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(+)-Fluprostenol

(+)-Fluprostenol
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Purity:99.56%
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(+)-Fluprostenol

Catalog No. T21224Cas No. 54276-17-4
(+)-Fluprostenol (AL-5848), an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycoprotein 1 (OVGP1).
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Pack SizePriceAvailabilityQuantity
1 mg$77In Stock
5 mg$189In Stock
10 mg$313In Stock
25 mg$578In Stock
50 mg$833In Stock
100 mg$1,150In Stock
1 mL x 10 mM (in DMSO)$223In Stock
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Related Compound Libraries of "(+)-Fluprostenol"

Product Introduction

Bioactivity
Description
(+)-Fluprostenol (AL-5848), an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycoprotein 1 (OVGP1).
In vivo
(+)-Fluprostenol(s.c. to rats on day 18 of pregnancy) increased cervical creep, or softness, by the following day. Doses of (+)-Fluprostenol 100-fold larger were necessary to increase uterine contractions. (+)-Fluprostenol produced falls in serum progesterone concentrations, increases in 20 alpha-dihydroprogesterone concentrations, no changes in oestradiol or relaxin concentrations and a reduction in the ovarian human chorionic gonadotrophin binding capacity in vitro. (+)-Fluprostenol was less potent in inducing cervical softness when administered per vaginam, and a dose which produced softening in pregnant rats was ineffective in ovariectomized steroid-maintained pregnant or pro-oestrous rats[3].
AliasFluprostenol, (+)-, Travoprost acid, AL-5848
Chemical Properties
Molecular Weight458.47
FormulaC23H29F3O6
Cas No.54276-17-4
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 325 mg/mL (708.88 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1812 mL10.9058 mL21.8117 mL109.0584 mL
5 mM0.4362 mL2.1812 mL4.3623 mL21.8117 mL
10 mM0.2181 mL1.0906 mL2.1812 mL10.9058 mL
20 mM0.1091 mL0.5453 mL1.0906 mL5.4529 mL
50 mM0.0436 mL0.2181 mL0.4362 mL2.1812 mL
100 mM0.0218 mL0.1091 mL0.2181 mL1.0906 mL

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