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CTAP

CTAP Structure
  • ₹14700.01 - ₹20978.85
  • Product name: CTAP
  • CAS: 103429-32-9
  • MF: C51H69N13O11S2
  • MW: 1104.3
  • EINECS:
  • MDL Number:MFCD00671434
  • Synonyms:H-D-PHE-CYS-TYR-D-TRP-ARG-THR-PEN-THR-NH2;D-PHE-CYS-TYR-D-TRP-ARG-THR-PEN-THR-NH2;CTAP;CYS2, TYR3, ARG5, PEN7-AMIDE;H-D-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2(Cys2-Pen7);7)-disulfide;M.W. 1104.30 C51H69N13O11S2;CTAP-NH2
3 prices
Selected condition:

Brand

  • Sigma-Aldrich
  • Sigma-Aldrich(India)

Package

  • 1MG
  • ManufacturerSigma-Aldrich
  • Product number5.08316
  • Product descriptionCTAP - CAS 103429-32-9 - Calbiochem
  • Packaging1MG
  • Price₹14700.01
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product number5.08316
  • Product descriptionCTAP - CAS 103429-32-9 - Calbiochem
  • Packaging1MG
  • Price₹14700.01
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product numberC6352
  • Product descriptionCTAP ≥95%
  • Packaging1MG
  • Price₹20978.85
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich 5.08316 CTAP - CAS 103429-32-9 - Calbiochem 1MG ₹14700.01 2022-06-14 Buy
Sigma-Aldrich(India) 5.08316 CTAP - CAS 103429-32-9 - Calbiochem 1MG ₹14700.01 2022-06-14 Buy
Sigma-Aldrich(India) C6352 CTAP ≥95% 1MG ₹20978.85 2022-06-14 Buy

Properties

storage temp. :-20°C
form :Solid
color :off-white
Water Solubility :Soluble to 1 mg/ml in water
Sequence :{d-Phe}-Cys-Tyr-{d-Trp}-Arg-Thr-{Pen}-Thr-NH2 (Disulfide bridge:Cys2-Pen7)
InChIKey :OFMQLVRLOGHAJI-FGHAYEPSSA-N

Safety Information

Symbol(GHS):
Signal word:
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
Precautionary statements:

Description

CTAP is a water soluble, cyclic octapeptide which acts as a receptor antagonist that is selective for the μ opioid receptor (IC50 = 3.5 nM) over the δ receptor (IC50 = 4,500 nM). It is a poor antagonist of the somatostatin receptor (IC50 = 14.3 μM). CTAP is at least 10-fold more potent than naltrexone as an antagonist of diverse compounds which have antinociceptive effects through the μ opioid receptor. It resists enzymatic metabolism in the blood and enters the brain and cerebrospinal fluid.

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