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  4. Bignoniaceae

Bignoniaceae

 

Bignoniaceae (53):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-N0560
    Oroxylin A 480-11-5 99.87%
    Oroxylin A is an active flavonoid compound with strong anti-cancer effects. Oroxylin A inhibits the IL-6/STAT3 pathway and NF-κB signaling, inhibits cell proliferation and induces apoptosis. Oroxylin A inhibits colitis-related carcinogenesis.
    Oroxylin A
  • HY-14589
    Chrysin 480-40-0 99.75%
    Chrysin is one of the most well known estrogen blockers.
    Chrysin
  • HY-N1435
    Oroxin B 114482-86-9 99.39%
    Oroxin B (OB) is a BBB-permeable flavonoid isolated from traditional Chinese herbal medicine Oroxylum indicum (L.) Vent. Oroxin B (OB) possesses obvious inhibitory effect and induces early apoptosis rather than late apoptosis on liver cancer cells through upregulation of PTEN, down regulation of COX-2, VEGF, PI3K, and p-AKT. Oroxin B (OB) selectively induces tumor-suppressive ER stress in malignant lymphoma cells.
    Oroxin B
  • HY-N6961
    Lapachol 84-79-7 99.49%
    Lapachol, a natural naphthoquinone, is an orally active, potent DHODH inhibitor. Lapachol has immunosuppressive activity on lymphocytes through its direct ability to block DHODH activity and inhibit pyrimidine synthesis. Lapachol is a vitamin K antagonist with antitumor activity and can inhibit DNA and RNA synthesis in neoplastic cells. Lapachol has anti-Leishmania activity.
    Lapachol
  • HY-N2025
    Oroxin A 57396-78-8 99.76%
    Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE). Oroxin A acts as a partial PPARγ agonist that can activate PPARγ transcriptional activation. Oroxin A activates PPARγ by docking into the PPARγ protein ligand-binding domain. Oroxin A also exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence.
    Oroxin A
  • HY-134537
    Vitamin K2(5) 957-78-8
    Vitamin K2 (5) (Compound 1) is a prenylogue of the Vitamin K2 (HY-109569) series that can be found in the heartwood of Tabebuia avellanedae.
    Vitamin K2(5)
  • HY-N19765
    (-)-Cycloolivil 6-O-β-D-glucopyranoside 151228-11-4
    (-)-Cycloolivil 6-O-β-D-glucopyranoside is a lignan glycoside that can be isolated from the leaves and branches of Stereospermum cylindricum.
    (-)-Cycloolivil 6-O-β-D-glucopyranoside
  • HY-N17850
    5-Hydroxy-6,7-dimethoxyflavone 2035-05-4
    5-Hydroxy-6,7-dimethoxyflavone is an orally active inhibitor of ferroptosis (Ferroptosis). 5-Hydroxy-6,7-dimethoxyflavone inhibits H1N1 virus-induced ferroptosis by upregulating the expression of SLC7A11 and GPX4. 5-Hydroxy-6,7-dimethoxyflavone alleviates inflammatory responses and inhibits apoptosis by suppressing the activation of the NF-κB and p38 MAPK signaling pathways. 5-Hydroxy-6,7-dimethoxyflavone can be used in studies related to H1N1 influenza virus infection.
    5-Hydroxy-6,7-dimethoxyflavone
  • HY-110398
    5,6,7-Trimethoxyflavone 973-67-1 98.76%
    5,6,7-Trimethoxyflavone is a flavonoid compound that can be isolated from plants Callicarpa japonica. 5,6,7-Trimethoxyflavone exhibits antiviral and anti-inflammatory activities through inhibition of NF-κB/AP-1/STAT signaling pathway.
    5,6,7-Trimethoxyflavone
  • HY-N2376
    Chrysin-7-O-glucuronide 35775-49-6 99.47%
