JKC-301
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
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})
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-#
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