2. Natural Products
  3. Plants
  4. Fabaceae

Fabaceae

 

Fabaceae (88):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-N8742
    Geraldol 21511-25-1 99.20%
    Geraldol is a Flavonoids product that can be isolated from the herbs of Lotus corniculatus L..
    Geraldol
  • HY-Y1783
    2-(Methylamino)ethanol 109-83-1 99.51%
    2-(Methylamino)ethanol (N-Methylethanolamine) is an alkaloid that can be isolated from lentil seeds. 2-(Methylamino)ethanol is used as an organic building block in chemical synthesis and as a solvent for removing carbon dioxide from gas streams.
    2-(Methylamino)ethanol
  • HY-N16506
    Koparin 65048-75-1 98.64%
    Koparin is a minor isoflavone constituent that can be isolated from the wood of Castanospermum austral.
    Koparin
  • HY-W719041
    1,6-Di-O-galloyl-β-D-glucose 23363-08-8
    1,6-Di-O-galloyl-β-D-glucose is a compound found in the fruit of Phyllanthus emblica. 1,6-Di-O-galloyl-β-D-glucose has HIV-1 reverse transcriptase (RT) inhibitory activity with an IC50 value of 270 μM. The inhibitory mechanism of 1,6-Di-O-galloyl-β-D-glucose is competitive inhibition of the template primer and non-competitive inhibition of the substrate (dTTP). 1,6-Di-O-galloyl-β-D-glucose can be used in anti-HIV research.
    1,6-Di-O-galloyl-β-D-glucose
  • HY-W021008
    Sotolone 28664-35-9
    Sotolone (Dimethylhydroxyfuranone) is an activator of the human olfactory receptor OR8D1. Sotolone activates the human olfactory receptor OR8D1, with EC50 values of 84.98 μM and 167.2 μM for its S-enantiomer and R-enantiomer, respectively. Sotolone has unique aroma profiles: (R)-sotolone exhibits smoky, burnt, herbal and grassy notes; (S)-sotolone presents sweet, milky, sour and nutty notes. Sotolone also acts as an antifungal agent, showing moderate inhibitory activity against Magnaporthe oryzae in vitro.
    Sotolone
  • HY-165443
    Cassaine 468-76-8
    Cassaine (Nervocidine) is a Na+/K+-ATPase inhibitor. Cassaine stabilizes phosphorylated intermediates, slows spontaneous dephosphorylation and blocks potassium-stimulated dephosphorylation. Cassaine exhibits non-competitive inhibition with respect to K+, shows inhibition enhanced by Pi and antagonized by Na+. Cassaine induces positive inotropic effects in perfused hearts with faster inotropy offset. Cassaine can be used for research on cardiac arrhythmias.
    Cassaine
  • HY-N9907
    7,3′-Dihydroxy-8,4′-dimethoxyisoflavone 53947-99-2
    7,3′-Dihydroxy-8,4′-dimethoxyisoflavone
  • HY-N19812
    Eryvarin F 568564-59-0
    Eryvarin F is a 3-phenoxychromone derivative found in the roots of Erythrina variegata.
    Eryvarin F
  • HY-131586
    3,7-Dihydroxyflavone 492-00-2 98.04%
    3,7-Dihydroxyflavone (Resogalangin) is a flavonoid phytoestrogen, which can be isolated from Adenophora species. 3,7-Dihydroxyflavone is a modulator of estrogen receptors and an inhibitor of human progesterone metabolizing enzyme AKR1C1 and fungal 17β-hydroxysteroid dehydrogenase and a redox inhibitor (IC50=0.6 and 6.0 μM, respectively). 3,7-Dihydroxyflavone is a fluorescent binding substrate for human serum albumin (HSA) with excitation wavelengths of 370 nm (pH 7.4) and 350 nm (pH 3.5), respectively, and emission wavelength of 515 nm.
    3,7-Dihydroxyflavone
  • HY-119846
    Afromosin 550-79-8 99.68%
    Afromosin is an isoflavone, that can be isolated from Millettia dielsiana Harms. Afromosin exhibits remarkable tumor inhibitory effects.
    Afromosin
  • HY-N17803
    Fisetin tetramethyl ether 17093-86-6
    Fisetin tetramethyl ether
  • HY-N12083
    Flemichapparin B 3187-53-9
    Flemichapparin B
  • HY-114341
    Kaempferol 5-glucoside 34157-80-7
    Kaempferol 5-glucoside (Kaempferol 5-O-β-D-glucopyranoside) is an orally active flavonol glycoside and immunomodulator. Kaempferol 5-glucoside is isolated from the aerial parts of Indigofera aspalathoides Vahl ex DC. Kaempferol 5-glucoside enhances delayed-type hypersensitivity in rats. Kaempferol 5-glucoside increases humoral antibody titers. Kaempferol 5-glucoside is used for the research of autoimmune diseases.
    Kaempferol 5-glucoside
  • HY-182559
    Candidin 1405-90-9
    Candidin is an antioxidant flavonoid, which can be found in the roots of Millettia brandisiana. Candidin induces cytotoxic activity in human cancer cells. Candidin mediates antioxidant activity via peroxyl radical scavenging. Candidin can be used for the research of liver cancer and lung cancer.
    Candidin
  • HY-N19257
    Cassaidine 26296-41-3
    Cassaidine is an alkaloid. Cassaidine can be isolated from Erythuouhleum species. Cassaidine is applicable to research related to nasopharyngeal carcinoma.
    Cassaidine
  • HY-N17895
    1-[2,4-Dihydroxy-5-(3-methyl-2-butenyl)phenyl]ethanone 28437-37-8
    1-[2,4-Dihydroxy-5-(3-methyl-2-butenyl)phenyl]ethanone
  • HY-N17999
    10-Hydroxypheophorbide A 83688-53-3
    10-Hydroxypheophorbide A is a chlorophyll-related compound found in the leaves of
    Neptunia oieracea. 10-Hydroxypheophorbide A inhibits the activation of tumor promoter-induced Epstein-Barr virus (EBV) activation. 10-Hydroxypheophorbide A exhibits photo-induced cytotoxicity in cancer cells.
    10-Hydroxypheophorbide A
  • HY-N17399
    Bis(2-methylheptyl) phthalate 2678-38-8
    Bis (2-methylheptyl) phthalate is an orally effective antiviral agent. Bis (2-methylheptyl) phthalate inhibits the pathogenic process of white spot syndrome virus (WSSV) in Penaeus monodon. Bis (2-methylheptyl) phthalate can be used in studies related to white spot syndrome.
    Bis(2-methylheptyl) phthalate
  • HY-N18311
    Caragiside B 1300025-60-8
    Caragiside B is an isoflavone glucoside that can be isolated from the whole plant of Caragana densa. Caragiside B inhibits arachidonic acid (HY-109590)-induced platelet aggregation by interfering with platelet aggregation pathways.
    Caragiside B
  • HY-N17637
    Machaeric acid 511-81-9
    Machaeric acid is a triterpenoid and triterpene sapogenin, which serves as the aglycone of Senegaloside A; it can be isolated from the seeds of Caragana microphylla Lam. and Acacia senegal(Mimosaceae). Machaeric acid exhibits remarkable biosafety, and even at concentrations as high as 200 μM, it does not induce cytotoxicity or reduce the viability of H4IIE rat hepatoma cells.
    Machaeric acid