    Chrysin-7-O-glucuronide is a flavonoid found in Scutellaria baicalensis. Chrysin-7-O-glucuronide inhibits α-glucosidase and α-amylase with IC50 values of 612.13 and 980.73 μg/mL. Chrysin-7-O-glucuronide suppresses NF-κB signaling activity. Chrysin-7-O-glucuronide scavenges free radicals, acts as a tight junction protector, and mitigates intestinal mucosal barrier injury. Chrysin-7-O-glucuronide can be used for the research of type 2 diabetes and severe acute pancreatitis-induced intestinal mucosal barrier injury.
    Chrysin-7-O-glucuronide
  • HY-N3592
    Citreorosein 481-73-2
    Citreorosein is a natural product that can be isolated from Xanthoria parietina.
    Citreorosein
  • HY-N3255
    Minecoside 51005-44-8 99.86%
    Minecoside is a CXCR4/STAT3 inhibitor with anticancer and anti-inflammatory activity. Minecoside decreases CXCR4 expression and suppresses STAT3 activation, thus to inhibit CXCL 12-induced invasion. Minecoside potently inhibits cancer metastasis and promotes apoptotic progression.
    Minecoside
  • HY-N2772
    8-Epideoxyloganic acid 88668-99-9 99.95%
    8-Epideoxyloganic acid (7-Deoxy-8-epiloganic acid), an iridoid glucoside, can be found in Incarvillea delavayi. 8-Epideoxyloganic acid exhibits weak antinociceptive activity.
    8-Epideoxyloganic acid
  • HY-14589R
    Chrysin (Standard) 480-40-0
    Chrysin (Standard) is the analytical standard of Chrysin. This product is intended for research and analytical applications. Chrysin is one of the most well known estrogen blockers.
    Chrysin (Standard)
  • HY-N12710
    Crenatoside 61276-16-2 98.0%
    Crenatoside is a phenylethanol glycoside compound that can be isolated from the ethyl acetate of the tree extract of T. stans var. stans with EC50 value of 34.78 μM. Crenatoside has anti-Zika virus activity.
    Crenatoside
  • HY-N3706
    Dehydro-α-lapachone 15297-92-4 98.77%
    Dehydro-α-lapachone can be isolated from the methanol extract of stems of Catalpa ovata G Don. Dehydro-α-lapachone inhibits mycelial growth of Botrytis cinerea with IC50 value 0.41 mg/L.
    Dehydro-α-lapachone
  • HY-N9854
    Icariside E4 126253-42-7 98.13%
    Icariside E4 is an antinociceptive agent, and can be isolated from Tabebuia roseo-alba. Icariside E4 has peripheral analgesic activity by ATP-sensitive K+ channel-dependent mechanisms. Icariside E4 also has anti-oxidant, anti-Alzheimer and anti-inflammatory effects.
    Icariside E4
  • HY-N3602
    Cleroindicin F 189264-47-9
    Cleroindicin F ((-)-Rengyolone), a cleroindicin, is an antimicrobial agent. Cleroindicin F shows relatively high anticandidal activity against Candida strains with a MIC value down to 12.5 µg/mL.
    Cleroindicin F
  • HY-N9731
    6-O-p-Hydroxybenzoylglutinoside 202337-44-8
    6-O-p-Hydroxybenzoylglutinoside acts as a selective NF-κB inhibitor that suppresses the transcriptional activity of TNF-α-activated NF-κB (IC50=52.78 μM). 6-O-p-Hydroxybenzoylglutinoside shows no significant inhibitory activity against sEH, AChE, or BChE. 6-O-p-Hydroxybenzoylglutinoside is a caged chlorinated iridoid glycoside identified from the seeds of Catalpa bungei (Manchurian catalpa).
    6-O-p-Hydroxybenzoylglutinoside
  • HY-N9726
    Campsiketalin 93675-96-8
    Campsiketalin (Compound 6) is a cyclohexylethanoid that can be found in the flowers of Campsis grandiflora.
    Campsiketalin