Product Information
Applications
Biological Information
Primary Targetu Opioid receptpr
Primary Target IC<sub>50</sub>3.5 nM
Purity≥95% by HPLC
Physicochemical Information
Peptide SequenceD-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 (2-7 disulfide bond)
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
Toxicity Standard Handling
Storage -20°C
Protect from Light Protect from light
Do not freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Packaging Information
Transport Information
Supplemental Information
Specifications

Documentation

CTAP - CAS 103429-32-9 - Calbiochem SDS

Title

Safety Data Sheet (SDS) 

References

Reference overview
Perry, C., et al., 2013. Behav. Neurosci. 127, 535.
Burkett, J. et al. 2011. Neuropsychopharm. 36, 2200.
Steinmiller, L., et al., 2008. Psychopharmacol. (Berl). 195, 497.
Sterious, S., et al., 2003. J. Pharmacol. Exp. Ther. 304, 301.
Abbruscato, T., et al. 1997. J. Pharmacol. 280, 402.
Data Sheet

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision25-October-2013 JSW
Synonymsµ opioid receptor antagonist, CTAP
DescriptionA highly potent octapeptide that acts as a selective and brain penetrating bioavailable µ opioid receptor antagonist (IC50 = 3.5 nM). Used in studies of reward systems and additions.
FormOff-white solid
CAS number103429-32-9
Chemical formulaC₅₁H₆₉N₁₃O₁₁S₂
Peptide SequenceD-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 (2-7 disulfide bond)
Purity≥95% by HPLC
SolubilityH₂O
Storage -20°C
Protect from light
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity Standard Handling
ReferencesPerry, C., et al., 2013. Behav. Neurosci. 127, 535.
Burkett, J. et al. 2011. Neuropsychopharm. 36, 2200.
Steinmiller, L., et al., 2008. Psychopharmacol. (Berl). 195, 497.
Sterious, S., et al., 2003. J. Pharmacol. Exp. Ther. 304, 301.
Abbruscato, T., et al. 1997. J. Pharmacol. 280, 402.

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Categories

Life Science Research > Inhibitors and Biochemicals > Small Molecules & Inhibitors > Neurochemicals > Antagonists