Basic information Safety Supplier Related

JKC-301

Basic information Safety Supplier Related

JKC-301 Basic information

Product Name:
JKC-301
Synonyms:
  • CYCLO(-D-ASP-PRO-D-ILE-LEU-D-TRP)
  • JKC 301 (CYCLO-[D-ASP-PRO-D-LLE-LEU-D-TR P]), SYNTHETIC, >99% PURITY
  • JKC-301
  • Cyclo(D-α-aspartyl-L-prolyl-D-isoleucyl-L-leucyl-D-tryptophyl)
  • JKC-301 Cyclo(-D-Asp-Pro-D-Ile-Leu-D-Trp)
CAS:
136553-96-3
MF:
C32H44N6O7
MW:
624.73
Mol File:
136553-96-3.mol
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JKC-301 Chemical Properties

Boiling point:
1052.2±65.0 °C(Predicted)
Density 
1.31±0.1 g/cm3(Predicted)
storage temp. 
-15°C
pka
4.04±0.10(Predicted)
Sequence
Cyclo({d-Asp}-Pro-{d-Ile}-Leu-{d-Trp})
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JKC-301 Usage And Synthesis

Uses

JKC 301 is a selective Endothelin A receptor antagonist. JKC 301 attenuates the pressor effects of nicotine in rats. JKC 301 can be used to study cardiovascular disease caused by smoking[1][2].

References

[1] Tanus-Santos JE, Sampaio RC, Hyslop S, Franchini KG, Moreno H Jr. Endothelin ET(A) receptor antagonism attenuates the pressor effects of nicotine in rats. Eur J Pharmacol. 2000 May 12;396(1):33-7. DOI:10.1016/s0014-2999(00)00194-1
[2] Ngoka LC, et al. Location of alkali metal binding sites in endothelin A selective receptor antagonists, cyclo(D-Trp-D-Asp-Pro-D-Val-Leu) and cyclo(D-Trp-D-Asp-Pro-D-Ile-Leu), from multistep collisionally activated decompositions. J Mass Spectrom. 2000 Feb;35(2):265-76. DOI:10.1002/(SICI)1096-9888(200002)35:2<265::AID-JMS946>3.0.CO;2-#

JKC-301Supplier

GL Biochem (Shanghai) Ltd
Tel
21-61263452 13641803416
Email
ymbetter@glbiochem.com
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Chemsky (shanghai) International Co.,Ltd
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021-50135380
Email
shchemsky@sina.com
Cellmano Biotech Limited
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0551-65326643 18156095617
Email
info@cellmano.com
Creative Peptides
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Email
info@creative-peptides.com