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163973-98-6

163973-98-6 structure
163973-98-6 structure
  • Name: Fsh receptor-binding inhibitor fragment(bi-10)
  • Chemical Name: L-Threonyl-L-α-glutamyl-L-asparaginyl-L-leucyl-L-α-glutamyl-L-prolyl-L-asparaginylglycyl-L-α-glutamylglycinamide
  • CAS Number: 163973-98-6
  • Molecular Formula: C42H67N13O19
  • Molecular Weight: 1058.06
  • Catalog: Signaling Pathways GPCR/G Protein GNRH Receptor
  • Create Date: 2018-06-02 17:38:22
  • Modify Date: 2025-08-25 20:53:17
  • FSH receptor-binding inhibitor fragment(bi-10) is a potent FSH antagonist. FSH receptor-binding inhibitor fragment(bi-10) blocks the binding of FSH to FSHR, and alteres FSH action at the receptor level. FSH receptor-binding inhibitor fragment(bi-10) results in the suppression of ovulation and causes follicular atresia of mice. FSH receptor-binding inhibitor fragment(bi-10) has the potential for utilizing to restrain the carcinogenesis of ovarian cancer by down-regulating overexpression of FSHR and ERβ in the ovaries[1].

Name L-Threonyl-L-α-glutamyl-L-asparaginyl-L-leucyl-L-α-glutamyl-L-prolyl-L-asparaginylglycyl-L-α-glutamylglycinamide
Synonyms Glycinamide, L-threonyl-L-α-glutamyl-L-asparaginyl-L-leucyl-L-α-glutamyl-L-prolyl-L-asparaginylglycyl-L-α-glutamyl-
L-Threonyl-L-α-glutamyl-L-asparaginyl-L-leucyl-L-α-glutamyl-L-prolyl-L-asparaginylglycyl-L-α-glutamylglycinamide
Description FSH receptor-binding inhibitor fragment(bi-10) is a potent FSH antagonist. FSH receptor-binding inhibitor fragment(bi-10) blocks the binding of FSH to FSHR, and alteres FSH action at the receptor level. FSH receptor-binding inhibitor fragment(bi-10) results in the suppression of ovulation and causes follicular atresia of mice. FSH receptor-binding inhibitor fragment(bi-10) has the potential for utilizing to restrain the carcinogenesis of ovarian cancer by down-regulating overexpression of FSHR and ERβ in the ovaries[1].
Related Catalog
In Vivo FSH receptor-binding inhibitor fragment(bi-10) (10, 20, 30, 40 mg/kg; 肌肉注射; 每天1次; 连续5天) 在大剂量 (30 mg/kg-40 mg/kg) 可抑制卵巢和卵泡发育,降低卵巢中 ERβ 和 FSHR mRNA 和蛋白质的表达水平,抑制 E2 的产生[1]。 Animal Model: Prepuberty Kunming female mice of 21-days old and body weight of 22.3±1.52g[1] Dosage: 10, 20, 30, 40 mg/kg Administration: Intramuscularly injection; once a day for five consecutive days Result: Could attenuate FSH promoting effect on the follicular development, resulting in the poor maturation of ovarian follicles. High dose (40mg/kg) treatment blocked the follicle development of mice. High dose of FRBI (40mg/kg) treatment blocked the follicle development of mice.
References

[1]. Gong Zhuandi, et al. FSH receptor binding inhibitor restrains follicular development and possibly attenuates carcinogenesis of ovarian cancer through down-regulating expression levels of FSHR and ERβ in normal ovarian tissues. Gene. 2018 Aug 20;668:174-181.  

Density 1.4±0.1 g/cm3
Boiling Point 1757.1±65.0 °C at 760 mmHg
Molecular Formula C42H67N13O19
Molecular Weight 1058.06
Flash Point 1016.4±34.3 °C
Exact Mass 1057.467651
LogP -5.91
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.578
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