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Alprostadil

Catalog No.
B2154
vasodilator
Grouped product items
SizePriceStock Qty
10mM (in 1mL DMSO)
$121.00
In stock
10mg
$113.00
In stock
50mg
$366.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Email: [email protected]

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Background

Alprostadil (CAS 745-65-3), also known as prostaglandin E1, is an endogenous prostaglandin analog that exerts potent vasodilatory activity by binding and activating prostaglandin E-type (EP) receptors, primarily EP2 and EP4. Upon receptor activation, intracellular cyclic adenosine monophosphate (cAMP) levels rise, mediating smooth muscle relaxation and vasodilation. Clinically, Alprostadil is investigated and utilized in research contexts addressing vascular biology, erectile dysfunction mechanisms, and cardiovascular function, offering insights into prostaglandin signaling pathways.

Product Citation

Chemical Properties

Physical AppearanceA solid
StorageStore at -20°C
M.Wt354.48
Cas No.745-65-3
FormulaC20H34O5
Solubilityinsoluble in H2O; ≥13.4 mg/mL in DMSO; ≥47.1 mg/mL in EtOH
Chemical Name7-[(1R,2R,3R)-3-hydroxy-2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopentyl]heptanoic acid
SDFDownload SDF
Canonical SMILESCCCCCC(C=CC1C(CC(=O)C1CCCCCCC(=O)O)O)O
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

Protocol

Cell experiment:[1]

Cell lines

Human umbilical vein endothelial cells (HUVECs)

Reaction Conditions

0 ~ 10 μM alprostadil

Applications

Alprostadil (1 nM ~ 10 μM; 48 h) concentration-dependently reduced HUVEC proliferation (up to 100% inhibition) in the presence of 20 ng/mL vascular endothelial growth factor (VEGF), with an IC50 of 400 nM. Alprostadil (0.01 ~ 10 μM; 6 h) also inhibited VEGF-induced HUVEC migration in a concentration dependent manner, with an IC50 of 500 nM.

Animal experiment:[1]

Animal models

Female C57/bl6 mice, 6 ~ 8 weeks of age

Dosage form

20 ng

Administered subcutaneously for 4 days

Applications

Alprostadil treatment (20 ng/animal/day; 4 days) significantly inhibited the fibroblast growth factor (FGF)-induced angiogenesis in mice. Alprostadil could be useful for diseases that require anti-angiogenic therapy, such as diabetic retinopathy and solid tumors.

Note

The technical data provided above is for reference only.

References:

1. Cattaneo MG, Pola S, Dehò V, et al. Alprostadil suppresses angiogenesis in vitro and in vivo in the murine Matrigel plug assay. British Journal of Pharmacology, 2003, 138(2): 377-385.

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