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  2. Metabolic or Endocrine Disease
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  5. FR 78844

FR 78844 is an orally active bone resorption inhibitor. FR 78844 attenuates metaphyseal bone mineral density decreases in Streptozotocin (HY-13753)-induced diabetic rats, and Heparin (HY-17567A)-induced osteopenia, but does not affect vitamin D-deficient rat bone loss. FR 78844 can be used for the research of osteopenia.

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

FR 78844

FR 78844 Chemical Structure

CAS No. : 112856-39-0

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Description

FR 78844 is an orally active bone resorption inhibitor. FR 78844 attenuates metaphyseal bone mineral density decreases in Streptozotocin (HY-13753)-induced diabetic rats, and Heparin (HY-17567A)-induced osteopenia, but does not affect vitamin D-deficient rat bone loss. FR 78844 can be used for the research of osteopenia[1][2].

In Vitro

FR 78844 potently inhibits PTH-induced calcium release from rat calvaria in vitro with an IC50 of 4.4 × 10-7 M[1].

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

In Vivo

FR 78844 (1-100 mg/kg; p.o.; 5 days a week; 4 weeks) significantly attenuates Streptozotocin-induced osteopenic bone loss in rats[1].
FR 78844 (1-100 mg/kg; p.o.; 5 days a week; 4 weeks) significantly attenuates ovariectomy-induced osteopenic bone loss in rats[1].
FR 78844 (1-100 mg/kg; p.o.; 5 days a week; 4 weeks) does not attenuate vitamin D deficiency-induced osteopenic bone loss in rats[1].
FR 78844 (1-100 mg/kg; p.o.; 5 days a week; 4 weeks) dose-dependently attenuates Heparin-induced osteopenia in rats[2].

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

Animal Model: Wistar rats (9-week-old female; Streptozotocin (STZ)-induced diabetic model)[1]
Dosage: 1; 10; 100 mg/kg
Administration: p.o.; 5 days a week; 4 weeks
Result: Attenuated the decrease in femur metaphyseal bone mineral density by 66% at 100 mg/kg dose compared to vehicle-treated STZ rats.
Did not produce a significant effect at 1 mg/kg and 10 mg/kg doses.
Animal Model: Wistar rats (9-week-old female; ovariectomized model)[1]
Dosage: 1; 10; 100 mg/kg
Administration: p.o.; 5 days a week; 4 weeks
Result: Attenuated the decrease in femur metaphyseal bone mineral density by 81% at 100 mg/kg dose compared to vehicle-treated ovariectomized rats.
Did not produce a significant effect at 1 mg/kg and 10 mg/kg doses.
Animal Model: Wistar rats (4-week-old female; vitamin D-deficient model)[1]
Dosage: 1; 10; 100 mg/kg
Administration: p.o.; 5 days a week; 4 weeks
Result: Did not produce a significant effect on femur metaphyseal bone mineral density at any tested dose compared to vehicle-treated vitamin D-deficient rats.
Animal Model: Wistar rats (female, 9 weeks old, osteopenia induced by Heparin sodium 2000 U/kg·day subcutaneously 5 days a week for 4 weeks)[2]
Dosage: 1; 10; 100 mg/kg
Administration: p.o.; 5 days a week; 4 weeks
Result: Attenuated the heparin-induced decrease in metaphyseal bone mineral density in a dose-dependent manner.
Produced a significant increase in metaphyseal bone mineral density at 100 mg/kg compared to the vehicle-treated heparinized group.
Showed a significant improvement in metaphyseal bone mineral density at 10 mg/kg relative to the vehicle group.
Molecular Weight

355.15

Formula

C8H9NNa2O6P2S

CAS No.
SMILES

S=C(NC1=CC=CC=C1)C(P(O)(O)=O)P(O[Na])(O[Na])=O

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

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Product Name:
FR 78844
Cat. No.:
HY-122075
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