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SOAT1

Catalog No Product Description CAS No. Purity Structural Formula
BP3174
Gymnemagenin
Gymnemagenin is a potent and selective antagonist for the β isoform of LXR, it has antihyperglycemic activity, it can be considered further for development into a potent anti-diabetic drug.
22467-07-8 98% Gymnemagenin
BP1072
Peimine
Peimine has good anti-inflammatory effects in vivo, it inhibits the production of inflammatory cytokines induced by LPS through blocking MAPKs and NF-κB signaling pathways. It also has antitussive and sedative actions, the action being suspected to be central in nature.
23496-41-5 98% Peimine
BP1109
Piperine
Piperine is a N-acylpiperidine that is piperidine substituted by a (1E,3E)-1-(1,3-benzodioxol-5-yl)-5-oxopenta-1,3-dien-5-yl group at the nitrogen atom. It is an alkaloid isolated from the plant Piper nigrum. It has a role as a NF-kappaB inhibitor, a plant metabolite, a food component and a human blood serum metabolite. It is a tertiary carboxamide, a piperidine alkaloid, a member of benzodioxoles and a N-acylpiperidine. It is functionally related to an (E,E)-piperic acid. Piperine, an inhibitor of human P-glycoprotein and/or CYP3A4, which has antinociceptive, antiarthritic, antidepressant, hepatoprotective, immunomodulatory , antitumor, anti-oxidative, anti-apoptotic, chemo-protective, and anti-inflammatoryactivities. Administration of piperine appears to reverse preexisting high-fat diet (HFD)-induced hepatic steatosis and insulin resistance, probably by activation of adiponectin-AMPK signalling.
94-62-2 98% Piperine
BP0140
Alkannin
Alkannin is a hydroxy-1,4-naphthoquinone. Alkannin, Found in Alkanna tinctoria as a food coloring agent. Alkannin has anti-cancer activity, inhibits cell cycle, and induces cell apoptosis.Alkannin improves liver inflammation in the Rho kinase pathway.
517-88-4 98% Alkannin
BP1419
Tussilagone
Tussilagone has anti-cancer, anti-oxidant and anti-inflammatory activities. Tussilagone inhibits dendritic cell function through the induction of heme oxygenase-1; it has potential treatment of neuro-inflammatory diseases through the inhibition of overproduction of nitric oxide and prostaglandin E(2).
104012-37-5 98% Tussilagone
BP1158
Protopine
Protopine acts as a potent inhibitor of thromboxane synthesis and PAF with hepatoprotective, antidepressant, antioxidant, antispasmodic and relaxant properties. Protopine is also a novel microtubule-stabilizing agent, causes mitotic arrest and apoptotic cell death in human hormone-refractory prostate cancer cell lines. Protopine blocks phosphorylation of mitogen-activated protein kinases (MAP kinases) and also blocks activation of a nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB). Protopine is a dibenzazecine alkaloid isolated from Fumaria vaillantii. It has a role as a plant metabolite.
130-86-9 98% Protopine
BP4259 82375-30-2 98% Humantenirine
BP0875
Liquiritin apioside
Liquiritin apioside has antioxidant property by inducing glutathione (GSH) biosynthesis via the inhibition of cytokines and protected lung epithelial cells against cigarette smoke-mediated oxidative stress, might be as protective agent against epithelial injury in COPD. Liquiritin apioside is a glycoside and a member of flavonoids.
74639-14-8 98% Liquiritin apioside
SBP04438 2130-17-8 Tetrahymanol
BP1006
Nordihydrocapsaicin
Capsaicin and dihydrocapsaicin are the major active components in pepper spray products, which are widely used for law enforcement and self-protection, they has cytotoxicity, they induces p53 protein and G1 phase cell cycle arrest. Dihydrocapsaicin induces hypothermia and substance P depletion, it or radiolabelled dihydrocapsaicin, may be a useful tool for investigating the mechanisms by which capsaicin alters thermoregulation and primary afferent neuron function.Capsaicin and dihydrocapsaicin have effect on in vitro blood coagulation and platelet aggregation. Nordihydrocapsaicin is a member of phenols and a member of methoxybenzenes.
28789-35-7 98% Nordihydrocapsaicin
SBP02717
Haplopine
Haplopine shows photo-activated antimicrobial activity against S. aureus. It exhibits potent melanogenesis-inhibitory activities with almost no toxicity to the cells. Haplopine is an organic heterotricyclic compound, an organonitrogen heterocyclic compound and an oxacycle.
