Natural Products
| Catalog No. | Information |
| CFN96626 | Tetrahydropapaverine hydrochloride Reference standards. |
| CFN96627 | Tetrahydrocannabivarin Tetrahydrocannabivarin is a neutral cannabis receptor subtype (CB1) receptor antagonist, it can increases neural responding to rewarding and aversive stimuli, this effect profile suggests therapeutic activity in obesity, perhaps with a lowered risk of depressive side effects. Tetrahydrocannabivarin exhibits anticonvulsant effects in a piriform cortical brain slice model of epileptiform activity. |
| CFN96628 | Taxuspine X Taxuspine X may have p-glycoprotein inhibitory activity. |
| CFN96629 | Taxuspine W Taxuspine W is a natural product from the Japanese yew Taxus cuspidata Sieb. et Zucc. |
| CFN96630 | Taxuspine B Taxuspine B is a natural product from the Japanese yew Taxus cuspidata Sieb. et Zucc. |
| CFN96631 | Taxumairol R Taxumairol R is a natural product from Taxus mairei. |
| CFN96632 | Taxumairol B Taxumairol B is a natural product from Taxus yunnanensis. |
| CFN96633 | Taxol C 1. Taxol C can reduce interaction with the P-glycoprotein transporter that may allow for increased permeation of taxanes into the brain. |
| CFN96634 | Taxinine M Taxinine M is a natural product from Chinese yew Taxus chinensis. |
| CFN96635 | Taxinine J Taxinine J possesses inhibitory activity on heptoma cell in vitro. |
| CFN96636 | Taxinine Taxinine and Taxinine B can inhibit the drug transport by P-glycoprotein in multidrug-resistant cells. |
| CFN96637 | Taxin B Taxin B has toxic effects. |
| CFN96638 | Taxezopidine L Taxezopidines K and taxezopidine L can markedly inhibit Ca2+-induced depolymerization of microtubules. |
| CFN96639 | Taxezopidine G Taxezopidine G is a natural product from Taxus cuspidata. |
| CFN96640 | Taxcultine Taxcultine can actively promote tubulin assembly. |
| CFN96641 | Taxagifine Taxagifine shows cytotoxic activity toward HepG2 cells; it can suppress the superoxide generation induced by N-formyl-methionyl-leucyl-phenylalanine (fMLP) and arachidonic acid (AA) in a concentration-dependent manner. |
| CFN96642 | Taxacin Taxacin shows strong inhibitory effects on platelet aggregation induced by arachidonic acid (IC(50):21.9 microM). Taxacin can suppress the superoxide generation induced by N-formyl-methionyl-leucyl-phenylalanine (fMLP) and arachidonic acid (AA) in a concentration-dependent manner. |
| CFN96643 | Taxachitriene B Taxachitriene B is a natural product from the Chinese yew Taxus chinensis. |
| CFN96644 | Taxachitriene A Taxachitriene A is a natural product from the Chinese yew Taxus chinensis. |
| CFN96645 | Tauroursodeoxycholic acid Tauroursodeoxycholic acid (TUDCA) may enhance the secretory capacity of cholestatic hepatocytes by stimulation of exocytosis and insertion of transport proteins into apical membranes via PKC-dependent mechanisms. TUDCA acts as a chemical chaperone to enhance protein folding and ameliorate ER stress, increases insulin sensitivity, it may be an effective pharmacological approach for treating insulin resistance. TUDCA has wide-range neuroprotective effects, it is a strong modulator of AbetaE22Q-triggered apoptosis, it may provide a potentially useful treatment in patients with hemorrhagic stroke and perhaps other acute brain injuries associated with cell death by apoptosis. |
| CFN96646 | Taurocholic acid Taurocholic acid feeding shows cytoprotective effects on the biliary tree after adrenergic denervation of the liver; taurocholic acid feeding prevents tumor necrosis factor-alpha-induced damage of cholangiocytes by a PI3K-mediated pathway. Rectal administration of taurocholic acid can stimulate glucagon-like peptide-1 and peptide YY by TGR5 receptor activation, which may have potential for the management of type 2 diabetes and obesity. |
| CFN96647 | Tasumatrol L Tasumatrol L is a natural product from Taxus sumatrana. |
| CFN96648 | Taspine Taspine shows antitumor activity by modulating the EGFR signaling pathway of Erk1/2 and Akt in vitro and in vivo, it can inhibit growth and induce apoptosis of HUVEC in a dose-dependent manner, it has shown meaningful angiogenesis activity. Taspine exhibits a dose-related cicatrizant effect and an ED50 of 0.375 mg/kg. |
