Calcicludine

Code:
4310-s
Name:
Calcicludine
CaC
Trp-Gln-Pro-Pro-Trp-Tyr-Cys-Lys-Glu-Pro-Val-Arg-Ile-Gly-Ser-Cys-Lys-Lys-Gln-Phe-Ser-Ser-Phe-Tyr-Phe-Lys-Trp-Thr-Ala-Lys-Lys-Cys-Leu-Pro-Phe-Leu-Phe-Ser-Gly-Cys-Gly-Gly-Asn-Ala-Asn-Arg-Phe-Gln-Thr-Ile-Gly-Glu-Cys-Arg-Lys-Lys-Cys-Leu-Gly-Lys (Disulfide bonds between Cys7-Cys57, Cys16-Cys40, and Cys32-Cys53)
(M.W. 6980.1) C321H476N86O78S6
Neuronal L-type Ca2+ Channel Blocker
Package Price(Yen) Availability
Vial 0.1 mg 30,000 contact us
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Purity:
≧97.0% (HPLC)
Storage:
-20 ℃
Source:
Green Mamba, Dendroaspis angusticeps
Production:
Synthetic Product

Solubility: H2O (10 μM)

more information

Category:
Biologically Active Peptides

reference

  1. H. Schweitz, C. Heurteaux, P. Bois, D. Moinier, G. Romey, and M. Lazdunski, Proc. Natl. Acad. Sci. USA, 91, 878 (1994). (Original)
  2. H. Nishio, Y. Nishiuchi, T. Inui, M. Nakao, T.X. Watanabe, T. Kimura, and S. Sakakibara, Peptide Chemistry 1995, 113 (1996). (Chem. Synthesis & Pharmacol.)
  3. O.D. Uchitel, Toxicon, 35, 1161 (1997). (Review)
  4. J. Santos-Torres, A. Fuente, J.M. Criado, A.S. Riolobos, M. Heredia, and J. Yajeya, J. Neurosci. Res., 85, 634 (2007). (Pharmacol.)

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