1. Cytoskeleton
  2. Integrin
    Toll-like Receptor (TLR)
    TNF Receptor
  3. Mumefural


Cat. No.: HY-N8903
Handling Instructions

Mumefural is a bioactive component of the processed fruit of Prunus mume Sieb. Mumefural inhibits platelet aggregation. Mumefural shows anti-thrombotic effects and ameliorates cognitive impairment.

For research use only. We do not sell to patients.

Mumefural Chemical Structure

Mumefural Chemical Structure

CAS No. : 222973-44-6

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Mumefural is a bioactive component of the processed fruit of Prunus mume Sieb. Mumefural inhibits platelet aggregation. Mumefural shows anti-thrombotic effects and ameliorates cognitive impairment[1][2].

IC50 & Target[1]











In Vivo

Mumefural (0.1-10 mg/kg; i.p.; once) shows anti-thrombotic effects in rats[1].
Mumefural (20-80 mg/kg; oral; daily for 42 days) ameliorates cognitive impairment in chronic cerebral hypoperfusion via regulating the septohippocampal cholinergic system and neuroinflammation[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: SD rats, FeCl3-induced arterial thrombosis model[1]
Dosage: 0.1, 1, or 10 mg/kg
Administration: Intraperitoneal injection, 30 min before 35% FeCl3 treatment
Result: Significantly improved blood flow by inhibiting occlusion and thrombus formation. Prevented collagen fiber damage in injured vessels and inhibited the expression of the platelet activation-related proteins P-selectin and E-selectin. Significantly reduced the increased inflammatory signal of nuclear factor (NF)-κB, toll-like receptor 4 (TLR4), tumor necrosis factor (TNF)-α, and interleukin (IL)-6 in blood vessels.
Animal Model: Male Wistar rats, Chronic cerebral hypoperfusion (CCH) model[2]
Dosage: 20, 40, or 80 mg/kg
Administration: Oral, once a day for 42 days
Result: Significantly improved cognitive impairment. Inhibited cholinergic system dysfunction, attenuated choline acetyltransferase-positive cholinergic neuron loss. Inhibited myelin basic protein degradation and increased the hippocampal expression of synaptic markers and cognition-related proteins. Reduced neuroinflammation, inhibited gliosis, and attenuated the activation of P2X7 receptor, TLR4/MyD88, NLRP3, and NF-κB.
Animal Model: SD rats[1]
Dosage: 2 or 10 mg/kg
Administration: IV or PO (Pharmacokinetic Analysis)
Result: Plasma pharmacokinetic parameters of Mumefural in SD rats[1]
T1/2 (h) Tmax (h) Cmax (ng/mL) AUC0-t (ng⋅h/mL) F (%)
IV (2 mg/kg) 0.14±0.05 0.08±0 1894.54±580.66 564.73±178.35 -
PO (2 mg/kg) 0.69±0.69 0.31±0.13 1731.61±290.64 1043.28±202.37 36.95±7.17

AUC(0–t): area under the curve from the time of dosing to infinity; Cmax: maximum concentration; F: bioavailability; T1/2: terminal half-life; Tmax: time of the maximum concentration; SD: standard deviation; F was calculated using the following formula
Molecular Weight







Room temperature in continental US; may vary elsewhere.


Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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