| CFN96649 | Tabernanthine Tabernanthine shows affinity for opiate receptors, it can decrease morphine and cocaine self-administration in rats, it may be effective in treating addiction to opioid and stimulant drugs.Tabernanthine tartrate has peripheral cardiovascular effects in anaesthetized rats. |
| CFN96650 | Taberdivarine H Taberdivarine H is a natural product from Tabernaemontana officinalis. |
| CFN96651 | Sulochrin Sulochrin shows antifungal and antibacterial activities, it can inhibit hepatitis C virus (HCV) infection in a dose-dependent manner without any apparent cytotoxicity up to 50 uM. Sulochrin has an inhibitory activity to eosinophil degranulation. |
| CFN96652 | Sugetriol 6,9-diacetate Reference standards. |
| CFN96653 | Sugeroside Sugeroside is a natural product from Achillea clypeolata. |
| CFN96654 | Sudan III C.I. Solvent Red 23, commercial Sudan III, is widely used in cosmetic products, it has mutagenic activities. Sudan III dye strongly induces CYP1A1 mRNA expression in HepG2 cells. |
| CFN96655 | Suavioside A Suavioside A tastes sweet, it could be used as a sweetener. |
| CFN96656 | Stylopine hydrochloride Stylopine is a protoberberine-type alkaloid that has potential biological activities, including anti-inflammatory activity. |
| CFN96657 | Strictosidinic acid Strictosidinic acid has an antiradical action against DPPH, it has a promising effect in the central nervous system. |
| CFN96658 | Stauntosaponin A Stauntosaponin A and stauntosaponin B show moderate inhibitory activities against Na+/K+-ATPase with IC50 values of 21 and 29 uM, respectively. |
| CFN96659 | Stachybotrylactam Stachybotrylactam has toxicity. |
| CFN96660 | Stachybotrolide Stachybotrolide is a natural product from Stachybotrys alternans. |
| CFN96661 | Stachybotramide Stachybotramide preferentially stimulate the plasma cholesteryl ester transfer protein (CETP)-mediated transfer of cholesteryl esters (CE) from high density lipoprotein (HDL) to both very low density lipoprotein (VLDL) and low density lipoprotein (LDL). |
| CFN96662 | Stachartin E Stachartin E is a natural product from the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. |
| CFN96663 | Stachartin D Stachartin D is a natural product from the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. |
| CFN96664 | Stachartin C Stachartin C is a natural product from the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. |
| CFN96665 | Stachartin B Stachartin B is a natural product from the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. |
| CFN96666 | Stachartin A Stachartin A is a natural product from the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. |
| CFN96667 | Spiratisanin C Spiratisanin C is a natural product from Spiraea japonica. |
| CFN96668 | Spiratisanin B Spiratisanin B is a natural product from Spiraea japonica. |
| CFN96669 | Spiratisanin A Spiratisanin A is a natural product from Spiraea japonica. |
| CFN96670 | Sorokinianin Sorokinianin is a phytotoxin, it has antifungal activity, it is highly effective in suppressing spore germination of F. solani (75%) at 100 ug/ml concentration. |
| CFN96671 | Sophoracarpan B Sophoracarpan B is a natural product from Sophora tomentosa L. |
| CFN96672 | Sophoracarpan A Sophoracarpan A is a natural product from Sophora tomentosa L. |
| CFN96673 | Sodium cholate Sodium cholate (Cholic acid) exhibits a strong spermicidal and antiviral [anti-human immunodeficiency virus (HIV)-1] activity. |
| CFN96674 | Siegeskaurolic acid Siegeskaurolic acid exhibits anti-inflammatory and antinociceptive effects, which due to the inhibition of iNOS and COX-2 expression in RAW 264.7 macrophages via NF-kappaB inactivation. |
| CFN96675 | Shizukaol B Shizukaol B exerts anti-inflammatory effects in LPS-activated microglia partly by modulating JNK-AP-1 signaling pathway; it also shows significant anti-neuroinflammatory effects by inhibiting nitric-oxide (NO) production in lipopolysaccharide (LPS)-stimulated murine BV-2 microglial cells with relatively low cytotoxicity. Shizukaol B exhibits anti-HIV-1 replication activities in both wild-type HIV-1 and two NNRTIs-resistant strains, it also has significant cytotoxicities against C8166 cells. Shizukaol B prevents monocyte adhesion to HUVEC through the inhibition of cell adhesion molecules expression stimulated by TNF-alpha. |
