130849-58-0

130849-58-0 structure
130849-58-0 structure
  • Name: Z-321
  • Chemical Name: Z-321
  • CAS Number: 130849-58-0
  • Molecular Formula: C19H24N2O2S
  • Molecular Weight: 344.471
  • Catalog: Research Areas Neurological Disease
  • Create Date: 2018-02-18 14:07:01
  • Modify Date: 2024-04-04 11:26:28
  • Z-321 is a prolylendopeptidase (PEP) inhibitor.

Name Z-321
Synonyms 2-(2,3-dihydro-1H-inden-2-yl)-1-[(4R)-4-(pyrrolidin-1-ylcarbonyl)-1,3-thiazolidin-3-yl]ethanone
2-(2,3-Dihydro-1H-inden-2-yl)-1-[(4R)-4-(1-pyrrolidinylcarbonyl)-1,3-thiazolidin-3-yl]ethanone
Ethanone, 2-(2,3-dihydro-1H-inden-2-yl)-1-[(4R)-4-(1-pyrrolidinylcarbonyl)-3-thiazolidinyl]-
M2V0Y789FK
Z-321
Description Z-321 is a prolylendopeptidase (PEP) inhibitor.
Related Catalog
Target

PEP[1]

In Vivo Z-321 is a prolylendopeptidase (PEP) inhibitor. In the 100 or 200 mg/kg Z-321-treated groups, mean lordosis quotient (LQ) decreases after administration. However, there is no statistical difference among the values before and after. In contrast, the mean LQ in the 300 mg/kg Z-321-treated females is lower than that before injection (P<0.005). Furthermore, when compare to that in the vehicle-treated control group, mean LQ is also significantly lower (p<0.05). The incidence of soliciting behavior decreases after treatment with 300 mg/kg Z-321, when compare to that before treatment, but there is no statistical difference. The present study also demonstrates that 300 mg/kg Z-321 is effective in inhibiting lordosis behavior without disturbance of locomotor activity[1].
Animal Admin Femal wistar rats (200 to 250 g) are used and housed under conditions of controlled temperature (23 to 26°C) and photoperiod (14: 10 h, light:dark). Fifty four rats are ovariectomized under ether anesthesia. Two weeks after ovariectomy, sexual behavioral tests are carried out before and after a treatment with Z-321 (100, 200 or 300 mg/kg). Another group of rats, 7 females are given 1 mL/kg of 10% gum arabic as control group[1].
References

[1]. Oosuka I, et al. Decrease of sexual receptivity by prolylendopeptidase inhibitor in female rats. Jpn J Pharmacol. 2000 May;83(1):82-5.

Density 1.3±0.1 g/cm3
Boiling Point 588.8±50.0 °C at 760 mmHg
Molecular Formula C19H24N2O2S
Molecular Weight 344.471
Flash Point 309.9±30.1 °C
Exact Mass 344.155853
LogP 2.60
Vapour Pressure 0.0±1.6 mmHg at 25°C
Index of Refraction 1.622
Storage condition 2-8℃