5876-17-5 98% Haplopine
BP0940
Methyleugenol
Methyleugenol (ME) is a natural constituent of the essential oils of a number of plants widely used in foodstuffs as flavouring agents, in view of the carcinogenic potential of ME, the need to check its presence in food products with effective analytical methods. ME has elaxant and antispasmodic actions on guinea-pig isolated ileum, it also has antinociceptive, anti-inflammatory, and insecticidal properties.ME can inhibit the production of nitric oxide and decreased the protein expression of inducible nitric oxide synthase, it down-regulates the production of pro-inflammatory cytokines in the ischemic brain as well as in immunostimulated mixed glial cells. O-methyleugenol is a phenylpropanoid. It is functionally related to a eugenol.
93-15-2 98% Methyleugenol
BP1111
Platycodin D
Platycodon D shows antinociceptive, and anti-inflammatory activities, it can induce autophagy in NCI-H460 and A549 cells through inhibiting PI3K/Akt/mTOR signaling pathway and activating JNK and p38 MAPK signaling pathways. Platycodon D can inhibit migration, invasion, and growth of MDA-MB-231 human breast cancer cells via suppression of EGFR-mediated Akt and MAPK pathways. Platycodin D is also a potent adjuvant of specific cellular and humoral immune responses against recombinant hepatitis B antigen. Platycodin D is a triterpenoid saponin. It has a role as a metabolite.
58479-68-8 98% Platycodin D
BP1417
Tuberostemonine
Tuberostemonine is a natural product found in Stemona phyllantha and Stemona tuberosa. It has a role as a metabolite.
6879-01-2 98% Tuberostemonine
BP0312
Capsaicin
Capsaicin, the main pungent ingredient in 'hot' chilli peppers, is a TRPV1 agonist with EC50 of 0.29±0.05 μM in HEK293 cells, which elicits a sensation of burning pain by selectively activating sensory neurons that convey information about noxious stimuli to the central nervous system, it may used as a pain therapy by the long-lasting and inhibitory effects on persistent pain. Capsaicin has antioxidant activity , it is more effective than melatonin in suppressing the formation of lipid hydroperoxides, it also reduces anxiety-like behaviours in rats and may be an admissible drug candidate for treating endometriosis. Capsaicin is a capsaicinoid. It has a role as a TRPV1 agonist, a non-narcotic analgesic and a voltage-gated sodium channel blocker.
404-86-4 98% Capsaicin
SBP03451
Evocarpine
Evocarpine shows antimycobacterial, and vasorelaxant effects, it can inhibit Ca2+ influx through voltage-dependent calcium channels.
15266-38-3 98% Evocarpine
SBP03048
Piperlotine A
Piperlotine A shows potent antiplatelet aggregation activity.
389572-70-7 98% Piperlotine A
BP0034
1-Octacosanol
1-Octacosanol is an ultra-long-chain primary fatty alcohol that is octacosane in which a hydrogen attached to one of the terminal carbons is replaced by a hydroxy group. It has a role as a plant metabolite. It is an ultra-long-chain primary fatty alcohol and a fatty alcohol 28:0. It derives from a hydride of an octacosane. 1-Octacosanol is reported to possess cholesterol-lowering effects, antiaggregatory properties, cytoprotective use, and ergogenic properties, it is used as a nutritional supplement. 1-Octacosanol is a straight chain aliphatic 28 carbon fatty alcohol and the main component of cholesterol lowering agent docosanol. 1-Octacosanol has various activities such as anti fatigue, anti angiogenesis, cholesterol lowering, and insecticidal.
557-61-9 95%GC 1-Octacosanol
BP0945
Methysticin
Methysticin is a potent NF-kappaB inhibitor in kava with minimum toxicity, it possesses hepatotoxic, anticonvulsant and neuroprotective properties, it contributes to CYP1A1 induction. Methysticin is an aromatic ether and a member of 2-pyranones.
495-85-2 98% Methysticin
BP1066
Parthenolide
Parthenolide exhibits anti-cancer, anti-inflammatory, immunomodulatory, anti-Leishmania, and antimigraine effects, it inhibits nociception and neurogenic vasodilatation in the trigeminovascular system by targeting the TRPA1 channel.Parthenolide is also an inhibitor of the nuclear factor-kappaB pathway, can ameliorate cardiovascular derangement and outcome in endotoxic shock in rodents. (1Ar,7aS,10aS,10bS)-1a,5-dimethyl-8-methylidene-2,3,6,7,7a,8,10a,10b-octahydrooxireno[9,10]cyclodeca[1,2-b]furan-9(1aH)-one is a germacranolide.
20554-84-1 98% Parthenolide