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Annonaceae

 

Annonaceae (80):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-N8241
    N-trans-Caffeoyltyramine 103188-48-3 99.71%
    N-TRANS-CaffeoyLtyramine is an effective inflammatory response regulator, which has antioxidant activity and anticoagulation effects.
    N-trans-Caffeoyltyramine
  • HY-N0649
    Narcissin 604-80-8 99.82%
    Narcissin (Narcissoside), a flavonol glycoside, exhibits evident scavenging activity against both authentic ONOO- and SIN-1-derived ONOO- with IC50s of 3.5 and 9.6 μM, respectively.
    Narcissin
  • HY-B0935
    Benzyl benzoate 120-51-4 99.94%
    Benzyl benzoate (Phenylmethyl benzoate) is an orally active anti-scabies agent, acaricide (EC50= 0.06 g/m2) and fungicide. Benzyl benzoate is an angiotensin II (Ang II) inhibitor with antihypertensive effects. Benzyl benzoate can be used in perfumes, pharmaceuticals and the food industry.
    Benzyl benzoate
  • HY-N8432
    Dipyrithione 3696-28-4 99.93%
    Dipyrithione is a potent antimicrobial agent. Dipyrithione shows antifungal activity and antiproliferative activity. Dipyrithione induces apoptosis and cycle arrest at G1 phase. Dipyrithione shows anti-inflammatory activity in vivo. Dipyrithione shows anti-tumor activity. Dipyrithione has the potential for the research of dermatophytosis.
    Dipyrithione
  • HY-N2877
    Annonacin 111035-65-5 98.09%
    Annonacin is an acetylgenin that is toxic by inhibiting the pathway of the mitochondrial complex. Annonacin increases tau phosphorylation in R406W+/+ mice. Annonacin acts as an inhibitor of the sodium/potassium and sarcoplasmic reticulum (SERCA) ATPase pumps. Annonacin has significant killing effect on ovarian cancer cell, cervical cancer cell, breast cancer cell, bladder cancer cell and skin cancer cell. Annonacin induces apoptosis through Bax and Caspase-3-related pathways.
    Annonacin
  • HY-N15524
    Thalictoside 74213-96-0
    Thalictoside is found in A. squamosa L. Thalictoside is a sEH inhibitor (IC50: 20.2 µM). Thalictoside exerts anti-osteoporotic effects through an estrogen-like mechanism. Thalictoside can be used in the research of cardiovascular and urinary diseases.
    Thalictoside
  • HY-N15525
    Arabinothalictoside 153287-94-6
    Arabinothalictoside is found in A. squamosa L. Arabinothalictoside is a sEH inhibitor (IC50: 47.1 µM). Arabinothalictoside can be used in the research of cardiovascular and urinary diseases.
    Arabinothalictoside
  • HY-N15527
    Staphylionoside D 663919-93-5
    Staphylionoside D is found in Annona squamosa L.. Staphylionoside D can inhibit the NO production and exhibit anti-inflammatory activity.
    Staphylionoside D
  • HY-N2318
    Podocarpic acid 5947-49-9 99.78%
    Podocarpic acid is a natural product, which has the best all-round positive effect and acts as a novel TRPA1 activator.
    Podocarpic acid
  • HY-126066
    (-)-Syringaresinol 6216-81-5 99.95%
    (-)-Syringaresinol is an orally active isomer of syringaresinol (HY-N8307) found in Annona Montana. (-)-Syringaresinol exhibits antioxidant, anti-inflammatory, and anticancer activities. (-)-Syringaresinol can alleviate ulcerative colitis via the PI3K-Akt/MAPK/Wnt signaling pathway. (-)-Syringaresinol inhibits HL-60 cell proliferation by arresting the G1 phase and inducing apoptosis. (-)-Syringaresinol inhibits LPS (HY-D1056)-induced microglial activation by downregulating the NF-κB p65 signaling pathway and its interaction with ERβ, exerting anti-neuroinflammatory effects.
    (-)-Syringaresinol
  • HY-N7227
    Anonaine 1862-41-5
    Anonaine is an antiparasitic agent. Anonaine also is a glutathione S-transferase (GST) inhibitor.
    Anonaine
  • HY-N7203
    N-Caffeoyl O-methyltyramine 189307-47-9 98.44%
    N-Caffeoyl O-methyltyramine is a class of alkaloid isolated from Cuscuta reflexa with strong inhibitory activity against α-glucosidase (IC50 of 103.58 μM).
    N-Caffeoyl O-methyltyramine
  • HY-N6805
    Isoeugenol acetate 93-29-8 99.92%
    Isoeugenol acetate (Acetyl isoeugenol) is a derivative of Isoeugenol (HY-N1952). Isoeugenol acetate is an inhibitor for ferroptosis.
    Isoeugenol acetate
  • HY-122930
    Lysicamine 15444-20-9 99.34%
    Lysicamine, a natural compound, possesses antibacterial, anticancer and anti-inflammation activity.
    Lysicamine
  • HY-N2051
    Zeylenone 193410-84-3 ≥98.0%
    Zeylenone, a naturally occurring cyclohexene oxide, inhibits proliferation and induces apoptosis in cervical carcinoma cells via PI3K/AKT/mTOR and MAPK/ERK pathways.
    Zeylenone
  • HY-N9499
    3-Methoxyflavone 7245-02-5 99.88%
    3-Methoxyflavone is a flavonoid compound isolated from Artemisia incanescens with antiviral activity.
    3-Methoxyflavone
  • HY-N7450
    Icariside D2 38954-02-8 ≥98.0%
    Icariside D2, isolated from Annona glabra fruit, inhibits angiotensin-converting enzyme. Icariside D2 shows significant cytotoxic activity on the HL-60 cell line with the IC50 value of 9.0 ± 1.0 μM. Icariside D2 induces apoptosis .
    Icariside D2
  • HY-119398
    Lanuginosine 23740-25-2 98.27%
    Lanuginosine (Compound 12) is an AChE inhibitor (IC50: 10.9 μM). Lanuginosine inhibits aggregation. Lanuginosine can be used for research of Alzheimer’s disease.
    Lanuginosine
  • HY-N10391
    (-)-Cleistenolide 1003600-48-3
    (-)-Cleistenolide is a α,β-unsaturated δ-lactone isolated from Cleistochlamys kirkii Oliver. (-)-Cleistenolide has antibacterial and antitumor activity.
    (-)-Cleistenolide
  • HY-N10606
    Uvagrandol
    Uvagrandol potently inhibits α-glucosidase and porcine lipase (IC50: 15.2 μM, 11.2 μM respectively). Uvagrandol can be used in the research of Type 2 diabetes and obesity.
    Uvagrandol