inflammatory conditions in animal models. Escin IIA additionally demonstrates gastroprotective effects by reducing ethanol-induced gastric mucosal lesions in rats, thereby supporting its role in the study of anti-inflammatory and gastroprotective mechanisms in preclinical research.

Escin IIB, a natural saponin compound isolated from the seeds of horse chestnut (Aesculus hippocastanum L.), exhibits biologically positive effects on acute inflammation in animal models. Escin IIB has also demonstrated strong gastroprotective properties by significantly reducing ethanol-induced gastric mucosal lesions, highlighting its potential application in the study of anti-inflammatory mechanisms and gastric mucosal defense pathways in preclinical research.

Sodium Aescinate (Escin sodium salt) is extracted from Aesculus wilsonii.

Isoescin IB (Standard) is a reference standard for research and analysis in studies involving Isoescin IB. Isoescin IB is a natural product from Aesculus hippocastanum L. Isoescin IB and Escin IB are the chief active ingredients in escin.

N1,N4-Di-p-coumaroylputrescine is a useful organic compound for research related to life sciences. The catalog number is T124929 and the CAS number is 37946-59-1.

Rescinnamine is an inhibitor of angiotensin-converting enzyme. It also is a vinca alkaloid obtained from Rauwolfia serpentina and other species of Rauwolfia. It used as an antihypertensive drug.

Isoescin IA, a triterpenoid saponin isolated from the seeds of Aesculus chinensis, exhibits anti-HIV-1 protease activity.

N-Acetylputrescine is a polyamine commonly occurring excreted in normal human urine

N,N′-Diferuloylputrescine acts as a pigment inhibitor, showing a 57% reduction in pigmentation. It also considerably diminishes the protein expression of MITF and displays potent antioxidant properties as a radical scavenger against reactive oxygen species [1].

N-trans-Feruloylputrescine, an alkaloid, can be isolated from Magnolia officinalis [1].

Isoescin Ie, a derivative of Aescine found in Aesculi Semen extract [1], exhibits properties related to the primary compound.

Feruloylputrescine is a natural product.

Rescinnamine (Standard) is a reference standard for research and analysis in studies involving Rescinnamine. Rescinnamine is an inhibitor of angiotensin-converting enzyme. It also is a vinca alkaloid obtained from Rauwolfia serpentina and other species of Rauwolfia. It used as an antihypertensive drug.

Isoescin IA (Standard) is a reference standard for research and analysis in studies involving Isoescin IA. Isoescin IA is a triterpenoid saponin isolated from the seeds of Aesculus chinensis. It has anti-HIV-1 protease activity.