| Cat.No. | Name | Information |
|---|---|---|
| M3997 | Nuciferine | Nuciferine is an antagonist at 5-HT2A (IC50=478 nM), 5-HT2C (IC50=131 nM), and 5-HT2B (IC50=1 μM), an inverse agonist at 5-HT7 (IC50=150 nM). Nuciferine possesses anti-hyperlipidemia, anti-hypotensive, anti-arrhythmic, and insulin secretagogue activities. |
| M3996 | Betulin | Betulin is a specific, small molecule inhibitor of SREBP (Sterol Regulatory Element-Binding Proteins). |
| M3995 | Jervine | Jervine is a naturally occuring steroidal alkaloid that causes cyclopia by blocking sonic hedgehog signaling. |
| M3994 | Hederagenin | Hederagenin is a derivative of oleanolic acid isolated from the leaves of ivy (Hedera helix L.) that has been shown to have potential anti-tumor activity. Hederagenin can inhibit LPS-stimulated expression of iNOS, COX-2, and NF-κB. |
| M3990 | Betulonic acid | Betulinic acid (Betulinic acid) is an inhibitor of eukaryotic cell topoisomerase I with IC50 value of 5 μM. It has anti-inflammatory, anti-malaria, anti-AIDS and anti-tumor activities. Betulinic acid is also a new nF-KB agonist. |
| M3987 | Ginsenoside Rb1 | Ginsenoside Rb1 is an ingredient in the Chinese medicine Panax ginseng. Ginsenoside inhibition Na, K-ATPase++ activityIC50 6.3±1.0 μM. Ginsenoside Rb1 also inhibits IRAK-1 activation and phosphorylation of NF-κB p65. |
| M3986 | Bruceantin | Bruceantin was first isolated from Brucea antidysenterica, a tree used in Ethiopia for the treatment of cancer. |
| M3983 | Puerarin | Puerarin is a 5-HT2C receptor antagonist. Puerarin inhibits the expression of LPS-induced iNOS, COX-2 and CRP proteins and also suppresses their mRNAs from RT-PCR experiments in RAW264.7 cells. |
| M3981 | Bilobalide | Bilobalide, a natural product extracted from Ginkgo biloba leaf, is known to exhibit a number of pharmacological activities. |
| M3980 | Dipsacoside B | Dipsacoside B is extracted from Lonicara confusa DC. dried buds and flowers. Dipsacoside B showes strong antimicrobial activity. |
| M3979 | Caffeic acid | Caffeic acid is an endogenous phenolic phytochemical compound that exists in plants and many foods. |
| M3978 | 10-Deacetylbaccatin III | 10-Deacetylbaccatin-III is an intermediate for taxol analog preparations. |
| M3977 | Chlorogenic acid | Chlorogenic acid is an orally active antioxidant activity, antibacterial, hepatoprotective, cardioprotective, anti-inflammatory, antipyretic, neuroprotective, anti-obesity, antiviral, anti-microbial, anti-hypertension compound. |
| M3976 | (20S)-Protopanaxadiol | (20S)-Protopanaxadiol (aPPD) is one of the aglycones of the ginsenosides and has a wide range of pharmacological activities. |
| M3974 | Ingenol | Ingenol is a extremely weak protein kinase C (PKC) activator. Starting material for synthesis of ingenol derivatives. |
| M3972 | Amygdalin | Laetrile is a glycoside initially isolated from the seeds of the tree Prunus dulcis, also known as bitter almonds. |
| M3971 | Isosteviol | Isosteviol is a tetracyclic diterpenoid obtained by acid hydrolysis of steviol glycoside extracts isolated from abundant Stevia rebaudiana plants. |
| M3968 | Dihydromyricetin | Dihydromyricetin is a natural antioxidant flavonoid from Ampelopsis grossedentata. |
| M3967 | α-Hederin | α-Hederin is a triterpene saponin which affects the binding behavior, dynamics, and regulation of beta 2-adrenergic receptors. |
| M3966 | Oxysophocarpine | Oxysophocarpine (OSC), a quinolizidine alkaloid extracted from leguminous plants of the genus Robinia, is traditionally used for various diseases including neuronal disorders. |
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