# Probing the Hydrophobic Part of Analogues of the Incadronate-Evidence of Their Interaction with Immunological System of Sheep

**Authors:** Ewa Chmielewska, Joanna Wietrzyk, Jan Kuryszko, Zdzisław Kiełbowicz, Paweł Kafarski

PMC · DOI: 10.3390/ph19020256 · 2026-02-01

## TL;DR

Researchers tested incadronate analogues on sheep and found mild antiosteoporotic effects but also a reduced immune response.

## Contribution

New aminomethylenebisphosphonic compounds were synthesized and tested for antiosteoporotic and immunological effects in sheep.

## Key findings

- Two compounds showed mild antiosteoporotic activity in sheep.
- A decrease in immune response to Corynebacterium pseudotuberculosis was observed as a side effect.
- The compounds demonstrated significant cytotoxic activity in vitro.

## Abstract

Background: Thirty-five analogues of a promising antiosteoporotic drug, incadronate, have been synthesized and evaluated for their antiproliferative activity against mouse macrophage-like J774E cells. These cells originated from identical precursors as osteoclasts and served to select the most active compounds. Two of them, n-heptyl- and n-octyl-aminomethylenebispohosphonic acids, were then used for the medication of sheep with induced osteoporosis. They demonstrated mild antiosteoporotic activity that was documented using bone histopathology. Additionally, a decrease in the immunological response to Corynebacterium pseudotuberculosis was observed as a major side effect accompanied by this medication. Methods: Aminomethylenebisphosphonates may be obtained in the three-component reaction of aliphatic amine, triethyl orthoformate and diethyl phosphite with the further acid hydrolysis of crude esters. The obtained N-substituted alkiloaminomethylenebisphosphonic acids are presented alongside with their in vitro activity toward mouse macrophages J774E. Results: The new families of aminomethylenebisphosphonic compounds synthesized by our approach may be of practical importance due to the significant cytotoxic activity in the cell cultures investigated. Two of them were chosen for further evaluation in the treatment of induced osteoporosis in sheep. Conclusions: In vivo studies confirmed the mild therapeutic effects of compounds 4 (N-(n-heptylamino)methylenebisphosphonic acid and 5 (N-(n-octylamino)methylenebisphosphonic acid; however, they are not suitable analogues of incadronate for consideration as potential drugs.

## Linked entities

- **Chemicals:** incadronate (PubChem CID 156594044), triethyl orthoformate (PubChem CID 31214), diethyl phosphite (PubChem CID 12977)
- **Diseases:** osteoporosis (MONDO:0005298)
- **Species:** Mus musculus (taxon 10090), Ovis aries (taxon 9940)

## Full-text entities

- **Genes:** PTH (parathyroid hormone) [NCBI Gene 5741] {aka FIH1, PTH1}, GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}
- **Diseases:** lymphadenitis (MESH:D008199), osteoporotic (MESH:D058866), cancer (MESH:D009369), skeletal disorder (MESH:C564967), skin injury (MESH:D000069836), fracture (MESH:D050723), injury to (MESH:D014947), infectious disease (MESH:D003141), estrogen deficiency (MESH:D056828), Osteoporosis (MESH:D010024), Bone (MESH:D001847), hypercalcemia (MESH:D006934), weight loss (MESH:D015431), cytotoxic (MESH:D064420), Osteonecrosis of the jaw (MESH:D059266), death (MESH:D003643)
- **Chemicals:** NaOH (MESH:D012972), 13C (MESH:C000615229), Epon 812 (MESH:C004875), ethanol (MESH:D000431), Bisphonal (MESH:C071542), sodium dodecyl sulfate (MESH:D012967), hydrochloric acid (MESH:D006851), alkanes (MESH:D000473), testosterone (MESH:D013739), Aminomethylenebisphosphonic acid (MESH:C487584), methylprednisolone (MESH:D008775), D2O (MESH:D017666), water (MESH:D014867), streptomycin (MESH:D013307), carbon (MESH:D002244), pentobarbital (MESH:D010424), esters (MESH:D004952), xylazine (MESH:D014991), EDTA (MESH:D004492), cortisol (MESH:D006854), nitrogen (MESH:D009584), oxygen (MESH:D010100), osmium tetroxide (MESH:D009993), CHP (MESH:C048279), phosphate (MESH:D010710), trypan blue (MESH:D014343), 3H (MESH:D014316), vitamin D (MESH:D014807), paraffin (MESH:D010232), calcium (MESH:D002118), formalin (MESH:D005557), Bisphosphonate (MESH:D004164), alcohol (MESH:D000438), H (MESH:D006859), calcitriol (MESH:D002117), dimethylformamide (MESH:D004126), CO2 (MESH:D002245), citric acids (MESH:D019343), steroid (MESH:D013256), L-glutamine (MESH:D005973), phosphonic acid (MESH:C570063), adenosine triphosphate (MESH:D000255), TMS (MESH:D013932), oil (MESH:D009821), acetone (MESH:D000096), amine (MESH:D000588), hydroxyapatite (MESH:D017886), H3PO4 (MESH:C030242), triethyl phosphite (MESH:C018680), MTT (MESH:C070243), penicillin (MESH:D010406), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MESH:C022616), 2H (MESH:D003903), C13H31NO6P2 (-)
- **Species:** Ovis aries (domestic sheep, species) [taxon 9940], Canis lupus familiaris (dog, subspecies) [taxon 9615], Mus musculus (house mouse, species) [taxon 10090], Corynebacterium pseudotuberculosis (species) [taxon 1719], Homo sapiens (human, species) [taxon 9606], Primates (primates, order) [taxon 9443], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** J744E — Homo sapiens (Human), Limb-girdle muscular dystrophy type 2B, Telomerase immortalized cell line (CVCL_VG60), J774E — Mus musculus (Mouse), Mouse reticulum cell sarcoma, Cancer cell line (CVCL_4692)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943640/full.md

---
Source: https://tomesphere.com/paper/PMC12943640